(en)Compositions and methods are provided for antisense modulation of interleukin-5 signal transduction. Antisense compounds, particularly antisense oligonucleotides, targeted to nucleic acids encoding interleukin-5 and interleukin-5 receptor a are preferred. Methods of using these compounds for modulation of interleukin-5 signal transduction and for treatment of diseases associated with interleukin-5 signal transduction are also provided.

1.ApplicationNumber: US-67953203-A
1.PublishNumber: US-2004121376-A1
2.Date Publish: 20040624
3.Inventor: DEAN NICHOLAS M.
KARRAS JAMES G.
MCKAY ROBERT
MANOHARAN MUTHIAH

4.Inventor Harmonized: DEAN NICHOLAS M(US)
KARRAS JAMES G(US)
MCKAY ROBERT(US)
MANOHARAN MUTHIAH(US)

5.Country: US
6.Claims:
(en)Compositions and methods are provided for antisense modulation of interleukin-5 signal transduction. Antisense compounds, particularly antisense oligonucleotides, targeted to nucleic acids encoding interleukin-5 and interleukin-5 receptor a are preferred. Methods of using these compounds for modulation of interleukin-5 signal transduction and for treatment of diseases associated with interleukin-5 signal transduction are also provided.

7.Description:
(en)[0001] This application is a continuation of U.S. application Ser. No. 09/800,629 filed Mar. 7, 2001 which is a continuation-in-part of PCT Application No. PCT/US00/07318 filed Mar. 17, 2000 which corresponds to U.S. application Ser. No. 09/280,799 filed Mar. 26, 1999 now issued U.S. Pat. No. 6,136,603.



