Methods for detection of a target nucleic acid by forming a cleavage structure using an RNA polymerase

• US 20090117540A1
• Filed: 06/22/2006
• Published: 05/07/2009
• Est. Priority Date: 10/29/1999
• Status: Active Grant

• Current Assignee: Hologic Incorporated
• Original Assignee: Stratagene California
• Inventors: Sorge, Joseph A.
• Granted Patent: US 7,824,859 B2
• Time in Patent Office: Days
• US Class Current: 435/6
• CPC Class Codes: C12Q 1/48 involving transferase
• CPC Class Codes: C12Q 1/6823 Release of bound markers
• CPC Class Codes: C12Q 2521/119 RNA polymerase
• CPC Class Codes: C12Q 2521/301 Endonuclease
• CPC Class Codes: C12Q 2521/307 Single strand endonuclease
• CPC Class Codes: C12Q 2525/161 incorporating target specific and non-target specific sites
• CPC Class Codes: C12Q 2525/301 Hairpin oligonucleotides
• CPC Class Codes: C12Q 2531/113 PCR
• CPC Class Codes: C12Q 2561/109 Invader technology
• CPC Class Codes: C12Q 2565/519 characterised by the capture moiety being a single stranded oligonucleotide
• CPC Class Codes: G01N 33/5308 for analytes not provided for elsewhere, e.g. nucleic acids, uric acid, worms, mites

Abstract

The invention relates to compositions and methods for generating a signal indicative of the presence of a target nucleic acid in a sample, where the compositions and methods include an RNA polymerase, a FEN nuclease, and a probe.

Claims

1. A composition for generating a signal indicative of the presence of a target nucleic acid sequence in a sample, said composition comprising an RNA polymerase, a FEN nuclease, a primer and a probe.

2. The composition of claim 1, wherein the FEN nuclease is a flap-specific nuclease.

3. The composition of claim 1, wherein the FEN nuclease is thermostable.

4. The composition of claim 1, wherein the probe comprises at least one labeled moiety capable of providing a signal.

5. The composition of claim 1, wherein the RNA polymerase is T7-RNA polymerase, SP6-RNA polymerase, T3 RNA polymerase and NS5B RNA polymerase.

6. A composition for performing a non-polymerase chain reaction process for simultaneously forming a cleavage structure comprising duplex and single-stranded nucleic acid, amplifying a target nucleic acid sequence in a sample and cleaving said cleavage structure, the composition comprising an RNA polymerase, a FEN nuclease, a labeled probe.

7. The composition of claim 6, wherein the FEN nuclease is a flap-specific nuclease.

8. The composition of claim 6, wherein the FEN nuclease is thermostable.

9. The composition of claim 6, wherein the probe comprises at least one labeled moiety capable of providing a signal.

10. The composition of claim 6, wherein the RNA polymerase is T7-RNA polymerase, SP6-RNA polymerase, T3 RNA polymerase or NS5B RNA polymerase

11. A kit for generating a signal indicative of the presence of a target nucleic acid sequence in a sample, the kit comprising a FEN nuclease, an RNA polymerase, a probe and a suitable buffer.

12. The kit of claim 11, wherein the FEN nuclease is a flap-specific nuclease.

13. The kit of claim 11, wherein the FEN nuclease is thermostable.

14. The kit of claim 11, wherein the probe comprises at least one labeled moiety capable of providing a signal.

15. The kit of claim 11, wherein the RNA polymerase is T7-RNA polymerase, SP6-RNA polymerase, T3 RNA polymerase or NS5B RNA polymerase

16. The kit of claim 11, wherein said FEN nuclease, said buffer and said RNA polymerase are in the same composition.

17. A composition for generating a signal indicative of the presence of a target nucleic acid sequence in a sample, the composition comprising an RNA polymerase, a FEN nuclease, and a probe that is complementary to the target nucleic acid.

18. The composition of claim 17, further comprising the target nucleic acid.

19. The composition of claim 17, wherein the probe has a 5′

flap.

