Claims
- 1. A viral vector comprising an expression cassette, wherein the expression cassette comprises a pot II promoter operably-linked to a nucleic acid sequence encoding a small interfering RNA molecule (siRNA) targeted against a gene of interest.
- 2. The viral vector of claim 1, wherein the siRNA forms a hairpin structure comprising a duplex structure and a loop structure.
- 3. The viral vector of claim 2, wherein the loop structure contains from 4 to 10 nucleotides.
- 4. The viral vector of claim 2, wherein the loop structure contains 4, 5 or 6 nucleotides.
- 5. The viral vector of claim 2, wherein the duplex is less than 30 nucleotides in length.
- 6. The viral vector of claim 2, wherein the duplex contains from 19 to 25 nucleotides.
- 7. The viral vector of claim 2, wherein the siRNA further comprises a 3′ overhang region or a 5′ overhang region.
- 8. The viral vector of claim 7, wherein the overhang region is from 1 to 10 nucleotides in length.
- 9. The viral vector of claim 1, wherein the pol II promoter is regulatable.
- 10. The viral vector of claim 1, wherein the pol II promoter is a constitutive promoter.
- 11. The viral vector of claim 1, wherein the pol II promoter is a CMV or RSV promoter.
- 12. The viral vector of claim 11, wherein the pol II promoter is a CMV promoter.
- 13. The viral vector of claim 11, wherein the promoter is a RSV promoter.
- 14 The viral vector of claim 1, wherein the expression cassette further comprises a polyadenylation signal.
- 15. The viral vector of claim 14, wherein the polyadenylation signal is a synthetic minimal polyadenylation signal.
- 16. The viral vector of claim 1, wherein the nucleic acid sequence further comprises a marker gene.
- 17. The viral vector of claim 1, wherein the viral vector is an adenoviral, lentiviral, adeno-associated viral (AAV), poliovirus, HSV, or murine Maloney-based viral vector.
- 18. The viral vector of claim 1, wherein the viral vector is an adenoviral vector.
- 19. The viral vector of claim 1, wherein the gene of interest is a gene associated with a condition amenable to siRNA therapy.
- 20. The viral vector of clam 19, wherein the condition amenable to siRNA therapy is a neurodegenerative disease.
- 21. The viral vector of claim 20, wherein the neurodegenerative disease is a trinucleotide-repeat disease.
- 22. The viral vector of claim 21, wherein the trinucleotide-repeat disease is a disease associated with polyglutamine repeats.
- 23. The viral vector of claim 21, wherein the trinucleotide-repeat disease is Huntington's disease or spinocerebellar ataxia.
- 24. The viral vector of claim 1, wherein the gene of interest encodes a ligand for a chemokine involved in the migration of a cancer cell, or a chemokine receptor.
- 25. A viral vector comprising an expression cassette, wherein the expression cassette comprises a pol II promoter operably-linked to a nucleic acid sequence encoding a first segment, a second segment located immediately 3′ of the first segment, and a third segment located immediately 3′ of the second segment, wherein the first and third segments are each less than 30 base pairs in length and each more than 10 base pairs in length, and wherein the sequence of the third segment is the complement of the sequence of the first segment, and wherein the nucleic acid sequence functions as a small interfering RNA molecule (siRNA) targeted against a gene of interest.
- 26. A method of reducing the expression of a gene product in a cell, comprising contacting a cell with viral vector comprising an expression cassette, wherein the expression cassette comprises a pol II promoter operably-linked to a nucleic acid sequence encoding a small interfering RNA molecule (siRNA) targeted against a gene, wherein expression from the targeted gene is reduced.
- 27. The method of claim 26, wherein the siRNA forms a hairpin structure comprising a duplex structure and a loop structure.
- 28. The method of claim 27, wherein the loop structure contains from 4 to 10 nucleotides.
- 29. The method of claim 27, wherein the loop structure contains 4, 5 or 6 nucleotides.
- 30. The method of claim 27, wherein the duplex is less than 30 nucleotides in length.
