Methods and compositions for generation of multiple copies of nucleic acid sequences and methods of detection thereof
View Patent ↗The present invention provides novel isothermal methods of generating multiple copies of, detecting and/or quantifying nucleic acid sequences of interest based on limited primer extension or attachment of oligonucleotide pairs using composite RNA/DNA primers. Methods for generating multiple copies of and/or detecting and/or quantifying nucleic acid sequences, wherein products of primer extension or attachment of oligonucleotide pairs comprising a cleavable portion are generated, and wherein cleavage of the products results in dissociation of cleaved products from target polynucleotides, are provided. The invention further provides compositions, kits and systems for practicing these methods.
1. A method of generating multiple copies of a nucleic acid sequence of interest, said method comprising the steps of:
(a) hybridizing a composite primer to a target polynucleotide, wherein the composite primer comprises an RNA portion and a 3′ DNA portion, the 3′ DNA portion comprising a 3′ most nucleotide, such that the 3′ most nucleotide of the 3′ DNA portion hybridizes from 1 to about 10 nucleotides from the sequence of interest;
(b) extending the composite primer with DNA polymerase under conditions that permit primer extension, whereby a primer extension product is produced; and
(c) cleaving the RNA portion of the primer extension product of(b) with an enzyme that cleaves RNA from an RNA/DNA hybrid such that the cleaved primer extension product dissociates from the target polynucleotide,
wherein the primer extension product is of a size that when the RNA is cleaved the cleaved primer extension product dissociates from the target polynucleotide under essentially the same conditions as those for primer extension, whereby multiple copies of the sequence of interest are produced.
2. The method of claim 1 , wherein said conditions that permit primer extension comprise at least one terminator deoxyribonucleotide triphosphate or analog thereof.
3. The method of claim 1 , wherein said conditions that permit primer extension comprise the absence of a nucleotide that must be provided for primer extension to continue.
4. The method of claim 1 , wherein the sequence of interest is a single nucleotide base.
5. The method of claim 1 , wherein the sequence of interest is more than a single nucleotide base.
6. The method of claim 1 , wherein the RNA portion of the composite primer is 5′ with respect to the 3′ DNA portion.
7. The method of claim 6 , wherein the 5′ RNA portion is adjacent to the 3′ DNA.
8. The method of claim 1 , wherein the enzyme that cleaves RNA is RNase H.
9. The method of claim 1 , wherein the DNA polymerase lacks strand displacement activity.
10. The method of claim 1 , wherein the target polynucleotide is DNA or cDNA.
11. The method of claim 1 , wherein the target polynucleotide is generated by amplification.
12. The method of claim 11 , wherein amplification occurs simultaneously with generating multiple copies of a sequence of interest.
13. The method of claim 11 , wherein amplification occurs prior to generating multiple copies of a sequence of interest.
14. A method of determining whether a nucleic acid sequence of interest is present or absent in a sample, said method comprising the steps of:
(a) hybridizing a composite primer to a target polynucleotide, wherein the composite primer comprises an RNA portion and a 3′ DNA portion, the 3′ DNA portion comprising a 3′ most nucleotide, such that the 3′ most nucleotide of the DNA portion of the composite primer hybridizes from 1 to about 10 nucleotides from the sequence of interest;
(b) extending the composite primer with DNA polymerase under conditions that permit primer extension, whereby a primer extension product comprising a detectable identifying characteristic is produced if the sequence of interest is present; and
(c) cleaving the RNA portion of the primer extension product of (b), if any, with an enzyme that cleaves RNA from an RNA/DNA hybrid such that the cleaved primer extension product dissociates from the target polynucleotide,
wherein the primer extension product is of a size that when the RNA is cleaved the cleaved primer extension product dissociates from the target polynucleotide under essentially the same conditions as those for primer extension, whereby detection of the cleaved primer extension product comprising the detectable identifying characteristic indicates the presence of the sequence of interest.
15. The method of claim 14 , wherein said conditions that permit primer extension comprise at least one terminator deoxyribonucleotide triphosphate or analog thereof.
