Kits for amplifying and detecting nucleic acid sequences

• US 8,445,664 B2
• Filed: 10/20/2005
• Issued: 05/21/2013
• Est. Priority Date: 06/24/1998
• Status: Expired due to Fees

• Current Assignee: Enzo Diagnostics, Inc.
• Original Assignee: Enzo Diagnostics, Inc.
• Inventors: Rabbani, Elazar, Stavrianopoulos, Jannis, Donegan, James J., Coleman, Jack, Walner, Marleen
• Primary Examiner(s): Babic, Christopher M.
• Application Number:
  US11/256,592
• Publication Number:
  US 20080070241A1
• Time in Patent Office: 2,770 Days
• Field of Search: None
• US Class Current: 536/24.33
• CPC Class Codes: C12Q 1/6844 Nucleic acid amplification reactions
• CPC Class Codes: C12Q 1/6853 using modified primers or templates
• 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 2531/119 Strand displacement amplification [SDA]

Abstract

This invention provides novel processes for amplifying nucleic acid sequences of interest, including linear and non-linear amplification. In linear amplification, a single initial primer or nucleic acid construct is utilized to carry out the amplification process. In non-linear amplification, a first initial primer or nucleic acid construct is employed with a subsequent initial primer or nucleic acid construct. In other non-linear amplification processes provided by this invention, a first initial primer or nucleic acid construct is deployed with a second initial primer or nucleic acid construct to amplify the specific nucleic acid sequence of interest and its complement that are provided. A singular primer or a singular nucleic acid construct capable of non-linear amplification can also be used to carry out non-linear amplification in accordance with this invention. Post-termination labeling process for nucleic acid sequencing is also disclosed in this invention that is based upon the detection of tagged molecules that are covalently bound to chemically reactive groups provided for chain terminators. A process for producing nucleic acid sequences having decreased thermodynamic stability to complementary sequences is also provided and achieved by this invention. Unique nucleic acid polymers are also disclosed and provided in addition to other novel compositions, kits and the like.

Claims

1. A kit for isothermal amplification of a sequence of a nucleic acid analyte in a sample, said kit comprising:

a first oligonucleotide primer comprising (i) a 3′

terminal nucleotide sequence that anneals to a single-stranded nucleic acid analyte and serves as the origin of synthesis for synthesizing a first single-stranded nucleic acid molecule complementary at least in part to the sample single-stranded nucleic acid analyte when said nucleic acid analyte is present in said sample, and (ii) a 5′

terminal nucleotide sequence that is complementary to an arbitrary region of the first single-stranded nucleic acid molecule, such that a stem loop can form between the 5′

terminal nucleotide sequence and the complementary region of the first single-stranded nucleic acid molecule;

a second oligonucleotide primer comprising a nucleotide sequence which anneals to a region of the single-stranded nucleic acid analyte located 3′

to where the first oligonucleotide primer anneals thereto;

a third oligonucleotide primer comprising (i) a 3′

terminal nucleotide sequence that anneals to the first single-stranded nucleic acid molecule prepared using the first oligonucleotide primer and serves as the origin of synthesis for synthesizing a second single-stranded nucleic acid molecule complementary at least in part to the first single-stranded nucleic acid molecule, and (ii) a 5′

terminal nucleotide sequence that is complementary to an arbitrary region of the second single-stranded nucleic acid molecule, such that a stem loop can form between the 5′

terminal nucleotide sequence and the complementary region of the second single-stranded nucleic acid molecule;

a polymerizing enzyme having strand displacement activity;

a positive control nucleic acid that comprises, in order, (a) a first sequence complementary to said second oligonucleotide primer, (b) a second sequence complementary to the 3′

terminal nucleotide sequence of said first oligonucleotide primer, (c) a third sequence identical to the 5′

segment of said terminal nucleotide sequence of said first oligonucleotide primer, (d) a fourth sequence complementary to the 5′

segment of said terminal nucleotide sequence of said third oligonucleotide primer, and (e) a fifth sequence identical to the 3′

terminal nucleotide sequence of said third oligonucleotide primer, and

one or more nucleotides which are used by the polymerizing enzyme to extend the primers, wherein

the complementarity of said 5′

terminal nucleotide sequence in said first oligonucleotide primer with sequences generated by extension of said first oligonucleotide primer and the complementarity of said 5′

terminal nucleotide sequence in said third oligonucleotide primer with sequences generated by extension of said third oligonucleotide primer isothermally amplifies sequences between the site on said nucleic acid analyte and said positive control nucleic acid that are complementary to the 3′

terminal nucleotide sequence of said first primer and the site on said first single-stranded nucleic acid molecule that is complementary to the 3′

terminal nucleotide sequence of said third primer, and

said isothermal amplification is provided by stem loop formation of said first and third oligonucleotide primers after template dependent primer extension.