20. The composition of claim 19, wherein the 5′

region of the probe is non complementary to the target nucleic acid.

21. The composition of claim 17;

wherein the probe comprises;

at least one labeled moiety capable of providing a signal.

22. The composition of claim 17, wherein the probe comprises a pair of interactive signal generating labeled moieties effectively positioned to quench the generation of a detectable signal, the labeled moieties being separated by a site susceptible to FEN nuclease cleavage.

23. The composition of claim 22, wherein the pair of interactive signal generating moieties comprises a quencher moiety and a fluorescent moiety.

24. The composition of claim 17, further comprising an upstream oligonucleotide primer, wherein the upstream oligonucleotide primer hybridizes upstream of the probe and is extended by the RNA polymerase.

25. The composition of claim 24, further comprising a reverse primer.

26. The composition of claim 17, wherein the FEN nuclease is selected from the group consisting of FEN nuclease enzyme derived from Archaeglobus fulgidus, Methanococcus jannaschii, Pyrococcus furiosus, Taq, Tfl and Bca.

27. The composition of claim 17, wherein the RNA polymerase is an RNA dependent polymerase.

28. The composition of claim 17, wherein the RNA polymerase is a DNA dependent polymerase.

29. The composition of claim 17, wherein the RNA polymerase is selected from the

group consisting of:

T7-RNA polymerase, SP6-RNA polymerase, T3 RNA polymerase, and NS5B RNA polymerase.

30. The composition of claim 17, wherein the RNA polymerase is thermostable.

31. A kit for generating a signal indicative of the presence of a target nucleic acid sequence in a sample, the composition comprising an RNA polymerase, a FEN nuclease, and a probe that is complementary to the target nucleic acid.

32. The kit of claim 31, wherein the probe comprises at least one labeled moiety capable of providing a signal.

33. The kit of claim 31, wherein the probe comprises a pair of interactive signal generating labeled moieties effectively positioned to quench the generation of a detectable signal, the labeled moieties being separated by a site susceptible to FEN nuclease cleavage.

34. The kit of claim 33, wherein the pair of interactive signal generating moieties comprises a quencher moiety and a fluorescent moiety.

35. The kit of claim 31, further comprising an upstream oligonucleotide primer, wherein the upstream oligonucleotide primer hybridizes upstream of the probe and is extended by said RNA polymerase.

36. The kit of claim 35, further comprising a reverse primer.

37. The kit of claim 31, wherein the FEN nuclease is selected from the group consisting of FEN nuclease enzyme derived from Archaeglobus fulgidus, Methanococcus jannaschii, Pyrococcus furiosus, Taq, Tfl and Bca.

38. The kit of claim 31, wherein the RNA polymerase is T7-RNA polymerase, SP6-RNA polymerase, T3 RNA polymerase and NS5B RNA polymerase.

39. The kit of claim 31, wherein the RNA polymerase is thermostable.

40. The kit of claim 31, wherein the RNA polymerase is an RNA dependent RNA polymerase.

41. The kit of claim 31, wherein the RNA polymerase is a DNA dependent RNA polymerase.

42. A method of generating a signal indicative of the presence of a target nucleic acid sequence in a sample, comprising forming a cleavage structure by incubating a sample comprising a target nucleic acid sequence with an RNA polymerase and cleaving the cleavage structure with a FEN nuclease to generate a signal, wherein generation of the signal is indicative of the presence of a target nucleic acid sequence in the sample.

44. The method of claim 42, wherein the RNA polymerase is thermostable

45. The method of claim 42, wherein the RNA polymerase is T7-RNA polymerase, SP6-RNA polymerase, T3 RNA polymerase or NS5B RNA polymerase.

46. The method of claim 42, wherein the FEN nuclease is a flap-specific nuclease.

47. The method of claim 42, wherein the FEN nuclease is thermostable.

48. The method of claim 42, wherein a cleavage structure is formed comprising at least one labeled moiety capable of providing a signal.