16. The method of claim 14 , wherein said conditions that permit primer extension comprise the absence of a nucleotide that must be provided for primer extension to continue.
17. The method of claim 14 , wherein the sequence of interest is a single nucleotide, and the conditions for primer extension comprise one terminator deoxyribonucleotide triphosphate or analog thereof.
18. The method of claim 14 , wherein the sequence of interest is a single nucleotide base.
19. The method of claim 14 , wherein the sequence of interest is more than a single nucleotide base.
20. The method of claim 14 , wherein the RNA portion of the composite primer is 5′ with respect to the 3′ DNA portion.
21. The method of claim 14 , wherein the 5′ RNA portion is adjacent to the 3′ DNA portion.
22. The method of claim 14 , wherein the enzyme that cleaves RNA is RNase H.
23. The method of claim 14 , wherein the DNA polymerase lacks strand displacement activity.
24. The method of claim 14 , wherein the target polynucleotide is DNA or cDNA.
25. The method of claim 14 , wherein the target polynucleotide is generated by amplification.
26. The method of claim 25 , wherein amplification occurs simultaneously with generating multiple copies of a sequence of interest.
27. The method of claim 25 , wherein amplification occurs prior to generating multiple copies of a sequence of interest.
28. The method of claim 14 , wherein the target polynucleotide is attached to an analyte.
29. The method of claim 28 , wherein the analyte is selected from the group consisting of a polypeptide, an antibody, an organic molecule and an inorganic molecule.
30. The method of claim 14 , wherein said detectable identifying characteristic is selected from the group consisting of size of the cleaved primer extension product, sequence of the cleaved primer extension product, and detectable signal associated with the cleaved primer extension product.
31. The method of claim 14 , wherein the detectable identifying characteristic comprises the sequence of the cleaved primer extension product, wherein the sequence is detected by hybridizing the cleaved primer extension product with a nucleic acid probe that is hybridizable to the cleaved primer extension product.
32. The method of claim 31 , wherein said nucleic acid probe comprises DNA.
33. The method of claim 31 , wherein the nucleic acid probe is provided as an array.
34. The method of claim 33 , wherein the array comprises the probe immobilized on a substrate fabricated from a material selected from the group consisting of paper, glass, plastic, polypropylene, nylon, polyacrylamide, nitrocellulose, silicon, polystyrene, and optical fiber.
35. The method of claim 30 , wherein said detectable signal is associated with a label on a deoxyribonucleotide triphosphate or analog thereof that is incorporated during primer extension.
36. The method of claim 30 , wherein said detectable signal is associated with interaction of two labels, wherein one label is on a deoxyribonucleotide triphosphate or analog thereof that is incorporated during primer extension and another label is on a deoxyribonucleotide triphosphate or analog thereof located in the primer portion of the primer extension product.
37. A method of generating multiple copies of a nucleic acid sequence of interest comprising:
incubating a reaction mixture, said reaction mixture comprising:
(a) a target polynucleotide;
(b) a composite primer that hybridizes to the target polynucleotide, said composite primer comprising an RNA portion and a 3′ DNA portion, the 3′ DNA portion comprising a 3′ most nucleotide, such that the 3′ most nucleotide of the 3′ DNA portion of the primer hybridizes from 1 nucleotide to about 10 nucleotides from the sequence of interest;
(c) a DNA polymerase; and
(d) an enzyme that cleaves RNA from an RNA/DNA hybrid,
wherein the incubation is under conditions that permit primer hybridization, primer extension and RNA cleavage, such that a primer extension product is produced, and wherein the primer extension product is of a size such that cleavage of RNA from the primer extension product results in dissociation of the cleaved primer extension product from the target polynucleotide.
38. The method of claim 37 , wherein said conditions that permit primer extension comprise at least one terminator deoxyribonucleotide triphosphate or analog thereof.
39. The method of claim 37 , wherein said conditions that permit primer extension comprise the absence of a nucleotide that must be provided for primer extension to continue.