FIELD OF THE INVENTION
[0002] The present invention provides compositions and methods for modulating interleukin-5 (IL-5) signaling through antisense modulation of IL-5 and/or IL-5 receptor a (IL-5a) expression. In particular, this invention relates to antisense compounds, particularly oligonucleotides, specifically hybridizable with nucleic acids encoding IL-5 or IL-5Ra. Such oligonucleotides have been shown to modulate the expression of IL-5 and IL-5Ra, respectively.
BACKGROUND OF THE INVENTION
[0003] Cytokines are relatively low molecular weight, pharmacologically active proteins that are secreted by cells for the purpose of altering either their own functions or those of adjacent cells. Cytokines are important regulators of hematopoiesis. They exert their actions by binding to specific receptors on the cell surface. Among the cytokines are a large number of interleukins as well as growth and colony-stimulating factors. Interleukin-5 (IL-5) is a critical cytokine for regulation of growth, activation, maturation, and survival of eosinophils, a type of leukocyte, and their release from the bone marrow. Eosinophils have been implicated in the pathogenesis of certain diseases (“eosinophilic syndromes”) characterized by long-term chronic inflammation of tissues, such as the lungs in the case of asthma or the muscles in the case of eosinophilia myalgia. Other eosinophilic syndromes in addition to these include allergic rhinitis and atopic dermatitis. Eosinophils have also been noted as a component of cellular infiltrates of malignant tumors. Eosinophils are attracted to sites of wounding or inflammation, where they undergo a process of activation. Because eosinophils play a seminal role in the pathogenesis of asthma, particularly the late-phase reaction of asthma, and other inflammatory and/or allergic conditions, IL-5 signal transduction is of clinical importance.
[0004] In humans, IL-5 is selective in specifically promoting eosinophil and basophilic differentiation and maturation. Blood and tissue eosinophilia is a characteristic abnormality in allergy and asthma and convincing evidence implicates IL-5 as the key cytokine regulating this selective eosinophilic inflammation. Thus, inhibition of IL-5 production or effector function will abolish the eosinophilic component in asthma and other eosinophilic diseases, likely preventing further tissue damage caused by release of eosinophil-specific inflammatory mediators and potentially providing clinical benefit. Indeed, it has been demonstrated neutralizing IL-5 with a monoclonal antibody can completely inhibit bronchoalveolar eosinophilia caused by allergen challenge in guinea pigs, mice, and monkeys. A correlation exists between pulmonary eosinophilia and asthma in man and it is clear that selective inhibition of IL-5 can block airway hyperresponsiveness in animal models.
[0005] Asthma is characterized by episodic airways obstruction, increased bronchial hyperresponsiveness, and airway inflammation. An association has been shown between the number of activated T cells and eosinophils in the airways and abnormalities in forced expiratory volume in one second (FEV1), a measure of pulmonary function, increased bronchial responsiveness, and clinical severity in asthma. It has been documented that both interleukin-5 (IL-5) mRNA and protein levels are increased in bronchial biopsies from both atopic and intrinsic asthmatics. IL-5 interacts with cells via the IL-5 receptor (IL-5R) on the cell surface. The IL-5 receptor is a heterodimer of a- and β-subunits. The IL-5 receptor a-subunit is specific to IL-5R, whereas the β-subunit is common to IL-3, IL-5, and granulocyte/macrophage colony-stimulating factor (GM-CSF) receptors. The human IL-5 receptor (IL-5R) is expressed in vitro on eosinophils, basophils, and B lymphocytes, although its role on B cells remains in question. Besides a membrane anchored form, two forms of soluble human IL-5Ra are produced. Only the membrane form of the a chain is complexed with the β chain, which is required for signaling.
[0006] The link between T cell derived IL-5 and lung eosinophilia is further strengthened by the observation that increased levels of IL-5 receptor a mRNA are also found in bronchial biopsies from asthmatics and that the eosinophil is the predominant site of this increased IL-5Ra expression. Further, the subset of eosinophils that express the membrane bound form of the IL-5 receptor inversely correlates with FEV1 while the subset expressing the soluble form of the receptor directly correlates with FEV1. These observations suggest that IL-5 receptor a isoform expression is of central importance in determining clinical prognosis. The soluble form of the receptor may be serving a beneficial role in asthmatic patients. It is therefore presently believed that an effective therapeutic approach to preventing eosinophilia in asthma and other eosinophilic syndromes would entail selective inhibition of membrane but not soluble IL-5 receptor expression. In addition, there are several animal and lung explant models of allergen-induced eosinophilia, late phase airway responses, and bronchial hyperresponsiveness which collectively support a link between IL-5 and airway eosinophilia and decreased pulmonary function.
[0007] Several approaches to inhibition of IL-5 function have been tried. Chimeric, humanized and other interleukin-5 (IL-5) monoclonal antibodies (mAbs), and pharmaceutical compositions and therapeutic methods are disclosed in WO 96/21000. Ribozymes for cleaving IL-5 mRNA are disclosed in WO 95/23225. A 16mer phosphodiester oligodeoxynucleotide with two phosphorothioate linkages, targeted to IL-5 mRNA, was used to inhibit IL-5 secretion by human peripheral blood mononuclear cells. Weltman and Karim, Allergy Asthma Proc., 1998, 19, 257-261; Sept.-Oct. 1998. Methods of treating airway disease by administering essentially adenosine-free antisense oligonucleotides to the airway epithelium are disclosed in WO 96/40162. IL-5 and IL-5 receptor are among the antisense targets disclosed.
[0008] Thus there remains a long-felt need for compositions and methods for modulating IL-5 signal transduction, particularly in the treatment and prevention of asthma and other reactive airway disease.
SUMMARY OF THE INVENTION
[0009] The present invention is directed to antisense compounds, particularly oligonucleotides, which are targeted to a nucleic acid encoding IL-5 or IL-5Ra, and which modulate the expression of these gene targets. Pharmaceutical and other compositions comprising the antisense compounds of the invention are also provided. Further provided are methods of modulating the expression of IL-5 and/or IL-5Ra in cells or tissues comprising contacting said cells or tissues with one or more of the antisense compounds or compositions of the invention. Further provided are methods of modulating IL-5 signaling in cells or tissues comprising contacting said cells or tissues with one or more of the antisense compounds or compositions of the invention. Further provided are methods of treating an animal, particularly a human, suspected of having or being prone to a disease or condition associated with IL-5 signaling or with expression of IL-5 or IL-5Ra by administering a therapeutically or prophylactically effective amount of one or more of the antisense compounds or compositions of the invention.
DETAILED DESCRIPTION OF THE INVENTION
[0010] The present invention comprehends antisense compounds capable of modulating IL-5 signal transduction, preferably by modulating expression of IL-5 or IL-5 receptor a. These compounds are useful for both research and therapeutic, including prophylactic, uses.
[0011] The human IL-5 receptor a gene contains 14 exons. A membrane-anchored form of the receptor and two soluble forms have been identified. The mRNA transcript encoding the membrane-anchored form of the human IL-5 receptor a contain exons 1-10 and 12-14. Exon 11 is spliced out by an alternative splicing event. The major soluble isoform (soluble form 1) is generated as a result of a normal splicing event and an in-frame stop codon in exon 11. The other soluble form (soluble form 2) is generated by the absence of splicing and therefore is generated by reading into intron 11. Tuypens et al. Eur. Cytokine Netw., 1992, 3, 451-459.
[0012] The mRNA encoding the membrane form of the mouse IL-5 receptor a contains 11 exons. The transmembrane domain of the receptor is encoded in exon 9. Two mRNAs encoding soluble (secreted) forms of the receptor result from differential splicing events. The mRNA encoding soluble form 1 of the receptor is missing exon 9 (exon 8 is spliced to exon 10)and the mRNA encoding soluble form 2 is missing exons 9 and 10 (exon 8 is spliced to exon 11). Imamura et al., DNA and Cell Biol., 1994, 13, 283-292.
[0013] In both mouse and humans, there are both soluble forms and a membrane-bound form of IL-5 receptor a. In mouse, the soluble form is expressed, though experiments are usually done by addition of exogenous recombinant soluble receptor. Recombinant murine soluble IL-5 receptor a binds IL-5, and does not inhibit proliferation of the IL-5-responsive Y16B cell line. In vivo, recombinant soluble murine IL-5 receptor a suppresses antigen-induced airway eosinophilia. In humans, recombinant human soluble IL-5 receptor a binds human IL-5 and inhibits its biological activity in vitro, i.e., prevents TF-1 proliferation and survival. In other words, in the human system, the soluble IL-5 receptor a acts as a sponge to bind the IL-5 cytokine and block its effects. Only the membrane-bound form of IL-5 receptor a is able to transduce the IL-5 signal. Soluble human IL-5 receptor a is not normally detected in human biological fluids; however, a direct correlation has been observed between the expression of soluble human IL-5 receptor a and pulmonary function in asthmatic subjects.
[0014] The present invention employs oligomeric antisense compounds, particularly oligonucleotides, for use in modulating IL-5 signal transduction. In preferred embodiments this is done by modulating the function of nucleic acid molecules encoding IL-5 or IL-5Ra, ultimately modulating the amount of IL-5 or IL-5Ra produced. Antisense compounds are provided which specifically hybridize with one or more nucleic acids encoding IL-5 or IL-5Ra. In preferred embodiments used herein, the term “nucleic acid encoding IL-5” encompasses DNA encoding IL-5, RNA (including pre-mRNA and mRNA) transcribed from such DNA, and also cDNA derived from such RNA. Similarly the term “nucleic acid encoding IL-5Ra” encompasses DNA encoding IL-5Ra, RNA (including pre-mRNA and mRNA) transcribed from such DNA, and also cDNA derived from such RNA. In the context of the present invention, the term “nucleic acid target” encompasses nucleic acids encoding either IL-5 or IL-5Ra, according to which of these the antisense compound is complementary. The specific hybridization of an oligomeric compound with its target nucleic acid interferes with the normal function of the nucleic acid. This modulation of function of a target nucleic acid by compounds which specifically hybridize to it is generally referred to as “antisense”. The functions of DNA to be interfered with include replication and transcription. The functions of RNA to be interfered with include all vital functions such as, for example, translocation of the RNA to the site of protein translation, translation of protein from the RNA, splicing of the RNA to yield one or more mRNA species, and catalytic activity which may be engaged in or facilitated by the RNA. The overall effect of such interference with target nucleic acid function is modulation of the expression of IL-5 or IL-5Ra. In the context of the present invention, “modulation” means either an increase (stimulation) or a decrease (inhibition) in the expression of a gene. In the context of the present invention, inhibition is the preferred form of modulation of gene expression and mRNA is a preferred target.
[0015] It is preferred to target specific nucleic acids for antisense. “Targeting” an antisense compound to a particular nucleic acid, in the context of this invention, is a multi step process. The process usually begins with the identification of a nucleic acid sequence whose function is to be modulated. This may be, for example, a cellular gene (or mRNA transcribed from the gene) whose expression is associated with a particular disorder or disease state, or a nucleic acid molecule from an infectious agent. In the present invention, the target is a nucleic acid molecule encoding IL-5 or IL-5Ra. The targeting process also includes determination of a site or sites within this gene for the antisense interaction to occur such that the desired effect, e.g., detection or modulation of expression of the protein, will result. Within the context of the present invention, a preferred intra genic site is the region encompassing the translation initiation or termination codon of the open reading frame (ORF) of the gene. Since, as is known in the art, the translation initiation codon is typically 5′-AUG (in transcribed mRNA molecules; 5′-ATG in the corresponding DNA molecule), the translation initiation codon is also referred to as the “AUG codon,” the “start codon” or the “AUG start codon”. A minority of genes have a translation initiation codon having the RNA sequence 5′-GUG, 5′-UUG or 5′-CUG, and 5′-AUA, 5′-ACG and 5′-CUG have been shown to function in vivo. Thus, the terms “translation initiation codon” and “start codon” can encompass many codon sequences, even though the initiator amino acid in each instance is typically methionine (in eukaryotes) or formylmethionine (in prokaryotes). It is also known in the art that eukaryotic and prokaryotic genes may have two or more alternative start codons, any one of which may be preferentially utilized for translation initiation in a particular cell type or tissue, or under a particular set of conditions. In the context of the invention, “start codon” and “translation initiation codon” refer to the codon or codons that are used in vivo to initiate translation of an mRNA molecule transcribed from a gene encoding IL-5 or IL-5Ra, regardless of the sequence(s) of such codons.
[0016] It is also known in the art that a translation termination codon (or “stop codon”) of a gene may have one of three sequences, i.e., 5′-UAA, 5′-UAG and 5′-UGA (the corresponding DNA sequences are 5′-TAA, 5′-TAG and 5′-TGA, respectively). The terms “start codon region” and “translation initiation codon region” refer to a portion of such an mRNA or gene that encompasses from about 25 to about 50 contiguous nucleotides in either direction (i.e., 5′ or 3′) from a translation initiation codon. Similarly, the terms “stop codon region” and “translation termination codon region” refer to a portion of such an mRNA or gene that encompasses from about 25 to about 50 contiguous nucleotides in either direction (i.e., 5′ or 3′) from a translation termination codon.
[0017] The open reading frame (ORF) or “coding region,” which is known in the art to refer to the region between the translation initiation codon and the translation termination codon, is also a region which may be targeted effectively. Other target regions include the 5′ untranslated region (5′UTR), known in the art to refer to the portion of an mRNA in the 5′ direction from the translation initiation codon, and thus including nucleotides between the 5′ cap site and the translation initiation codon of an mRNA or corresponding nucleotides on the gene, and the 3′ untranslated region (3′UTR), known in the art to refer to the portion of an mRNA in the 3′ direction from the translation termination codon, and thus including nucleotides between the translation termination codon and 3′ end of an mRNA or corresponding nucleotides on the gene. The 5′ cap of an mRNA comprises an N7-methylated guanosine residue joined to the 5′-most residue of the mRNA via a 5′-5′ triphosphate linkage. The 5′ cap region of an mRNA is considered to include the 5′ cap structure itself as well as the first 50 nucleotides adjacent to the cap. The 5′ cap region may also be a preferred target region.
[0018] Although some eukaryotic mRNA transcripts are directly translated, many contain one or more regions, known as “introns,” which are excised from a transcript before it is translated. The remaining (and therefore translated) regions are known as “exons” and are spliced together to form a continuous mRNA sequence. mRNA splice sites, i.e., intron-exon junctions, may also be preferred target regions, and are particularly useful in situations where aberrant splicing is implicated in disease, or where an overproduction of a particular mRNA splice product is implicated in disease.
[0019] Aberrant fusion junctions due to rearrangements or deletions are also preferred targets. It has also been found that introns can also be effective, and therefore preferred, target regions for antisense compounds targeted, for example, to DNA or pre-mRNA.
[0020] Once one or more target sites have been identified, oligonucleotides are chosen which are sufficiently complementary to the target, i.e., hybridize sufficiently well and with sufficient specificity, to give the desired effect.
[0021] In the context of this invention, “hybridization” means hydrogen bonding, which may be Watson-Crick, Hoogsteen or reversed Hoogsteen hydrogen bonding, between complementary nucleoside or nucleotide bases. For example, adenine and thymine are complementary nucleobases which pair through the formation of hydrogen bonds. “Complementary,” as used herein, refers to the capacity for precise pairing between two nucleotides. For example, if a nucleotide at a certain position of an oligonucleotide is capable of hydrogen bonding with a nucleotide at the same position of a DNA or RNA molecule, then the oligonucleotide and the DNA or RNA are considered to be complementary to each other at that position. The oligonucleotide and the DNA or RNA are complementary to each other when a sufficient number of corresponding positions in each molecule are occupied by nucleotides which can hydrogen bond with each other. Thus, “specifically hybridizable” and “complementary” are terms which are used to indicate a sufficient degree of complementarity or precise pairing such that stable and specific binding occurs between the oligonucleotide and the DNA or RNA target. It is understood in the art that the sequence of an antisense compound need not be 100% complementary to that of its target nucleic acid to be specifically hybridizable. An antisense compound is specifically hybridizable when binding of the compound to the target DNA or RNA molecule interferes with the normal function of the target DNA or RNA to cause a loss of utility, and there is a sufficient degree of complementarity to avoid non-specific binding of the antisense compound to non-target sequences under conditions in which specific binding is desired, i.e., under physiological conditions in the case of in vivo assays or therapeutic treatment, and, in the case of in vitro assays, under conditions in which the assays are performed.
[0022] Antisense compounds are commonly used as research reagents and diagnostics. For example, antisense oligonucleotides, which are able to inhibit gene expression with exquisite specificity, are often used by those of ordinary skill to elucidate the function of particular genes. Antisense compounds are also used, for example, to distinguish between functions of various members of a biological pathway. Antisense modulation has, therefore, been harnessed for research use.
[0023] The specificity and sensitivity of antisense is also harnessed by those of skill in the art for therapeutic uses. Antisense oligonucleotides have been employed as therapeutic moieties in the treatment of disease states in animals and man. Antisense oligonucleotides have been safely and effectively administered to humans and numerous clinical trials are presently underway. It is thus established that oligonucleotides can be useful therapeutic modalities that can be configured to be useful in treatment regimes of cells, tissues and animals, especially humans. In the context of this invention, the term “oligonucleotide” refers to an oligomer or polymer of ribonucleic acid (RNA) or deoxyribonucleic acid (DNA) or mimetics thereof. This term includes oligonucleotides composed of naturally-occurring nucleobases, sugars and covalent internucleoside (backbone) linkages as well as oligonucleotides having non-naturally-occurring portions which function similarly. Such modified or substituted oligonucleotides are often preferred over native forms because of desirable properties such as, for example, enhanced cellular uptake, enhanced affinity for nucleic acid target and increased stability in the presence of nucleases.
[0024] While antisense oligonucleotides are a preferred form of antisense compound, the present invention comprehends other oligomeric antisense compounds, including but not limited to oligonucleotide mimetics such as are described below. The antisense compounds in accordance with this invention preferably comprise from about 8 to about 30 nucleobases. Particularly preferred are antisense oligonucleotides comprising from about 8 to about 30 nucleotides). As is known in the art, a nucleoside is a base-sugar combination. The base portion of the nucleoside is normally a heterocyclic base. The two most common classes of such heterocyclic bases are the purines and the pyrimidines. Nucleotides are nucleosides that further include a phosphate group covalently linked to the sugar portion of the nucleoside. For those nucleosides that include a pentofuranosyl sugar, the phosphate group can be linked to either the 2-, 3- or 5-hydroxyl moiety of the sugar. In forming oligonucleotides, the phosphate groups covalently link adjacent nucleosides to one another to form a linear polymeric compound. In turn the respective ends of this linear polymeric structure can be further joined to form a circular structure. However, open linear structures are generally preferred. Within the oligonucleotide structure, the phosphate groups are commonly referred to as forming the internucleoside backbone of the oligonucleotide. The normal linkage or backbone of RNA and DNA is a 3- to 5-phosphodiester linkage.
[0025] Specific examples of preferred antisense compounds useful in this invention include oligonucleotides containing modified backbones or non-natural internucleoside linkages. As defined in this specification, oligonucleotides having modified backbones include those that retain a phosphorus atom in the backbone and those that do not have a phosphorus atom in the backbone. For the purposes of this specification, and as sometimes referenced in the art, modified oligonucleotides that do not have a phosphorus atom in their internucleoside backbone can also be considered to be oligonucleosides.
[0026] Preferred modified oligonucleotide backbones include, for example, phosphorothioates, chiral phosphorothioates, phosphoro-dithioates, phosphotri-esters, aminoalkyl-phosphotri-esters, methyl and other alkyl phosphonates including 3-alkylene phosphonates and chiral phosphonates, phosphinates, phosphoramidates including 3-amino phosphoramidate and aminoalkylphosphoramidates, thionophosphoramidates, thionoalkylphosphonates, thionoalkylphosphotriesters, and boranophosphates having normal 3-5-linkages, 2-5-linked analogs of these, and those having inverted polarity wherein the adjacent pairs of nucleoside units are linked 3-5- to 5-3- or 2-5- to 5-2-. Various salts, mixed salts and free acid forms are also included.
[0027] Representative United States patents that teach the preparation of the above phosphorus-containing linkages include, but are not limited to, U.S. Pat. Nos. 3,687,808; 4,469,863; 4,476,301; 5,023,243; 5,177,196; 5,188,897; 5,264,423; 5,276,019; 5,278,302; 5,286,717; 5,321,131; 5,399,676; 5,405,939; 5,453,496; 5,455,233; 5,466,677; 5,476,925; 5,519,126; 5,536,821; 5,541,306; 5,550,111; 5,563,253; 5,571,799; 5,587,361; and 5,625,050, each of which is herein incorporated by reference.
[0028] Preferred modified oligonucleotide backbones that do not include a phosphorus atom therein have backbones that are formed by short chain alkyl or cycloalkyl internucleoside linkages, mixed heteroatom and alkyl or cycloalkyl internucleoside linkages, or one or more short chain heteroatomic or heterocyclic internucleoside linkages. These include those having morpholino linkages (formed in part from the sugar portion of a nucleoside); siloxane backbones; sulfide, sulfoxide and sulfone backbones; formacetyl and thioformacetyl backbones; methylene formacetyl and thioformacetyl backbones; alkene containing backbones; sulfamate backbones; methyleneimino and methylenehydrazino backbones; sulfonate and sulfonamide backbones; amide backbones; and others having mixed N, O, S and CH 2 component parts.
[0029] Representative United States patents that teach the preparation of the above oligonucleosides include, but are not limited to, U.S. Pat. Nos. 5,034,506; 5,166,315; 5,185,444; 5,214,134; 5,216,141; 5,235,033; 5,264,562; 5,264,564; 5,405,938; 5,434,257; 5,466,677; 5,470,967; 5,489,677; 5,541,307; 5,561,225; 5,596,086; 5,602,240; 5,610,289; 5,602,240; 5,608,046; 5,610,289; 5,618,704; 5,623,070; 5,663,312; 5,633,360; 5,677,437; and 5,677,439, each of which is herein incorporated by reference.
[0030] In other preferred oligonucleotide mimetics, both the sugar and the internucleoside linkage, i.e., the backbone, of the nucleotide units are replaced with novel groups. The base units are maintained for hybridization with an appropriate nucleic acid target compound. One such oligomeric compound, an oligonucleotide mimetic that has been shown to have excellent hybridization properties, is referred to as a peptide nucleic acid (PNA). In PNA compounds, the sugar-backbone of an oligonucleotide is replaced with an amide containing backbone, in particular an aminoethylglycine backbone. The nucleobases are retained and are bound directly or indirectly to aza nitrogen atoms of the amide portion of the backbone. Representative United States patents that teach the preparation of PNA compounds include, but are not limited to, U.S. Pat. Nos. 5,539,082; 5,714,331; and 5,719,262, each of which is herein incorporated by reference. Further teaching of PNA compounds can be found in Nielsen et al., Science, 1991, 254, 1497-1500.
[0031] Most preferred embodiments of the invention are oligonucleotides with phosphorothioate backbones and oligonucleosides with heteroatom backbones, and in particular —CH 2 —NH—O—CH 2 —, —CH 2 —N(CH 3 )—O—CH 2 — [known as a methylene (methylimino) or MMI backbone], —CH 2 —O—N(CH 3 )—CH 2 —, —CH 2 —N(CH 3 )—N(CH 3 )—CH 2 — and —O—N(CH 3 )—CH 2 —CH 2 — [wherein the native phosphodiester backbone is represented as —O—P—O—CH 2 —] of the above referenced U.S. Pat. No. 5,489,677, and the amide backbones of the above referenced U.S. Pat. No. 5,602,240. Also preferred are oligonucleotides having morpholino backbone structures of the above-referenced U.S. Pat. No. 5,034,506.
[0032] Modified oligonucleotides may also contain one or more substituted sugar moieties. Preferred oligonucleotides comprise one of the following at the 2′ position: OH; F; O-, S-, or N-alkyl; O-, S-, or N-alkenyl; O-, S- or N-alkynyl; or O-alkyl-O-alkyl, wherein the alkyl, alkenyl and alkynyl may be substituted or unsubstituted C 1 to C 10 alkyl or C 2 to C 10 alkenyl and alkynyl. Particularly preferred are O[(CH 2 ) n O] m CH 3 , O(CH 2 ) n OCH 3 , O(CH 2 ) n NH 2 , O(CH 2 ) n CH, 3 O(CH) 2 O NH, 2 and O(CH 2 ) n ON[(CH 2 ) n CH 3 )] 2 , where n and m are from 1 to about 10. Other preferred oligonucleotides comprise one of the following at the 2-position: C 1 to C 10 lower alkyl, substituted lower alkyl, alkaryl, aralkyl, O-alkaryl or O-aralkyl, SH, SCH 3 , OCN, Cl, Br, CN, CF 3 , OCF 3 , SOCH 3 , SO 2 CH 3 , ONO 2 , NO 2 , N 3 , NH 2 , heterocycloalkyl, heterocycloalkaryl, aminoalkylamino, polyalkylamino, substituted silyl, an RNA cleaving group, a reporter group, an intercalator, a group for improving the pharmacokinetic properties of an oligonucleotide, or a group for improving the pharmacodynamic properties of an oligonucleotide, and other substituents having similar properties. A preferred modification includes an alkoxyalkoxy group, 2′-methoxyethoxy (2′-O—CH 2 CH 2 OCH 3 , also known as 2′-O-(2-methoxyethyl) or 2′-MOE) (Martin et al., Helv. Chim. Acta, 1995, 78, 486-504). Further preferred modifications include 2-dimethylaminooxyethoxy, i.e., a 2′-O(CH 2 ) 2 ON(CH 3 ) 2 group, also known as 2′-DMAOE and 2′-dimethylaminoethoxyethoxy, i.e., 2′-O—CH 2 —O—CH 2 —N(CH 2 ) 2 .
[0033] Other preferred modifications include 2′-methoxy (2′-O—CH 3 ), 2′-aminopropoxy (2′-OCH 2 CH 2 CH 2 NH 2 ) and 2′-fluoro (2′-F). Similar modifications may also be made at other positions on the oligonucleotide, particularly the 3′ position of the sugar on the 3′ terminal nucleotide or in 2-5-linked oligonucleotides and the 5′ position of 5′ terminal nucleotide. Oligonucleotides may also have sugar mimetics such as cyclobutyl moieties in place of the pentofuranosyl sugar. Representative United States patents that teach the preparation of such modified sugar structures include, but are not limited to, U.S. Pat. Nos. 4,981,957; 5,118,800; 5,319,080; 5,359,044; 5,393,878; 5,446,137; 5,466,786; 5,514,785; 5,519,134; 5,567,811; 5,576,427; 5,591,722; 5,597,909; 5,610,300; 5,627,0531 5,639,873; 5,646,265; 5,658,873; 5,670,633; and 5,700,920, each of which is herein incorporated by reference.
[0034] Oligonucleotides may also include nucleobase (often referred to in the art simply as “base”) modifications or substitutions. As used herein, “unmodified” or “natural” nucleobases include the purine bases adenine (A) and guanine (G), and the pyrimidine bases thymine (T), cytosine (C) and uracil (U). Modified nucleobases include other synthetic and natural nucleobases such as 5-methylcytosine (5-me-C), 5-hydroxymethyl cytosine, xanthine, hypoxanthine, 2-aminoadenine, 6-methyl and other alkyl derivatives of adenine and guanine, 2-propyl and other alkyl derivatives of adenine and guanine, 2-thiouracil, 2-thiothymine and 2-thiocytosine, 5-halouracil and cytosine, 5-propynyl uracil and cytosine, 6-azo uracil, cytosine and thymine, 5-uracil (pseudouracil), 4-thiouracil, 8-halo, 8-amino, 8-thiol, 8-thioalkyl, 8-hydroxyl and other 8-substituted adenines and guanines, 5-halo particularly 5-bromo, 5-trifluoromethyl and other 5-substituted uracils and cytosines, 7-methylguanine and 7-methyladenine, 8-azaguanine and 8-azaadenine, 7-deazaguanine and 7-deazaadenine and 3-deazaguanine and 3-deazaadenine. Further nucleobases include those disclosed in U.S. Pat. No. 3,687,808, those disclosed in Kroschwitz, J. I., The Concise Encyclopedia Of Polymer Science And Engineering , ed. John Wiley & Sons, 1990, pages 858-859, those disclosed by Englisch et al., Angewandte Chemie, International Edition, 1991, 30, 613, and those disclosed by Sanghvi, Y. S., Crooke, S. T., and Lebleu, B. eds., Antisense Research and Applications , CRC Press, Boca Raton, 1993, pp. 289-302. Certain of these nucleobases are particularly useful for increasing the binding affinity of the oligomeric compounds of the invention. These include 5-substituted pyrimidines, 6-azapyrimidines and N-2, N-6 and O-6 substituted purines, including 2-aminopropyl-adenine, 5-propynyluracil and 5-propynylcytosine. 5-methylcytosine substitutions have been shown to increase nucleic acid duplex stability by 0.6-1.2° C. (Sanghvi, Y. S., Crooke, S. T. and Lebleu, B., eds., Antisense Research and Application , CRC Press, Boca Raton, 1993, pp. 276-278) and are presently preferred base substitutions, even more particularly when combined with 2′-O-methoxyethyl sugar modifications.
[0035] Representative United States patents that teach the preparation of certain of the above noted modified nucleobases as well as other modified nucleobases include, but are not limited to, the above noted U.S. Pat. No. 3,687,808, as well as U.S. Pat. Nos. 4,845,205; 5,130,302; 5,134,066; 5,175,273; 5,367,066; 5,432,272; 5,457,187; 5,459,255; 5,484,908; 5,502,177; 5,525,711; 5,552,540; 5,587,469; 5,594,121; 5,596,091; 5,614,617; 5,681,941; and 5,750,692, each of which is herein incorporated by reference.
[0036] Another modification of the oligonucleotides of the invention involves chemically linking to the oligonucleotide one or more moieties or conjugates which enhance the activity, cellular distribution or cellular uptake of the oligonucleotide. Such moieties include but are not limited to lipid moieties such as a cholesterol moiety (Letsinger et al., Proc. Natl. Acad. Sci. USA, 1989, 86, 6553-6556), cholic acid (Manoharan et al., Bioorg. Med. Chem. Let., 1994, 4, 1053-1060), a thioether, e.g., hexyl-S-tritylthiol (Manoharan et al., Ann. N.Y. Acad. Sci., 1992, 660, 306-309; Manoharan et al., Bioorg. Med. Chem. Let., 1993, 3, 2765-2770), a thiocholesterol (Oberhauser et al., Nucl. Acids Res., 1992, 20, 533-538), an aliphatic chain, e.g., dodecandiol or undecyl residues (Saison-Behmoaras et al., EMBO J., 1991, 10, 1111-1118; Kabanov et al., FEBS Lett., 1990, 259, 327-330; Svinarchuk et al., Biochimie, 1993, 75, 49-54), a phospholipid, e.g., di-hexadecyl-rac-glycerol or triethyl-ammonium 1,2-di-O-hexadecyl-rac-glycero-3-H-phosphonate (Manoharan et al., Tetrahedron Lett., 1995, 36, 3651-3654; Shea et al., Nucl. Acids Res., 1990, 18, 3777-3783), a polyamine or a polyethylene glycol chain (Manoharan et al., Nucleosides & Nucleotides, 1995, 14, 969-973), or adamantane acetic acid (Manoharan et al., Tetrahedron Lett., 1995, 36, 3651-3654), a palmityl moiety (Mishra et al., Biochim. Biophys. Acta, 1995, 1264, 229-237), or an octadecylamine or hexylamino-carbonyl-oxycholesterol moiety (Crooke et al., J. Pharmacol. Exp. Ther., 1996, 277, 923-937.
[0037] Representative United States patents that teach the preparation of such oligonucleotide conjugates include, but are not limited to, U.S. Pat. Nos. 4,828,979; 4,948,882; 5,218,105; 5,525,465; 5,541,313; 5,545,730; 5,552,538; 5,578,717, 5,580,731; 5,580,731; 5,591,584; 5,109,124; 5,118,802; 5,138,045; 5,414,077; 5,486,603; 5,512,439; 5,578,718; 5,608,046; 4,587,044; 4,605,735; 4,667,025; 4,762,779; 4,789,737; 4,824,941; 4,835,263; 4,876,335; 4,904,582; 4,958,013; 5,082,830; 5,112,963; 5,214,136; 5,082,830; 5,112,963; 5,214,136; 5,245,022; 5,254,469; 5,258,506; 5,262,536; 5,272,250; 5,292,873; 5,317,098; 5,371,241, 5,391,723; 5,416,203, 5,451,463; 5,510,475; 5,512,667; 5,514,785; 5,565,552; 5,567,810; 5,574,142; 5,585,481; 5,587,371; 5,595,726; 5,597,696; 5,599,923; 5,599,928 and 5,688,941, each of which is herein incorporated by reference.
[0038] It is not necessary for all positions in a given compound to be uniformly modified, and in fact more than one of the aforementioned modifications may be incorporated in a single compound or even at a single nucleoside within an oligonucleotide. The present invention also includes antisense compounds which are chimeric compounds. “Chimeric” antisense compounds or “chimeras,” in the context of this invention, are antisense compounds, particularly oligonucleotides, which contain two or more chemically distinct regions, each made up of at least one monomer unit, i.e., a nucleotide in the case of an oligonucleotide compound. These oligonucleotides typically contain at least one region wherein the oligonucleotide is modified so as to confer upon the oligonucleotide increased resistance to nuclease degradation, increased cellular uptake, and/or increased binding affinity for the target nucleic acid. An additional region of the oligonucleotide may serve as a substrate for enzymes capable of cleaving RNA:DNA or RNA:RNA hybrids. By way of example, RNase H is a cellular endonuclease which cleaves the RNA strand of an RNA:DNA duplex. Activation of RNase H, therefore, results in cleavage of the RNA target, thereby greatly enhancing the efficiency of oligonucleotide inhibition of gene expression. Cleavage of the RNA target can be routinely detected by gel electrophoresis and, if necessary, associated nucleic acid hybridization techniques known in the art.
[0039] Chimeric antisense compounds of the invention may be formed as composite structures of two or more oligonucleotides, modified oligonucleotides, oligonucleosides and/or oligonucleotide mimetics as described above. Such compounds have also been referred to in the art as hybrids or gapmers. Representative United States patents that teach the preparation of such hybrid structures include, but are not limited to, U.S. Pat. Nos. 5,013,830; 5,149,797; 5,220,007; 5,256,775; 5,366,878; 5,403,711; 5,491,133; 5,565,350; 5,623,065; 5,652,355; 5,652,356; and 5,700,922, each of which is herein incorporated by reference.
[0040] The antisense compounds used in accordance with this invention may be conveniently and routinely made through the well-known technique of solid phase synthesis. Equipment for such synthesis is sold by several vendors including, for example, Applied Biosystems (Foster City, Calif.). Any other means for such synthesis known in the art may additionally or alternatively be employed. It is well known to use similar techniques to prepare oligonucleotides such as the phosphorothioates and alkylated derivatives.
[0041] The antisense compounds of the invention are synthesized in vitro and do not include antisense compositions of biological origin, or genetic vector constructs designed to direct the in vivo synthesis of antisense molecules.
[0042] The compounds of the invention may also be admixed, encapsulated, conjugated or otherwise associated with other molecules, molecule structures or mixtures of compounds, as for example, liposomes, receptor targeted molecules, oral, rectal, topical or other formulations, for assisting in uptake, distribution and/or absorption. Representative United States patents that teach the preparation of such uptake, distribution and/or absorption assisting formulations include, but are not limited to, U.S. Pat. Nos. 5,108,921; 5,354,844; 5,416,016; 5,459,127; 5,521,291; 5,543,158; 5,547,932; 5,583,020; 5,591,721; 4,426,330; 4,534,899; 5,013,556; 5,108,921; 5,213,804; 5,227,170; 5,264,221; 5,356,633; 5,395,619; 5,416,016; 5,417,978; 5,462,854; 5,469,854; 5,512,295; 5,527,528; 5,534,259; 5,543,152; 5,556,948; 5,580,575; and 5,595,756, each of which is herein incorporated by reference.
[0043] The antisense compounds of the invention encompass any pharmaceutically acceptable salts, esters, or salts of such esters, or any other compound which, upon administration to an animal including a human, is capable of providing (directly or indirectly) the biologically active metabolite or residue thereof. Accordingly, for example, the disclosure is also drawn to prodrugs and pharmaceutically acceptable salts of the compounds of the invention, pharmaceutically acceptable salts of such prodrugs, and other bioequivalents.
[0044] The term “prodrug” indicates a therapeutic agent that is prepared in an inactive form that is converted to an active form (i.e., drug) within the body or cells thereof by the action of endogenous enzymes or other chemicals and/or conditions. In particular, prodrug versions of the oligonucleotides of the invention are prepared as SATE [(S-acetyl-2-thioethyl) phosphate] derivatives according to the methods disclosed in WO 93/24510 or in WO 94/26764.
[0045] The term “pharmaceutically acceptable salts” refers to physiologically and pharmaceutically acceptable salts of the compounds of the invention: i.e., salts that retain the desired biological activity of the parent compound and do not impart undesired toxicological effects thereto. Pharmaceutically acceptable base addition salts are formed with metals or amines, such as alkali and alkaline earth metals or organic amines. Examples of metals used as cations are sodium, potassium, magnesium, calcium, and the like. Examples of suitable amines are N,N′-dibenzylethylenediamine, chloroprocaine, choline, diethanolamine, dicyclohexylamine, ethylenediamine, N-methylglucamine, and procaine (see, for example, Berge et al., “Pharmaceutical Salts,” J. of Pharma Sci., 1977, 66, 1-19). The base addition salts of said acidic compounds are prepared by contacting the free acid form with a sufficient amount of the desired base to produce the salt in the conventional manner. The free acid form may be regenerated by contacting the salt form with an acid and isolating the free acid in the conventional manner. The free acid forms differ from their respective salt forms somewhat in certain physical properties such as solubility in polar solvents, but otherwise the salts are equivalent to their respective free acid for purposes of the present invention. As used herein, a “pharmaceutical addition salt” includes a pharmaceutically acceptable salt of an acid form of one of the components of the compositions of the invention. These include organic or inorganic acid salts of the amines. Preferred addition salts are acid salts such as the hydrochlorides, acetates, salicylates, nitrates and phosphates. Other suitable pharmaceutically acceptable salts are well known to those skilled in the art and include basic salts of a variety of inorganic and organic acids, such as, for example, with inorganic acids, such as for example hydrochloric acid, hydrobromic acid, sulfuric acid or phosphoric acid; with organic carboxylic, sulfonic, sulfo or phospho acids or N-substituted sulfamic acids, for example acetic acid, propionic acid, glycolic acid, succinic acid, maleic acid, hydroxymaleic acid, methylmaleic acid, fumaric acid, malic acid, tartaric acid, lactic acid, oxalic acid, gluconic acid, glucaric acid, glucuronic acid, citric acid, benzoic acid, cinnamic acid, mandelic acid, salicylic acid, 4-aminosalicylic acid, 2-phenoxybenzoic acid, 2-acetoxybenzoic acid, embolic acid, nicotinic acid or isonicotinic acid; and with amino acids, such as the 20 alpha-amino acids involved in the synthesis of proteins in nature, for example glutamic acid or aspartic acid, and also with phenylacetic acid, methanesulfonic acid, ethanesulfonic acid, 2-hydroxyethanesulfonic acid, ethane-1,2-disulfonic acid, benzenesulfonic acid, 4-methylbenzenesulfoic acid, naphthalene-2-sulfonic acid, naphthalene-1,5-disulfonic acid, 2- or 3-phosphoglycerate, glucose-6-phosphate, N-cyclohexylsulfamic acid (with the formation of cyclamates), or with other acid organic compounds, such as ascorbic acid. Pharmaceutically acceptable salts of compounds may also be prepared with a pharmaceutically acceptable cation. Suitable pharmaceutically acceptable cations are well known to those skilled in the art and include alkaline, alkaline earth, ammonium and quaternary ammonium cations. Carbonates or hydrogen carbonates are also possible.
[0046] For oligonucleotides, preferred examples of pharmaceutically acceptable salts include but are not limited to (a) salts formed with cations such as sodium, potassium, ammonium, magnesium, calcium, polyamines such as spermine and spermidine, etc.; (b) acid addition salts formed with inorganic acids, for example hydrochloric acid, hydrobromic acid, sulfuric acid, phosphoric acid, nitric acid and the like; (c) salts formed with organic acids such as, for example, acetic acid, oxalic acid, tartaric acid, succinic acid, maleic acid, fumaric acid, gluconic acid, citric acid, malic acid, ascorbic acid, benzoic acid, tannic acid, palmitic acid, alginic acid, polyglutamic acid, naphthalenesulfonic acid, methanesulfonic acid, p-toluenesulfonic acid, naphthalenedisulfonic acid, polygalacturonic acid, and the like; and (d) salts formed from elemental anions such as chlorine, bromine, and iodine.
[0047] The antisense compounds of the present invention can be utilized for diagnostics, therapeutics, prophylaxis and as research reagents and kits. For therapeutics, an animal, preferably a human, suspected of having a disease or disorder which can be treated by modulating IL-5 signaling is treated by administering one or more antisense compounds in accordance with this invention. The compounds of the invention can be utilized in pharmaceutical compositions by adding an effective amount of an antisense compound to a suitable pharmaceutically acceptable diluent or carrier. Use of the antisense compounds and methods of the invention may also be useful prophylactically, e.g., to prevent or delay infection, inflammation or tumor formation, for example.
[0048] The antisense compounds of the invention are useful for research and diagnostics, because these compounds hybridize to nucleic acids encoding IL-5 or IL-5Ra, enabling sandwich and other assays to easily be constructed to exploit this fact. Hybridization of the antisense oligonucleotides of the invention with a nucleic acid encoding IL-5 or IL-5Ra can be detected by means known in the art. Such means may include conjugation of an enzyme to the oligonucleotide, radiolabelling of the oligonucleotide or any other suitable detection means. Kits using such detection means for detecting the level of IL-5 or IL-5Ra in a sample may also lo be prepared.
[0049] The present invention also includes pharmaceutical compositions and formulations which include the antisense compounds of the invention. The pharmaceutical compositions of the present invention may be administered in a number of ways depending upon whether local or systemic treatment is desired and upon the area to be treated. Administration may be topical (including ophthalmic and to mucous membranes including vaginal and rectal delivery), pulmonary, e.g., by inhalation or insufflation of powders or aerosols, including by nebulizer; intratracheal, intranasal, epidermal and transdermal), oral or parenteral. Parenteral administration includes intravenous, intraarterial, subcutaneous, intraperitoneal or intramuscular injection or infusion; or intracranial, e.g., intrathecal or intraventricular, administration. Oligonucleotides with at least one 2′-O-methoxyethyl modification are believed to be particularly useful for oral administration.
[0050] Pharmaceutical compositions and formulations for topical administration may include transdermal patches, ointments, lotions, creams, gels, drops, suppositories, sprays, liquids and powders. Conventional pharmaceutical carriers, aqueous, powder or oily bases, thickeners and the like may be necessary or desirable. Coated condoms, gloves and the like may also be useful.
[0051] Compositions and formulations for oral administration include powders or granules, suspensions or solutions in water or non-aqueous media, capsules, sachets or tablets. Thickeners, flavoring agents, diluents, emulsifiers, dispersing aids or binders may be desirable.
[0052] Compositions and formulations for parenteral, intrathecal or intraventricular administration may include sterile aqueous solutions which may also contain buffers, diluents and other suitable additives such as, but not limited to, penetration enhancers, carrier compounds and other pharmaceutically acceptable carriers or excipients.
[0053] Pharmaceutical compositions and/or formulations comprising the oligonucleotides of the present invention may also include penetration enhancers in order to enhance the alimentary delivery of the oligonucleotides. Penetration enhancers may be classified as belonging to one of five broad categories, i.e., fatty acids, bile salts, chelating agents, surfactants and non-surfactants (Lee et al., Critical Reviews in Therapeutic Drug Carrier Systems, 1991, 8, 91-192; Muranishi, Critical Reviews in Therapeutic Drug Carrier Systems, 1990, 7, 1-33). One or more penetration enhancers from one or more of these broad categories may be included.
[0054] Various fatty acids and their derivatives which act as penetration enhancers include, for example, oleic acid, lauric acid, capric acid, myristic acid, palmitic acid, stearic acid, linoleic acid, linolenic acid, dicaprate, tricaprate, recinleate, monoolein (a.k.a. 1-monooleoyl-rac-glycerol), dilaurin, caprylic acid, arichidonic acid, glyceryl 1-monocaprate, 1-dodecylazacycloheptan-2-one, acylcarnitines, acylcholines, mono- and di-glycerides and physiologically acceptable salts thereof (i.e., oleate, laurate, caprate, myristate, palmitate, stearate, linoleate, etc.) (Lee et al., Critical Reviews in Therapeutic Drug Carrier Systems, 1991, 8:2, 91-192; Muranishi, Critical Reviews in Therapeutic Drug Carrier Systems, 1990, 7:1, 1-33; El-Hariri et al., J. Pharm. Pharmacol., 1992, 44, 651-654). Examples of some presently preferred fatty acids are sodium caprate and sodium laurate, used singly or in combination at concentrations of 0.5 to 5%.
[0055] The physiological roles of bile include the facilitation of dispersion and absorption of lipids and fat-soluble vitamins (Brunton, Chapter 38 In: Goodman & Gilman's The Pharmacological Basis of Therapeutics, 9th Ed., Hardman et al., eds., McGraw-Hill, New York, N.Y., 1996, pages 934-935). Various natural bile salts, and their synthetic derivatives, act as penetration enhancers. Thus, the term “bile salt” includes any of the naturally occurring components of bile as well as any of their synthetic derivatives. A presently preferred bile salt is chenodeoxycholic acid (CDCA) (Sigma Chemical Company, St. Louis, Mo.), generally used at concentrations of 0.5 to 2%.
[0056] Complex formulations comprising one or more penetration enhancers may be used. For example, bile salts may be used in combination with fatty acids to make complex formulations. Preferred combinations include CDCA combined with sodium caprate or sodium laurate (generally 0.5 to 5%).
[0057] Chelating agents include, but are not limited to, disodium ethylenediaminetetraacetate (EDTA), citric acid, salicylates (e.g., sodium salicylate, 5-methoxysalicylate and homovanilate), N-acyl derivatives of collagen, laureth-9 and N-amino acyl derivatives of beta-diketones (enamines)(Lee et al., Critical Reviews in Therapeutic Drug Carrier Systems, 1991, 8:2, 92-192; Muranishi, Critical Reviews in Therapeutic Drug Carrier Systems, 1990, 7:1, 1-33; Buur et al., J. Control Rel., 1990, 14, 43-51). Chelating agents have the added advantage of also serving as DNase inhibitors.
[0058] Surfactants include, for example, sodium lauryl sulfate, polyoxyethylene-9-lauryl ether and polyoxyethylene-20-cetyl ether (Lee et al., Critical Reviews in Therapeutic Drug Carrier Systems, 1991, 8:2, 92-191); and perfluorochemical emulsions, such as FC-43 (Takahashi et al., J. Pharm. Pharmacol., 1988, 40, 252-257).
[0059] Non-surfactants include, for example, unsaturated cyclic ureas, 1-alkyl- and 1-alkenylazacyclo-alkanone derivatives (Lee et al., Critical Reviews in Therapeutic Drug Carrier Systems, 1991, 8:2, 92-191); and non-steroidal anti-inflammatory agents such as diclofenac sodium, indomethacin and phenylbutazone (Yamashita et al., J. Pharm. Pharmacol., 1987, 39, 621-626).
[0060] As used herein, “carrier compound” refers to a nucleic acid, or analog thereof, which is inert (i.e., does not possess biological activity per se) but is recognized as a nucleic acid by in vivo processes that reduce the bioavailability of a nucleic acid having biological activity by, for example, degrading the biologically active nucleic acid or promoting its removal from circulation. The coadministration of a nucleic acid and a carrier compound, typically with an excess of the latter substance, can result in a substantial reduction of the amount of nucleic acid recovered in the liver, kidney or other extracirculatory reservoirs, presumably due to competition between the carrier compound and the nucleic acid for a common receptor. For example, the recovery of a partially phosphorothioated oligonucleotide in hepatic tissue is reduced when it is coadministered with polyinosinic acid, dextran sulfate, polycytidic acid or 4-acetamido-4′-isothiocyano-stilbene-2,2′-disulfonic acid (Miyao et al., Antisense Res. Dev., 1995, 5, 115-121; Takakura et al., Antisense & Nucl. Acid Drug Dev., 1996, 6, 177-183).
[0061] In contrast to a carrier compound, a “pharmaceutically acceptable carrier” (excipient) is a pharmaceutically acceptable solvent, suspending agent or any other pharmacologically inert vehicle for delivering one or more nucleic acids to an animal. The pharmaceutically acceptable carrier may be liquid or solid and is selected with the planned manner of administration in mind so as to provide for the desired bulk, consistency, etc., when combined with a nucleic acid and the other components of a given pharmaceutical composition. Typical pharmaceutically acceptable carriers include, but are not limited to, binding agents (e.g., pregelatinized maize starch, polyvinyl-pyrrolidone or hydroxypropyl methylcellulose, etc.); fillers (e.g., lactose and other sugars, microcrystalline cellulose, pectin, gelatin, calcium sulfate, ethyl cellulose, polyacrylates or calcium hydrogen phosphate, etc.); lubricants (e.g., magnesium stearate, talc, silica, colloidal silicon dioxide, stearic acid, metallic stearates, hydrogenated vegetable oils, corn starch, polyethylene glycols, sodium benzoate, sodium acetate, etc.); disintegrates (e.g., starch, sodium starch glycolate, etc.); or wetting agents (e.g., sodium lauryl sulphate, etc.). Sustained release oral delivery systems and/or enteric coatings for orally administered dosage forms are described in U.S. Pat. Nos. 4,704,295; 4,556,552; 4,309,406; and 4,309,404.
[0062] The compositions of the present invention may additionally contain other adjunct components conventionally found in pharmaceutical compositions, at their art-established usage levels. Thus, for example, the compositions may contain additional compatible pharmaceutically-active materials such as, e.g., antipruritics, astringents, local anesthetics or anti-inflammatory agents, or may contain additional materials useful in physically formulating various dosage forms of the composition of present invention, such as dyes, flavoring agents, preservatives, antioxidants, opacifiers, thickening agents and stabilizers. However, such materials, when added, should not unduly interfere with the biological activities of the components of the compositions of the invention.
[0063] In certain embodiments of this invention, the antisense compounds of the invention may be administered in combination with a conventional anti-asthma medication. Typically, two types of medication are used in attempts to control asthma: quick-relief medications (short-acting bronchodilators) that work fast to stop attacks or relieve symptoms and long-term preventive medications (especially anti-inflammatory agents) that keep symptoms and attacks from starting. Examples of the short-acting bronchodilators are short-acting β2-agonists, for example, albuterol, bitolterol, fenoterol isoetharine, metaproterenol, pirbuterol, salbutamol and terbutaline; anticholinergics, for example ipratropium bromide and oxitropium bromide; short-acting theophyllines, for example, aminophylline; and epinephrine/adrenaline. Examples of long-term preventive medications are inhaled or oral corticosteroids, for example, beclomethasone, budesonide, fluticasone triamcinolone, prednisolone, prednisone and methylprednisolone; sodium cromoglycate or cromolyn sodium; nedocromil; oral or inhaled long-acting β2-agonists, for example salmeterol, formoterol, terbutaline, salbutamol; sustained-release theophyllines, for example, aminophylline, methylxanthine and xanthine; and ketotifen. Antisense compounds of the present inventions may be administered in combination or conjunction with these or any of the asthma medications known in the art.
[0064] The compounds of the invention may also be administered in combination with another inhibitor of IL-5 signal transduction, preferably an antibody directed to IL-5. Such antibodies are known in the art.
[0065] Regardless of the method by which the antisense compounds of the invention are introduced into a patient, colloidal dispersion systems may be used as delivery vehicles to enhance the in vivo stability of the compounds and/or to target the compounds to a particular organ, tissue or cell type. Colloidal dispersion systems include, but are not limited to, macromolecule complexes, nanocapsules, microspheres, beads and lipid-based systems including oil-in-water emulsions, micelles, mixed micelles, liposomes and lipid:oligonucleotide complexes of uncharacterized structure. A preferred colloidal dispersion system is a plurality of liposomes. Liposomes are microscopic spheres having an aqueous core surrounded by one or more outer layer(s) made up of lipids arranged in a bilayer configuration (see, generally, Chonn et al., Current Op. Biotech., 1995, 6, 698-708).
[0066] Certain embodiments of the invention provide for liposomes and other compositions containing (a) one or more antisense compounds and (b) one or more other chemotherapeutic agents which function by a non-antisense mechanism. Examples of such chemotherapeutic agents include, but are not limited to, anticancer drugs such as daunorubicin, dactinomycin, doxorubicin, bleomycin, mitomycin, nitrogen mustard, chlorambucil, melphalan, cyclophosphamide, 6-mercaptopurine, 6-thioguanine, cytarabine (CA), 5-fluorouracil (5-FU), floxuridine (5-FUdR), methotrexate (MTX), colchicine, vincristine, vinblastine, etoposide, teniposide, cisplatin and diethylstilbestrol (DES). See, generally, The Merck Manual of Diagnosis and Therapy, 15th Ed., Berkow et al., eds., 1987, Rahway, N.J., pp. 1206-1228. Anti-inflammatory drugs, including but not limited to nonsteroidal anti-inflammatory drugs and corticosteroids, and antiviral drugs, including but not limited to ribovirin, vidarabine, acyclovir and ganciclovir, may also be combined in compositions of the invention. See, generally, The Merck Manual of Diagnosis and Therapy, 15th Ed., Berkow et al., eds., 1987, Rahway, N.J., pp. 2499-2506 and 46-49, respectively. Other non-antisense chemotherapeutic agents are also within the scope of this invention. Two or more combined compounds may be used together or sequentially.
[0067] In another related embodiment, compositions of the invention may contain one or more antisense compounds, particularly oligonucleotides, targeted to a first nucleic acid and one or more additional antisense compounds targeted to a second nucleic acid target. Two or more combined compounds may be used together or sequentially.
[0068] The formulation of therapeutic compositions and their subsequent administration is believed to be within the skill of those in the art. Dosing is dependent on severity and responsiveness of the disease state to be treated, with the course of treatment lasting from several days to several months, or until a cure is effected or a diminution of the disease state is achieved. Optimal dosing schedules can be calculated from measurements of drug accumulation in the body of the patient. Persons of ordinary skill can easily determine optimum dosages, dosing methodologies and repetition rates. Optimum dosages may vary depending on the relative potency of individual oligonucleotides, and can generally be estimated based on EC 50 s found to be effective in in vitro and in vivo animal models. In general, dosage is from 0.01 μg to 100 g per kg of body weight, and may be given once or more daily, weekly, monthly or yearly, or even once every 2 to 20 years. Persons of ordinary skill in the art can easily estimate repetition rates for dosing based on measured residence times and concentrations of the drug in bodily fluids or tissues. Following successful treatment, it may be desirable to have the patient undergo maintenance therapy to prevent the recurrence of the disease state, wherein the oligonucleotide is administered in maintenance doses, ranging from 0.01 μg to 100 g per kg of body weight, once or more daily, to once every 20 years.
[0069] While the present invention has been described with specificity in accordance with certain of its preferred embodiments, the following examples serve only to illustrate the invention and are not intended to limit the same.



