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Last Updated: March 28, 2024

Claims for Patent: 7,696,406


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Summary for Patent: 7,696,406
Title:Expression of a recombinant transgene
Abstract: A system for expression of a heterologous polypeptide in a transgenic host cell is disclosed. The system is based upon a transgene comprising a eukaryotic promoter operably linked to a DNA sequence comprising, in the 5\' to 3\' direction, a DNA sequence complementary to a sequence encoding a heterologous polypeptide, a DNA sequence complementary to an internal ribosome entry site, and a DNA sequence corresponding to a 3\' untranslated region of a positive strand single-stranded RNA virus. Following introduction of a stimulus, the host cell synthesizes an RNA molecule complementary to a recombinant RNA encoded by the transgene. The stimulus can be a positive strand single-stranded RNA virus or a nucleic acid thereof. Because the complement of the recombinant RNA comprises an internal ribosome entry site and a sequence encoding a heterologous polypeptide, the host cell can synthesize the heterologous polypeptide.
Inventor(s): Allison; Richard F. (Leslie, MI)
Assignee: Board of Trustees Operating Michigan State University (East Lansing, MI)
Application Number:10/561,720
Patent Claims:1. A method of producing a heterologous polypeptide, the method comprising: a) providing a transgenic plant or a transgenic plant cell comprising a recombinant DNA molecule comprising, in the 5' to 3' direction, i) a plant promoter; ii) a sequence complementary to a coding sequence for a heterologous polypeptide; iii) a sequence complementary to a plant virus internal ribosome entry site; and iv) a 3' UTR sequence having a sequence encoding a viral RNA replication initiation site; b) growing the transgenic plant or transgenic plant cell; c) producing an RNA transcript of the DNA sequence in the transgenic plant or the transgenic plant cell, the RNA transcript being a complementary RNA copy of the DNA sequence; d) infecting the transgenic plant or the transgenic plant cell with an RNA nucleic acid encoding an RNA-dependent RNA polymerase operable to recognize the viral RNA replication initiation site and convert the RNA transcript produced by the transgenic plant or the transgenic plant cell to a translatable mRNA, the mRNA having a RNA sequence comprising, in the 5' to 3' direction: i) a sequence complementary to the 3' UTR sequence; ii) a coding sequence of the plant virus internal ribosome entry site; and iii) a coding sequence of the heterologous polypeptide; and e) translating the translatable mRNA in the transgenic plant or the transgenic plant cell to form the heterologous polypeptide.

2. The method of producing a heterologous polypeptide of claim 1, wherein the plant promoter is a selected from the group consisting of a constitutive promoter and an inducible promoter.

3. The method of producing a heterologous polypeptide of claim 2, wherein the constitutive promoter is a cauliflower mosaic virus 35S promoter.

4. The method of producing a heterologous polypeptide of claim 1, wherein the coding sequence for the heterologous polypeptide encodes a polypeptide selected from the group consisting of a hormone, an enzyme, a cell toxin, a viral polypeptide, a cell surface polypeptide, and an intracellular polypeptide.

5. The method of producing a heterologous polypeptide of claim 1, wherein the internal ribosome entry site is selected from the group consisting of a turnip mosaic potyvirus IRES, a tobamovirus IRES, and a hibiscus chlorotic ringspot virus IRES.

6. The method of producing a heterologous polypeptide of claim 1, wherein the sequence complementary to an internal ribosome entry site is a sequence complementary to a picornavirus internal ribosome entry site.

7. The method of producing a heterologous polypeptide of claim 1, wherein the 3' UTR sequence is obtained from a positive strand single-stranded RNA plant virus RNA with no DNA stage.

8. The method of producing a heterologous polypeptide of claim 1, further comprising a sequence complementary to an intron.

9. The method of producing a heterologous polypeptide of claim 1, wherein said DNA sequence further comprises a transcription termination signal sequence.

10. The method of producing a heterologous polypeptide of claim 1, wherein the transgenic plant is a dicotyledonous plant.

11. The method of producing a heterologous polypeptide of claim 10, wherein the dicotyledonous plant is a Nicotiana plant.

12. The method of producing a heterologous polypeptide of claim 11, wherein the Nicotiana plant is a Nicotiana benthamiana plant.

13. The method of producing a heterologous polypeptide of claim 1, wherein the infecting the transgenic plant or the transgenic plant cell for synthesis of an RNA complementary to an RNA transcript of the recombinant DNA comprises infecting the transgenic plant or the transgenic plant cell with a positive strand single-stranded RNA plant virus operable to recognize the viral RNA replication initiation site and convert the RNA transcript produced by the transgenic plant or the transgenic plant cell to a translatable mRNA.

14. The method of producing a heterologous polypeptide of claim 13, wherein the positive strand single-stranded RNA plant virus is a positive strand single-stranded RNA plant virus having no DNA stage.