40. The method of claim 37 , wherein the sequence of interest is a single nucleotide base.
41. The method of claim 37 , wherein the sequence of interest is more than a single nucleotide base.
42. The method of claim 37 , wherein the RNA portion of the composite primer is 5′ with respect to the 3′ DNA portion.
43. The method of claim 37 , wherein the 5′ RNA portion is adjacent to the 3′ DNA portion.
44. The method of claim 37 , wherein the enzyme that cleaves RNA is RNase H.
45. The method of claim 37 , wherein the DNA polymerase lacks strand displacement activity.
46. The method of claim 37 , wherein the target polynucleotide is DNA or cDNA.
47. The method of claim 37 , wherein the target polynucleotide is generated by amplification.
48. The method of claim 47 , wherein amplification occurs simultaneously with generating multiple copies of a sequence of interest.
49. The method of claim 47 , wherein amplification occurs prior to generating multiple copies of a sequence of interest.
50. A method of determining whether a nucleic acid sequence of interest is present or absent in a sample comprising incubating a reaction mixture, said reaction mixture comprising:
(a) a target polynucleotide;
(b) a composite primer that hybridizes to the target polynucleotide, said composite primer comprising an RNA portion and a 3′ DNA portion, the 3′ DNA portion comprising a 3′ most nucleotide, such that the 3′ most nucleotide of the 3′ DNA portion of the primer hybridizes from 1 nucleotide to about 10 nucleotides from the sequence of interest;
(c) a DNA polymerase; and
(d) an enzyme that cleaves RNA from an RNA/DNA hybrid,
wherein the incubation is under conditions that permit primer hybridization, primer extension to generate a primer extension product comprising a detectable identifying characteristic, and RNA cleavage, such that the primer extension product comprising a detectable identifying characteristic is produced, and wherein the primer extension product is of a size such that cleavage of RNA from the primer extension product results in dissociation of the cleaved primer extension product from the target polynucleotide, whereby detection of the cleaved primer extension product comprising the detectable identifying characteristic indicates presence of the nucleotide sequence of interest.
51. The method of claim 50 , wherein said conditions that permit primer extension comprise at least one terminator deoxyribonucleotide triphosphate or analog thereof.
52. The method of claim 50 , wherein said conditions that permit primer extension comprise the absence of a nucleotide that must be provided for primer extension to continue.
53. The method of claim 50 , wherein the sequence of interest is a single nucleotide, and the conditions for primer extension comprise one terminator deoxyribonucleotide triphosphate or analog thereof.
54. The method of claim 50 , wherein the sequence of interest is a single nucleotide base.
55. The method of claim 50 , wherein the sequence of interest is more than a single nucleotide base.
56. The method of claim 50 , wherein the RNA portion of the composite primer is 5′ with respect to the 3′ DNA portion.
57. The method of claim 50 , wherein the 5′ RNA portion is adjacent to the 3′ DNA portion.
58. The method of claim 50 , wherein the enzyme that cleaves RNA is RNase H.
59. The method of claim 50 , wherein the DNA polymerase lacks strand displacement activity.
60. The method of claim 50 , wherein the target polynucleotide is DNA or cDNA.
61. The method of claim 50 , wherein the target polynucleotide is generated by amplification.
62. The method of claim 61 , wherein amplification occurs simultaneously with generating multiple copies of a sequence of interest.
63. The method of claim 61 , wherein amplification occurs prior to generating multiple copies of a sequence of interest.
64. The method of claim 50 , wherein the target polynucleotide is attached to an analyte.
65. The method of claim 64 , wherein the analyte is selected from the group consisting of a polypeptide, an antibody, an organic molecule and an inorganic molecule.
66. The method of claim 50 , wherein said detectable identifying characteristic is selected from the group consisting of size of the cleaved primer extension product, sequence of the cleaved primer extension product, and detectable signal associated with the cleaved primer extension product.
67. The method of claim 50 , wherein the detectable identifying characteristic comprises the sequence of the cleaved primer extension product, wherein the sequence is detected by hybridizing the cleaved primer extension product with a nucleic acid probe that is hybridizable to the cleaved primer extension product.