2. The kit according to claim 1, further comprising:

a fourth oligonucleotide primer comprising a nucleotide sequence which anneals to a region of the first single-stranded nucleic acid molecule located 3′

to where the third oligonucleotide primer anneals thereto.

3. The kit according to claim 1, wherein said polymerizing enzyme comprises a DNA polymerase, RNA polymerase, reverse transcriptase, DNA ligase, or a combination of any of the foregoing.

4. The kit according to claim 1, wherein said DNA polymerase has reverse transcriptase activity.

5. The kit according to claim 1, further comprising reagents for carrying out strand extension.

6. The kit according to claim 1, further comprising a detector that generates a change in signal from primer extension.

7. The kit according to claim 1, wherein any of said oligonucleotide primers comprise a detectable label or labels.

8. The kit according to claim 1, wherein said one or more nucleotides are labeled.

9. The kit according to claim 1, further comprising a detector for detection of a product of nucleic acid synthesis.

10. The kit according to claim 1, further comprising a melting temperature regulator.

11. The kit according to claim 10, wherein the melting temperature regulator comprises betaine.

12. The kit according to claim 11, wherein said betaine comprises an effective concentration thereof.

13. The kit according to claim 12, wherein the effective concentration of betaine in reaction solution is about 0.55 M.

27. The kit according to claim 1, wherein said isothermal amplification is provided by stem loop formation, at 53°

C. or higher, of said first and third oligonucleotide primers after template dependent primer extension.

14. A kit for amplifying a target nucleotide sequence under isothermal conditions, the kit comprising:

a first oligonucleotide primer comprising (i) a 3′

terminal nucleotide sequence that anneals to a single-stranded nucleic acid analyte and serves as the origin of synthesis for synthesizing a first single-stranded nucleic acid molecule complementary at least in part to the sample single-stranded nucleic acid analyte when said nucleic acid analyte is present in said sample, and (ii) a 5′

terminal nucleotide sequence that is complementary to an arbitrary region of the first single-stranded nucleic acid molecule, such that a stem loop can form between the 5′

terminal nucleotide sequence and the complementary region of the first single-stranded nucleic acid molecule;

a second oligonucleotide primer comprising a nucleotide sequence which anneals to a region of the single-stranded nucleic acid analyte located 3′

to where the first oligonucleotide primer anneals thereto;

a third oliqonucleotide primer comprising (i) a 3′

terminal nucleotide sequence that anneals to the first single-stranded nucleic acid molecule prepared using the first oligonucleotide primer and serves as the origin of synthesis for synthesizing a second single-stranded nucleic acid molecule complementary at least in part to the first single-stranded nucleic acid molecule, and (ii) a 5′

terminal nucleotide sequence that is complementary to an arbitrary region of the second single-stranded nucleic acid molecule, such that a stem loop can form between the 5′

terminal nucleotide sequence and the complementary region of the second single-stranded nucleic acid molecule;

a polymerizing enzyme having strand displacement activity; and

one or more nucleotides which are used by the polymerizing enzyme to extend the primers, wherein

the complementarity of said 5′

terminal nucleotide sequence in said first oliqonucleotide primer with sequences generated by extension of said first oligonucleotide primer and the complementarity of said 5′

terminal nucleotide sequence in said third oligonucleotide primer with sequences generated by extension of said third oligonucleotide primer isothermally amplifies sequences between the site on said nucleic acid analyte that are complementary to the 3′

terminal nucleotide sequence of said first primer and the site on said first single-stranded nucleic acid molecule that is complementary to the 3′

terminal nucleotide sequence of said third primer, and

said isothermal amplification is provided by stem loop formation, at 53°

C. or higher, of said first and third oliqonucleotide primers after template dependent primer extension.

15. The kit according to claim 14, further comprising:

a fourth oligonucleotide primer comprising a nucleotide sequence which anneals to a region of the first single-stranded nucleic acid molecule located 3′

to where the third oligonucleotide primer anneals thereto.

16. The kit according to claim 14, wherein said polymerizing enzyme comprises a DNA polymerase, RNA polymerase, reverse transcriptase, DNA ligase, or a combination of any of the foregoing.

17. The kit according to claim 14, wherein said DNA polymerase has reverse transcriptase activity.

18. The kit according to claim 14, further comprising reagents for carrying out strand extension.

19. The kit according to claim 14, further comprising a detector that generates a change in signal from primer extension.