15. The method of producing a heterologous polypeptide of claim 14, wherein the positive strand single-stranded RNA plant virus having no DNA stage is selected from the group consisting of a Bromovirus, a Tobacco etch virus, a Tobacco vein mottle virus, and a Pepper mottle virus.

16. The method of producing a heterologous polypeptide of claim 1, wherein the heterologous polypeptide produced in a cell infected with the RNA nucleic acid when compared as a molar ratio to the amount of the heterologous polypeptide produced in a cell not provided the RNA nucleic acid, ranges at least from about 50:1 to about 10,000:1.

17. The method of producing a heterologous polypeptide of claim 1, wherein said method of producing a heterologous polypeptide in a transgenic plant is used to confer disease resistance to a transgenic plant further comprising conferring resistance to subsequent infection from a second positive strand single-stranded RNA virus.

18. A recombinant DNA molecule comprising, in the 5' to 3' direction: a) a plant promoter; b) a sequence complementary to a coding sequence for a heterologous polypeptide; c) a sequence complementary to a plant internal ribosome entry site; and d) a 3' UTR sequence comprising a DNA sequence of a 3' UTR RNA sequence of a positive strand single-stranded RNA plant virus.

19. The recombinant DNA molecule of claim 18, wherein the plant promoter is selected from the group consisting of a constitutive promoter and an inducible promoter.

20. The recombinant DNA molecule of claim 19, wherein the constitutive promoter is a cauliflower mosaic virus 35S promoter.

21. The recombinant DNA molecule of claim 18, wherein the coding sequence for the heterologous polypeptide encodes a polypeptide selected from the group consisting of a hormone, an enzyme, a cell toxin, a viral polypeptide, a cell surface polypeptide, and an intracellular polypeptide.

22. The recombinant DNA molecule of claim 18, wherein the sequence complementary to a plant internal ribosome entry site is a sequence complementary to a plant internal ribosome entry site (IRES) selected from the group consisting of a turnip mosaic potyvirus IRES, a tobamovirus IRES, and a hibiscus chlorotic ringspot virus IRES.

23. The recombinant DNA molecule of claim 18, wherein the sequence complementary to a plant internal ribosome entry site is a sequence complementary to a tobamovirus internal ribosome entry site.

24. The recombinant DNA molecule of claim 18, wherein the 3' UTR DNA sequence is a DNA copy of a positive strand single-stranded RNA plant virus RNA having no DNA stage.

25. The recombinant DNA molecule of claim 24, wherein the positive strand single-stranded RNA virus RNA having no DNA stage is a 3' UTR of a bromovirus.

26. The recombinant DNA molecule of claim 18, further comprising a sequence complementary to an intron.

27. The recombinant DNA molecule of claim 18, further comprising a transcription termination signal.

28. A transgenic plant comprising the recombinant DNA molecule of claim 18.

29. A transgenic plant cell of claim 28.

30. The transgenic plant of claim 28, wherein the transgenic plant is a transgenic dicotyledonous plant.

31. The transgenic dicotyledonous plant of claim 30, wherein the transgenic dicotyledonous plant is a transgenic Nicotiana plant.

32. Transgenic seed comprising the recombinant DNA molecule of claim 18.

33. A vector having at least one site for insertion of a recombinant DNA construct having inserted therein the recombinant DNA molecule of claim 18.

34. A vector according to claim 33, wherein the at least one site for insertion further comprises a recombination site.

35. A vector according to claim 34, wherein the recombination site is selected from the group consisting of a bacteriophage lambda att site and a topoisomerase I-based recombination site.

36. A vector according to claim 33, wherein the at least one site for insertion further comprises at least one restriction enzyme recognition site.

37. A vector according to claim 36, wherein the at least one restriction enzyme recognition site comprises a polylinker.

38. A recombinant RNA molecule comprising, in the 5' to 3' direction: a) an RNA sequence comprising a sequence complementary to a coding sequence for a heterologous polypeptide; b) a sequence complementary to an internal ribosome entry site; and c) a 3' UTR of a positive strand single-stranded RNA virus.

39. The recombinant RNA molecule of claim 38, wherein the coding sequence for a heterologous polypeptide encodes a polypeptide selected from the group consisting of a hormone, an enzyme, a cell toxin, a viral polypeptide, a cell surface polypeptide, and an intracellular polypeptide.