68. The method of claim 67 , wherein said nucleic acid probe comprises DNA.
69. The method of claim 67 , wherein the nucleic acid probe is immobilized on a surface.
70. The method of claim 69 , wherein the surface comprises a substrate fabricated from a material selected from the group consisting of paper, glass, plastic, polypropylene, nylon, polyacrylamide, nitrocellulose, silicon, polystyrene, and optical fiber.
71. The method of claim 66 , wherein said detectable signal is associated with a label on a deoxyribonucleotide triphosphate or analog thereof that is incorporated during primer extension.
72. The method of claim 66 , wherein said detectable signal is associated with interaction of two labels, wherein one label is on a deoxyribonucleotide triphosphate or analog thereof that is incorporated during primer extension and another label is on a deoxyribonucleotide triphosphate or analog thereof located in the primer portion of the primer extension product.
73. The method of claims 14 or 50 , wherein said method comprises determining whether two or more sequences of interest are present or absent in a sample, said method comprising using one or more different composite primers, wherein the detectable identifying characteristics of the cleaved primer extension products corresponding to two different sequences of interest are different from each other.
74. The method of claim 73 , wherein said method comprises at least two different composite primers.
75. The method of claim 73 , wherein at least one of the sequences of interest is a variant of the sequence of interest.
76. A method for identifying an altered sequence of interest in a sample comprising incubating a reaction mixture, said mixture comprising:
(a) a target polynucleotide;
(b) a composite primer that hybridizes to the target polynucleotide, said composite primer comprising an RNA portion and a 3′ DNA portion, the 3′ DNA portion comprising a 3′ most nucleotide, such that the 3′ most nucleotide of the 3′ DNA portion of the primer hybridizes from 1 nucleotide to about 10 nucleotides from the altered sequence of interest;
(c) a DNA polymerase; and
(d) an enzyme that cleaves RNA from an RNA/DNA hybrid,
wherein the incubation is under conditions that permit primer hybridization and primer extension to generate a primer extension product comprising a detectable identifying characteristic, and RNA cleavage, such that a primer extension product comprising a detectable identifying characteristic is produced, and
wherein the primer extension product is of a size that when RNA is cleaved from the primer extension product, the cleaved primer extension product dissociates from the target polynucleotide, whereby the cleaved primer extension product is characterized to identify the altered sequence of interest.
77. The method of claim 76 , wherein the cleaved primer extension product produced from the target polynucleotide comprises a different detectable identifying characteristic as compared with a detectable identifying characteristic of a cleaved primer extension product produced from a reference template containing the sequence of interest, wherein the characterization comprises comparing the detectable identifying characteristics.
78. A method of identifying an altered sequence of interest in a sample, said method comprising incubating a reaction mixture, said reaction mixture comprising:
(a) a target polynucleotide;
(b) a composite primer that hybridizes to the target polynucleotide, said composite primer comprising an RNA portion and a 3′ DNA portion, the 3′ DNA portion comprising a 3′ most nucleotide, such that the 3′ most nucleotide of the 3′ DNA portion of the primer hybridizes from 1 nucleotide to about 10 nucleotides from the altered sequence of interest;
(c) a DNA polymerase; and
(d) an enzyme that cleaves RNA from an RNA/DNA hybrid,
wherein the incubation is under conditions that permit primer hybridization, and primer extension to generate a primer extension product comprising a detectable identifying characteristic, and RNA cleavage, such that the primer extension product comprising a detectable identifying characteristic is produced, and
wherein the primer extension product is of a size that when RNA is cleaved from the primer extension product, the cleaved primer extension product dissociates from the target polynucleotide, and
wherein production of detectably fewer cleaved primer extension products from the target as compared to the amount of cleaved primer extension products produced from a reference template comprising the sequence of interest indicates that the target polynucleotide contains an altered sequence of interest.
79. The method of claim 78 , further comprising characterizing the sequence of the template polynucleotide 1 to about 10 nucleotides 5′ from the sequence hybridizable to the composite primer.