EXAMPLES
Example 1
Nucleoside Phosphoramidites for Oligonucleotide Synthesis Deoxy and 2-alkoxy amidites
[0070] 2-Deoxy and 2-methoxy β-cyanoethyldiisopropyl phosphoramidites were purchased from commercial sources (e.g. Chemgenes, Needham Mass. or Glen Research, Inc. Sterling Va.). Other 2′-O-alkoxy substituted nucleoside amidites are prepared as described in U.S. Pat. No. 5,506,351, herein incorporated by reference. For oligonucleotides synthesized using 2-alkoxy amidites, the standard cycle for unmodified oligonucleotides was utilized, except the wait step after pulse delivery of tetrazole and base was increased to 360 seconds.
[0071] Oligonucleotides containing 5-methyl-2′-deoxycytidine (5-Me-C) nucleotides were synthesized according to published methods (Sanghvi, et. al., Nucleic Acids Research, 1993, 21, 3197-3203] using commercially available phosphoramidites (Glen Research, Sterling Va. or ChemGenes, Needham Mass.).
2-Fluoro amidites
2-Fluorodeoxyadenosine amidites
[0072] 2′-fluoro oligonucleotides are synthesized as described previously by Kawasaki, et. al., J. Med. Chem., 1993, 36, 831-841 and U.S. Pat. No. 5,670,633, herein incorporated by reference. Briefly, the protected nucleoside N6-benzoyl-2′-deoxy-2′-fluoroadenosine is synthesized utilizing commercially available 9-beta-D-arabinofuranosyladenine as starting material and by modifying literature procedures whereby the 2-alpha-fluoro atom is introduced by a S N 2-displacement of a 2-beta-trityl group. Thus N6-benzoyl-9-beta-D-arabinofuranosyladenine was selectively protected in moderate yield as the 3′,5′-ditetrahydropyranyl (THP) intermediate. Deprotection of the THP and N6-benzoyl groups is accomplished using standard methodologies and standard methods are used to obtain the 5′-dimethoxytrityl-(DMT) and 5′-DMT-3′-phosphoramidite intermediates.
2-Fluorodeoxyguanosine
[0073] The synthesis of 2′-deoxy-2′-fluoroguanosine is accomplished using tetraisopropyldisiloxanyl (TPDS) protected 9-beta-D-arabinofuranosylguanine as starting material, and conversion to the intermediate diisobutyryl-arabinofuranosylguanosine. Deprotection of the TPDS group is followed by protection of the hydroxyl group with THP to give diisobutyryl di-THP protected arabinofuranosylguanine. Selective O-deacylation and triflation is followed by treatment of the crude product with fluoride, then deprotection of the THP groups. Standard methodologies are used to obtain the 5′-DMT- and 5′-DMT-3′-phosphoramidites.
2-Fluorouridine
[0074] Synthesis of 21-deoxy-21-fluorouridine is accomplished by the modification of a literature procedure in which 2,2′-anhydro-A1-beta-D-arabinofuranosyluracil is treated with 70% hydrogen fluoride-pyridine. Standard procedures were used to obtain the 5′-DMT and 5′-DMT-3′phosphoramidites.
2-Fluorodeoxycytidine
[0075] 2′-deoxy-2′-fluorocytidine is synthesized via amination of 2′-deoxy-2′-fluorouridine, followed by selective protection to give N4-benzoyl-2′-deoxy-2′-fluorocytidine. Standard procedures are used to obtain the 5′-DMT and 5′-DMT-3′phosphoramidites.
2-O-(2-Methoxyethyl) modified amidites
[0076] 2′-O-Methoxyethyl-substituted nucleoside amidites were prepared as follows, or alternatively, as per the methods of Martin, P., Helvetica Chimica Acta, 1995, 78, 486-504.
2,2′-Anhydro [1-(beta-D-arabinofuranosyl)-5-methyluridine]
[0077] 5-Methyluridine (ribosylthymine, commercially available through Yamasa, Choshi, Japan) (72.0 g, 0.279 M), diphenyl-carbonate (90.0 g, 0.420 M) and sodium bicarbonate (2.0 g, 0.024 M) were added to DMF (300 mL). The mixture was heated to reflux, with stirring, allowing the evolved carbon dioxide gas to be released in a controlled manner. After 1 hour, the slightly darkened solution was concentrated under reduced pressure. The resulting syrup was poured into diethylether (2.5 L), with stirring. The product formed a gum. The ether was decanted and the residue was dissolved in a minimum amount of methanol (ca. 400 mL). The solution was poured into fresh ether (2.5 L) to yield a stiff gum. The ether was decanted and the gum was dried in a vacuum oven (60° C. at 1 mm Hg for 24 hours) to give a solid that was crushed to a light tan powder (57 g, 85% crude yield). The NMR spectrum was consistent with the structure, contaminated with phenol as its sodium salt (ca. 5%). The material was used as is for further reactions or purified further by column chromatography using a gradient of methanol in ethyl acetate (10-25%) to give a white solid, mp 222-4° C.
2′-O-Methoxyethyl-5-methyluridine
[0078] 2,2′-Anhydro-5-methyluridine (195 g, 0.81 M), tris(2-methoxyethyl)borate (231 g, 0.98 M) and 2-methoxyethanol (1.2 L) were added to a 2 L stainless steel pressure vessel and placed in a pre-heated oil bath at 160° C. After heating for 48 hours at 155-160° C., the vessel was opened and the solution evaporated to dryness and triturated with MeOH (200 mL). The residue was suspended in hot acetone (1 L). The insoluble salts were filtered, washed with acetone (150 mL) and the filtrate evaporated. The residue (280 g) was dissolved in CH 3 CN (600 mL) and evaporated. A silica gel column (3 kg) was packed in CH 2 Cl 2 /Acetone/MeOH (20:5:3) containing 0.5% Et 3 NH. The residue was dissolved in CH 2 Cl 2 (250 mL) and adsorbed onto silica (150 g) prior to loading onto the column. The product was eluted with the packing solvent to give 160 g (63%) of product. Additional material was obtained by reworking impure fractions.
2′-O-Methoxyethyl-5′-O-dimethoxytrityl-5-methyluridine
[0079] 2′-O-Methoxyethyl-5-methyluridine (160 g, 0.506 M) was co-evaporated with pyridine (250 mL) and the dried residue dissolved in pyridine (1.3 L). A first aliquot of dimethoxytrityl chloride (94.3 g, 0.278 M) was added and the mixture stirred at room temperature for one hour. A second aliquot of dimethoxytrityl chloride (94.3 g, 0.278 M) was added and the reaction stirred for an additional one hour. Methanol (170 mL) was then added to stop the reaction. HPLC showed the presence of approximately 70% product. The solvent was evaporated and triturated with CH 3 CN (200 mL). The residue was dissolved in CHCl 3 (1.5 L) and extracted with 2×500 mL of saturated NaHCO 3 and 2×500 mL of saturated NaCl. The organic phase was dried over Na 2 SO 4 , filtered and evaporated. 275 g of residue was obtained. The residue was purified on a 3.5 kg silica gel column, packed and eluted with EtOAc/Hexane/Acetone (5:5:1) containing 0.5% Et 3 NH. The pure fractions were evaporated to give 164 g of product. Approximately 20 g additional was obtained from the impure fractions to give a total yield of 183 g (57%).
3′-O-Acetyl-21-O-methoxyethyl-5′-O-dimethoxytrityl-5-methyluridine
[0080] 2′-O-Methoxyethyl-5′-O-dimethoxytrityl-5-methyluridine (106 g, 0.167 M), DMF/pyridine (750 mL of a 3:1 mixture prepared from 562 mL of DMF and 188 mL of pyridine) and acetic anhydride (24.38 mL, 0.258 M) were combined and stirred at room temperature for 24 hours. The reaction was monitored by tlc by first quenching the tlc sample with the addition of MeOH. Upon completion of the reaction, as judged by tlc, MeOH (50 mL) was added and the mixture evaporated at 35° C. The residue was dissolved in CHCl 3 (800 mL) and extracted with 2×200 mL of saturated sodium bicarbonate and 2×200 mL of saturated NaCl. The water layers were back extracted with 200 mL of CHCl 3 . The combined organics were dried with sodium sulfate and evaporated to give 122 g of residue (approx. 90% product). The residue was purified on a 3.5 kg silica gel column and eluted using EtOAc/Hexane(4:1). Pure product fractions were evaporated to yield 96 g (84%). An additional 1.5 g was recovered from later fractions.
3′-O-Acetyl-2′-O-methoxyethyl-5′-O-dimethoxytrityl-5-methyl-4-triazoleuridine
[0081] A first solution was prepared by dissolving 3′-O-acetyl-2′-O-methoxyethyl-5′-O-dimethoxytrityl-5-methyluridine (96 g, 0.144 M) in CH 3 CN (700 mL) and set aside. Triethylamine (189 mL, 1.44 M) was added to a solution of triazole (90 g, 1.3 M) in CH 3 CN (1 L), cooled to −5° C. and stirred for 0.5 hours using an overhead stirrer. POCl 3 was added dropwise, over a 30 minute period, to the stirred solution maintained at 0-10° C., and the resulting mixture stirred for an additional 2 hours. The first solution was added dropwise, over a 45 minute period, to the latter solution. The resulting reaction mixture was stored overnight in a cold room. Salts were filtered from the reaction mixture and the solution was evaporated. The residue was dissolved in EtOAc (1 L) and the insoluble solids were removed by filtration. The filtrate was washed with 1×300 mL of NaHCO 3 and 2×300 mL of saturated NaCl, dried over sodium sulfate and evaporated. The residue was triturated with EtOAc to give the title compound.
2′-O-Methoxyethyl-5′-O-dimethoxytrityl-5-methylcytidine
[0082] A solution of 3′-O-acetyl-2′-O-methoxyethyl-5′-O-dimethoxytrityl-5-methyl-4-triazoleuridine (103 g, 0.141 M) in dioxane (500 mL) and NH 4 OH (30 mL) was stirred at room temperature for 2 hours. The dioxane solution was evaporated and the residue azeotroped with MeOH (2×200 mL). The residue was dissolved in MeOH (300 mL) and transferred to a 2 liter stainless steel pressure vessel. MeOH (400 mL) saturated with NH 3 gas was added and the vessel heated to 100° C. for 2 hours (tlc showed complete conversion). The vessel contents were evaporated to dryness and the residue was dissolved in EtOAc (500 mL) and washed once with saturated NaCl (200 mL). The organics were dried over sodium sulfate and the solvent was evaporated to give 85 g (95%) of the title compound.
N4-Benzoyl-2′-O-methoxyethyl-5′-O-dimethoxytrityl-5-methylcytidine
[0083] 2′-O-Methoxyethyl-5′-O-dimethoxytrityl-5-methylcytidine (85 g, 0.134 M) was dissolved in DMF (800 mL) and benzoic anhydride (37.2 g, 0.165 M) was added with stirring. After stirring for 3 hours, tlc showed the reaction to be approximately 95% complete. The solvent was evaporated and the residue azeotroped with MeOH (200 mL). The residue was dissolved in CHCl 3 (700 mL) and extracted with saturated NaHCO 3 (2×300 mL) and saturated NaCl (2×300 mL), dried over MgSO 4 and evaporated to give a residue (96 g). The residue was chromatographed on a 1.5 kg silica column using EtOAc/Hexane (1:1) containing 0.5% Et 3 NH as the eluting solvent. The pure product fractions were evaporated to give 90 g (90%) of the title compound.
N4-Benzoyl-2′-O-methoxyethyl-5′-O-dimethoxytrityl-5-methylcytidine-3′-amidite
[0084] N4-Benzoyl-2′-O-methoxyethyl-5′-O-dimethoxytrityl-5-methylcytidine (74 g, 0.10 M) was dissolved in CH 2 Cl 2 (1 L). Tetrazole diisopropylamine (7.1 g) and 2-cyanoethoxy-tetra-(isopropyl)phosphite (40.5 mL, 0.123 M) were added with stirring, under a nitrogen atmosphere. The resulting mixture was stirred for 20 hours at room temperature (tlc showed the reaction to be 95% complete). The reaction mixture was extracted with saturated NaHCO 3 (1×300 mL) and saturated NaCl (3×300 mL). The aqueous washes were back-extracted with CH 2 Cl 2 (300 mL), and the extracts were combined, dried over MgSO 4 and concentrated. The residue obtained was chromatographed on a 1.5 kg silica column using EtOAc/Hexane (3:1) as the eluting solvent. The pure fractions were combined to give 90.6 g(87%) of the title compound.
Example 2
Oligonucleotide Synthesis
[0085] Unsubstituted and substituted phosphodiester (P—O) oligonucleotides are synthesized on an automated DNA synthesizer (Applied Biosystems model 380B) using standard phosphoramidite chemistry with oxidation by iodine.
[0086] Phosphorothioates (P—S) are synthesized as per the phosphodiester oligonucleotides except the standard oxidation bottle was replaced by 0.2 M solution of 3H-1,2-benzodithiole-3-one 1,1-dioxide in acetonitrile for the stepwise thiation of the phosphite linkages. The thiation wait step was increased to 68 seconds and was followed by the capping step. After cleavage from the CPG column and deblocking in concentrated ammonium hydroxide at 55° C. (18 hr), the oligonucleotides were purified by precipitating twice with 2.5 volumes of ethanol from a 0.5 M NaCl solution.
[0087] Phosphinate oligonucleotides are prepared as described in U.S. Pat. No. 5,508,270, herein incorporated by reference.
[0088] Alkyl phosphonate oligonucleotides are prepared as described in U.S. Pat. No. 4,469,863, herein incorporated by reference.
[0089] 3-Deoxy-3-methylene phosphonate oligonucleotides are prepared as described in U.S. Pat. Nos. 5,610,289 or 5,625,050, herein incorporated by reference. Phosphoramidite oligonucleotides are prepared as described in U.S. Pat. No. 5,256,775 or U.S. Pat. No. 5,366,878, herein incorporated by reference.
[0090] Alkylphosphonothioate oligonucleotides are prepared as described in published PCT applications PCT/US94/00902 and PCT/US93/06976 (published as WO 94/17093 and WO 94/02499, respectively), herein incorporated by reference.
[0091] 3′-Deoxy-3′-amino phosphoramidate oligonucleotides are prepared as described in U.S. Pat. No. 5,476,925, herein incorporated by reference.
[0092] Phosphotriester oligonucleotides are prepared as described in U.S. Pat. No. 5,023,243, herein incorporated by reference.
[0093] Borano phosphate oligonucleotides are prepared as described in U.S. Pat. Nos. 5,130,302 and 5,177,198, both herein incorporated by reference.
Example 3
Oligonucleoside Synthesis
[0094] Methylenemethylimino linked oligonucleosides, also identified as MMI linked oligonucleosides, methylenedimethyl-hydrazo linked oligonucleosides, also identified as MDH linked oligonucleosides, methylenecarbonylamino linked oligonucleosides, also identified as amide-3 linked oligonucleosides, and methyleneaminocarbonyl linked oligo-nucleosides, also identified as amide-4 linked oligonucleo-sides, as well as mixed backbone compounds having, for instance, alternating MMI and P—O or P—S linkages are prepared as described in U.S. Pat. Nos. 5,378,825, 5,386,023, 5,489,677, 5,602,240 and 5,610,289, all of which are herein incorporated by reference.
[0095] Formacetal and thioformacetal linked oligonucleosides are prepared as described in U.S. Pat. Nos. 5,264,562 and 5,264,564, herein incorporated by reference.
[0096] Ethylene oxide linked oligonucleosides are prepared as described in U.S. Pat. No. 5,223,618, herein incorporated by reference.
Example 4
PNA Synthesis
[0097] PNA oligomers were synthesized in a 10 μmol scale on a 433A Peptide Synthesizer (ABI, Perkin-Elmer Corp.) using commercially available Boc/Cbz-protected monomers (Perseptive Biosystems, Perkin-Elmer Corp). The coupling reaction was performed using 7 eqv. (70 μmol) monomer (0.25 M in DMF), 6.8 eqv. (68 μmol) O-(7-azabenzotriazol-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate (HATU, 0.223 M in DMF) as the condensing reagent and a coupling time of 10 min. The coupling efficiency was monitored qualitatively and the coupling step was repeated if the test indicated yields below 99-100% using the following conditions: To increase the concentration of activated monomer, HATU (68 μmol, 25.9 mg) was added to the monomer solution (70 μmol, ca. 150 μl) as a solid. The synthesis cycle was continued adding DIEA (140 μmol, 0.5 M in pyridine), pre-activation of the monomer for 1 min, and a coupling time of 40 min. After cleavage and deprotection the PNA oligomers were purified by RP-HPLC using a 306 Piston Pump System, a 811C Dynamic Mixer, a 170 Diode Array Detector and a 215 Liquid Handler from Gilson (Middleton, Wis.). The system was operated with Unipoint 1.8 Software. The HPLC conditions were as follows: Column: Zorbax SB-C18 (250×7.8 mm, 5 μ, 300 A); column temperature: 55° C.; Solvent A: 0.1% TFA in H 2 O; Solvent B: CH 3 CN/H 2 O (80:20); Gradient: 0-40 min 0-40% B. After chromatographic purification the oligomers were lyophilized and stored at −20° C.
[0098] Peptide nucleic acids (PNAs), including conjugation of amino acids to PNAs, can be prepared in accordance with any of the various procedures referred to in Peptide Nucleic Acids (PNA): Synthesis, Properties and Potential Applications, Bioorganic & Medicinal Chemistry, 1996, 4, 5-23. They may also be prepared in accordance with U.S. Pat. Nos. 5,539,082, 5,700,922, and 5,719,262, herein incorporated by reference.
Example 5
Synthesis of Chimeric Oligonucleotides
[0099] Chimeric oligonucleotides, oligonucleosides or mixed oligonucleotides/oligonucleosides of the invention can be of several different types. These include a first type wherein the “gap” segment of linked nucleosides is positioned between 5′ and 3′ “wing” segments of linked nucleosides and a second “open end” type wherein the “gap” segment is located at either the 3′ or the 5′ terminus of the oligomeric compound. Oligonucleotides of the first type are also known in the art as “gapmers” or gapped oligonucleotides. Oligonucleotides of the second type are also known in the art as “hemimers” or “wingmers”.
[2′-O-Me]--[2′-deoxy]--[2′-O-Me] Chimeric Phosphorothioate Oligonucleotides
[0100] Chimeric oligonucleotides having 2′-O-alkyl phosphorothioate and 2′-deoxy phosphorothioate oligonucleotide segments are synthesized using an Applied Biosystems automated DNA synthesizer Model 380B, as above. Oligonucleotides are synthesized using the automated synthesizer and 2-deoxy-5′-dimethoxytrityl-3′-O-phosphoramidite for the DNA portion and 5′-dimethoxytrityl-2′-O-methyl-3′-O-phosphoramidite for 5′ and 3′ wings. The standard synthesis cycle is modified by increasing the wait step after the delivery of tetrazole and base to 600 s repeated four times for RNA and twice for 2′-O-methyl. The fully protected oligonucleotide is cleaved from the support and the phosphate group is deprotected in 3:1 Ammonia/Ethanol at room temperature overnight then lyophilized to dryness. Treatment in methanolic ammonia for 24 hours at room temperature is then done to deprotect all bases and sample was again lyophilized to dryness. The pellet is resuspended in 1M TBAF in THF for 24 hours at room temperature to deprotect the 2′ positions. The reaction is then quenched with 1M TEAA and the sample is then reduced to k volume by 30 rotovac before being desalted on a G25 size exclusion column. The oligo recovered is then analyzed spectrophotometrically for yield and for purity by capillary electrophoresis and by mass spectrometry.
[2′-O-(2-Methoxyethyl)]--[2′-deoxy]--[2′-O-(2-Methoxyethyl)] Chimeric Phosphorothioate Oligonucleotides
[0101] [2′-O-(2-methoxyethyl)]--[2′-deoxy]--[-2′-O-(methoxy-ethyl)] chimeric phosphorothioate oligonucleotides were prepared as per the procedure above for the 2-O-methyl chimeric oligonucleotide, with the substitution of 2-O-(methoxyethyl) amidites for the 2-O-methyl amidites.
[2′-O-(2-Methoxyethyl)Phosphodiester]--[2′-deoxy Phosphorothioate]--[2′-O-(2-Methoxyethyl) Phosphodiester] Chimeric Oligonucleotides
[0102] [2′-O-(2-methoxyethyl phosphodiester]--[2′-deoxy phosphorothioate]--[2′-O-(methoxyethyl) phosphodiester] chimeric oligonucleotides are prepared as per the above procedure for the 2-O-methyl chimeric oligonucleotide with the substitution of 2-O-(methoxyethyl) amidites for the 2-O-methyl amidites, oxidization with iodine to generate the phosphodiester internucleotide linkages within the wing portions of the chimeric structures and sulfurization utilizing 3,H-1,2 benzodithiole-3-one 1,1 dioxide (Beaucage Reagent) to generate the phosphorothioate internucleotide linkages for the center gap.
[0103] Other chimeric oligonucleotides, chimeric oligonucleosides and mixed chimeric oligonucleotides/oligonucleosides are synthesized according to U.S. Pat. No. 5,623,065, herein incorporated by reference.
Example 6
Oligonucleotide Isolation
[0104] After cleavage from the controlled pore glass column (Applied Biosystems) and deblocking in concentrated ammonium hydroxide at 55° C. for 18 hours, the oligonucleotides or oligonucleosides were purified by precipitation twice out of 0.5 M NaCl with 2.5 volumes ethanol. Synthesized oligonucleotides were analyzed by polyacrylamide gel electrophoresis on denaturing gels and judged to be at least 85% full length material. The relative amounts of phosphorothioate and phosphodiester linkages obtained in synthesis were periodically checked by 31 p nuclear magnetic resonance spectroscopy, and for some studies oligonucleotides were purified by HPLC, as described by Chiang et al., J. Biol. Chem. 1991, 266, 18162-18171. Results obtained with HPLC-purified material were similar to those obtained with non-HPLC purified material.
Example 7
Analysis of Oligonucleotide Inhibition of IL-5 or IL-5Ra Expression
[0105] Antisense modulation of IL-5 or IL-5Ra expression can be assayed in a variety of ways known in the art. For example, IL-5 or IL-5Ra mRNA levels can be quantitated by Northern blot analysis, RNAse protection assay (RPA), competitive polymerase chain reaction (PCR), or real-time PCR (RT-PCR). RNA analysis can be performed on total cellular RNA or poly(A)+ mRNA. Methods of RNA isolation are taught in, for example, Ausubel, et al., Current Protocols in Molecular Biology , Volume 1, John Wiley & Sons, Inc., 1993, pp. 4.1.1-4.2.9 and 4.5.1-4.5.3. Northern blot analysis is routine in the art and is taught in, for example, Ausubel, et al., Current Protocols in Molecular Biology , Volume 1, John Wiley & Sons, Inc., 1996, pp. 4.2.1-4.2.9. Real-time quantitative (PCR) can be conveniently accomplished using the commercially available ABI PRISMJ 7700 Sequence Detection System, available from PE-Applied Biosystems, Foster City, Calif. and used according to manufacturer's instructions. Other methods of PCR are also known in the art.
[0106] IL-5 or IL-5Ra protein levels can be quantitated in a variety of ways well known in the art, such as immunoprecipitation, Western blot analysis (immunoblotting), ELISA, flow cytometry or fluorescence-activated cell sorting (FACS). Antibodies directed to IL-5 or IL-5Ra can be identified and obtained from a variety of sources, such as PharMingen Inc., San Diego Calif., or can be prepared via conventional antibody generation methods. Methods for preparation of polyclonal antisera are taught in, for example, Ausubel, et al., Current Protocols in Molecular Biology , Volume 2, John Wiley & Sons, Inc., 1997, pp. 11.12.1-11.12.9. Preparation of monoclonal antibodies is taught in, for example, Ausubel, et al., Current Protocols in Molecular Biology , Volume 2, John Wiley & Sons, Inc., 1997, pp. 11.4.1-11.11.5.
[0107] Immunoprecipitation methods are standard in the art and can be found at, for example, Ausubel, et al., Current Protocols in Molecular Biology , Volume 2, John Wiley & Sons, Inc., 1998, pp. 10.16.1-10.16.11. Western blot (immunoblot) analysis is standard in the art and can be found at, for example, Ausubel, et al., Current Protocols in Molecular Biology , Volume 2, John Wiley & Sons, Inc., 1997, pp. 10.8.1-10.8.21. Enzyme-linked immunosorbent assays (ELISA) are standard in the art and can be found at, for example, Ausubel, et al., Current Protocols in Molecular Biology , Volume 2, John Wiley & Sons, Inc., 1991, pp. 11.2.1-11.2.22.
Example 8
Poly(A)+ mRNA Isolation
[0108] Poly(A)+ mRNA is isolated according to Miura et al., Clin. Chem., 1996, 42, 1758-1764. Other methods for poly(A)+ mRNA isolation are taught in, for example, Ausubel, et al., Current Protocols in Molecular Biology , Volume 1, John Wiley & Sons, Inc., 1993, pp. 4.5.1-4.5.3. Briefly, for cells grown on 96-well plates, growth medium is removed from the cells and each well is washed with 200 μL cold PBS. 60 μL lysis buffer (10 mM Tris-HCl, pH 7.6, 1 mM EDTA, 0.5 M NaCl, 0.5% NP-40, 20 mM vanadyl-ribonucleoside complex) is added to each well, the plate is gently agitated and then incubated at room temperature for five minutes. 55 μL of lysate is transferred to Oligo d(T) coated 96-well plates (AGCT Inc., Irvine Calif.). Plates are incubated for 60 minutes at room temperature, washed 3 times with 200 μL of wash buffer (10 mM Tris-HCl pH 7.6, 1 mM EDTA, 0.3 M NaCl). After the final wash, the plate is blotted on paper towels to remove excess wash buffer and then air-dried for 5 minutes. 60 μL of elution buffer (5 mM Tris-HCl pH 7.6), preheated to 70° C. is added to each well, the plate is incubated on a 90° C. hot plate for 5 minutes, and the eluate is then transferred to a fresh 96-well plate.
[0109] Cells grown on 100 mm or other standard plates may be treated similarly, using appropriate volumes of all solutions.
Example 9
Total RNA Isolation
[0110] Total mRNA is isolated using an RNEASY 96J kit and buffers purchased from Qiagen Inc. (Valencia Calif.) following the manufacturer's recommended procedures. The kit can be used with cells grown on a variety of sizes of plate or bottle, including 96-well plates. Briefly, for cells grown on 96-well plates, growth medium is removed from the cells and each well is washed with 200 μL cold PBS. 100 μL Buffer RLT is added to each well and the plate vigorously agitated for 20 seconds. 100 μL of 70% ethanol is then added to each well and the contents mixed by pipetting three times up and down. The samples are then transferred to the RNEASY 96J well plate attached to a QIAVACJ manifold fitted with a waste collection tray and attached to a vacuum source. Vacuum is applied for 15 seconds. 1 mL of Buffer RW1 is added to each well of the RNEASY 96J plate and the vacuum again applied for 15 seconds. 1 mL of Buffer RPE is then added to each well of the RNEASY 96J plate and the vacuum applied for a period of 15 seconds. The Buffer RPE wash is then repeated and the vacuum is applied for an additional 10 minutes. The plate is then removed from the QIAVACJ manifold and blotted dry on paper towels. The plate is then re-attached to the QIAVACJ manifold fitted with a collection tube rack containing 1.2 mL collection tubes. RNA is then eluted by pipetting 60 μL water into each well, incubating 1 minute, and then applying the vacuum for 30 seconds. The elution step is repeated with an additional 60 μL water.
MOUSE IL-5
Example 10
Antisense Inhibition of Murine IL-5 Expression
[0111] In accordance with the present invention, a series of antisense oligonucleotides were designed to target different regions of murine IL-5 RNA, using published sequences (Genbank Accession No. X06271 incorporated herein as SEQ ID NO: 1). The oligonucleotides are shown in Table 1. Target sites are indicated by nucleotide numbers, as given in the sequence source reference (Genbank Accession No. X06271) to which the oligonucleotide binds. All compounds in Table 1 are chimeric oligonucleotides (“gapmers”) 20 nucleotides in length, composed of a central “gap” region consisting of ten 2′-deoxynucleotides, which is flanked on both sides (5′ and 3′ directions) by five-nucleotide “wings”. The wings (shown in bold) are composed of 2′-O-methoxyethyl (2′-MOE) nucleotides. The internucleoside (backbone) linkages are phosphorothioate (P—S) throughout the oligonucleotide. Cytidine residues in the 2′-MOE regions are 5-methylcytidines but cytidines in the 2′-deoxy regions are unmodified unless otherwise indicated.
TABLE 1 Murine IL-5 Antisense Oligonucleotides SEQ ISIS NUCLEOTIDE SEQUENCE 1 ID TARGET TARGET NO. (5′->3′) NO SITE 2 REGION 16975 CCCAA GCAATTTATT CTCTC 2 510-529 5′UTR 16976 TCAGC AAAGGAAGAG CGCAG 3 544-563 Coding 16977 CACTG TGCTCATGGG AATCT 4 654-673 Coding 16978 ACTTT ACCTCATTGC TTGTC 5 718-737 Coding 16979 TCAGA GCGGTATAGC AAGGT 6 774-793 Coding 16980 CTCAT CGTCTGCAAA GGAAA 7 1548-1567 Coding 16981 TATGA GTAGGGACAG GAAGC 8 1568-1587 Coding 16982 ATTTT TATGAGTACG GACAG 9 1573-1592 Coding 16983 AGCAC GGCAGTAAAG AATAA 10 1598-1617 Coding 16984 ACAAG GAAAACAAAG AGAGG 11 2380-2399 Coding 16985 CTGGT GCTGAAAGAA GATTA 12 3454-3473 Coding 16986 CCACG GACAGTTTGA TCCTT 13 3513-3532 Coding 16987 AATGA CAGGTTTTGG AATAG 14 3549-3568 Coding 16988 GCGGT CAATGTATTT CTTTA 15 3571-3590 Coding 16989 GGAAC TTACTTTTTG GCGGT 16 3586-3605 Coding 16990 CAGAC TGTCAGGTTG GCTCC 17 3644-3663 Coding 16991 TCCTC GCCACACTTC TCCTG 18 3673-3692 Coding 16992 AACTG CCTCGTCCTC CGTCT 19 3694-3713 Coding 16993 TACTC ATCACACCAA GGAAC 20 3732-3751 Coding 16994 CTCAG CCTCAGCCTT CCATT 21 3762-3781 Stop 16995 TTAAA TTGTGAAGTC CTGTC 22 3794-3813 3′-UTR 16996 AAATA TAAATGGAAA CAGCA 23 3874-3893 3′-UTR 16997 CTACA GGACATAAAT ATAAA 24 3885-3904 3′-UTR 16998 TATA CAAAAAGGTTA AACAC 25 3938-3957 3′-UTR 16999 GGTTA TCCTTGGCTA CATTA 26 4001-4020 3′-UTR