40. The recombinant RNA molecule of claim 38, wherein the sequence complementary to an internal ribosome entry site is a sequence complementary to an IRES selected from the group consisting of a picornavirus IRES, a foot-and-mouth disease virus IRES, an encephalomyocarditis virus IRES, a hepatitis A virus IRES, a hepatitis C virus IRES, a human rhinovirus IRES, a poliovirus IRES, a swine vesicular disease virus IRES, a turnip mosaic potyvirus IRES, a human fibroblast growth factor 2 mRNA IRES, a pestivirus IRES, a Leishmania RNA virus IRES, a Moloney murine leukemia virus IRES a human rhinovirus IRES, aphthovirus IRES, a human immunoglobulin heavy chain binding protein mRNA IRES, a Drosophila Antennapedia mRNA IRES, a human fibroblast growth factor 2 mRNA IRES, a hepatitis G virus IRES, a tobamovirus IRES, a vascular endothelial growth factor mRNA IRES, a Coxsackie B group virus IRES, a c-myc protooncogene mRNA IRES, a human MYT2 mRNA IRES, a human parechovirus type 1 virus IRES, a human parechovirus type 2 virus IRES, a eukaryotic initiation factor 4GI mRNA IRES, a Plautia stali intestine virus IRES, a Theiler's murine encephalomyelitis virus IRES, a bovine enterovirus IRES, a connexin 43 mRNA IRES, a homeodomain protein Gtx mRNA IRES, an AML1 transcription factor mRNA IRES, an NF-kappa B repressing factor mRNA IRES, an X-linked inhibitor of apoptosis mRNA IRES, a cricket paralysis virus RNA IRES, a p58(PITSLRE) protein kinase mRNA IRES, an ornithine decarboxylase mRNA IRES, a connexin-32 mRNA IRES, a bovine viral diarrhea virus IRES, an insulin-like growth factor I receptor mRNA IRES, a human immunodeficiency virus type 1 gag gene IRES, a classical swine fever virus IRES, a Kaposi's sarcoma-associated herpes virus IRES, a short IRES selected from a library of random oligonucleotides, a Jembrana disease virus IRES, an apoptotic protease-activating factor 1 mRNA IRES, a Rhopalosiphum padi virus IRES, a cationic amino acid transporter mRNA IRES, a human insulin-like growth factor 11 leader 2 mRNA IRES, a giardiavirus IRES, a Smad5 mRNA IRES, a porcine teschovirus-1 talfan IRES, a Drosophila Hairless mRNA IRES, an hSNM1 mRNA IRES, a Cbfa1/Runx2 mRNA IRES, an Epstein-Barr virus IRES, a hibiscus chlorotic ringspot virus IRES, a rat pituitary vasopressin V1b receptor mRNA IRES, and a human hsp70 mRNA IRES.

41. The recombinant RNA molecule of claim 38, wherein the sequence complementary to an internal ribosome entry site is a sequence complementary to a picornavirus internal ribosome entry site.

42. The recombinant RNA molecule of claim 38, wherein the 3' UTR of a positive strand single-stranded RNA virus is a 3' UTR of a positive strand single-stranded RNA virus having no DNA stage.

43. The recombinant RNA molecule of claim 42, wherein the 3' UTR of a positive strand single-stranded RNA virus having no DNA stage is a 3' UTR of a bromovirus.

44. The recombinant RNA molecule of claim 38, further comprising a sequence complementary to an intron.

45. A transgenic cell or transgenic plant comprising the recombinant RNA molecule of claim 38.

46. The transgenic cell of claim 45, wherein the transgenic cell is a transgenic plant cell.

47. The transgenic plant of claim 45, wherein the transgenic plant is a transgenic dicotyledonous plant.

48. The transgenic dicotyledonous plant of claim 47, wherein the transgenic dicotyledonous plant is a transgenic Nicotiana plant.

49. The transgenic Nicotiana plant of claim 48, wherein the transgenic Nicotiana plant is a transgenic Nicotiana benthamiana plant.

50. The method of producing a heterologous polypeptide of claim 1, wherein infecting the transgenic plant or the transgenic plant cell with an RNA nucleic acid comprises infecting the transgenic plant or the transgenic plant cell with a positive strand single-stranded RNA plant virus having a RNA genome operable to recognize and activate the viral RNA replication initiation site and convert the RNA transcript produced by the transgenic plant or transgenic plant cell to a translatable mRNA.

51. The method of producing a heterologous polypeptide of claim 1, wherein infecting the transgenic plant or the transgenic plant cell with an RNA nucleic acid comprises transfecting the transgenic plant or the transgenic plant cell with a RNA of a positive strand single-stranded virus operable to recognize and activate the viral RNA replication initiation site and convert the RNA transcript produced by the transgenic plant or transgenic plant cell to a translatable mRNA.

Details for Patent 7,696,406

Applicant Tradename Biologic Ingredient Dosage Form BLA Approval Date Patent No. Expiredate
Merck Sharp & Dohme Corp. INTRON A interferon alfa-2b For Injection 103132 06/04/1986 ⤷  Try a Trial 2039-02-26
Merck Sharp & Dohme Corp. INTRON A interferon alfa-2b For Injection 103132 ⤷  Try a Trial 2039-02-26
Merck Sharp & Dohme Corp. INTRON A interferon alfa-2b Injection 103132 ⤷  Try a Trial 2039-02-26
>Applicant >Tradename >Biologic Ingredient >Dosage Form >BLA >Approval Date >Patent No. >Expiredate

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