Methods and compositions for transcription-based nucleic acid amplification

• US 20040203019A1
• Filed: 10/14/2003
• Published: 10/14/2004
• Est. Priority Date: 06/26/2000
• Status: Active Grant

• Current Assignee: NuGEN Technologies, Inc. (Tecan Group AG)
• Original Assignee: NuGEN Technologies, Inc. (Tecan Group AG)
• Inventors: Kurn, Nurith
• Granted Patent: US 7,294,461 B2
• Time in Patent Office: Days
• US Class Current: 435/6
• CPC Class Codes: C12Q 1/6865 Promoter-based amplification, e.g. nucleic acid sequence amplification [NASBA], self-sustained sequence replication [3SR] or transcription-based amplification system [TAS]
• CPC Class Codes: C12Q 1/6876 Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
• CPC Class Codes: C12Q 2525/143 incorporating a promoter sequence
• CPC Class Codes: C12Q 2525/186 incorporating a non-extendable or blocking moiety
• CPC Class Codes: C12Q 2531/119 Strand displacement amplification [SDA]

Abstract

Methods for isothermal exponential amplification of a target polynucleotide are disclosed. The methods employ two transcription modules, the first module providing linear amplification resulting in RNA transcripts, and a second module providing for further (generally cyclical) amplification resulting in more RNA transcripts. In one aspect, the amplification of the first module is composite primer based. In a second aspect, the amplification of the first module is based on target switching to generate a primer extension product comprising a promoter sequence. In all aspects, the RNA transcripts of the first transcription module are subjected to further amplification by creating an intermediate product comprising a double stranded promoter region from which transcription can occur. The invention further provides compositions and kits for practicing said methods, as well as methods which use the amplification results.

Claims

1-16. -16 (canceled)

17. A method of generating multiple copies of a nucleic acid sequence of interest, said method comprising the steps of:

(a) hybridizing a single stranded target polynucleotide comprising the sequence of interest with a first primer;

(b) hybridizing a propromoter template switch oligonucleotide (TSO) comprising a propromoter sequence and a region that is hybridizable to a region of the target polynucleotide which is 5′

with respect to hybridization of the first primer to the target polynucleotide;

(c) extending the first primer with DNA polymerase such that a first primer extension product comprising a sequence complementary to the propromoter sequence of the propromoter TSO is produced, whereby a complex of first primer extension product, target polynucleotide and propromoter TSO is generated, wherein said complex comprises a double stranded promoter region;

(d) transcribing from the double stranded promoter region with a DNA-dependent RNA polymerase to generate a sense RNA transcript;

(e) hybridizing a second primer to the sense RNA transcript of step (d);

(f) extending the second primer with RNA-dependent DNA polymerase to generate a complex comprising a second primer extension product and an RNA transcript;

(g) cleaving RNA in the complex of step (f) with an enzyme that cleaves RNA in an RNA/DNA hybrid;

(h) hybridizing a single stranded second primer extension product with a propromoter polynucleotide, wherein the propromoter polynucleotide comprises a propromoter and a region which hybridizes to the single stranded second primer extension product under conditions which allow transcription to occur by RNA polymerase, such that sense RNA transcripts comprising the sequence of interest are produced;

whereby multiple copies of the nucleic acid sequence of interest are produced.

18. A method of generating multiple copies of a nucleic acid sequence of interest, said method comprising the steps of:

(a) combining;

the complex of step (c) of claim 17;

an RNA polymerase;

a second primer that is hybridizable to a sense RNA transcript comprising the sequence of interest;

an RNA-dependent DNA polymerase;

an enzyme that cleaves RNA from an RNA/DNA hybrid; and

a propromoter polynucleotide comprising a propromoter and a region which hybridizes to a second primer extension product; and

(b) incubating the mixture of step (a) under conditions that permit primer hybridization and extension, RNA cleavage, hybridization of a propromoter polynucleotide to a primer extension product to form a complex comprising a primer extension product and a propromoter polynucleotide, and RNA transcription, whereby multiple copies of the nucleic acid sequence of interest are generated.