[0112] Oligonucleotides were tested in EL-4 T cells (ATCC TIB-39, American Type Culture Collection, Manassas, Va.) by Northern blot analysis as described in previous examples using a commercially available murine IL-5 probe. These cells are PHA responsive and PMA plus cAMP elevating agents induce a several hundredfold increase in IL-5 synthesis by these cells. Cells were maintained and stimulated to express IL-5 according to published methods and transfected with oligonucleotide via electroporation.
[0113] Oligonucleotides were tested at a concentration of 10 μM. The results are shown in Table 2:
TABLE 2 Effect of Antisense Oligonucleotides on Murine IL-5 mRNA Levels ISIS SEQ NO. ID NO: TARGET REGION % CONTROL % INHIB 16975 2 5′ UTR 89.4 10.6 16976 3 Coding 93.2 6.8 16977 4 Coding 107.8 — 16978 5 Coding 95 5 16979 6 Coding 96.9 3.1 16980 7 Coding 91 9 16981 8 Coding 55.8 44.2 16982 9 Coding 60 40 16983 10 Coding 67.6 32.4 16984 11 Coding 73.2 26.8 16985 12 Coding 71.6 28.4 16986 13 Coding 74.2 25.8 16987 14 Coding 104 — 16988 15 Coding 98.8 1.2 16989 16 Coding 107 — 16990 17 Coding 148 — 16991 18 Coding 107 — 16992 19 Coding 70 30 16993 20 Coding 78.1 21.9 16994 21 Stop 79.4 20.6 16995 22 3′-UTR 95.7 4.3 16996 23 3′-UTR 113 — 16997 24 3′-UTR 122 — 16998 25 3′-UTR 110 — 16999 26 3′-UTR 68.1 31.9

[0114] SEQ ID NO 8, 9, 10, 19 and 26 (ISIS 16981, 16982, 16983, 16992 and 16999, respectively) showed at least 30% inhibition of IL-5 expression in this assay and are therefore preferred.
Example 11
Dose Response Comparison of ISIS 16992 and 16999 for Reduction of Murine IL-5 mRNA Levels
[0115] ISIS 16992 and 16999 (SEQ ID NO: 19 and 26, respectively) were screened at concentrations of 5 to 25 μM in EL-4 T cells for the ability to decrease IL-5 mRNA levels. Oligonucleotides were introduced to cells by electroporation and mRNA levels were measured by Northern blot analysis.
[0116] An IC50 (oligonucleotide concentration at which mRNA was decreased by 50% compared to control) of approximately 15 AM was obtained for ISIS 16992 and approximately 18 μM for ISIS 16999.
[0117] ISIS 16999 was compared to 1, 3, and 5-mismatch control sequences (ISIS Nos 17983, 17984 and 17985; SEQ ID Nos: 30, 31 and 32, respectively) in dose-response measurements of IL-5 mRNA levels after oligonucleotide treatment. In this experiment ISIS 16999 had an IC50 of approximately 9 μM and ISIS 17983, the 1-base mismatch control, had an IC50 of approximately 13 μM. IC50s were not obtainable for the 3- and 5-base mismatch controls which reduced IL-5 mRNA levels only by 8% and 17%, respectively.
Example 12
Dose Response Comparison of ISIS 16992 and 16999 for Reduction of Murine IL-5 Protein Levels
[0118] ISIS 16992 and 16999 (SEQ ID NO: 19 and 26, respectively) were screened at concentrations of 5 to 25 μM in EL-4 T cells for the ability to decrease IL-5 protein levels. Oligonucleotides were introduced to cells by electroporation and protein levels were measured by ELISA assay using a murine IL-5 ELISA kit (Endogen, Woburn, MA). Starting IL-5 concentrations in the absence of oligonucleotide were approximately 2300 pg/ml and this was decreased to approximately 200 pg/ml at 25 μM ISIS 16992 and 400 pg/ml at 25 μM ISIS 16999. An IC50 of approximately 13 μM was obtained for ISIS 16992 and approximately 15 μM for ISIS 16999.
Example 13
Effect of ISIS 16999 on IL-5 Secretion by EL-4 Cells
[0119] EL-4 cells were treated with ISIS 16999 at doses from 5 to 20 μM as described in previous examples. Secreted IL-5 in the medium was detected by ELISA assay as in previous examples.
[0120] Secreted IL-5 levels were reduced by 13.5-fold as oligonucleotide concentration was increased from zero to 10 μM. ISIS 16989, which did not reduce IL-5 mRNA levels (see Table 2 above), showed much lesser reduction (approximately 2.5-fold) in secreted IL-5 levels. IL-5 levels stayed low for at least 72 hours after treatment with ISIS 16999.
Example 14
Optimization of Antisense Inhibition of Murine IL-5 Expression
[0121] An additional series of oligonucleotides targeted to murine IL-5 was synthesized. The oligonucleotide sequences are those previously tested but with modified gap placement. Sequences are shown in Table 3. Target sites in this table refer back to the ISIS number of the parent compound of the same sequence shown in previous tables.
TABLE 3 Optimization of Antisense Modulation of Murine IL-5 Expression SEQ ISIS NUCLEOTIDE SEQUENCE 1 ID TARGET NO. (5′->3′) NO SITE 2 CHEMISTRY 117858 TATGAGTAGGGACAGGAAGC 8 ISIS P-S; 2′- 16981 MOE 17859 TATGAGTAGG GACAGGAAGC 8 ISIS P-S; 2′- 16981 MOE /2′- deoxy 17860 TATGAGTAGG GACAGGAAGC 8 ISIS P-S; 2′- 16981 MOE /2′- deoxy 17861 TATGAGT AGGGACAGGA AGC 8 ISIS P-S; 2′- 16981 MOE /2′ deoxy 17862 TAT GAGTAGGGA CAGGAAGC 8 ISIS P-S; 2′- 16981 MOE /2′- deoxy 17863 AACTGCCTCGTCCTCCGTCT 19 ISIS P-S; 2′- 16992 MOE 17864 AACTGCCTCG TCCTCCGTCT 19 ISIS P-S; 2′- 16992 MOE /2′- deoxy 17865 AACTGCCTCG TCCTCCGTCT 19 ISIS P-S; 2′- 16992 MOE /2′- deoxy 17866 AACTGCC TCGTCCTCCG TCT 19 ISIS P-S; 2′- 16992 MOE /2′- deoxy 17867 AAC TGCCTCGTCC TCCGTCT 19 ISIS P-S; 2′- 16992 MOE /2′- deoxy 17868 GGTTATCCTTGGCTACATTA 26 ISIS P-S; 2′- 16999 MOE 17869 GGTTATCCTT GGCTACATTA 26 ISIS P-S; 2′- 16999 MOE /2′- deoxy 17870 GGTTATCCTT GGCTACATTA 26 ISIS P-S; 2′- 16999 MOE /2′- deoxy 17871 GGTTATC CTTGGCTACA TTA 26 ISIS P-S; 2′- 16999 MOE /2′- deoxy 17872 GGT TATCCTTGGC TACATTA 26 ISIS P-S; 2′- 16999 MOE /2′- deoxy 17980 AACTG CCTC C TCCTC CGTCT 27 ISIS P-S; 2′- 16992 MOE /2′- mismatch deoxy; 17931 AACTG CC A C C T G CTC CGTCT 23 ISIS P-S; 2′- 16992 3 MOE /2′- mismatch deoxy; 17982 AACTG G C A C C T G C A C CGTCT 29 ISIS P-S; 2′- 16992 5 MOE /2′- mismatch deoxy; 17983 GGTTA TCCT A GGCTA CATTA 30 ISIS P-S; 2′- 16999 1 MOE /2′- mismatch deoxy; 17984 GGTTA TC G T A GC C TA CATTA 31 ISIS P-S; 2′- 16999 3 MOE /2′- mismatch deoxy; 17985 GGTTA A C G T A G C C A A CATTA 32 ISIS P-S; 2′- 16999 5 MOE /2′- mismatch deoxy; 17994 AACTGCCTCCTCCTCCGTCT 19 ISIS P-S; 2′- 16992 deoxy 17995 GGTTATCGTAGCCTACATTA 26 ISIS P-S; 2′- 16999 deoxy 18242 GGT TATCCTTGGC TACATTA 26 ISIS PS; 2′- 16999 MOE /2′- deoxy; All C- 5meC 18243 GGTTATC CTTGGCTACA TTA 26 ISIS PS; 2′- 16999 MOE /2′- deoxy; All C- 5meC 18244 AAC TGCCTCGTCC TCCGTCT 19 ISIS PS; 2′- 16992 MOE /2′- deoxy; All C- 5meC 18245 AACTGCC TCGTCCTCCG TCT 19 ISIS PS; 2′- 16992 MOE /2′- deoxy; All C- 5meC 18246 TAT GAGTAGGGAC AGGAAGC 8 ISIS PS; 2′- 16981 MOE /2′- deoxy; All C- 5meC 18247 TATGAGT AGGCACAGGA AGC 8 ISIS PS; 2′- 16981 MOE /2′- deoxy; All C- 5meC 20391 GGTTA TCCTTGGCTA CATTA 26 ISIS PS; 2′- 16999 MOE /2′- deoxy, All C- 5meC 20392 GGTTA TCCTTGGCTA CATTA 26 ISIS 2′-MOE, 16999 P-O /2′- deoxy/P- S; All C- 5meC 20393 GGTTA A C G T A G C C A ACATTA 32 ISIS PS; 2′- 16999 MOE /2′- 5 deoxy; mismatch All C- 5meC; 20394 GGTTA A C G T A G C C A ACATTA 32 ISIS 2′-MOE, 16999 5 P-O /2′- mismatch deoxy/P- S; All C- 5meC; 20564 GGTTA TCCTTCGCTA CATTA 26 ISIS P-O; 2′- 16999 MOE /2′- deoxy; All C- 5meC; 21437 GGTTA TCCTTGGCTA CATTA 26 ISIS P-S; 2′- 16999 MOE /2′- deoxy; 5′FITC 21882 GGTT ATCCTTCCCTA CATTA 26 ISIS P-O; 2′- 16999 MOE /2′- deoxy; All C- 5meC; 21966 AACTG CCTCGTCCTC CGTCT 19 ISIS 2′-MOE, 16992 P-O /2′- deoxy/ P- S; All C- 5meC; 21967 AACTG CCTCGTCCTC CGTCT 19 ISIS PS; 2′- 16992 MOE /2′- deoxy; All C- 5meC 21968 AACTG CCTCGTCCTC CGTCT 19 ISIS P-O; 2′- 16992 MOE /2′- deoxy; All C- 5meC 21970 GGTTA A C G T A G C C A A CATTA 32 ISIS P-O; 2′- 16999 5 MOE /2′- mismatch deoxy; All C- 5meC; 22087 AACTG G C A C C T G C A C CGTCT 29 ISIS 2′-MOE, 16992 5 P-O/2′- mismatch deoxy/P- S; All C- 5meC; 22088 AACTG G C A C C T G C A C CGTCT 29 ISIS P-C; 2′- 16992 5 MOE /2′- mismatch deoxy; All C- 5meC; 24232 b AACTGGCACCTGCAC CGTCT 29 ISIS PS; 2′- 16992 5 MOE /2′- mismatch deoxy; All C- 5meC;

[0122] ISIS 17868, 17869, 17860, 18242 and 18243, all gap variants of ISIS 16999 (SEQ ID NO: 26), were tested and compared to the parent oligonucleotide, ISIS 16999 for ability to reduce IL-5 mRNA levels in EL-4 cells. In a screen at 15 μM oligonucleotide concentration (the IC50 for ISIS 16999), ISIS 18243 gave comparable activity to ISIS 16999. ISIS 17870 and 18242 were slightly less active, ISIS 17869 showed modest activity and ISIS 17868 was virtually inactive. In a subsequent dose-response assay, ISIS 17870 and 18243 showed activity comparable to or slightly better than that of ISIS 16999.
[0123] ISIS 17858, 17859, 17860, 18246 and 18247, all gap variants of ISIS 16981 (SEQ ID NO: 8), were tested and compared to the parent oligonucleotide, ISIS 16981, for ability to reduce IL-5 mRNA levels in EL-4 cells. In a screen at 15 μM oligonucleotide concentration, ISIS 17859 and 18246 showed activity comparable to the parent, ISIS 16981, with ISIS 18247 only slightly less active. ISIS 17858 and 17860 were more active than the parent compound. All of the ISIS 16981 gap variants tested are therefore preferred.
[0124] ISIS 17863, 17864, 17865, 18244 and 18245, all gap variants of ISIS 16992 (SEQ ID NO: 19), were tested and compared to the parent oligonucleotide, ISIS 16992. In a screen at 15 μM oligonucleotide concentration, ISIS 18245 showed activity only slightly (approx 20%) less than the parent compound. ISIS 17863 and 18244 were modestly active and ISIS 17864 and 17865 were nearly inactive. Thus ISIS 18245 is also preferred.
[0125] ISIS 16999 was also compared to ISIS 20391, a compound of the same sequence, backbone and gap placement but with 5-methyl cytosines in place of every cytosine (in both the deoxy gap and the 2′-methoxyethoxy regions), and to ISIS 20392, which was identical to ISIS 20391 except the backbone was phosphodiester (P—O) in the 2′ methoxyethoxy regions and phosphorothioate (P—S) in the deoxy gap. Oligos were compared at doses of 5, 15 and 25 μM for ability to reduce IL-5 mRNA levels in EL-4 cells. Both ISIS 20391 and 20392 showed roughly comparable activity to ISIS 16999, with 20392 slightly more active than the parent. Both of these compounds are therefore preferred. 5-base mismatches of both ISIS 20391 and 20392 were inactive at all concentrations. ISIS 20564, a full phosphodiester compound, was virtually inactive at these concentrations in a separate experiment.
Example 15
Effect of IL-5 Antisense Oligonucleotide ISIS 20391 on In Vivo T Cell IL-5 mRNA Expression
[0126] IL-5 mRNA expression was measured in EL-4 T cells by real-time quantitative PCR using the TaqMan system on a Perkin-Elmer ABI PRISM 7700. Relative IL-5 levels were normalized to GAPDH levels. The primer and probe sequences were as follows:
murine IL5: Probe: 5′-6-FAM DYE-AG TGT TCT GAC TCT CAG CTG TGT CTG GGC-TAMRA DYE-3′ (SEQ ID NO: 33) Sense: 5′-TTC AGA GTC ATG AGA AGG ATG CTT-3′ (SEQ ID NO:34) Antisense: 5′ACC ACT GTG CTC ATG GGA ATC T-3′ (SEQ ID NO: 35) GAPDH: Probe: 5′-6-FAM DYE-AAG GCC GAG AAT GGG AAG CTT GTC ATC-TAMRA DYE-3′ (SEQ ID NO: 36) Sense: 5′-GGC AAA TTC AAC GGC ACA GT-3′ (SEQ ID NO: 37) Antisense: 5′-GGG TCT CGC TCC TGG AAG AT-3′. (SEQ ID NO: 38)

[0127] ISIS 20391 reduced IL-5 mRNA levels by 75% compared to ovalbumin-induced IL-5 levels, whereas the mismatch oligonucleotide ISIS 20393 reduced IL-5 mRNA by only 40%.
Example 16
Effect of ISIS 20391 (Targeted to Murine IL-5) on Ovalbumin-Induced Peritonitis in Balb/c Mice
[0128] An eosinophil peroxidase (EPO) calorimetric assay was used to measure the effect of oligonucleotides on eosinophilia in peritoneal lavage fluid after ovalbumin immunization and challenge. The method used is a modification of Strath et al., J. Immunol. Meth., 1985, 83, 209-215. Briefly, the substrate solution consists of 0.05 M o-phenylenediamine dihydrochloride (OPD, Sigma Chem. Co., St. Louis, Mo.) in 0.05 M Tris buffer containing 1 mM hydrogen peroxide and 0.1% Triton X-100. Reaction mixture is added to cells, incubated in the dark for 30 minutes and the reaction was stopped by addition of {fraction (1/4)} volume of 4 M sulfuric acid. The EPO was measured as the absorbance at 492 nm, blanked against substrate solution. Using this assay, EPO levels are proportional to number of eosinophils present. Mice were dosed chronically with oligonucleotides. Ovalbumin challenge increased EPO levels in peritoneal lavage fluid over sixteenfold. ISIS 20391 dosed chronically at 5 mg/kg reduced EPO levels after ovalbumin induction by 47%. The mismatch control reduced EPO by approximately 12.6%.
[0129] A dose-dependent reduction of EPO by ISIS 20391 was obtained, with approximately 75% reduction at 10mg/kg oligonucleotide dose compared to 29% reduction by the mismatch control. The IL-5 oligonucleotide correspondingly reduced eosinophil infiltration into the peritoneal cavity by 86% compared to the ovalbumin challenge control, while the mismatch only reduced infiltration by 26%. Using chronic subcutaneous administration (5 mg/kg/day for 15 days using implanted minipumps) a slight but reproducible inhibitory effect of the IL-5 oligonucleotide on eosinophilia in an ovalbumin lung challenge model has also been obtained.
Example 17
Reduction of IL-5 Protein in Peritoneal Lavage Fluid by ISIS 20391 Following 7 Day Dosing Schedule
[0130] Mice were dosed daily with ISIS 20391 at 5 or 20 mg/kg for 7 days. Following peritoneal lavage, IL-5 protein levels were measured using an ELISA assay. IL-5 levels in ovalbumin-treated mice were approximately 160 pg/ml. Treatment with ISIS 20391 at 5 and 20 mg/kg reduced IL-5 concentrations in peritoneal fluid to 110 and 80 pg/ml, respectively. A control oligonucleotide at 5 and 20 mg/kg reduced IL-5 levels to 160 and 130 pg/ml.
Example 18
Effect of IL-5 Antisense Oligonucleotide on Ovalbumin-Induced Murine Lung Asthma Model
[0131] Airway inflammation is observed in patients with allergic asthma. A murine model of allergic asthma has been developed, (Hessel et al. J. Immunol. 1998, 160, 2998-3005). Sensitization of BALB/c mice with ovalbumin induces a high level of ovalbumin-specific IgE in serum. Inhalation of ovalbumin in sensitized mice causes an immediate bronchoconstrictive response. Repeated inhalation of ovalbumin in sensitized animals induces nonspecific airway hyperresponsiveness in vivo, and infiltration of leukocytes in airway tissue.
[0132] Pathogen-free male BALB/c ByJ mice were obtained from Jackson Laboratories. Active sensitization is performed by IP injection of 20 ?g of ovalbumin (Sigma Chemical Co, St. Louis, Mo., grade II) in aluminum hydroxide adjuvant on days 2 and 9 of 16 days of daily oligonucleotide treatment. This produces high titers of total IgE in mouse serum of which 80% is ovalbumin-specific IgE (Hessel et al., J. Immunol., 1998, 160, 2998-3005). On day 16 of treatment, mice are exposed either 2% ovalbumin aerosol for 1 minute. The aerosol is generated with a nebulizer such as Medix 8001 (Sussex, UK). Oligonucleotides were dissolved in saline and injected daily i.v. in the tail vein by bolus infusion at the indicated doses from 2 days before antigen sensitization through challenge.
[0133] Bronchoalveolar lavage (BAL) is used to measure the leukocyte infiltration of airway tissue. 24 hours after the ovalbumin aerosol, mice were euthanized, tracheal cannulation was performed and saline washes collected. Percent eosinophils in BAL were determined.
[0134] Unsensitized mice had 1.6% eosinophils in BAL fluid; after ovalbumin sensitization this increased to 37.6%. ISIS 20391 at 5, 10 and 20 mg/kg reduced eosinophilia in BAL to 11.8%, 5.5% and 3.8%, respectively. The latter two are statistically significant reductions. Mismatch control oligonucleotide ISIS 20393 at 10 and 20 mg/kg yielded BAL eosinophil counts of 33.6% and 28.4%, respectively. The positive control, dexamethasone, reduced eosinophil counts to 5.8%.
[0135] Airway responsiveness to methacholine is measured in vivo 24 hours after the last aerosol exposure. Baseline nebulized methacholine dose response curves were constructed at day 0 before antigen sensitization for all groups of animals. Pulmonary function was monitored using a Buxco BioSystem Plethysmograph (Buxco, Troy N.Y.) and expressed as enhanced pause (Penh) which correlates to measured airway resistance (Hamelmann et al., Am. J. Respir. Crit. Care Med., 1997, 156, 766-775). Following challenge with aerosolized albumin, pulmonary function recordings were performed for 30 minutes to examine the early phase allergic response. For the late phase reaction, recordings were performed every hour from 2 hours to 9 hours after ovalbumin challenge. Airway responsiveness was measured at 24 hours after antigen challenge by measuring the airway response to methacholine for 3 minutes at each dose. Post-challenge recordings were compared to baseline recordings for each group to generate a Penh stimulation index. As a positive control, dexamethasone was administered i.p., 25 mg/kg, 1 day before the sensitization , 2 hours before the challenge, and 18 hours after the challenge.
[0136] Plethysmography results showed that ISIS 20391 at 10 or 20 mg/kg inhibited the methacholine-induced allergic airway hyperresponsiveness, reducing the peak Penh index from approximately 2.0 (no oligo) to approximately 1.25 after oligonucleotide treatment in several experiments. Dexamethasone, the positive control, reduced the Penh to approximately 1.0.
[0137] Data from one experiment was expressed another way, in terms of PC100, (provocation challenge 100 ) the concentration of methacholine needed to give a twofold increase in airway hyper reactivity. Unsensitized mice had a PC100 of 40.1 mg/ml methacholine. After ovalbumin sensitization, the PC100 was 9.84, indicating that much lower doses of methacholine caused the same increase in airway reactivity. This effect was reversible in part by ISIS 20391. At 5 mg/kg ISIS 20391 the PC100 was 10.6, but at 10 and 20 mg/kg the PC100 was increased to 30.7 and 41.6 mg/kg showing a reverse in airway hyper reactivity. Dexamethasone had a PC100 of 29.8 mg/kg methacholine.
Example 19
Early and Late Phase Allergic Airway Response in Mouse Whole Body Plethysmography Model
[0138] Ovalbumin challenge produces a two-phased response with separate and distinct peaks in airway hyper reactivity at approximately 2 minutes and approximately 2 hours after ovalbumin challenge. The first peak is about a twofold increase in Penh and the second peak is larger, a three- to four-fold increase in Penh. The late phase response was mitigated by ISIS 20391 at doses of 10 and 20 mg/kg. In particular, the late response, in which Penh reaches approximately 0.7 two hours after ovalbumin challenge (compared to 0.25 for unsensitized mice) was reduced by ISIS 20391 at 10 mg/kg to a Penh of approximately 0.4, which was a statistically significant reduction. Dexamethasone reduced the Penh to approximately 0.3. The mismatch control, ISIS 20393 at 10 mg/kg showed a statistically insignificant reduction of late phase Penh to approximately 0.5. In a higher-dose experiment, ISIS 20391 at 20 mg/kg reduced the Penh 2 hours after ovalbumin challenge from 0.7 to 0.425, which was statistically significant. Mismatch control ISIS 20393 at 20 mg/kg reduced Penh to approximately 0.6 which was not significant, and dexamethasone (positive control) reduced the response to approximately 0.25.
Human IL-5
Example 20
Human IL-5 Antisense Oligonucleotides
[0139] A series of antisense compounds were designed to target mRNA encoding human IL-5. These compounds are shown in Table 4.
TABLE 4 Nucleotide Sequences of Human IL-5 Oligonucleotides SEQ ISIS NUCLEOTIDE SEQUENCE 1 ID TARGET TARGET NO. (5′->3′) NO SITE 2 REGION 16071 CTTTG GCAAAGAAAG TGCAT 39 0509-0528 5′-UTR 16072 CGTTC TGCGTTTGCC TTTGG 40 0523-0542 5′-UTR 16073 TCCTC ATGGCTCTGA AACGT 41 0540-0559 AUG 16074 AAGAA AATTACCTCA TTGGC 42 0688-0707 Coding 16075 TTACA GCACACCAGC ATTCA 43 0857-0876 Coding 16076 TCCTC AGAGTCTGGA GAGGA 44 0895-0914 Coding 16077 GGAA CAGGAATCCTC AGAGT 45 0905-0924 Coding 16078 TTTAA CTTACATTTT TATGT 46 0928-0947 Coding 16079 TTTAC TTATTCATGC CATCA 47 0964-0983 Coding 16080 GACA CGATGCTCTTT GGGAA 48 1161-1180 Coding 16081 CATTT TAATATGACC AGGCA 49 1407-1426 Coding 16082 TTCTA GGCAACAAAC CACCA 50 1627-1646 Coding 16083 ACAGT TGGTGCTAAA TGAGG 51 1873-1892 Coding 16084 TTCTT CAGTGCACAG TTGGT 52 1884-1903 Coding 16085 ACCCC CTTGCACAGT TTGAC 53 1932-1951 Coding 16086 TGGCC GTCAATGTAT TTCTT 54 1988-2007 Coding 16087 TGTAA CTTACTTTTT GGCCG 55 2002-2021 Coding 16088 TCCAT AGAAATAGGC ACAGC 56 2051-2070 Coding 16089 CACAC TTTTTCTGTG AAAAA 57 2108-2127 Coding 16090 ATTGG TTTACTCTCC GTCTT 58 2135-2154 Coding 16091 TTATC CACTCGGTGT TCATT 59 2186-2205 Coding 16092 TCCTT CTCCTCCAAA ATCTT 60 2241-2260 3′-UTR 16093 TGGCC CTCATTCTCA CTGCA 61 2269-2288 3′-UTR 16094 TCTGG CAAAGTGTCA GTATG 62 2352-2371 3′-UTR 16095 TTGCC TGGAGGAAAA TACTT 63 2416-2435 3′-UTR 16096 CTTTGGCAAAGAAAGTGCAT 64 0509-0528 5′-UTR 16097 CGTTCTGCGTTTGCCTTTGG 65 0523-0542 5′-UTR 16098 AAGAAAATTACCTCATTGGC 66 0688-0707 Coding 16099 TCCTCAGAGTCTGGAGAGGA 67 0895-0914 Coding 16100 TTTAACTTACATTTTTATGT 68 0928-0947 Coding 16101 ACAGTTGGTGCTAAATGAGG 69 1873-1892 Coding 16102 TGTAACTTACTTTTTGGCCG 70 2002-2021 Coding 16103 CACACTTTTTCTGTGAAAAA 71 2108-2127 Coding 17986 TCTGG CAAACTGTCA GTATG 72 mismatch 16094 17987 TCTGG CATACTCTCA GTATG 73 mismatch 16094 17988 TCTGG CATACTCTGA GTATG 74 mismatch 16094 17989 TTGCC TGGACGAAAA TACTT 75 mismatch 16095 17990 TTGCC TGCACCTAAA TACTT 76 mismatch 16095 17991 TTGCC AGCACGTATA TACTT 77 mismatch 16095