49. The method of claim 42, wherein a cleavage structure is formed comprising a pair of interactive signal generating labeled moieties effectively positioned to quench the generation of a detectable signal, the labeled moieties being separated by a site susceptible to FEN nuclease cleavage, thereby allowing the nuclease activity of the FEN nuclease to separate the first interactive signal generating labeled moiety from the second interactive signal generating labeled moiety by cleaving at the site susceptible to FEN nuclease, thereby generating a detectable signal.

50. The method of claim 49, wherein the pair of interactive signal generating moieties comprises a quencher moiety and a fluorescent moiety.

51. The method of claim 42, wherein a cleavage structure comprises an RNA extension product and a downstream probe with a 5′

flap.

43. A method of detecting or measuring a target nucleic acid sequence, comprising forming a cleavage structure by incubating a sample comprising a target nucleic acid sequence with an RNA polymerase, cleaving the cleavage structure with a FEN nuclease to release a nucleic acid fragment and detecting and/or measuring the release of the fragment as an indication of the presence of the target sequence in the sample.

52. A method for detecting a target nucleic acid sequence in a sample, comprising:

mixing a probe, a target nucleic acid having a promoter region, a FEN nuclease and an RNA polymerase, under conditions which are permissive for the steps of (i) binding of the RNA polymerase to the promoter region in the target nucleic acid sequence and annealing of the probe to the target, (ii) synthesizing an RNA polymerase extension product, (iii) forming a cleavage structure, and (iv) and cleaving the cleavage structure with the FEN nuclease and detecting and/or measuring the release of labeled fragments or cleavage of the probe as an indication of the presence of the target sequence in the sample.

54. The method of claim 52 or 53, wherein the FEN nuclease is selected from the group consisting of FEN nuclease enzyme derived from Archaeglobus fulgidus, Methanococcus jannaschii, Pyrococcus furiosus, Taq, Tfl and Bca.

55. The method of claim 52 or 53, wherein the RNA polymerase is thermostable.

56. The method of claim 52 or 53, wherein the RNA polymerase is T7-RNA polymerase, SP6-RNA polymerase, T3 RNA polymerase and NS5B RNA polymerase.

57. The method of claim 52 or 53, wherein the probe comprises at least one labeled moiety capable of providing a signal.

58. The method of claim 52 or 53, wherein the probe comprises a pair of interactive signal generating labeled moieties effectively positioned to quench the generation of a detectable signal, the labeled moieties being separated by a site susceptible to FEN nuclease cleavage, thereby allowing the nuclease activity of the FEN nuclease to separate the first interactive signal generating labeled moiety from the second interactive signal generating labeled moiety by cleaving at the site susceptible to FEN nuclease, thereby generating a detectable signal.

59. The method of claim 58, wherein the pair of interactive signal generating moieties comprises a quencher moiety and a fluorescer moiety.

60. The method of claim 52 or 53, wherein the step of detecting and/or measuring the release of labeled fragments comprises detecting a change in fluorescence between an interactive pair of labels.

61. The method of claim 52 or 53, wherein the RNA polymerases displaces at least a portion of the downstream probe.

62. The method of claim 52 or 53, wherein the probe has a 5′

flap.

63. The method of claim 52 or 53, wherein the RNA polymerase polymerizes nucleotides complementary to a length of the target sufficient to form a cleavage structure so that the polymerized complementary RNA is adjacent at its 3′

end to the probe.

53. A method for detecting a target nucleic acid sequence in a sample, comprising:

mixing a probe, a target nucleic acid, a FEN nuclease, a primer and an RNA polymerase, under conditions which are permissive for the steps of (i) annealing of the primer and probe to the target nucleic acid, (ii) synthesizing an RNA polymerase extension product from said primer, (iii) forming a cleavage structure, and (iv) and cleaving the cleavage structure with the FEN nuclease and detecting and/or measuring the release of labeled fragments or cleavage of the probe as an indication of the presence of the target sequence in the sample.