19. A method of generating multiple copies of a nucleic acid sequence of interest, said method comprising the steps of:

(a) combining;

an RNA transcript of step (d) of claim 17;

a second primer that is hybridizable to the RNA transcript;

an RNA-dependent DNA polymerase;

an enzyme that cleaves RNA from an RNA/DNA hybrid;

a propromoter polynucleotide comprising a propromoter and a region which hybridizes to a second primer extension product; and

an RNA polymerase; and

(b) incubating the mixture of step (a) under conditions that permit primer hybridization and extension, RNA cleavage, hybridization of a propromoter polynucleotide to a primer extension product to form a complex comprising a primer extension product and a propromoter polynucleotide, and RNA transcription, whereby multiple copies of the nucleic acid sequence of interest are generated.

21. The method of claim 17, wherein the target polynucleotide is DNA.

22. The method of claim 17, wherein the target polynucleotide is RNA.

23. The method of claim 17, wherein the first and second primers are the same.

24. The method of claim 17, wherein the first and second primers are different.

25. The method of claim 17, wherein the first and second primers hybridize to different complementary sequences.

26. The method of claim 17, wherein the RNA-dependent DNA polymerase is reverse transcriptase.

27. The method of claim 17, wherein the target polynucleotide is RNA, and RNA in the complex of step (c) is cleaved with an enzyme that cleaves RNA in an RNA/DNA hybrid.

28. The method of claim 17, wherein the propromoter polynucleotide comprising a propromoter and a region which hybridizes to a second primer extension product is a propromoter TSO.

29. The method of claim 17, wherein the propromoter polynucleotide comprising a propromoter and a region which hybridizes to a second primer extension product is a propromoter template oligonucleotide (PTO).

30. The method of claim 17, wherein at least one type of rNTP used is a labeled rNTP, whereby labeled RNA products are generated.

32. The method of claim 17, wherein the DNA polymerase of step (c) is a DNA-dependent DNA polymerase, and wherein the DNA-dependent DNA polymerase and the RNA-dependent DNA polymerase are one enzyme.

33. The method of claim 17, wherein the RNA-dependent DNA polymerase and enzyme that cleaves RNA from an RNA/DNA hybrid are the same enzyme.

35. The method of claim 17, wherein the DNA polymerase of step (c) is a DNA-dependent DNA polymerase, and wherein the DNA-dependent DNA polymerase and enzyme that cleaves RNA from an RNA/DNA hybrid are the same enzyme.

37. The method of claim 17, wherein the DNA polymerase of step (c) is a DNA-dependent DNA polymerase, and wherein the DNA-dependent DNA polymerase, the RNA-dependent DNA polymerase and enzyme that cleaves RNA from an RNA/DNA hybrid are the same enzyme.

38. A method of sequencing a target polynucleotide, said method comprising (a) amplifying a target polynucleotide by the method of claim 17 in the presence of a mixture of rNTPs and rNTP analogs such that transcription is terminated upon incorporation of an rNTP analog;

and (b) analyzing the amplification products to determine sequence.

39. A method of sequencing a target polynucleotide, said method comprising (a) amplifying a target polynucleotide by the method of claim 17, wherein RNA transcripts generated from a first primer extension product are amplified in the presence of a mixture of rNTPs and rNTP analogs such that transcription is terminated upon incorporation of an rNTP analog;

and (b) analyzing the amplification products to determine sequence.

40. A method of detecting a mutation in a target polynucleotide by single stranded conformation polymorphism, comprising (a) amplifying the target polynucleotide by the method of claim 17;

and (b) analyzing the amplification products for single stranded conformation, wherein a difference in conformation as compared to a reference single stranded polynucleotide indicates a mutation in the target polynucleotide.

45. A method of producing a microarray, comprising (a) amplifying a target polynucleotide by the method of claim 17;

and (b) immobilizing the amplification products on a substrate to fabricate a microarray comprising the amplification products.

46. A method of characterizing a sequence of interest, comprising (a) amplifying a target polynucleotide by the method of claim 30;

and (b) analyzing the labeled RNA products.