[0140] These oligonucleotides were electroporated into human HSB-2 cells and tested for effect on IL-5 mRNA by Northern blot analysis as described in previous examples. The HSB-2 T-cell line was obtained from the American Type Culture Collection and cells are cultured according to ATCC recommendations. They produce IL-5 upon induction with PMA+ionomycin. Oligonucleotides were tested by Northern blot analysis at a concentration of 10 μM for their ability to block IL-5 mRNA expression. The results are shown in Table 5.
TABLE 5 Activity of Antisense Oligonucleotides Targeted to Human IL-5 ISIS SEQ ID TARGET NO. NO: REGION % CONTROL % INHIB 16071 39 5′-UTR 124 — 16072 40 5′-UTR 93.1 — 16073 41 AUG 101 — 16074 42 Coding 146 — 16075 43 Coding 144 — 16076 44 Coding 296 — 16077 45 Coding 157 — 16078 46 Coding 166 — 16079 47 Coding 75 25 16080 48 Coding 224 — 16081 49 Coding 215 — 16082 50 Coding 94.3 5.7 16083 51 Coding 110 — 16084 52 Coding 22.2 77.8 16085 53 Coding 45.4 54.6 16086 54 Coding 158 — 16087 55 Coding 98.7 1.3 16088 56 Coding 88.4 11.6 16089 57 Coding 139 — 16090 58 Coding 72 28 16091 59 Coding 125 — 16092 60 3′-UTR nd nd 16093 61 3′-UTR 78.5 21.5 16094 62 3′-UTR 58.1 41.9 16095 63 3′-UTR 157 — 16096 64 5′-UTR 164 — 16097 65 5′-UTR 286 — 16098 66 Coding 117 — 16099 67 Coding 157 — 16100 68 Coding 163 — 16101 69 Coding 94.4 5.6 16102 70 Coding 109 — 16103 71 Coding 172 —

[0141] ISIS 16084, 16085 and 16094 inhibited IL-5 mRNA expression by at least 40%.
[0142] A dose-response curve was generated for inhibition of human IL-5 protein expression in HSB-2 cells by ISIS 16085. Cells untreated with oligonucleotide were found to express approximately 47 pg/ml IL-5. After treatment with ISIS 16085 at 5, 15 and 25 μM doses, IL-5 levels dropped to 21, 0 and 0 pg/ml, respectively. Treatment with a 1-mismatch control oligonucleotide at 5, 15 and 25 μM doses gave IL-5 levels of 26, 25 and 20 pg/ml, respectively. Treatment with a 3-mismatch control oligonucleotide at 5, 15 and 25 μM doses gave IL-5 levels of 52, 48 and 46 pg/ml, respectively. A 5-mismatch oligonucleotide did not inhibit, and at some doses stimulated, IL-5 protein expression.
Example 21
Inhibition of IL-5 Expression by ISIS 16085 in Human CEM T Cells
[0143] Using an RNAse protection assay (RiboquantJ hCK4, Pharmingen, La Jolla Calif.), it was determined that ISIS 16085 inhibited IL-5 expression in a second T cell line, CEM (obtained from American Type Culture Collection) with an IC50 estimated at approximately 25 μM. IL-5 expression is induced in these cells by treatment with PMA plus ionomycin in the presence of IL-2, anti-CD28 crosslinking antibody, and dibutyryl cAMP. Dose response analysis of ISIS 16085 vs. its 5-mismatch control in stimulated CEM cells showed a dose-dependent decrease in IL-5 mRNA of about 50% at 25 μM oligonucleotide, compared with about 22% reduction with the mismatch control. No decreases were seen in other cytokine gene products measured in this assay panel.
Example 22
Optimization of Oligonucleotides Targeted to Human IL-5
[0144] Additional 2′-methoxyethoxy gapmer oligonucleotides were designed to optimize placement and size of 2′ deoxy regions. These are shown in Table 6.
TABLE 6 Nucleotide Analogues of Human IL-5 Oligonucleotides SEQ ISIS NUCLEOTIDE SEQUENCE 1 ID TARGET TARGET NO. (5′->3′) NO: SITE 2 REGION 16090 ATTGG TTTACTCTCC GTCTT 58 2135-2154 Coding 17873 ATTGGTTTACTCTCCGTCTT ″ ″ ″ 17874 ATTGGTTTAC TCTCCCTCTT ″ ″ ″ 17875 ATTGCTTTAC TCTCCGTCTT ″ ″ ″ 17876 ATTGCTT TACTCTCCGT CTT ″ ″ ″ 17877 ATT GGTTTACTCT CCGTCTT ″ ″ ″ 16094 TCTGG CAAAGTGTCA GTATG 62 235214 2371 3-′UTR 17878 TCTGGCAAAGTGTCAGTATG 62 ″ ″ 17879 TCTGGCAAAG TCTCAGTATG ″ ″ ″ 17880 TCTGCCAAAC TGTCAGTATG ″ ″ ″ 17881 TCTGCCA AAGTGTCAGT ATG ″ ″ ″ 17882 TCT GGCAAAGTGT CACTATC ″ ″ ″ 17992 TCTCCCAAAGTGTCAGTATG ″ ″ ″ 16095 TTGCC TGGAGGAAAA TACTT 63 2416-2435 3′-UTR 17883 TTGCCTGGAGGAAAATACTT ″ ″ ″ 17884 TTGCCTGGAG GAAAATACTT ″ ″ ″ 17885 TTGCCTGGAG GAAAATACTT ″ ″ ″ 17886 TTGCCTG GAGGAAAATA CTT ″ ″ ″ 17887 TTG CCTGGAGGAA AATACTT ″ ″ ″ 17993 TTGCCTGGAGGAAAATACTT ″ ″ ″ 18248 TTG CCTGGAGGAA AATACTT ″ ″ ″ 18249 TTGCCTG GAGGAAAATACTT ″ ″ ″ 18250 TCT GGCAAAGTGT CAGTATG 62 2352-2371 3-′UTR 18251 TCTGGCA AAGTGTCAGT ATG ″ ″ ″ 18252 ATT GGTTTACTCT CCGTCTT 58 2135-2154 Coding 18253 ATTGGTT TACTCTCCGT CTT ″ ″ ″

TABLE 7
Nucleotide Analogues of Human IL-5 Oligonucleotides
[0145] Mixed backbone [phosphorothioate (P—S) and phosphodiester (P—O)] or all-phosphodiester (P—O) backbone analogs of ISIS 16095 and its mismatch control were also designed. These are shown in Table 7.
TABLE 7 SEQ ISIS NUCLEOTIDE SEQUENCE 1 ID TARGET NO. (5′->3′) NO: REGION 21883 TTGCC TGGAGGAAAA TACTT 64 mixed backbone; P-O in 2′ MOE regions and P-S in 2′deoxy gap 22103 TTGCC AGCACGTATA TACTT 77 mixed backbone; P-O in 2′ MOE regions and P-S in 2′deoxy gap; 21883 mismatch 23114 TTGCC TGGAGGAAAA TACTT 63 P-O throughout 23115 TTGCC AGCACGTATA TACTT 77 P-O throughout; 23114 mismatch

MOUSE IL-5 RECEPTOR
Example 23
Mouse IL-5 Receptor A Oligos
[0146] The mRNA encoding the membrane form of the mouse IL-receptor a contains 11 exons. The transmembrane domain of the receptor is encoded in exon 9. Two mRNAs encoding soluble (secreted) forms of the receptor result from differential splicing events. The mRNA encoding soluble form 1 of the receptor is missing exon 9 (exon 8 is spliced to exon 10)and the mRNA encoding soluble form 2 is missing exons 9 and 10 (exon 8 is spliced to exon 11). Imamura et al., DNA and Cell Biology, 13, 283-292.
[0147] Murine BCL 1 cells were chosen for screening antisense oligonucleotides targeted to murine IL-5 receptor a. These are B-cell leukemia cells derived from a spontaneously arising tumor of BALB/c origin, and proliferate in response to murine or human IL-5. This is a CD5+ line which resembles a subset of human chronic lymphocytic leukemia tumors and secretes IgM upon lipopolysaccharide stimulation. Cells were obtained from the American Type Culture Collection and cultured in RPMI 1640 medium supplemented with 10% heat-inactivated fetal bovine serum (Sigma Chemical Co., St. Louis, Mo.), 10 mM Hepes, pH 7.2, 50 μM 2-ME, 2 mM L-glutamine, 100 U/ml penicillin and 100 μg/ml streptomycin (Gibco, Grand Island, N.Y.).
[0148] A series of antisense oligonucleotides were designed to target the murine IL-5 receptor. All are chimeric “gapmers” with 2′-methoxyethoxy flanks and central 10-base deoxy “gaps” and a phosphorothioate backbone throughout. Cells (1×10 7 cells in PBS) were transfected with oligonucleotides by electroporation at 200V, 1000 μF using a BTX Electro Cell Manipulator 600 (Genetronics, San Diego Calif.). Antisense oligonucleotide sequences are shown in Table 8.
TABLE 8 Nucleotide sequences of mouse IL-5 receptor a oligonucleotides SEQ ISIS NUCLEOTIDE SEQUENCE 1 ID TARGET TARGET NO. (5′->3′) NO: SITE REGION 16924 GACCT GTCCAGTGAG CTTCT 79 11 0112-0131 2 5′-UTR 16925 TAGCC GAATACTGGA AAGGT 80 0281-0300 5′-UTR 16926 AACAC AGGCACCATG GTAGC 81 0297-0316 AUG 16927 CTCTT GGTCAGGATT TGGGT 82 0445-0464 Coding 16928 TCCTC ACGCTAGCTG CAAAG 83 0572-0591 Coding 16929 ATGGC CTTAAGTGGG TGTGG 84 0719-0738 Coding 16930 GAGCC ATTAATGTGC ACAGC 85 0927-0946 Coding 16931 TCCAC TCGCCCCACC TTCCT 86 1250-1269 Coding 16932 AACAA GACGAAGCAG GCAGC 87 1338-1357 Coding 16933 CCGGA ACCGGTGGAA ACAAC 88 1400-1419 Coding 16934 CCAAC CTCTTCCACA CAATG 89 1500-1519 Coding 16935 TCCCA TGACTTCAAA TCCAA 90 1516-1535 Coding 16936 GCAAA ATGCCATCAA AACGT 91 1542-1561 STOP 16937 CGAGC TCTACCACCG CCTGG 92 1651-1670 3′-UTR 16938 CAAGC TGGCCTCGAA CTCAG 93 1712-1731 3′-UTR 16939 GGATG GGTTGGTGAC TTGCA 94 1835-1854 3′-UTR 16940 TGAGG AAACCAAAGG CCCAT 95 1946-1965 3′-UTR 16941 TGTCT CCCACTTGCG TCAGG 96 2164-2183 3′-UTR 16942 TTGAA CAGGCCTATG GAACA 97 2306-2325 3′-UTR 16943 TCTTT TTCACCCCAG GCACG 98 2359-2378 3′-UTR 16944 AATTC CCATGCATCC TCTTG 99 2515-2534 3′-UTR 16945 ATCCA CCAATCACCT CCAAA 100 2794-2813 3′-UTR 16946 TGTTC AGCCCATCAA AAAGA 101 2984-3003 3′-UTR 16947 ATTTG GCTGACAGGA CCCCG 102 3140-3159 3′-UTR 16948 TCCAG AGACTGCCCC ACCCA 103 3216-3235 3′-UTR 16949 CATCT GCTTCTGTAT TGCCA 104 3381-3400 3′-UTR 16950 CCTTT TAGCTCCTTG GGTAC 105 3456-3475 3′-UTR 16951 CATTT CTGAGGGTTG CTGGG 106 3513-3532 3′-UTR 18278 CATCT GATTGTGTCT TGCCA 107 mismatch 16949 18279 CATCT CCTTGTGTAT TGCCA 108 ″″ 18280 CACCT GATTGTGTCT TGTCA 109 ″ ″ 17652 TGTCC CTCCTTTTGG TGGGG 110 11 0741-0760 3 Coding 17653 TTAGC TCTGTCTCTG CTGAT 111 0071-0090 Coding 17654 AACTG CTGGCCAGAG TTGTA 112 0611-0630 Coding 17655 CATAG TTAAAGCAAT GATCT 113 1091-1110 Coding 17656 GTTTC TCATATTCAG TAACC 114 1451-1470 Coding 17657 GGAGT CCTGTATGAG TTCAT 115 1571-1590 3′-UTR 17658 TCTGT GCATCCCAGG TGCTG 116 1681-1700 3′-UTR 17659 CTGGC TGTCCTGGAA CTCAC 117 1741-1760 3′-UTR 17660 TTCAA GGTAACTCAA GCAAC 118 2001-2020 3′-UTR 17661 CTGAT CGCTACCACT GGCAA 119 2081-2100 3′-UTR 17662 CACTC TCAATGAGTT CTATC 120 2121-2140 3′-UTR 17663 TGATG CTGGTTGATC AATCT 121 2411-2430 3′-UTR 17664 TCAAT AGGGAATGGT GTCTT 122 2681-2700 3′-UTR 17665 TTCCA GAGTACCTAG AAGCC 123 2741-2760 3′-UTR 17666 CCAAC AGGTTGCCAT GAAGG 124 2851-2870 3′-UTR 17667 AGAGA TTAGAATTGA CTAAG 125 2881-2900 3′-UTR 17668 ACTAT TGCATATACT AGCAA 126 3161-3180 3′-UTR 17669 CCATC CAATATACAA CCACC 127 3191-3210 3′-UTR 17670 CTCAT GGAAGGAGTT ACAGA 128 3271-3290 3′-UTR 17671 TGTGG ATACTTCACT GCTTC 129 3311-3330 3′-UTR 17672 ATCCA ATAGATGACT GTGAG 130 3401-3420 3′-UTR 17673 GTTCA TATTGTTGTT CCTGC 131 3491-3510 3′-UTR

[0149] Total cellular RNA was isolated using the RNeasyJ kit (Qiagen, Santa Clara CA). mRNA was analyzed by RNAse protection assay (RPA) using the Riboquant Kit and a customized riboprobe spanning exon 9 of the IL-5 receptor a (PharMingen, La Jolla Calif.). The cDNA probes were generated from oligonucleotides matching the exon sequences of either exons 2, 8,9 or 10. Signals were quantitated using a Molecular Dynamics PhosphorImager. Results are shown in Table 9.
TABLE 9 Antisense inhibition of mouse IL-5 receptor a mRNA expression ISIS SEQ ID TARGET NO. NO: REGION % CONTROL % INHIB 16924 79 5′-UTR 98 2 16925 80 5′-UTR 86 14 16926 81 AUG 75 25 16927 82 Coding 74 26 16928 83 Coding 91 9 16929 84 Coding 87 13 16930 85 Coding 90 10 16931 86 Coding 108 — 16932 87 Coding 93 7 16933 88 Coding 102 — 16934 89 Coding 55 45 16935 90 Coding 108 — 16936 91 STOP 76 24 16937 92 3′-UTR 91 9 16938 93 3′-UTR 80 20 16939 94 3′-UTR 83 17 16940 95 3′-UTR 81 19 16941 96 3′-UTR 98 2 16942 97 3′-UTR 91 9 16943 98 3′-UTR 81 19 16944 99 3′-UTR 88 12 16945 100 3′-UTR 65 35 16946 101 3′-UTR 82 18 16947 102 3′-UTR 75 25 16948 103 3′-UTR 89 11 16949 104 3′-UTR 52 48 16950 105 3′-UTR 87 13 16951 106 3′-UTR 99 1

[0150] In this assay, ISIS 16926, 16927, 16934, 16936, 16945, 16947 and 16949 gave at least approximately 25% inhibition of IL-5Ra mRNA expression and are preferred. Of these, ISIS 16934, 16945 and 16949 gave at least 35% inhibition and are more preferred.
[0151] ISIS 16934, 16945 and 16949 were chosen for further study. These demonstrated IC50s for inhibition of murine IL-5 receptor a mRNA in BCL 1 cells of approximately 2.5 μM, 1.5 μM and 1 μM, respectively. ISIS 16949 was tested for effects on IL-5 receptor a protein expression and showed nearly complete inhibition.
Example 24
Antisense Oligonucleotides Targeted to Exon 9 of Mouse IL-5 Receptor
[0152] A series of antisense oligonucleotides were designed to “walk” the entire exon 9 of the coding region of murine IL-5 receptor a mRNA. Oligonucleotides were targeted to regions starting approximately every 10 nucleobases along the exon 9 sequence, which extends from nucleotides 1288 to 1381 on the sequence given as Genbank accession no. D90205. Oligonucleotides are shown in Table 10.
TABLE 10 Nucleotide Sequences of Mouse IL-5R Oligonucleotides-2′MOE gapmers SEQ ISIS NUCLEOTIDE SEQUENCE 1 ID TARGET TARGET NO. (5′->3′) NO: SITE 2 REGION 18001 CAAGG ACTTCCTTTC CTTTC 134 1288-1307 Coding/ exon 9 18002 GCCAT TCTACCAACG ACTTC 135 1298-1317 Coding/ exon 9 18003 ACAAT GAGATGCCAT TCTAC 136 1308-1327 Coding/ exon 9 18004 TGTTG GGAGCACAAT GAGAT 137 1318-1337 Coding/ exon 9 18005 AGCAG GCAGCTGTTG GGAGC 138 1328-1347 Coding/ exon 9 18006 TGAGA AGATTAACAA GACGA 139 1348-1367 Coding/ exon 9 18007 TGCAG ATGAGTGAGA AGATT 140 1358-1377 Coding/ exon 9 18008 ACTCT GCAGATGAGT GAGAA 141 1362-1381 Coding/ exon 9

[0153] Effect of these compounds on both membrane and soluble forms of murine IL-5 receptor a were measured and are shown in Table 11. Oligonucleotides were screened in BCL 1 cells at a dose of 10 μM and IL-5 receptor a mRNA was measured by RPA. Percent inhibition is compared to untreated (no oligonucleotide) control.
TABLE 11 Effect of 2′-MOE gapmers targeted to murine IL-5 receptor a mRNA exon 9 on membrane and soluble IL-5 receptor a mRNA expression SEQ ISIS % inhibition of % inhibition of ID NO. membrane IL-5 Ra soluble 1 IL-5 Ra NO: 18001 35 39 134 18002 5 8 135 18003 15 20 136 18004 10 20 137 18005 55 59 138 18006 59 65 139 18007 65 65 140 18008 75 75 141

Example 25
Effect of Fully 2′-MOE Oligonucleotides Targeted to Murine IL-5 Receptor a mRNA Exon 9 on Membrane and Soluble IL-5 Receptor A mRNA Expression
[0154] Additional oligonucleotides were designed to target exon 9 and intron/exon boundaries; these were uniformly 2′-methoxyethoxy modified with phosphorothioate backbones throughout. These are shown in Table 12 below.
TABLE 12 Nucleotide Sequences of Mouse IL-5R Oligonucleotides uniform 2′ MOE SEQ TARGET ISIS NUCLEOTIDE SEQUENCE 1 ID SITE TARGET NO. (5′->3′) NO: REGION 21750 GACTTCCTTTCCTTTCCTGG 142 1284-13032 I8/E9 21751 CAAGGACTTCCTTTCCTTTC 134 1288-1307 18001 21752 GCCATTCTACCAAGGACTTC 135 1298-1317 18002 21753 ACAATGAGATGCCATTCTAC 136 1308-1327 18003 21754 TGTTGGGAGCACAATGAGAT 137 1318-1337 18004 21755 AGCAGGCAGCTGTTGGGAGC 138 1328-1347 18005 21756 AACAAGACGAAGCAGGCAGC 143 1338-1357 Exon 9 21757 TGAGAAGATTAACAAGACGA 139 1348-1367 18006 21758 TGCAGATGAGTGAGAAGATT 140 1358-1377 18007 21759 ACTCTGCAGATGAGTGAGAA 141 1362-1381 18008 21760 CTACACTCTGCAGATCAGTG 144 1366-1383 E9/E10 21761 CGATCAGTTTTTCCTTCTAA 145 1145-1164 3 E7/E8 21762 TCACCCACATAAATAGGTTG 146 1272-1288 E8/E9 21763 GGTCCATAAATGACACCTGA 147 1382-1397 E9/E10 21764 TTACCTCATATTCAGTAACC 148 1451-1466 E10/E11 23235 GCCATTCTATCAAGGACTTC 149 mismatch 21752 23236 GCCATGCTATCAAGCACTTC 150 ″ ″ 23237 GCTATCCTATCAAGCACGTC 151 ″ ″ 23238 GACTTCCTTACCTTTCCTGG 152 mismatch 21750 23239 GACTTCCTCTTCTTCCCTGG 153 ″ ″ 23240 GACCTCTTTCCCTCTTCTGG 154 ″ ″

[0155] BCL 1 cells were treated with 10M of the full-2′-methoxyethoxy, full phosphorothioate oligonucleotides for 24 hours and total RNA was extracted and analyzed by RPA. Results are shown in Table 13.
TABLE 13 Effect of 2′ MOE uniformly modified oligonucleotides targeted to murine IL-5 receptor a mRNA exon on IL-5 mRNA % control % inhib'n % control % inhib'n SEQ ISIS membrane membrane soluble soluble ID NO. IL-5 Ra IL-5 Ra IL-5 Ra IL-5 Ra NO: 21750 8 92 197 — 142 21751 9 91 191 — 134 21752 6 94 194 — 135 21753 6 94 175 — 136 21754 8 92 184 — 137 21755 16 84 181 — 138 21756 6 94 166 — 143 21757 19 81 144 — 139 21758 31 69 116 — 140 21759 34 66 134 — 141 21760 55 45 116 — 144