20. The kit according to claim 14, wherein any of said oligonucleotide primers comprise a detectable label or labels.

21. The kit according to claim 14, wherein said one or more nucleotides are labeled.

22. The kit according to claim 14, further comprising a detector for detection of a product of nucleic acid synthesis.

23. The kit according to claim 14, further comprising a melting temperature regulator.

24. The kit according to claim 23, wherein the melting temperature regulator comprises betaine.

25. The kit according to claim 24, wherein said betaine comprises an effective concentration thereof.

26. The kit according to claim 25, wherein the effective concentration of betaine in reaction solution is about 0.55 M.

28. A kit for isothermal amplification of a sequence of a nucleic acid analyte in a sample, said kit comprising:

a first oligonucleotide primer comprising (i) a 3′

terminal nucleotide sequence that anneals to a single-stranded nucleic acid analyte and serves as the origin of synthesis for synthesizing a first single-stranded nucleic acid molecule complementary at least in part to the sample single-stranded nucleic acid analyte when said nucleic acid analyte is present in said sample, and (ii) a 5′

terminal nucleotide sequence that is complementary to an arbitrary region of the first single-stranded nucleic acid molecule, such that a stem loop can form between the 5′

terminal nucleotide sequence and the complementary region of the first single-stranded nucleic acid molecule;

a second oligonucleotide primer comprising (i) a 3′

terminal nucleotide sequence that anneals to the first single-stranded nucleic acid molecule prepared using the first oligonucleotide primer and serves as the origin of synthesis for synthesizing a second single-stranded nucleic acid molecule complementary at least in part to the first single-stranded nucleic acid molecule, and (ii) a 5′

terminal nucleotide sequence that is complementary to an arbitrary region of the second single-stranded nucleic acid molecule, such that a stem loop can form between the 5′

terminal nucleotide sequence and the complementary region of the second single-stranded nucleic acid molecule;

a polymerizing enzyme having strand displacement activity;

a positive control nucleic acid that comprises, in order, (a) a first sequence complementary to the 3′

terminal nucleotide sequence of said first oligonucleotide primer, (b) a second sequence identical to the 5′

segment of said terminal nucleotide sequence of said first oligonucleotide primer, (c) a third sequence complementary to the 5′

segment of said terminal nucleotide sequence of said second oligonucleotide primer, and (d) a fourth sequence identical to the 3′

terminal nucleotide sequence of said third oligonucleotide primer, and

one or more nucleotides which are used by the polymerizing enzyme to extend the primers, wherein

the complementarity of said 5′

terminal nucleotide sequence in said first oligonucleotide primer with sequences generated by extension of said first oligonucleotide primer and the complementarity of said 5′

terminal nucleotide sequence in said second oligonucleotide primer with sequences generated by extension of said second oligonucleotide primer isothermally amplifies sequences between the site on said nucleic acid analyte and said positive control nucleic acid that are complementary to the 3′

terminal nucleotide sequence of said first primer and the site on said first single-stranded nucleic acid molecule that is complementary to the 3′

terminal nucleotide sequence of said second primer, and

said isothermal amplification is provided by stem loop formation of said first and second oligonucleotide primers after template dependent primer extension.

29. The kit according to claim 28, further comprising a third oligonucleotide primer complementary to said analyte and said positive control nucleic acid.

30. The kit according to claim 29, wherein the region of said analyte and said positive control nucleic acid that is complementary to said third primer is 5′

to where said first oligonucleotide primer binds to said analyte or said control nucleic acid and said third prime displaces said first oligonucleotide primer after said first oligonucleotide primer has undergone template dependent primer extension.

31. The kit according to claim 30, further comprising a fourth oligonucleotide primer complementary to a complementary copy of said analyte and said control nucleic acid.

32. The kit according to claim 29, wherein the region of said complementary copy of said analyte and said control nucleic acid that is complementary to said fourth primer is 5′

to where said second oligonucleotide primer binds to said complementary copy and said fourth primer displaces said second oligonucleotide primer after said second oligonucleotide primer has undergone template dependent primer extension.

33. The kit according to claim 28, further comprising a third oligonucleotide primer complementary to a loop formed during said isothermal amplification.

34. The kit according to claim 33, further comprising a fourth oligonucleotide complementary to a loop formed during said isothermal amplification.

35. The kit according to claim 28, wherein said isothermal amplification is provided by stem loop formation, at 53°

C. or higher, of said first and second oligonucleotide primers after template dependent primer extension.