- 31. The method of claim 30, wherein the duplex is from 19 to 25 nucleotides in length.
- 32. The method of claim 26, wherein the siRNA further comprises an overhang region.
- 33. The method of claim 26 wherein the siRNA further comprises a 3′ overhang region or a 5′ overhang region.
- 34. The method of claim 33, wherein the overhang region is from 1 to 10 nucleotides in length.
- 35. The method of claim 26, wherein the pol II promoter is regulatable.
- 36. The method of claim 26, wherein the pol II promoter is a constitutive promoter.
- 37. The method of claim 26, wherein the pol II promoter is a CMV or RSV promoter.
- 38. The method of claim 37, wherein the pol II promoter is a CMV promoter.
- 39. The method of claim 37, wherein the pol II promoter is a RSV promoter.
- 40. The method of claim 26, wherein the expression cassette further comprises a polyadenylation signal.
- 41. The method of claim 40, wherein the polyadenylation signal is a synthetic minimal poyladenylation signal.
- 42. The method of claim 26, wherein the nucleic acid sequence further comprises a marker gene.
- 43. The method of claim 26, wherein the viral vector is an adenoviral, lentiviral, adeno-associated viral (AAV), poliovirus, HSV, or murine Maloney-based viral vector.
- 44. The method of claim 26, wherein the viral vector is an adenoviral vector.
- 45. The method of claim 26, wherein the expression is from a gene associated with a neurodegenerative disease.
- 46. The method of claim 45, wherein the neurodegenerative disease is a trinucleotide-repeat disease.
- 47. The method of claim 46, wherein the trinucleotide-repeat disease is a disease associated with polyglutamine repeats.
- 48. The method of claim 47, wherein the trinucleotide-repeat disease is Huntington's disease or spinocerebellar ataxia.
- 49. The method of claim 26, wherein the gene of interest encodes a ligand for a chemokine involved in the migration of a cancer cell, or a chemokine receptor.
- 50. A method of reducing the expression of a gene product in a cell, comprising contacting a cell with viral vector comprising an expression cassette, wherein the expression cassette comprises a pol II promoter operably-linked to a nucleic acid sequence encoding a first segment, a second segment located immediately 3′ of the first segment, and a third segment located immediately 3′ of the second segment, wherein the first and third segments are each less than 30 base pairs in length and each more than 10 base pairs in length, and wherein the sequence of the third segment is the complement of the sequence of the first segment, and wherein the nucleic acid sequence functions as a small interfering RNA molecule (siRNA) targeted against a gene of interest.
- 51. A method of treating a patient, comprising administering to the patient a composition comprising a viral vector, wherein the viral vector comprises an expression cassette, wherein the expression cassette comprises a pol II promoter operably-linked to a nucleic acid sequence encoding a small interfering RNA molecule (siRNA) targeted against a gene, wherein expression from the targeted gene is reduced.
- 52. A method of treating a patient, comprising administering to the patient a composition comprising a viral vector, wherein the viral vector comprises an expression cassette, wherein the expression cassette comprises a pol II promoter operably-linked to a nucleic acid sequence encoding a first segment, a second segment located immediately 3′ of the first segment, and a third segment located immediately 3′ of the second segment, wherein the first and third segments are each less than 30 base pairs in length and each more than 10 base pairs in length, and wherein the sequence of the third segment is the complement of the sequence of the first segment, and wherein the nucleic acid sequence functions as a small interfering RNA molecule (siRNA) targeted against a gene of interest.
CLAIM OF PRIORITY
[0001] This application is a continuation of U.S. Applicatoin Ser. No. 10/322,086 filed on Dec. 17, 2002, and a continuation-in-part application of U.S. application Ser. No. 10/212,322, filed Aug. 5, 2002.
Continuations (1)
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Number |
Date |
Country |
Parent |
10322086 |
Dec 2002 |
US |
Child |
10430351 |
May 2003 |
US |
Continuation in Parts (1)
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Number |
Date |
Country |
Parent |
10212322 |
Aug 2002 |
US |
Child |
10430351 |
May 2003 |
US |