[0156] All of the fully modified 2′-methoxyethoxy oligonucleotides targeted to murine IL-5 receptor a mRNA exon reduced expression of the membrane form of IL-5 receptor a and increased expression of the soluble form of the receptor. The potencies of these concurrent effects were coordinately diminished as the antisense target site moved toward the 3′ end of the exon. The overall amount of IL-5 receptor a transcription is unaffected. This demonstrates that fully 2′-methoxyethoxy-modified oligonucleotides targeted to exon 9 just distal to the intronic 3′ splice acceptor site blocked inclusion of exon 9 in the splice product and redirect the splicing machinery to the next downstream splice acceptor site (in intron 9). Reduction of the membrane form of IL-5 receptor a, particularly with no decrease or more particularly with an increase in the soluble form, is believed to have therapeutic utility in diseases associated with IL-5 signal transduction, especially asthma. These results show that splicing has been redirected by use of uniformly 2′-methoxyethoxy oligonucleotides targeted to exon 9 to cause exclusion (skipping) of exon 9 from the spliced mRNA products, resulting in controlled alteration of the ratio of soluble/membrane IL-5 receptor produced.
[0157] It was also shown that conversion of an RNAse H-dependent compound (the 2′ MOE gapmer ISIS 18002) to an RNAse H-independent compound (the fully-2′ MOE compound 21752) converted this oligonucleotide sequence from an inhibitor of both forms of IL-5 receptor a to one which selectively inhibits of the membrane form via splice redirection.
[0158] ISIS 21752 was chosen for further study. In dose response experiments, an IC50 of approximately 4 μM was obtained for inhibition of the membrane form of IL-5 receptor a mRNA. A 1-base mismatch (ISIS 23235) gave an IC50 of approximately 10.5 μM and 3- and 5-base mismatches did not inhibit membrane IL-5 receptor mRNA at any concentration.
Example 26
Effect of Fully 2′-MOE Peptide Nucleic Acid Oligonucleotides Targeted to Murine IL-5 Receptor A mRNA Exon 9 on Membrane and Soluble IL-5 Receptor A mRNA Expression
Example 27
Oligonucleotides Targeted to Exon-Exon Boundaries of Various Forms of Mouse IL-5 Receptor A mRNA
[0159] Oligonucleotides, either 2′ MOE gapmers or uniform 2′ MOE, were designed to target exon-exon boundaries of the mature IL-5 receptor a mRNA. The mRNA encoding the membrane form of the mouse IL-5 receptor a contains 11 exons. The transmembrane domain of the receptor is encoded in exon 9. Two mRNAs encoding soluble (secreted) forms of the receptor result from differential splicing events. The mRNA encoding soluble form 1 of the receptor is missing exon 9 (exon 8 is spliced to exon 10)and the mRNA encoding soluble form 2 is missing exons 9 and 10 (exon 8 is spliced to exon 11). In Table 14, the target region designated “E7-E8” indicates that the oligonucleotide is targeted to the exon 7-8 boundary, and so forth.
TABLE 14 Nucleotide Sequences of Mouse IL-5R Oligonucleotides SEQ ISIS NUCLEOTIDE SEQUENCE 1 ID TARGET TARGET NO. (5′−>3′) NO: SITE 2 REGION 21847 GTTTTTCCTTCTGAATGTGA 155 1139-1158 E7-E8 21848 GTTTT TCCTTCTGAATGTGA ″ 21847 21849 CTTTCCTTTCCCACATAAAT 156 1278-1297 E8-E9 21850 CTTTC CTTTCCCACA TAAAT ″ 21849 21851 TAAATGACACACTCTGCAGA 157 1372-1391 E9-E10 21852 TAAAT GACACACTCT GCAGA ″ 21851 21853 TAAATGACACCCACATAAAT 158 E8-E10 (soluble form 1) 21854 TAAAT GACACCCACA TAAAT ″ 21853 21855 TCGAAGGTTTCCACATAAAT 159 E8-E11 (soluble form 2) 21856 TCGAA GGTTTCCACA TAAAT ″ 21855 21969 CACCT GATTGTGTCT TGTCA 109 mismatch 16949 21972 CATCT GCTTCTGTAT TGCCA 104 16949 22089 TTACC TCATATTCAG TAACC 148 21764 22090 GGTCC ATAAATGACA CCTGA 147 21763 22091 TCACC CACATAAATA GGTTG 146 21762 22092 CGATC AGTTTTTCCT TCTAA 145 21761 22093 CTACA CTCTGCAGAT GAGTG 144 21760 22094 GACTT CCTTTCCTTT CCTGG 142 21750 23232 GCCAT TCTATCAAGG ACTTC 149 mismatch 21752 23233 GCCAT GCTATCAAGC ACTTC 150 ″ ″ 23234 GCTAT CCTATCAAGC ACGTC 151 ″ ″ d

[0160] These compounds were tested at 10 μM dose for ability to reduce membrane or soluble IL-5 receptor a mRNA by RPA. Results for compounds tested are shown in Table 15.
TABLE 15 Activity of Mouse IL-5R Oligonucleotides against Soluble and membrane IL-5 receptor a mRNA % INHIB'N % INHIB'N SEQ MEMBRANE SOLUBLE ISIS ID CHEM- IL-5 IL-5 TARGET NO. NO: ISTRY RECEPTOR RECEPTOR REGION 21847 155 uniform 23 20 E7-E8 2′-MOE (common) 21848 155 2′ MOE/ 89 86 21847 deoxy gapmer 21849 156 uniform 70 5 E8-E9 2′-MOE (membrane) 21850 156 2′ MOE/ 39 25 21849 deoxy gapmer 21851 157 uniform 61 0 E9-E10 2′-MOE (membrane) 21852 157 2′ MOE/ 20 14 21851 deoxy gapmer 21853 158 uniform 14 45 E8-E10 2′-MOE (soluble form 1) 21854 158 2′ MOE/ 11 14 21853 deoxy gapmer 21855 159 uniform 14 25 E8-E11 2′-MOE (soluble form 2)

[0161] As shown in Table 15, selective reduction of expression of the soluble form of IL-5 receptor a could be achieved with antisense oligonucleotides targeted to the exon 8-exon 10 boundary, or, to a lesser extent to the exon 8-exon 11 boundary, both of which junctions are only found in the soluble receptor mRNA. Selective reduction of expression of the membrane form of IL-5 receptor a could be achieved with antisense oligonucleotides targeted to the exon 8-exon 9 boundary or exon 9-exon 10 boundary, both of which are only present in the mRNA targeting the membrane form of IL-5 receptor a. Placement of the fully-2′ MOE oligonucleotides across the intron/exon boundaries of exon 9 resulted in similar effects as were obtained with fully-modified oligonucleotides positioned inside exon 9.
Example 28
Effect of Antisense Oligonucleotides on Expression of Membrane Form of IL-5 Receptor a Protein in Murine BCL 1 Cells
[0162] BCL 1 cells were treated with antisense oligonucleotide for 48 hours. Oligonucleotides used were ISIS 16949 (“common” oligonucleotide targeted to both soluble and membrane forms of IL-5 receptor), ISIS 21752, targeted only to the membrane form and ISIS 21853 and 21855, targeted only to the soluble forms of IL-5 receptor a. Oligonucleotides were introduced by electroporation as described in previous examples. Effect on levels of the membrane form of the receptor was examined by Western blot analysis. Membrane-enriched fractions were prepared as Triton X-100 insoluble material and separated by SDS-PAGE using 8% gels. Antibody to mouse IL-5 receptor a was purchased from Santa Cruz Biotechnology (Santa Cruz, Calif.) and used at 1:1000 dilution.
[0163] Compared to control (no oligonucleotide), ISIS 21752 nearly completely ablated the membrane IL-5 receptor. ISIS 21853 and 21855 together had little to no effect; both target the soluble receptor isoforms specifically. The common sequence oligonucleotide, ISIS 16949, reduced the soluble receptor by 75%.
[0164] Transfection with a fully 2′-MOE oligonucleotide targeted to the 5′ intron splice site for either exon 8, 9 or 10 resulted in specific exclusion of that particular downstream exon but not others adjacent or upstream. Thus targeting the 5′ intron splice sites with high-affinity antisense compounds such as fully 2′-MOE oligonucleotides allows selective deletion of individual exons of the mRNA transcript.
Example 29
Reduction of Eosinophils in Blood and Peritoneal Lavage Fluid of Mice Treated with IL-5 Receptor A Antisense Oligonucleotide
[0165] Mice received daily injections of recombinant mouse IL-5 for 5 days, with or without ISIS 21972 or its mismatch control, ISIS 21969. Percent eosinophils in blood and peritoneal lavage fluid were measured. In control mice (no IL-5, no oligonucleotide) eosinophil levels were 4% in peritoneal lavage fluid and 2% in blood. After IL-5 treatment, eosinophils increased to 13.5% in lavage fluid and 9.5% in blood. Treatment with mismatch oligonucleotide did not change this significantly (13.5% in lavage fluid, 10.5% in blood) but treatment with IL-5 receptor a antisense oligonucleotide reduced eosinophil levels to 8.5% in peritoneal lavage fluid and 7% in blood.
Human IL-5 Receptor
Example 30
Antisense Oligonucleotides Targeted to Human IL-5 Receptor A
[0166] The human IL-5 receptor a gene contains 14 exons. A membrane-anchored form of the receptor and two soluble forms have been identified. The membrane form is active in signal transduction and the soluble forms can act antagonistically. The mRNA transcript encoding the membrane-anchored form of the human IL-5 receptor a contain exons 1-10 and 12-14. Exon 11 is spliced out by an alternative splicing event. The major soluble isoform (soluble form 1) is generated as a result of a normal splicing event and an in-frame stop codon in exon 11. The other soluble form (soluble form 2) is generated by the absence of splicing and therefore is generated by reading into intron 11.
[0167] mRNA transcripts encoding the membrane form of the human IL-5 receptor a contain exons 1-10 and 12-14. Exon 11 is spliced out. It is, therefore, possible to target sequences in exons 1-10 which are common to both soluble and membrane forms of the receptor, or to selectively target sequences only present in the membrane form (exons 12-14). A series of antisense oligonucleotides were designed to be specific to only the membrane form of human IL-5 receptor a (IL-5Ra). These oligonucleotides target regions downstream of exon 11 (i.e., exons 12-14 and intervening introns, stop codon and 3′ untranslated region). Tavernier et al., Proc. Natl. Acad. Sci., 1992, 89, 7041-7045. These are shown in Table 16.
TABLE 16 Nucleotide Sequences of Human IL-5 receptor a membrane-specific antisense oligonucleotides SEQ ISIS NUCLEOTIDE SEQUENCE 1 ID TARGET TARGET NO. (5′−>3′) NO: SITE 2 REGION 16767 AACCA CTCTCTCAAG GGCTT 160 1070-1089 Coding 16768 TGCTG GAATTGGTGG AAACA 161 1173-1192 Coding 17769 GTCTC AACTCCAGGC TTCTC 162 1283-1302 Coding 16770 TCAAA ACACAGAATC CTCCA 163 1305-1324 STOP 16771 AGGAT GCCAAAGTGA CAGTC 164 1323-1342 STOP 16772 ATCCC TGTTCTTTTC ACTGA 165 1371-1390 3′-UTR 16773 CGCAG GTAAATTGAG TGTTG 166 1426-1445 3′-UTR 16774 TGAGG CGATTTGGAT GAAGC 167 1495-1514 3′-UTR 16775 TGGAC GTTAGCCTTA AAAGC 168 1651-1670 3′-UTR 16776 AGCTT AAACAGCCAA ACGGG 169 1693-1712 3′-UTR 16777 CTCCA GGCTGATGCA AAATG 170 1751-1770 3′-UTR 16778 GGGTG AGGAATTTGT GGCTC 171 1817-1836 3′-UTR 16779 CTGGA TCAGGCCTCT GGAGC 172 1936-1955 3′-UTR 18012 GGGTG AGGATTTTGT GGCTC 173 mismatch 16778 18013 GGGTG ATGATTTGGT GGCTC 174 ″ ″ 18014 GGCTG ATGATTTGGT GGGTC 175 ″ ″

[0168] These cells were tested in an IL-5 receptor-expressing subclone of TF-1 cells (provided by Dr. Christoph Walker, Novartis Research Centre, Horsham, UK. Cells were cultured in RPMI 1640 medium supplemented with 10% heat-inactivated fetal bovine serum (Sigma Chemical Company, St. Louis, Mo.), 10 mM Hepes, pH 7.2, 50 μM 2-ME, 2 mM L-glutamine, 100 U/ml penicillin, 100 μg/ml streptomycin (Gibco, Grand Island, N.Y.) and 10 ng/ml recombinant human IL-5 (R & D Systems, Minneapolis, Minn.) added every 48-72 hours. TF-1 cells (1×10 7 cells in PBS) were transfected with oligonucleotides by electroporation at 250V, 1000 μF using a BTX ElectroCell Manipulator 600 (Genetronics, San Diego Calif.).
[0169] Total cellular RNA was isolated using the RNeasyJ kit (Qiagen, Santa Clarita Calif.). Northern blotting was performed using standard methods using a full-length cDNA probe or a cDNA probe corresponding to the membrane isoform-specific exon sequences prepared from HL-60 cell RNA by standard RT-PCR followed by a nested primer reaction. Signals were quantitated using a Molecular Dynamics PhosphorImager. Results are shown in Table 17.
TABLE 17 Activity of Human IL-5 receptor a membrane-specific antisense oligonucleotides on IL-5 receptor mRNA expression % control % inhib. % control % inhib. SEQ ISIS membrane membrane soluble soluble ID NO. IL-5 Ra IL-5 Ra IL-5 Ra IL-5 Ra NO: 16767 86 14 95 5 160 16768 72 28 97 3 161 16769 48 52 100 0 162 16770 69 31 84 16 163 16771 66 34 78 22 164 16772 66 34 92 8 165 16773 48 52 84 16 166 16774 55 45 103 — 167 16775 100 0 95 5 168 16776 59 41 81 19 169 16777 31 69 84 16 170 16778 41 59 92 8 171 16779 55 45 95 5 172

[0170] ISIS 16769, 16773, 16774, 16776, 16777, 16778 and 16779 inhibited the membrane form of IL-5 receptor a by at least 40% and are preferred. Of these, ISIS 16769, 16774, 16778 and 16779 are more preferred because of their minimal effect on the soluble form of IL-5Ra.
[0171] The effect of ISIS 16778 on expression of human IL-5 receptor a protein on the surface of TF-1 cells was measured by flow cytometry. Following electroporation with oligonucleotide, TF-1 cells were incubated for 24 hours or as indicated, collected by centrifugation and washed with cold PBS. Cells were transferred to 12×75 mm polystyrene tubes and washed in 2% bovine serum albumin, 0.2% sodium azide in PBS at 41 C. Cells were centrifuged at 200× g and the supernatant was decanted. Specific antibody was then added at 1:100 for human IL-5 receptor a-phycoerythrin and the isotype control antibody in 0.1 mL of the above buffer. Antibodies were incubated with the cells for 30 minutes at 41 C in the dark with gentle agitation. Cells were then washed as above and resuspended in 0.3 mL of FacsFlow buffer (Becton Dickinson, Franklin Lakes, N.J.) with 0.5% formaldehyde. Cells were analyzed on a Becton-Dickinson FACScan. Results are expressed as the percentage of control expression based on mean fluorescence intensity, subtracting basal expression.
[0172] In dose-response experiments to determine the effect of this oligonucleotide on human IL-5 receptor a cell surface protein expression in TF-1 cells, ISIS 16778 demonstrated an IC50 of approximately 5 μM. A 1-mismatch control had an IC50 of 7.5 μM and 3- and 5-mismatch controls did not inhibit IL-5 receptor a below 75% of control.
[0173] An additional set of oligonucleotides was designed to target both membrane and soluble forms of human IL-5 receptor. These oligonucleotides, targeted to exons 1-10 and intervening introns, are sometimes referred to as “common” IL-5 receptor oligonucleotides. Sequences are shown in Table 18.
TABLE 18 Human IL-5R “Common” Antisense Oligonucleotides SEQ ISIS NUCLEOTIDE SEQUENCE 1 ID TARGET TARGET NO. (5′−>3′) NO SITE 2 REGION 16780 CCTGA GAAATGCGGT GGCCA 177 0019-0038 5′-UTR 16781 GTGTC TATGCTCGTG GCTGC 178 0093-0112 5′-UTR 16782 CGATC CTCTTGTTCC GACCA 179 0148-0167 5′-UTR 16783 ATGCG CCACGATGAT CATAT 180 0248-0267 AUG 16784 GCAGT ATCTCAGTGG CCCCC 181 0285-0304 Coding 16785 TGCTC TTGATCAGGA TTTGG 182 0403-0422 Coding 16786 CAGGA TGGTCCGCAC ACTTG 183 0536-0555 Coding 16787 GGGCA TGAAGTTCAG CAGAA 184 0591-0610 Coding 16788 GCCAG GTGCAGTGAA GGGAA 185 0702-0721 Coding 16789 CTCCC CAGTGTGTCT TTGCT 186 0805-0824 Coding 16790 AAGCC AGTCACGCCC TTTGC 187 0863-0882 Coding 16791 AAACA GCTGATCAAA GGGCC 188 0923-0942 Coding 16792 ATGGA TTGGAAAAGC AGACA 189 1034-1053 Coding 16793 TCTGC ACATGGAGCT CACTG 190 1181-1200 Coding 16794 AGGTT GGCTCCACTC ACTCC 191 1214-1233 Coding 18015 TCTGC ACATGTAGCT CACTG 192 mismatch 16793 18016 TCTGC ACGTGTAACT CACTG 193 ″ ″ 18017 TATGC ACGTGTAACT CCCTG 194 ″ ″

[0174] TABLE 19 Activity of Human IL-5 receptor a “Common” antisense oligonucleotides on IL-5 receptor mRNA expression % control % inhib'n % control % inhib'n SEQ ISIS membrane membrane soluble soluble ID NO. IL-5 Ra IL-5 Ra IL-5 Ra IL-5 Ra NO: 16780 86 14 84 16 177 16781 42 58 39 61 178 16782 41 59 39 61 179 16783 49 51 47 53 180 16784 92 8 89 11 181 16785 19 81 32 68 182 16786 14 86 13 87 183 16787 49 51 47 53 184 16788 22 78 21 79 185 16789 14 86 12 88 186 16790 22 78 21 79 187 16791 46 54 45 55 188 16792 35 65 34 66 189 16793 14 86 13 87 190 16794 38 62 37 63 191
[0175] In this assay, ISIS 16781, 16782, 16783, 16785, 16786, 16787, 16788, 16789, 16790, 16791, 16792, 16793 and 16794 inhibited both membrane and soluble IL-5 receptor a isoforms by greater than 50% and are preferred. Of these, ISIS 16786, 16788, 16789, 16790 and 16793 inhibited both isoforms by greater than 75%.
[0176] ISIS 16793 was chosen for further study. It totally inhibited expression of both soluble and membrane forms of human IL-5 receptor a mRNA. This compound was found to have an IC50 of approximately 2 μM for reduction of IL-5 receptor a cell surface protein in TF-1 cells. A 1-mismatch control had an IC50 of approximately 3 μM and 3- and 5-mismatch controls did not inhibit IL-5 receptor a expression below 75% of control.
Example 30
Antisense Oligonucleotides Targeted to Splice Sites in the Human IL-5 Receptor a mRNA
[0177] The human IL-5 receptor a gene contains 14 exons. A membrane-anchored form of the receptor and two soluble forms have been identified. As with the mouse receptor, the membrane form is active in signal transduction and the soluble forms are not, and can act antagonistically. The mRNA transcript encoding the membrane-anchored form of the human IL-5 receptor a contain exons 1-10 and 12-14. Exon 11 is spliced out by an alternative splicing event. The major soluble isoform (soluble form 1) is generated as a result of a normal splicing event and an in-frame stop codon in exon 11. The other soluble form (soluble form 2) is generated by the absence of splicing and therefore is generated by reading into intron 11.
[0178] Transcripts encoding soluble forms of human IL-5 receptor a do not contain exons 12, 13 or 14. It is, therefore, possible to target sequences in exons 1-10 which are common to both soluble and membrane forms of the receptor, or to selectively target sequences only present in the membrane form (exons 12-14). Oligonucleotides were also designed to target various intron/exon boundaries downstream of exon 11, with the intention of preventing successful splicing downstream of exon 11 and thus redirecting splice products away from the membrane form and in favor of the soluble form of IL-5 receptor a. A series of oligonucleotides were designed to target various splice sites or (intron-exon boundaries) in the IL-5 receptor mRNA. These are shown in Table 20 and their effect on IL-5 receptor mRNA and cell surface protein levels is shown in Tables 21 and 22.
TABLE 20 Nucleotide Sequences of Human IL-5R Oligonucleotides NUCLEOTIDE SEQUENCE 1 TARGET ISIS NO. (5′−>3′) SEQ ID NO: REGION 2 16746 ACCCAGCTTTCTGCAAAACA 196 I13/E14 16747 ACCCAGCTTT CTGCAAAACA ″ 16748 ACCCA GCTTTCTGCA AAACA ″ 16749 TCAACATTACCTCATAGTTA 197 E13/I13 16750 TCAACATTACC TCATAGTTA ″ 16751 TCAA CATTACCTCAT AGTTA ″ 16752 TAAATGACATCTGAAAACAG 198 I12/E13 16753 TAAATGACAT CTGAAAACAG ″ 16754 TAAAT GACATCTGAA AACAG ″ 16755 GAACACTTACATTTTACAGA 199 E12/I12 16756 GAACACTTAC ATTTTACAGA ″ 16757 GAACA CTTACATTTT ACAGA ″ 16758 TCATCATTTCCTGGTGGAAA 200 I11/E12 16759 TCATCATTTCC TGGTGGAAA ″ 16760 TCATC ATTTCCTGGT GGAAA ″ 18009 TCATCATTTACTGGTGGAAA 201 mismatch 18010 TCAGCATTTACTGGTGTAAA 202 mismatch 18011 TCAGCAGTTACTTGTGTAAA 203 mismatch # intron 12. I11/E12 indicates the junction between the 3′ end of intron 11 and the 5′ end of exon 12. Target sequences are from FIG. 2 of Tuypens, T., et al., Eur. Cytokine Netw., 1992, 3, 451-459.

[0179] TABLE 21 Modulation of Human IL-5 receptor a membrane form mRNA expression by Splice Site Oligonucleotides (18 hr) SEQ ISIS ID TARGET NO: NO: REGION % of CONTROL % INHIB 16746 196 I13/E14 36% 64% 16747 ” 66 34 16748 ” 25 75 16749 197 E13/I13 101 — 16750 ” 96 4 16751 ” 96 4 16752 198 I12/E13 101 — 16753 ” 98 2 16754 ” 101 — 16755 199 E12/I12 15.5 84 16756 ” 96 4 16757 ” 91 9 16758 200 I11/E12 176 — 16759 ” 81 19 16760 ” 76 24
[0180] ISIS 16746, 16748 and 16755 inhibited IL-5 membrane receptor mRNA expression by over 50% and are therefore preferred in this assay. Northern blot analysis indicated that ISIS 16755 inhibited the membrane receptor transcript without significantly inhibiting the soluble form. Thus it is believed that ISIS 16755 redirects splicing in favor of the membrane form, as is consistent with data obtained with other non-RNAse H (e.g., uniform 2′-methoxyethoxy) oligonucleotides targeted to splice sites.
TABLE 22 Modulation of Human IL-5 receptor a protein expression on the Cell Surface by Splice Site Oligonucleotides (36 hr) SEQ % of ISIS NUCLEOTIDE SEQUENCE 1 ID TARGET CON- % NO. (5′−>3′) NO REGION TROL INHIB 16746 ACCCAGCTTTCTGCAAAACA 196 I13/E14 35 65% 16747 ACCCAGCTTT CTGCAAAACA ″ 80.5 19.5 16748 ACCCA GCTTTCTGCA AAACA ″ 40.5 59.5 16749 TCAACATTACCTCATAGTTA 197 E13/I13 75 25 16750 TCAACATTACCTC ATAGTTA ″ 91 9 16751 TCAA CATTACCTCAT AGTTA ″ 101 — 16752 TAAATGACATCTGAAAACAG 198 I12/E13 100.5 — 16753 TAAATGACAT CTGAAAACAG ″ 96 4 16754 TAAAT GACATCTGAA AACAG ″ 100.5 — 16755 GAACACTTACATTTTACAGA 199 E12/I12 10.5 89.5 16756 GAACACTTAC ATTTTACAGA ″ 101 — 16757 GAACA CTTACATTTT ACAGA ″ 81 19 16758 TCATCATTTCCTGGTGGAAA 200 I11/E12 5.5 94.5 16759 TCATCATTTC CTGGTGGAAA ″ 75.5 24.5 16760 TCATC ATTTCCTGGT GGAAA ″ 71 29 # 5′end of intro junction between the 3′ end of intron 11 and the 5′ end of exon 12.