47. The method of claim 46, wherein step (b) comprises contacting the labeled RNA products with at least one probe.

48. The method of claim 47, wherein the at least one probe is provided as a microarray.

49. The method of claim 48, wherein the microarray comprises at least one probe immobilized on a substrate fabricated from a material selected from the group consisting of paper, glass, plastic, polypropylene, nylon, polyacrylamide, nitrocellulose, silicon, and optical fiber.

50. The method of claim 49, wherein the probe is immobilized on the substrate in a two-dimensional configuration or a three-dimensional configuration comprising pins, rods, fibers, tapes, threads, beads, particles, microtiter wells, capillaries, and cylinders.

51. The method of claim 46, wherein step (b) of analyzing the labeled RNA products comprises determining amount of said products, whereby the amount of the sequence of interest present in a sample is quantified.

52. A method of determining gene expression profile in a sample, said method comprising:

(a) amplifying at least two sequences of interest in the sample using the method of claim 17;

and

(b) determining amount of amplification products of each sequence of interest, wherein each said amount is indicative of amount of each sequence of interest in the sample, whereby the gene expression profile in the sample is determined.

53. The method of claim 52, wherein each target polynucleotide is a cDNA.

64. A kit comprising a propromoter TSO and a first primer, wherein both are hybridizable to a target polynucleotide, and instructions for amplifying the target polynucleotide according to the method of claim 17.

65. The kit of claim 64 further comprising a second primer.

66. A method of determining sequence of a sequence of interest comprising sequencing a nucleic acid amplification product, wherein said nucleic acid amplification product is generated by the method of claim 17.

67. A method of detecting presence of a nucleic acid sequence of interest in a sample, said method comprising detecting presence of the sequence of interest in a nucleic acid amplification product, wherein said nucleic acid amplification product is generated by the method of claim 17.

20. A method of generating multiple copies of a nucleic acid sequence of interest, said method comprising the steps of:

(a) combining;

a target polynucleotide;

a first primer which is hybridizable to the target polynucleotide;

a propromoter template switch oligonucleotide comprising a propromoter sequence and a region that is hybridizable to a region of the target polynucleotide which is 5′

with respect to hybridization of the first primer to the target polynucleotide;

optionally a DNA-dependent DNA polymerase;

an RNA polymerase;

a second primer that is hybridizable to a sense RNA transcript comprising the sequence of interest;

an RNA-dependent DNA polymerase;

an enzyme that cleaves RNA from an RNA/DNA hybrid; and

a propromoter polynucleotide comprising a propromoter and a region which hybridizes to a second primer extension product; and

(b) incubating the mixture of step (a) under conditions that permit primer hybridization and extension, RNA cleavage, hybridization of a propromoter polynucleotide to a primer extension product to form a complex comprising a primer extension product and a propromoter polynucleotide, and RNA transcription, whereby multiple copies of the nucleic acid sequence of interest are generated.

31. (canceled)

34. (canceled)

36. (canceled)

41-44. -44. (canceled)

54-55. -55. (canceled)

56. A system for amplifying a sequence of interest, comprising:

(a) a propromoter TSO;

(b) a first primer;

(c) optionally a DNA-dependent DNA polymerase;

(d) an RNA-dependent DNA polymerase;

(e) an enzyme that cleaves RNA from an RNA/DNA hybrid;

(f) optionally a second primer;

(g) an RNA polymerase.

57. The system of claim 56, wherein the DNA-dependent DNA polymerase and the RNA-dependent DNA polymerase are the same enzyme.

58. The system of claim 56, wherein the DNA-dependent DNA polymerase and enzyme that cleaves RNA from an RNA/DNA hybrid are the same enzyme.

59. The system of claim 56, wherein the RNA-dependent DNA polymerase and enzyme that cleaves RNA from an RNA/DNA hybrid are the same enzyme.

60. The system of claim 56, wherein the RNA-dependent DNA polymerase, DNA-dependent DNA polymerase and enzyme that cleaves RNA from an RNA/DNA hybrid are the same.

61-63. -63. (canceled)