[0181] ISIS 16746, 16748, 16755 and 16758 inhibited human IL-5 receptor a protein by over 50% in this assay and are therefore preferred. ISIS 16758 and 16755 were chosen for further study. ISIS 16758 was found to have an IC50 of approximately 5 μM for reduction of IL-5 receptor a cell surface protein in TF-1 cells. A 1-mismatch control had an IC50 of 10 μM and 3- and 5-mismatch controls did not inhibit IL-5 receptor a expression. ISIS 16758 inhibited IL-5 receptor a protein expression without reducing mRNA levels, consistent with an RNAse H-independent mechanism as predicted for a uniformly 2′-methoxyethoxy modified oligonucleotide.
Example 31
Induction of Apoptosis in TF-1 Cells Treated with IL-5 Receptor A Oligonucleotide
[0182] 1×10 6 TF-1 cells cultured in IL-5 (0.5 ng/ml) were collected 48 hours following oligonucleotide treatment (transfection was by electroporation as described in previous examples) and phosphatidylserine expression was detected as a measure of apoptosis using the Annexin-V flow cytometry kit (Clontech, Palo Alto, Calif.) according to the manufacturer's instructions. Briefly, cells were resuspended in 0.2 ml of staining buffer (10 mM Hepes, pH 7.4, 140 mM NaCl, 5 mM CaCl 2 ) and 10 μM of propidium iodide (50 μg/ml) and 5 μl of Annexin V reagent were added at 41 C for 10 minutes. The samples were diluted with FacsFlow (Becton Dickinson, Franklin Lakes N.J.) buffer and analyzed on a Becton Dickinson FACScan. Results are shown in Table 23.
TABLE 23 Apoptosis induction mediated by antisense to human IL-5 receptor a % ISIS Oligo dose Apoptotic SEQ ID No. Chemistry (μM) cells NO: No 14 oligo 16793 2′-MOE gapmer 5 19.8 190 “common” sequence ” 10 49.2 ” ” 15 62.3 ” 18017 5-mismatch 5 20.5 194 for 16793 ” 10 17.5 ” ” 15 20.3 ” 16758 Uniform 2′- 10 33.1 200 MOE ” 15 40.1 ” ” 20 50.4 ” 18011 5-mismatch 10 19 203 for 16758 ” 15 23.6 ” ” 20 21.8 ” 16778 2′-MOE gapmer 7.5 29.9 171 Membrane- specific ” 12.5 49.2 ” 18014 5-mismatch 7.5 38 175 for 16778 ” 12.5 32.2 ”

[0183] Apoptosis was shown to be induced in TF-1 cells cultured in the presence of IL-5 by antisense oligonucleotide inhibitors of IL-5 receptor a.
Example 32
Effect of IL-5 Receptor Oligonucleotides on Cell Proliferation
[0184] 2.5×10 4 TF-1 cells were incubated in 96-well plates in 200 μl complete RPMI in the absence of IL-5 for 16 hours following electroporation. IL-5 (0.5 ng/ml) was added and the cultures were pulsed with 1 μCi of [ 3 H]-thymidine for the last 8 hours of a 48-hour culture period. The cells were harvested on glass fiber filters and analyzed for thymidine incorporation (proportional to cell proliferation) by liquid scintillation counting. Results are shown in Table 24. Results are compared to thymidine incorporation in untreated controls.
TABLE 24 Inhibition of IL-5-induced TF-1 cell proliferation by human IL-5 receptor a antisense oligonucleotides % of Oligo control dose thymidine SEQ ID ISIS No. Chemistry (μM) incorporation NO: 16793 2′-MOE 5 44.5 190 gapmer “common” sequence ” 10 11.1 ” 18017 5- 5 89.1 194 mismatch for 16793 ” 10 92.8 ” 16758 Uniform 10 42.8 200 2′-MOE ” 15 39.2 ” ” 20 19.9 ” 18011 5- 10 95.6 203 mismatch for 16758 ” 15 97.9 ” ” 20 84.6 ”

[0185] These data demonstrate that antisense inhibitors of IL-5 receptor a greatly reduce cellular response to IL-5, i.e., cell proliferation in response to IL-5. Control oligonucleotides were ineffective.
Example 33
Oligonucleotides Targeted to Human IL-5 Receptor A
[0186] Oligonucleotides were designed to target the 5′ untranslated region of the IL-5 receptor a. These are shown in Table 25. Both 21-methoxyethoxy gapmers and uniform 2′-methoxyethoxy compounds were designed.
TABLE 25 Nucleotide Sequences of Human IL-5R Oligonucleotides SEQ ISIS NUCLEOTIDE SEQUENCE 1 ID TARGET TARGET NO. (5′−>3′) NO SITE 2 REGION 16963 AGCGGCAGAGCATTGAGAAC 204 0562-0581 5′UTR 16964 AGCGG CAGAGCATTG AGAAC 205 ″ ″ 16965 GAAGCAGCGGCAGAGCATTG 206 0567-0586 5′-UTR 16966 GAAGC AGCGGCAGAG CATTG 207 ″ ″

Example 34
Mixed Backbone Oligonucleotides Were Designed to Target Human IL-5 Receptor. These are Shown in Table 26.
[0187] TABLE 26 Mixed Backbone Nucleotide Analogues of Human IL-5R Oligonucleotides ISIS NUCLEOTIDE SEQUENCE 1 BACKBONE SEQ TARGET NO. (5′−>3′) CHEMISTRY ID NO: REGION 18018 TCATCATTTCCTGGTGGAAA P—S 200 16758 18019 TCATCATTTCCTGGTGGAAA P—O ″ ″ 18020 GGGTGAGGAATTTGTGGCTC P—S 171 16778 18021 GGGTG AGGAATTTGT GGCTC P—O /P—S ″ ″ 18022 TCTGCACATGGAGCTCACTG P—S 190 16793 18023 TCTGC ACATGGAGCT CACTG P—O /P—S ″ ″
Example 35
Optimization of Human IL-5 Receptor A Oligonucleotides
[0188] A series of antisense oligonucleotides were designed based on active sequences, with various placements of 2′ methoxyethoxy regions. These are shown in Table 27.
TABLE 27 Nucleotide Analogues of Human IL-5R Oligonucleotides NUCLEOTIDE SEQUENCE 1 TARGET ISIS NO. (5′−>3′) SEQ ID NO REGION 18024 AGCTTAA ACAGCCAAAC GGG 169 16776 18025 AGC TTAAACAGCC AAACGGG ″ ″ 18026 AGCTTAAACA GCCAAACGGG ″ ″ 18027 AGCTTAAACA GCCAAACGGG ″ ″ 18028 AGCTT AAACAGCCAA ACGGG ″ ″ 18029 AGCTTAAACAGCCAAACGGG ″ ″ 18030 CGCAGGT AAATTGAGTG TTG 166 16773 18031 CGC AGGTAAATTG AGTGTTG ″ ″ 18032 CGCAGGTAAA TTGAGTGTTG ″ ″ 18033 CGCAGGTAAA TTGAGTGTTG ″ ″ 18034 CGCAG GTAAATTGAG TGTTG ″ ″ 18035 CGCAGGTAAATTGAGTGTTG ″ ″ 18036 GGGTGAGG AATTTGTGG CTC 172 16778 18037 GGG TGAGGAATTT GTGGCTC ″ ″ 18038 GGGTGAGGAA TTTGTGGCTC ″ ″ 18039 GGGTGAGGAA TTTGTGGCTC ″ ″ 18040 GGGTG AGGAATTTGT GGCTC ″ ″ 18041 GGGTGAGGAATTTGTGGCTC ″ ″ 18042 AAGCCAG TCACGCCCTT TGC 187 16790 18043 AAG CCAGTCACGC CCTTTGC ″ ″ 18044 AAGCCAGTCA CGCCCTTTGC ″ ″ 18045 AAGCCAGTCA CGCCCTTTGC ″ ″ 18046 AAGCC AGTCACGCCC TTTGC ″ ″ 18047 AAGCCAGTCACGCCCTTTGC ″ ″ 18048 CAGGATGGTCCGCACACTTG 183 16786 18049 CAGGATG GTCCGCACACTTG ″ ″ 18050 CAG GATGGTCCGC ACACTTG ″ ″ 18051 CAGGATGGTC CGCACACTTG ″ ″ 18052 CAGGATGGTC CGCACACTTG ″ ″ 18053 CAGGA TGGTCCGCAC ACTTG ″ ″ 18054 TCTGCAC ATGGAGCTCA CTG 190 16793 18055 TCT GCACATGGAG CTCACTG ″ ″ 18056 TCTGCACATG GAGCTCACTG ″ ″ 18057 TCTGCACATG GAGCTCACTG ″ ″ 18058 TCTGC ACATGGAGCT CACTG ″ ″ 18059 TCTGCACATGGAGCTCACTG ″ ″ 18060 GAACACT TACATTTTAC AGA 199 16755 18061 GAACACTTAC ATTTTACAGA ″ ″ 18062 GAACACTTAC ATTTTACAGA ″ ″ 18063 CAACA CTTACATTTT ACAGA ″ ″ 18064 TCATCAT TTCCTGGTGG AAA 200 16758 18065 TCA TCATTTCCTG GTGGAAA ″ ″ 18066 TCA TCATTTCCTG GTGGAAA ″ ″ 18067 TCATC ATTTCCTGG TGGAAA ″ ″

Example 36
Modulation of mRNA Splicing of IL-5 Receptor a by Antisense Peptide Nucleic Acids (PNAs)
[0189] In order to determine the effectiveness of peptide nucleic acids as selective modulators of alternative mRNA splicing, a series of PNA oligonucleotide mimetics having the same nucleobase sequence (SEQ ID NO: 135) as an antisense sequence shown to produce exclusion of exon 9 from the IL-5 Receptor a processed mRNA were synthesized and evaluated.
[0190] Murine BCL 1 cells were chosen for screening PNA oligonucleotides targeted to murine IL-5 receptor a and were maintained in RPMI 1640 medium supplemented with 10% heat-inactivated fetal bovine serum (Sigma Chemical Company, St. Louis, Mo.), 10 mM Hepes, pH 7.2, 50 uM 2-ME, 2 mM L-glutamine, 100 U/mL penicillin and 100 ug/mL streptomycin.
[0191] BCL 1 cells were transfected by electroporation as described previously with 0.25, 0.5, 1, 5 and 10 μM of each of the compounds in Table 28. ISIS 110790 (SEQ ID NO: 209) is a shortmer (15 bp) of ISIS 21752 (SEQ ID NO: 135, described previously) lacking the first five nucleobases and having the same internucleoside linkages and modifications as ISIS 21752. ISIS 32297 (SEQ ID NO: 209) is a peptide nucleic acid with the nucleobase sequence of ISIS 110790 while ISIS 28496, a peptide nucleic acid with the same nucleobase sequence of ISIS 32297, contains the amino acid lysine conjugated to the COOH terminal end. The control peptide nucleic acid, ISIS 32304 (SEQ ID NO: 210) is a 3 base pair mismatch of ISIS 28496. At 24 hours, total RNA was extracted and analyzed by RPA. The results are shown in Table 29. Expression data for both isoforms are expressed as a percent of control. “N.D.” indicates no data.
TABLE 28 PNA oligonucleotide mimetics SEQ ISIS ID Number Nucleotide Sequence NO Backbone 21752 GCCATTCTACCAAGGACTTC 135 2′-O-MOE/P-S 110790 TCTACCAAGGACTTC 209 2′-O-MOE/P-S 32297 H-TCTACCAAGGACTTC-NH 2 209 PNA 28496 H-TCTACCAAGGACTTC-Lys-NH 2 209 PNA 32304 H-TCAACCTAGAACTTC-Lys-NH 2 210 PNA

[0192] TABLE 29 Alteration of splicing IL5Ra splicing pattern by PNAs ISIS Membrane Isoform Soluble Isoform Number 0.25 0.5 1 5 10 0.25 0.5 1 5 10 21752 N.D. 58 35 5 3 N.D. 119 150 170 160 110790 N.D. 75 59 7 7 N.D. 119 140 158 160 32297 78 55 41 15 N.D. 110 122 135 140 N.D. 28496 85 59 42 6 N.D. 119 135 150 138 N.D. 32304 110 102 95 95 N.D. 110 105 95 100 N.D.
[0193] These data show that peptide nucleic acids (PNAs) of shorter length and/or with the additional lysine modification are more potent in reducing expression and redirecting splicing of IL-5 Receptor a than their 2′-O-MOE-modified counterparts of the same sequence. Treatment of cells with antisense PNA resulted in dose-dependent, specific down regulation of the membrane isoform and enhanced expression of the soluble isoform with an effective concentration (EC50) lower than that observed with the corresponding 2′-O-MOE antisense oligonucleotides. These properties makes PNAs and modified PNAs a promising new class of lower molecular weight splicing modulators.



1


210


1
6727
DNA
Mus musculus

1

tgtacctccc acatctgctg gtgtgtacca ccacacctag taagatattc tcaacattta 60

tgtattttag cctaaccctg ttggaggtat acatttgaat acattttttc tcactttatc 120

aggaattgag tttaacacat attaaagcag gtgtggggca gggagggggg gataaaaaag 180

aaggtgctca agaaaagccg atcacgctcc caagagtgtg agcatgggcg tctctagaga 240

gatccgccat atatgcacaa cttttaaaga gaaattcaat aaccagaatg gagtgtaaat 300

gtggatcaaa gttgtagaaa cattctttta tgttatagaa aatgcttttt aagcaggggt 360

gggggtcaag atgttaacta ttattaaaga gcaaaaaaaa aaaaatgcat tttgtttgaa 420

gacccagggc actggaaacc ctgagtttca ggactcgcct ttattaggtg tcctctatct 480

gattgttagc aattattcat ttcctcagag agagaataaa ttgcttgggg attcggccct 540

gctctgcgct cttcctttgc tgaaggccag cgctgaagac ttcagagtca tgagaaggat 600

gcttctgcac ttgagtgttc tgactctcag ctgtgtctgg gccactgcca tggagattcc 660

catgagcaca gtggtgaaag agaccttgac acagctgtcc gctcaccgag ctctgttgac 720

aagcaatgag gtaaagtata acttattcct tcagctttgt ttttaagatc aggaccttgc 780

tataccgctc tgactggcct caaacttgct atgtagggta ggctgtccta acccctacca 840

gatctcctta cctatgtctc ccaaatacta ggattacaga cacattacct tgcctgacgc 900

tatggttctt cagaatgcat aaatagctgc atttggcctt taatcccaga acttgggagg 960

cagggtcagg tggatctctg tgagttcaag gccagacttg tctacgtggc cagttacagg 1020

acagccagag ctaaagcaag accctgattc aaaataattt tttttcaaaa caaaaaaaaa 1080

aaacccaaac catttgtggc aattcatttc taaacataaa gatctgcttt aaatagtgca 1140

attatggctt gttcccttgc cttcttgctc ccgttctgtc ctcttgtccc actctctccc 1200

cattccaccc ccaccatgtg ctcatggccc gcatctctac ttctctactc tctttctctc 1260

cctctcccct ccttcttcct ttccctctct ctctccctct tcttctcctc ctctctttct 1320

ctctctctcc ctctctctct ctctttctct ctctctctgc ttttttctat ctctactacc 1380

ctctcaactc ccctctccat gccctgaata agctctattc tatactaaaa aaaaaaaagt 1440

gcaattatga atgtgttagt gttaatgcac aggtgataac cctatcacca gcaagcattg 1500

cattaaaaaa ggcaacggac tctctttagg atgaccctat gatgttcttt cctttgcaga 1560

cgatgaggct tcctgtccct actcataaaa atgtaagtta ttctttactg ccgtgcttgc 1620

atgagtaagt cagcttcgca tactaagcta taagtcatct gcatctagct ttctggtgtt 1680

gtgtgtgtct gggatgggga cctctctagg tctcaagctc ctgggttcaa gtgattctct 1740

tgccttgata gagcagctgg gacacaggcc tgtgccacca cacccagcag agcttttgat 1800

ttcagttaaa ctgtttgact ttcttggaaa agaaaattta tgtaggtaga tatgaaagtt 1860

tgtgcttata aataaaaaga atatgagagt ggcaaattat gtaatcccag tacttgggag 1920

ccaaaggcag gggtagtctg agtctagggc cagcttagat acattgccct gtatgtatca 1980

aaagtaaatc ctataaataa ataaacaaaa acattagagg gctggagata taagctctgt 2040

tgatagatgg cctaatatgc tgggttgact cttagcaccc cataaactaa acatggaagt 2100

acctggctgt aatctcatga tggtgaaatg gaggcgggaa gatcataggt tcaaggtcat 2160

cctcagctac atttttgagc tagaggccag cctgggctat gagacacgca aaaaccacca 2220

gccaattaat attaggaatg gctttgagct agatctgtta tgtaagtggc cagctggagc 2280

tgtcagtcat acatctcaca gcctcacaag attctttgca tggcgagagg tcctgctggg 2340

ctccctttgg ctctgtccat ggctctcttc atcctagtgc ctctctttgt tttccttgtc 2400

ttatttctta ctgctgagga tcaagcccag ggccttcagt gtgtgaagtg agcactctac 2460

cactgaattc cagagcccgc ccactctaat gcctttctga aagtattaag agtttagggt 2520

tatatattcc ttttgtttat tttatgtgta tgagcatttt gcctgcatat atatatatat 2580

atatatatat atatatatat gtgtgtgtgt gtgtgtgtgt gtgtgtatat atatatgtat 2640

gtatgtatgt atgtatgtat gtatgtatat gtgtgtgtgt gtgtgtgtgt gtgtgtgtgt 2700

gttccacgta tgtgtctatg tgtctggtgt tcctgaaggc taaaagaagg gcatcagatc 2760

acctggggct ggatatgcag atggttgtga gccaaccatc tggatgctgg gaactgcatc 2820

aagtgttctt aaccactgag ccatctctcc cgctcagagg gttatattct taggtaatga 2880

tagaaagaca taaaaatatc atgaatgcct ttattaataa tttctaaaca gtttaatgaa 2940

tatgactatg tagtgatatt gtatacattt caatattatc ttattctagc gtaaagtaca 3000

ttatttaact ttttctaaat agaagaaaat tcatcagcct aaatttcaaa agaaaatatt 3060

aatatgggtg tggtaccact cacctttaat ccagatggtt gtgagccacc acaagggtgc 3120

tggtaactga acccaggtcc tctggaagag gacccagtga tcttaaccac tgagccatct 3180

ccccagcccc aatcctaact ttgggttcat ttttttgaaa tgatctcatg tagcactagc 3240

tggcctcaaa ctctatgtat cagaggctgg ccttcaactc ctgatcctct tacctcaact 3300

tcctgaatgc tggcattaca gataagcacc atcacatctt gtattgtctg gggtttttta 3360

ttgatgcatt taaattgcat gtatttattg catatggcat gatatttcaa aatatgtgta 3420

cgttgtgggc agtctgatct atttgcttct tgataatctt ctttcagcac cagctatgca 3480

ttggagaaat ctttcagggg ctagacatac tgaagaatca aactgtccgt gggggtactg 3540

tggaaatgct attccaaaac ctgtcattaa taaagaaata cattgaccgc caaaaagtaa 3600

gttccccagg gaccctgtga atccggctgc agctggttct ccaggagcca acctgacagt 3660

ctgttctttt cacaggagaa gtgtggcgag gagagacgga ggacgaggca gttcctggat 3720

tacctgcaag agttccttgg tgtgatgagt acagagtggg caatggaagg ctgaggctga 3780

gctgctccat ggtgacagga cttcacaatt taagttaaat tgtcaacaga tgcaaaaacc 3840

ccacaaaact gtgcaaatgc aagggatacc atatgctgtt tccatttata tttatgtcct 3900

gtagtcagtt aaacctatct atgtccatat atgcaaagtg tttaaccttt ttgtatacgc 3960

ataaaagaaa ttcctgtagc gcaggctggc ctcaaactgg taatgtagcc aaggataacc 4020

ttgaatttct gatcctcctg cctcctcttc ctgaaggctg aggttacaga catgcaccat 4080

tgccactagt tcatgaagtg ctggagatgg aacccaaggc tttgtgcatg ttaccaactg 4140

agttatactc cctccccctc atcctcttcg ttgcatcagg gtctcaagta ttccaggctg 4200

actttgaact cagtgtgtag ccaagggtga ccctgaactc ttggtccaga tggacgcagg 4260

aggatcacat acccaacctt agcatccttt ctcctagccc ctttagatag atgatactta 4320

atgactctct tgctgaggga tgccacaccg gggcttcctg ctcctatcta acttcaattt 4380

aatacccact agtcaatctc tcctcaactc cctgctactc tccccaaact ctagtaagcc 4440

cacttctatt tcttggggag agagaaggtt gacttttctt atgtcctatg tatgaatcag 4500

actgtgccat gactgtgcct ctgtgcctgg agcagctgga ttttggaaaa gaaaagggac 4560

atctccttgc agtgtgaatg agagccagcc acatgctggg ccttacttct ccgtgtaact 4620

gaacttaaga agcaaagtaa ataccacaac cttactaccc catgccaaca gaaagcataa 4680

aatggttggg atgttattca ggtatcaggg tcactggaga agcctccccc agtttactcc 4740

aggaaaaaca gatgtatgct tttatttaat tctgtaagat gttcatatta tttatgatgg 4800

attcagtaag ttaatattta ttacaacgta tataatattc taataaagca gaagggacaa 4860

ctcaaattca gtttgctatt ggtcttttct aaccctgggt gtgtgcaggg acccagagga 4920

gagactgagt atgtcctgac taagcacttt cagctcctta gagcttcagg gagcaccaag 4980

ggtggacttg gtagtggtat cgggagcaag aacaagggct gggactgagc ctggatctcc 5040

ctatgtagga gtatgtccag atggctcagg gtgaacagga gaggaatgaa tgagaggatg 5100

aatgaatgaa tgaataaatg aatgaatggg agatcgctcc attaataaag tgcttgctgt 5160

acaaggatga agagctgagt tcgagctcca aaacccattt cagaaagctg ggcatggtgg 5220

gggcacactt gtagtcctga cactgggaga cagaaatagc cagatccctg gggctctctg 5280

ttcagccaac ctaaatgaat tggtgagttc tggaccagtg agagatcttc tctcaaaaag 5340

caaggtggaa gccgagcgtg gtgacacacg cctttaattc cagcacttgg gaggcagagg 5400

caggcggatt tctgagttcg aggccagcct ggtctacaaa gtgagttcca ggacagccag 5460

ggctacacag agaaaccctg tctcaaaaaa caaacaaaca aacaaacaaa caaaccacca 5520

tgaactacct gtgtatgcat gttgtgtgtg cttgcattgt gcaggtcaaa tgaacacact 5580

gggactcttc cactaacact ctctacctcg ttccctaaga gggtctcctg ctgaacatgg 5640

agtttcccat ttcttttggt taggctggca gccagccagc aagtcccagc gatcctcctg 5700

tctcctcttc ctcctgctca gccccagggg tggagtctta ggtatgcgtg gccatgccag 5760

gctttttcca tgggtgctgg agatccagac gcagcttctc atgttcgcgc agtggcactc 5820

ttgcccactg aagcatcttc catcttgccc actgaagcat ctcccatctt acccactcaa 5880

gcatcttcca tcttacccac tcaagcatct tccatcttac ccactcaagc atcttccatc 5940

ttacccactc aagcatcttc cagctcctta gtatgttttt tttttaaaca tgtacttggc 6000

tttttaaaat tgtaataaac taaaggtata caatatgtat tgattgatat gcttacttat 6060

gtatttatct ttattttctt atttttttaa aaaatttatt ttatttatat gaatacactg 6120

tagctgactt cagacacacc agaacagggc attggatccc attacggatg gttgtgagcc 6180

accatgtggt tgctgggaat tgaactcagg acctttggaa gaacagtctc tctggctctg 6240

tagttatctt tcagtatact tttccttgaa aattttatat gtctgtgcga tctattctgg 6300

tcctaccatt cactctcact cttcctggac ttcccagtat ggccccctcc cgatttcaaa 6360

tcttctcact cttatttttt agcccactga gttcagttag tgttgtccct atgagcacgt 6420

gtggaccatc tacttgagct taggcaacct accagtggcc acatccctac aggaaaggta 6480

ctcttcctct cttggtggcc ataaaccccc aacgggtcct cacatagggc aggagcctta 6540

ggagtttccc tccccattca tactaaactt tggttggctt gatggtgtga agataaccac 6600

agctgctgtg aggtcctgag tacaagggcc aagtcacgtc caggaggcag catctcacag 6660

tacttacccc cagtctctgg ctcgaacatc cttcccacca tcccccttca tcatgttcct 6720

taagctt 6727



2
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


2

cccaagcaat ttattctctc 20



3
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


3

tcagcaaagg aagagcgcag 20



4
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


4

cactgtgctc atgggaatct 20



5
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


5

actttacctc attgcttgtc 20



6
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


6

tcagagcggt atagcaaggt 20



7
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


7

ctcatcgtct gcaaaggaaa 20



8
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


8

tatgagtagg gacaggaagc 20



9
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


9

atttttatga gtagggacag 20



10
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


10

acaaggaaaa taaagaataa 20



11
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


11

acaaggaaaa caaagagagg 20



12
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


12

ctggtgctga aagaagatta 20



13
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


13

ccacggacag tttgatcctt 20



14
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


14

aatgacaggt tttggaatag 20



15
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


15

gcggtcaatg tatttcttta 20



16
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


16

ggaacttact ttttggcggt 20



17
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


17

cagactgtca ggttggctcc 20



18
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


18

tcctcgccac acttctcctg 20



19
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


19

aactgcctcg tcctccgtct 20



20
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


20

tactcatcac accaaggaac 20



21
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


21

ctcagcctca gccttccatt 20



22
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


22

ttaaattgtg aagtcctgtc 20



23
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


23

aaatataaat ggaaacagca 20



24
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


24

ctacaggaca taaatataaa 20



25
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


25

tatacaaaaa ggttaaacac 20



26
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


26

ggttatcctt ggctacatta 20



27
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


27

aactgcctcc tcctccgtct 20



28
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


28

aactgccacc tgctccgtct 20



29
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


29

aactggcacc tgcaccgtct 20



30
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


30

ggttatccta ggctacatta 20



31
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


31

ggttatcgta gcctacatta 20



32
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


32

ggttaacgta gccaacatta 20



33
29
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


33

agtgttctga ctctcagctg tgtctgggc 29



34
24
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


34

ttcagagtca tgagaaggat gctt 24



35
22
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


35

accactgtgc tcatgggaat ct 22



36
27
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


36

aaggccgaga atgggaagct tgtcatc 27



37
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


37

ggcaaattca acggcacagt 20



38
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


38

gggtctcgct cctggaagat 20



39
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


39

ctttggcaaa gaaagtgcat 20



40
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


40

cgttctgcgt ttgcctttgg 20



41
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


41

tcctcatggc tctgaaacgt 20



42
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


42

aagaaaatta cctcattggc 20



43
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


43

ttacagcaca ccagcattca 20



44
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


44

tcctcagagt ctggagagga 20



45
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


45

ggaacaggaa tcctcagagt 20



46
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


46

tttaacttac atttttatgt 20



47
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


47

tttacttatt catgccatca 20



48
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


48

gacacgatgc tctttgggaa 20



49
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


49

cattttaata tgaccaggca 20



50
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


50

ttctaggcaa caaaccacca 20



51
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


51

acagttggtg ctaaatgagg 20



52
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


52

ttcttcagtg cacagttggt 20



53
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


53

acccccttgc acagtttgac 20



54
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


54

tggccgtcaa tgtatttctt 20



55
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


55

tgtaacttac tttttggccg 20



56
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


56

tccatagaaa taggcacagc 20



57
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


57

cacacttttt ctgtgaaaaa 20



58
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


58

attggtttac tctccgtctt 20



59
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


59

ttatccactc ggtgttcatt 20



60
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


60

tccttctcct ccaaaatctt 20



61
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


61

tggccctcat tctcactgca 20



62
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


62

tctggcaaag tgtcagtatg 20



63
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


63

ttgcctggag gaaaatactt 20



64
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


64

ctttggcaaa gaaagtgcat 20



65
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


65

cgttctgcgt ttgcctttgg 20



66
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


66

aagaaaatta cctcattggc 20



67
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


67

tcctcagagt ctggagagga 20



68
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


68

tttaacttac atttttatgt 20



69
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


69

acagttggtg ctaaatgagg 20



70
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


70

tgtaacttac tttttggccg 20



71
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


71

cacacttttt ctgtgaaaaa 20



72
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


72

tctggcaaac tgtcagtatg 20



73
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


73

tctggcatac tctcagtatg 20



74
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


74

tctgggatac tctgagtatg 20



75
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


75

ttgcctggac gaaaatactt 20



76
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


76

ttgcctgcac gtaaatactt 20



77
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


77

ttgccagcac gtatatactt 20



78
3230
DNA
Homo sapiens

78

atcctaatca agaccccagt gaacagaact cgaccctgcc aaggcttggc atttccattt 60

caatcactgt cttcccacca gtattttcaa tttcttttaa gacagattaa tctagccaca 120

gtcatagtag aacatagccg atcttgaaaa aaaacattcc caatatttat gtattttagc 180

ataaaattct gtttagtggt ctaccttata ctttgttttg cacacatctt ttaagaggaa 240

gttaattttc tgattttaag aaatgcaaat gtggggcaat gatgtattaa cccaaagatt 300

ccttccgtaa tagaaaatgt ttttaaaggg gggaaacagg gatttttatt attaaaagat 360

aaaagtaaat ttatttttta agatataagg cattggaaac atttagtttc acgatatgcc 420

attattaggc attctctatc tgattgttag aaattattca tttcctcaaa gacagacaat 480

aaattgactg gggacgcagt cttgtactat gcactttctt tgccaaaggc aaacgcagaa 540

cgtttcagag ccatgaggat gcttctgcat ttgagtttgc tagctcttgg agctgcctac 600

gtgtatgcca tccccacaga aattcccaca agtgcattgg tgaaagagac cttggcactg 660

ctttctactc atcgaactct gctgatagcc aatgaggtaa ttttctttat gattcctaca 720

gtctgtaaag tgcataggta atcatttgtg atggttcctt tactatatat agagatctgt 780

tataaataat aagattctga gcacattagt acatgggtga taactacatc accagcaaac 840

attctgttaa aagttatgaa tgctggtgtg ctgtaaaaat gattgtattt cctttcctct 900

ccagactctg aggattcctg ttcctgtaca taaaaatgta agttaaatta tgattcagta 960

aaatgatggc atgaataagt aaatttcctg ttttaagctg taaatcatta gttatcattg 1020

gaactattta attttctata ttttgttttc atatgggtgg ctgtgaatgt ctgtacttat 1080

aaatatgagg aatgactttt tatcaagtag aatcctttaa acaagtggat taggctcttt 1140

ggtgatgttg ttagtttgcc ttcccaaaga gcatcgtgtc aggattcttt ccagaaggat 1200

tccacactga gtgagaggtg cgtgctagtc tccgtgcagt tctgactctt tctcactcta 1260

acgtgtttct gaaagtatta gcaactcaga attatatttt tagaaccatg atcagtagac 1320

attaaaatat ataacaaatg ccctatatta ataattctgc atacttaaat aattatgact 1380

atatgatggt gtgtatgcat tgaatatgcc tggtcatatt aaaatgtaaa atatatagtt 1440

tattagtcta aatagaataa aactaccagc tagaactgta gaaacacatt gatatgagtt 1500

taatgtataa tgcattacac ttccaaaaca tttttttcca gttacataat taagttatat 1560

cctttataaa actcctcagt aatcatataa gcttcatcta ctttttgaaa attttatctt 1620

aatatgtggt ggtttgttgc ctagaaaaca aacaaaaaac tctttggaga agggaactca 1680

tgtaaatacc acaaaacaaa gcctaacttt gtggaccaaa attgttttaa taattatttt 1740

ttaattgatg aattaaaaag tatatatatt tattgtgtac aatatgatgt tttgaagtat 1800

gtatacattg cagaatggac aatggaccaa atttttatac cttgtcttga ttatttgcat 1860

tttaaaaatt ttcctcattt agcaccaact gtgcactgaa gaaatctttc agggaatagg 1920

cacactggag agtcaaactg tgcaaggggg tactgtggaa agactattca aaaacttgtc 1980

cttaataaag aaatacattg acggccaaaa agtaagttac acacattcaa tggaagctat 2040

atttgtcctg gctgtgccta tttctatgga attgacagtt tcctgtaata cctattgtca 2100

tttttctttt ttcacagaaa aagtgtggag aagaaagacg gagagtaaac caattcctag 2160

actacctgca agagtttctt ggtgtaatga acaccgagtg gataatagaa agttgagact 2220

aaactggttt gttgcagcca aagattttgg aggagaagga cattttactg cagtgagaat 2280

gagggccaag aaagagtcag gccttaattt tcaatataat ttaacttcag agggaaagta 2340

aatatttcag gcatactgac actttgccag aaagcataaa attcttaaaa tatatttcag 2400

atatcagaat cattgaagta ttttcctcca ggcaaaattg atatactttt ttcttattta 2460

acttaacatt ctgtaaaatg tctgttaact taatagtatt tatgaaatgg ttaagaattt 2520

ggtaaattag tatttattta atgttatgtt gtgttctaat aaaacaaaaa tagacaactg 2580

ttcaatttgc tgctggcctc tgtccttagc aatttgaagt tagcacagtc cattgagtac 2640

atgcccagtt tggaggaagg gtctgagcac atgtggctga gcatccccat ttctctggag 2700

aagtctcaag gttgcaaggc acaccagagg tggaagtgat ctagcaggac ttagtgggga 2760

tgtggggagc agggacacag gcaggaggtg aacctggttt tctctctaca gtatatccag 2820

aacctgggat ggtcgaaggg taaatggtag ggaataaatg aatgaatgtc gtttccaaga 2880

tgattgtaga actaaaatga gttgtaagct cccctggaag aagggatgtg gaacctgtaa 2940

ctaggttcct gcccagcctg tgagaagaat ttggcagatc atctcattgc cagtatagag 3000

aggaagccag aaaccctctc tgccaaggcc tgcaggggtt cttaccacct gaccctgcac 3060

cataacaaaa ggacagagag acatggtagg gcagtcccat tagaaagact gagttccgta 3120

ttcccggggc agggcagcac caggccgcac aacatccatt ctgcctgctt atggctatca 3180

gtagcatcac tagagattct tctgtttgag aaaacttctc tcaaggatcc 3230



79
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


79

gacctgtcca gtgagcttct 20



80
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


80

tagccgaata ctggaaaggt 20



81
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


81

aacacaggca ccatggtagc 20



82
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


82

ctcttggtca ggatttgggt 20



83
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


83

tcctcacgct agctgcaaag 20



84
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


84

atggccttaa gtgggtgtgg 20



85
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


85

gagccattaa tgtgcacagc 20



86
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


86

tccactcgcc ccaccttcct 20



87
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


87

aacaagacga agcaggcagc 20



88
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


88

ccggaaccgg tggaaacaac 20



89
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


89

ccaacctctt ccacacaatg 20



90
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


90

tcccatgact tcaaatccaa 20



91
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


91

gcaaaatgcc atcaaaacgt 20



92
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


92

cgagctctac caccgcctgg 20



93
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


93

caagctggcc tcgaactcag 20



94
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


94

ggatgggttg gtgacttgca 20



95
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


95

tgaggaaacc aaaggcccat 20



96
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


96

tgtctcccac ttgcgtcagg 20



97
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


97

ttgaacaggc ctatggaaca 20



98
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


98

tctttttcac cccaggcacg 20



99
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


99

aattcccatg gatcctcttg 20



100
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


100

atccagcaat cacctccaaa 20



101
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


101

tgttcagccc atcaaaaaga 20



102
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


102

atttggctga caggaccccg 20



103
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


103

tccagagact gccccaccca 20



104
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


104

catctgcttc tgtattgcca 20



105
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


105

ccttttagct ccttgggtac 20



106
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


106

catttctgag ggttgctggg 20



107
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


107

catctgattg tgtcttgcca 20



108
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


108

catctgcttg tgtattgcca 20



109
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


109

cacctgattg tgtcttgtca 20



110
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


110

tgtccctcct tttggtgggg 20



111
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


111

ttagctctgt ctctgctgat 20



112
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


112

aactgctggc cagagttgta 20



113
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


113

catagttaaa gcaatgatct 20



114
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


114

gtttctcata ttcagtaacc 20



115
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


115

ggagtcctgt atgagttcat 20



116
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


116

tctgtgcatc ccaggtgctg 20



117
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


117

ctggctgtcc tggaactcac 20



118
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


118

ttcaaggtaa gtcaagcaac 20



119
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


119

ctgatggcta ccactggcaa 20



120
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


120

cactctcaat gagttctatc 20



121
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


121

tgatgctggt tgatcaatct 20



122
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


122

tcaataggga atggtgtctt 20



123
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


123

ttccagagta cctagaagcc 20



124
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


124

ccaacaggtt gccatgaagg 20



125
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


125

agagattaga attgactaag 20



126
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


126

actattgcat atactagcaa 20



127
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


127

ccatccaata tacaaccacc 20



128
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


128

ctcatggaag gagttacaga 20



129
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


129

tgtggatact tcactgcttc 20



130
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


130

atccaataga tgactgtgag 20



131
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


131

gttcatattg ttgttcctgc 20



132
3571
DNA
Mus musculus

132

gaaataattg gtaaacacag aaaatgtttc aatagaaaaa agaggaaaca gaacactgtg 60

tagccctgtt atcagcagag acagagctaa cgctggggat accaaactag aagaagctca 120

ctggacaggt cccggtatgc agttctattt ttgttgatgg ctctgtatct aatgtgttca 180

tttgtaccaa ggatctaacc agggtcttcc agagtctgag caagcttctc ccactgagct 240

acatcacagc cccctgttta ttggaagaag aaatacttac acctttccag tattcggcta 300

ccatggtgcc tgtgttacta attcttgtgg gagctttggc aacactgcaa gctgacttac 360

ttaatcacaa aaagttttta cttctaccac ctgtcaattt taccattaaa gccactggat 420

tagctcaagt tcttttacac tgggacccaa atcctgacca agagcaaagg catgttgatc 480

tagagtatca cgtgaaaata aatgccccac aagaagacga atatgatacc agaaagactg 540

aaagcaaatg tgtgaccccc cttcatgaag gctttgcagc tagcgtgagg accattctga 600

agagcagcca tacaactctg gccagcagtt gggtttctgc tgaactcaaa gctccaccag 660

gatctcctgg aacctcggtt acgaatttaa cttgtaccac acacactgtt gtaagtagcc 720

acacccactt aaggccatac caagtgtccc ttcgttgcac ctggcttgtt gggaaggatg 780

cccctgagga cacacagtat ttcctatact acaggtttgg tgttttgact gaaaaatgcc 840

aagaatacag cagagatgca ctgaacagaa atactgcatg ctggtttccc aggacattta 900

tcaacagcaa agggtttgaa cagcttgctg tgcacattaa tggctcaagc aagcgtgctg 960

caatcaagcc ctttgatcag ctgttcagtc cacttgccat tgaccaagtg aatcctccaa 1020

ggaatgtcac agtggaaatt gaaagcaatt ctctctatat acagtgggag aaaccacttt 1080

ctgcctttcc agatcattgc tttaactatg agctgaaaat ttacaacaca aaaaatggtc 1140

acattcagaa ggaaaaactg atcgccaata agttcatctc aaaaattgat gatgtttcta 1200

catattccat tcaagtgaga gcagctgtga gctcaccttg cagaatgcca ggaaggtggg 1260

gcgagtggag tcaacctatt tatgtgggaa aggaaaggaa gtccttggta gaatggcatc 1320

tcattgtgct cccaacagct gcctgcttcg tcttgttaat cttctcactc atctgcagag 1380

tgtgtcattt atggaccagg ttgtttccac cggttccggc cccaaagagt aacatcaaag 1440

atctccctgt ggttactgaa tatgagaaac cttcgaatga aaccaaaatt gaagttgtac 1500

attgtgtgga agaggttgga tttgaagtca tgggaaattc cacgttttga tggcattttg 1560

ccattctgaa atgaactcat acaggactcc gtgataagag caaggactgc tatttcttgg 1620

caaggaggta tttcaaatga acactcagag ccaggcggtg gtagagctcg cctttaatac 1680

cagcacctgg gatgcacaga cgggaggatt tctgagttcg aggccagctt ggtctataaa 1740

gtgagttcca ggacagccag agctacacag agaaaccctg tctcgaaaaa acaaacaaac 1800

aaacaaacaa acaaaaatga acactcaatt tgaatgcaag tcaccaaccc atccagacat 1860

gagtcaccaa tgtcccattt cataaagtgt gcatgcctca ctcaaacctc cttgctcaca 1920

gcatagcacc agactcaccc agagcatggg cctttggttt cctacccaga gtaccatgtt 1980

ataccagtgt gtctttgaaa gttgcttgac ttaccttgaa ctttttgcac aggagacagt 2040

ttttttaagc taatgtcaca catgtttact ttgggttaag ttgccagtgg tagcactcag 2100

ctacagtgac aggaggaaag gatagaactc attgagagtg aacccaaatt caagactgtc 2160

tttcctgacg caagtgggag acacaatttc atggtgcttt tcccctttca gttctagaat 2220

agtttccttt ctagaactgt gcctgtgtct taaagcataa ggtaacattg aggcaaaaac 2280

aaagactatg tcccacatgt ccctgtgttc cataggcctg ttcaaggaaa tgtctaagcc 2340

aaagtaagtt taagtcaccg tgcctggggt gaaaaagatg gttcagatga cgaagaagca 2400

tgagggcctg agattgatca accagcatca agaaacaaca acaacaacag cagcagcaac 2460

aacaaaacag tgcaagaagc acattcctat aaccccagag ttgggagata aagacaagag 2520

gatccatggg aattgtagtt caaccagttt agccaattat gttatctcta ggttcactga 2580

gagaaatggt cttaaaaatt taaggtggag agtgactagg cagatcctct gatactgact 2640

tctgccctaa atatgcatac acatgtacac acacaacaca aagacaccat tccctattga 2700

gagagaagac agaagcttgt tcaaggatta aattcttcaa ggcttctagg tactctggaa 2760

atgacctgag aaagacattg aaaataattc tgctttggag gtgattgctg gatctagaat 2820

gtacttccca aagagatgtt gatgaaagag ccttcatggc aacctgttgg tcaactcatg 2880

cttagtcaat tctaatctct taaattaggg tttcctatac atattacaat tgtataaaaa 2940

tgtattctct aaatatcttc attaatgaag ctgtatctat aggtcttttt gatgggctga 3000

acatagaagc aaacacactt atgtgttggg aagaggaata agtagtgata gagggaccta 3060

gtggtagtta ttttacatag tcctgaagag ctaaagacaa tgaaagaaga aatggtactc 3120

acaagagaga gagctatgtc ggggtcctgt cagccaaatc ttgctagtat atgcaatagt 3180

gtctgggttt ggtggttgta tattggatgg ttccctgggt ggggcagtct ctggatggtc 3240

tttccttcca tcacagctct gaaatttgtc tctgtaactc cttccatgag tattttgttc 3300

cccattctaa gaagcagtga agtatccaca ctttggtctt ccttcttctt gagtttcatg 3360

tgttttgcaa attgtgtgcc tggcaataca gaagcagatg ctcacagtca tctattggat 3420

gaaacacagg gcccctaatg aaggagccag agaaagtacc caaggagcta aaagggtctg 3480

caaccctata gcaggaacaa caatatgaac tacccagcaa ccctcagaaa tgtaaatgaa 3540

gaaaatatct aataaaaaaa aaaaaaaaaa a 3571



133
965
DNA
Mus musculus

133

gccttggaga ctgtcactgt cagggctgat gacggatgag ctgggtcagg ctagatagac 60

cctagcaatt tattagagcc agactcctag gcaattctct ctctacatgt tcacttaagg 120

gttcagagct tcataacaaa gcagaagtca ggagtctcag aaatgcactt caaaatcagg 180

gtggaggaac ctgcccatgt gtcaggccct gtgacctatc aactcacaag ccttctgttg 240

ggatattgac caaacacagt atctttgctt atatgcaagc acacacttgc gtgcaacaca 300

cacacacaca cacacacaca cacacacaca cacacacaca cacacaccag gctaaagctc 360

gcagagttct cagattgtgg tatatgaagg agcaagcctt tgtcagtgaa cagtatgatc 420

actaagactc tagtgtgggc cctctctaat gggttgctct cttgggaatc ttcttccaaa 480

gagcagttgt gtggtctttc cattgtaaga gaaactgcag gtgtcttctt aaccatgaca 540

gttctgatga tgaaagtgta aagaacccgc cttaaagtca aacaccagtg cacccagaaa 600

gtagatgcac agctgcaggc tcagagctcg gcagccactg tacttcttag taaccaggaa 660

tcaaacgttt gactcactgt ggggttggta gggcagataa ataccttttt ctatgactag 720

gctggagaca cgcccaggac ccccaccaaa aggagggaca ggaaaagaga aataattggt 780

aaacacagaa aatgtttcaa tagaaaaaag aggaaacaga acactgtgta gccctgttat 840

cagcagagac agagctaacg ctggggatac caaactagaa gaagctcact ggacaggtcc 900

cggtatgcag ttctattttt gttgatggct ctgtatctaa tgtgttcatt tgtaccaagg 960

tgagt 965



134
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


134

caaggacttc ctttcctttc 20



135
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


135

gccattctac caaggacttc 20



136
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


136

acaatgagat gccattctac 20



137
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


137

tgttgggagc acaatgagat 20



138
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


138

agcaggcagc tgttgggagc 20



139
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


139

tgagaagatt aacaagacga 20



140
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


140

tgcagatgag tgagaagatt 20



141
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


141

actctgcaga tgagtgagaa 20



142
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


142

gacttccttt cctttcctgg 20



143
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


143

aacaagacga agcaggcagc 20



144
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


144

ctacactctg cagatgagtg 20



145
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


145

cgatcagttt ttccttctaa 20



146
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


146

tcacccacat aaataggttg 20



147
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


147

ggtccataaa tgacacctga 20



148
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


148

ttacctcata ttcagtaacc 20



149
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


149

gccattctat caaggacttc 20



150
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


150

gccatgctat caagcacttc 20



151
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


151

gctatcctat caagcacgtc 20



152
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


152

gacttcctta cctttcctgg 20



153
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


153

gacttcctct tcttccctgg 20



154
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


154

gacctctttc cctcttctgg 20



155
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


155

gtttttcctt ctgaatgtga 20



156
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


156

ctttcctttc ccacataaat 20



157
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


157

taaatgacac actctgcaga 20



158
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


158

taaatgacac ccacataaat 20



159
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


159

tcgaaggttt ccacataaat 20



160
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


160

aaccactctc tcaagggctt 20



161
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


161

tgctggaatt ggtggaaaca 20



162
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


162

gtctcaactc caggcttctc 20



163
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


163

tcaaaacaca gaatcctcca 20



164
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


164

aggatgccaa agtgacagtc 20



165
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


165

atccctgttc ttttcactga 20



166
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


166

cgcaggtaaa ttgagtgttg 20



167
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


167

tgaggcgatt tggatgaagc 20



168
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


168

tggacgttag ccttaaaagc 20



169
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


169

agcttaaaca gccaaacggg 20



170
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


170

ctccaggctg atgcaaaatg 20



171
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


171

gggtgaggaa tttgtggctc 20



172
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


172

ctggatcagg cctctggagc 20



173
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


173

gggtgaggat tttgtggctc 20



174
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


174

gggtgatgat ttggtggctc 20



175
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


175

ggctgatgat ttggtgggtc 20



176
2006
DNA
Homo sapiens

176

cggtcctcgc catcttctgt tgagtactgg tcggaacaag aggatcgtct gtagacagga 60

tatgatcatc gtggcgcatg tattactcat ccttttgggg gccactgaga tactgcaagc 120

tgacttactt cctgatgaaa agatttcact tctcccacct gtcaatttca ccattaaagt 180

tactggtttg gctcaagttc ttttacaatg gaaaccaaat cctgatcaag agcaaaggaa 240

tgttaatcta gaatatcaag tgaaaataaa cgctccaaaa gaagatgact atgaaaccag 300

aatcactgaa agcaaatgtg taaccatcct ccacaaaggc ttttcagcaa gtgtgcggac 360

catcctgcag aacgaccact cactactggc cagcagctgg gcttctgctg aacttcatgc 420

cccaccaggg tctcctggaa cctcagttgt gaatttaact tgcaccacaa acactacaga 480

agacaattat tcacgtttaa ggtcatacca agtttccctt cactgcacct ggcttgttgg 540

cacagatgcc cctgaggaca cgcagtattt tctctactat aggtatggct cttggactga 600

agaatgccaa gaatacagca aagacacact ggggagaaat atcgcatgct ggtttcccag 660

gacttttatc ctcagcaaag ggcgtgactg gcttgcggtg cttgttaacg gctccagcaa 720

gcactctgct atcaggccct ttgatcagct gtttgccctt cacgccattg atcaaataaa 780

tcctccactg aatgtcacag cagagattga aggaactcgt ctctctatcc aatgggagaa 840

accagtgtct gcttttccaa tccattgctt tgattatgaa gtaaaaatac acaatacaag 900

gaatggatat ttgcagatag aaaaattgat gaccaatgca ttcatctcaa taattgatga 960

tctttctaag tacgatgttc aagtgagagc agcagtgagc tccatgtgca gagaggcagg 1020

gctctggagt gagtggagcc aacctattta tgtgggaaat gatgaacaca agcccttgag 1080

agagtggttt gtcattgtga ttatggcaac catctgcttc atcttgttaa ttctctcgct 1140

tatctgtaaa atatgtcatt tatggatcaa gttgtttcca ccaattccag caccaaaaag 1200

taatatcaaa gatctctttg taaccactaa ctatgagaaa gctgggtcca gtgagacgga 1260

aattgaagtc atctgttata tagagaagcc tggagttgag accctggagg attctgtgtt 1320

ttgactgtca ctttggcatc ctctgatgaa ctcacacatg cctcagtgcc tcagtgaaaa 1380

gaacagggat gctggctctt ggctaagagg tgttcagaat ttaggcaaca ctcaatttac 1440

ctgcgaagca atacacccag acacaccagt cttgtatctc ttaaaagtat ggatgcttca 1500

tccaaatcgc ctcacctaca gcagggaagt tgactcatcc aagcattttg ccatgttttt 1560

tctccccatg ccgtacaggg tagcacctcc tcacctgcca atctttgcaa tttgcttgac 1620

tcacctcaga cttttcattc acaacagaca gcttttaagg ctaacgtcca gctgtattta 1680

cttctggctg tgcccgtttg gctgtttaag ctgccaattg tagcactcag ctaccatctg 1740

aggaagaaag cattttgcat cagcctggag tgaatcatga acttggattc aagactgtct 1800

tttctatagc aagtgagagc cacaaattcc tcacccccct acattctaga atgatctttt 1860

tctaggtaga ttgtgtatgt gtgtgtatga gagagagaga gagagagaga gagagagaga 1920

gagaaattat ctcaagctcc agaggcctga tccaggatac atcatttgaa accaactaat 1980

ttaaaagcat aatagagcta atatat 2006



177
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


177

cctgagaaat gcggtggcca 20



178
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


178

gtgtctatgc tcgtggctgc 20



179
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


179

cgatcctctt gttccgacca 20



180
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


180

atgcgccacg atgatcatat 20



181
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


181

gcagtatctc agtggccccc 20



182
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


182

tgctcttgat caggatttgg 20



183
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


183

caggatggtc cgcacacttg 20



184
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


184

gggcatgaag ttcagcagaa 20



185
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


185

gccaggtgca gtgaagggaa 20



186
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


186

ctccccagtg tgtctttgct 20



187
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


187

aagccagtca cgccctttgc 20



188
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


188

aaacagctga tcaaagggcc 20



189
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


189

atggattgga aaagcagaca 20



190
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


190

tctgcacatg gagctcactg 20



191
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


191

aggttggctc cactcactcc 20



192
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


192

tctgcacatg tagctcactg 20



193
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


193

tctgcacgtg taactcactg 20



194
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


194

tatgcacgtg taactccctg 20



195
1998
DNA
Homo sapiens

195

ccgctgcttc tcatcgcatg gccaccgcat ttctcaggcc aggcacattg agcattggtc 60

ctgtgcctga cgctatgcta gatgctgggg ttgcagccac gagcatagac acgacagaca 120

cggtcctcgc catcttctgt tgagtactgg tcggaacaag aggatcgtct gtagacaggc 180

tacagattgt tttagattga agtttcctgt catgttcact catctttaaa tcctcatagt 240

aaaaaggata tgatcatcgt ggcgcatgta ttactcatcc ttttgggggc cactgagata 300

ctgcaagctg acttacttcc tgatgaaaag atttcacttc tcccacctgt caatttcacc 360

attaaagtta ctggtttggc tcaagttctt ttacaatgga aaccaaatcc tgatcaagag 420

caaaggaatg ttaatctaga atatcaagtg aaaataaacg ctccaaaaga agatgactat 480

gaaaccagaa tcactgaaag caaatgtgta accatcctcc acaaaggctt ttcagcaagt 540

gtgcggacca tcctgcagaa cgaccactca ctactggcca gcagctgggc ttctgctgaa 600

cttcatgccc caccagggtc tcctggaacc tcaattgtga atttaacttg caccacaaac 660

actacagaag acaattattc acgtttaagg tcataccaag tttcccttca ctgcacctgg 720

cttgttggca cagatgcccc tgaggacacg cagtattttc tctactatag gtatggctct 780

tggactgaag aatgccaaga atacagcaaa gacacactgg ggagaaatat cgcatgctgg 840

tttcccagga cttttatcct cagcaaaggg cgtgactggc tttcggtgct tgttaacggc 900

tccagcaagc actctgctat caggcccttt gatcagctgt ttgcccttca cgccattgat 960

caaataaatc ctccactgaa tgtcacagca gagattgaag gaactcgtct ctctatccaa 1020

tgggagaaac cagtgtctgc ttttccaatc cattgctttg attatgaagt aaaaatacac 1080

aatacaagga atggatattt gcagatagaa aaattgatga ccaatgcatt catctcaata 1140

attgatgatc tttctaagta cgatgttcaa gtgagagcag cagtgagctc catgtgcaga 1200

gaggcagggc tctggagtga gtggagccaa cctatttatg tgggaaatga tgaacacaag 1260

cccttgagag agtggtttgt cattgtgatt atggcaacca tctgcttcat cttgttaatt 1320

ctctcgctta tctgtaaaat atgtcattta tggatcaagt tgtttccacc aattccagca 1380

ccaaaaagta atatcaaaga tctctttgta accactaact atgagaaagc tgggtccagt 1440

gagacggaaa ttgaagtcat ctgttatata gagaagcctg gagttgagac cctggaggat 1500

tctgtgtttt gactgtcact ttggcatcct ctgatgaact cacacatgcc tcagtgcctc 1560

agtgaaaaga acagggatgc tggctcttgg ctaagaggtg ttcagaattt aggcaacact 1620

caatttacct gcgaagcaat acacccagac acaccagtct tgtatctctt aaaagtatgg 1680

atgcttcatc caaatcgcct cacctacagc agggaagttg actcatccaa gcattttgcc 1740

atgttttttc tccccatgcc gtacagggta gcacctcctc acctgccaat ctttgcaatt 1800

tgcttgactc acctcagact ttcattcaca acagacagct tttaaggcta acgtccagct 1860

gtatttactt ctggctgtgc cgtttggctg tttaagctgc caattgtagc actcagctac 1920

catctgagga agaaagcatt ttgcatcagc ctggagtgaa ccatgaactt ggattcaaga 1980

ctgtcttttc tatagcaa 1998



196
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


196

acccagcttt ctgcaaaaca 20



197
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


197

tcaacattac ctcatagtta 20



198
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


198

taaatgacat ctgaaaacag 20



199
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


199

gaacacttac attttacaga 20



200
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


200

tcatcatttc ctggtggaaa 20



201
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


201

tcatcattta ctggtggaaa 20



202
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


202

tcagcattta ctggtgtaaa 20



203
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


203

tcagcagtta cttgtgtaaa 20



204
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


204

agcggcagag cattgagaac 20



205
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


205

agcggcagag cattgagaac 20



206
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


206

gaagcagcgg cagagcattg 20



207
20
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


207

gaagcagcgg cagagcattg 20



208
612
DNA
Homo sapiens

208

ggtaccagac ctgctcacaa agcagagaag agctaaggcg gttctctaag ggcagagaat 60

tgctgctatt gcctagtgag tggggagagg gtactcctca ggccttactt cctatcaaat 120

catgtgtcag tgttgcctag gagacagagg cacagtaact actgtagcca aacaaggcac 180

ataaacaaaa cagaaatgca acgctttaga gtacccacgg aaaacttgtt taccttgtca 240

ccatgagtaa aagttaattc ccactcctga agagagcaaa ccaactctga aagagagtga 300

aaatgcagac aagacagtta tcagataatg gctatctgga cgagagattc tttcgtttga 360

cagcagtttg gttgttggga gttccagttc agctcctgca cagttgctct gtacaaatcc 420

tcctccatat ttgcttagag aaaacgtgtt gccatcccat catgaaggaa gctgcctgag 480

agtttttaac cattacagcc gtgatgatga aagagtgaag aaccgcctct aagttaaaaa 540

gtgcacccag agataaggtt cgttctcaat gctctgccgc tgcttctcat cgcatggcca 600

ccgcatttct ca 612



209
15
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


209

tctaccaagg acttc 15



210
15
DNA
Artificial Sequence

Description of Artificial SequenceSynthetic


210

tcaacctaga acttc 15