Methods and compositions for amplifying nucleic acids

• US 20070020667A1
• Filed: 06/29/2006
• Published: 01/25/2007
• Est. Priority Date: 06/30/2005
• Status: Abandoned Application

• Current Assignee: Applied Biosystems LLC (Thermo Fisher Scientific Incorporated)
• Original Assignee: Applied Biosystems LLC (Thermo Fisher Scientific Incorporated)
• Inventors: Shannon, Mark, Ruff, David
• Application Number:
  US11/478,840
• Publication Number:
  US 20070020667A1
• Time in Patent Office: Days
• US Class Current: 435/6
• CPC Class Codes: C12P 19/34 Polynucleotides, e.g. nucleic acids, oligoribonucleotides
• CPC Class Codes: C12Q 1/6846 Common amplification features

Abstract

Methods and compositions for amplifying nucleic acids are provided.

Claims

1. A method of amplifying a plurality of target nucleic acid sequences comprising:

forming a reaction composition comprising (a) a plurality of target nucleic acid sequences, (b) at least one set of primers, and (c) at least one polymerase;

incubating the reaction composition under conditions wherein one or more of the plurality of target nucleic acid sequences are amplified;

wherein at least one of the at least one set of primers comprises a plurality of primers, wherein each primer of the plurality of primers comprises at least one designed portion and at least one random portion;

wherein one of the at least one designed portions consists of two nucleotides at the 5′

portion of the primer.

2. The method of claim 1, wherein at least one of the at least one random portions comprises eight random nucleotides.

3. The method of claim 1, wherein the at least one polymerase is selected from at least one of phi29 DNA polymerase, taq polymerase, stoffel fragment, and Bst DNA polymerase.

4. The method of claim 1, wherein the two nucleotides at the 5′

portion of the primer comprise pyrimidines.

5. The method of claim 4, wherein at least one of the at least one set of primers comprises primers of the sequence CTN₈.

6. The method of claim 1, wherein the two nucleotides at the 5′

portion of the primer comprise purines.

7. The method of claim 6, wherein at least one of the at least one set of primers comprises primers of the sequence GAN₈.

8. The method of claim 1 wherein at least one of the at least one set of primers comprises primers of the sequence SSN₈.

9. The method of claim 1, wherein the at least one DNA polymerase is inactive and is subsequently activated at a given temperature.

10. The method of claim 1, wherein at least one of the at least one random portions is between 6 nucleotides and 9 nucleotides in length.

11. The method of claim 1, wherein the plurality of target nucleic acid sequences comprises genomic DNA.

12. The method of claim 1, wherein the plurality of target nucleic acid sequences are amplified under isothermal reaction conditions.

13. The method of claim 12, wherein the isothermic conditions comprise a temperature of about 50°

C.

14. The method of claim 1, wherein the plurality of target nucleic acid sequences comprises mitochondrial DNA.

15. The method of claim 1, further comprising treating at least one of the plurality of target nucleic acid sequences with a modifying agent before forming the reaction composition.

16. The method of claim 15, wherein the modifying agent is bisulfite.

17. The method of claim 1, wherein the plurality of target nucleic acid sequences comprises one or more forensic markers.

18. The method of claim 1, wherein the reaction composition has only one set of primers.

19. A composition for amplifying a plurality of target nucleic acid sequences comprising:

(a) a plurality of target nucleic acid sequences;

(b) at least one set of primers; and

(c) at least one DNA polymerase;

wherein at least one of the at least one set of primers comprises a plurality of primers, wherein each primer of the plurality of primers comprises at least one designed portion and at least one random portion;

wherein one of the at least one designed portions consists of two nucleotides at the 5′

portion of the primer.

20. The composition of claim 19, wherein one of the at least one random portions comprises eight random nucleotides.

21. The composition of claim 19, wherein the at least one DNA polymerase is selected from at least one of phi29 DNA polymerase, taq polymerase, stoffel fragment, and Bst DNA polymerase.

22. The composition of claim 19, wherein the two nucleotides at the 5′

portion of the primer comprise pyrimidines.

23. The composition of claim 22, wherein at least one of the at least one sets of primers comprises primers of the sequence CTN₈.

24. The composition of claim 19, wherein the two nucleotides at the 5′

portion of the primer comprise purines.

25. The composition of claim 24, wherein one of the at least one primer sets comprises primers of the sequence GAN₈.

26. The method of claim 19 wherein at least one of the at least one set of primers comprises primers of the sequence SSN₈.

27. The composition of claim 19, wherein one of the at least one random portions is between 6 nucleotides and 9 nucleotides in length.

28. The composition of claim 19, wherein the plurality of target nucleic acid sequences comprises genomic DNA.

29. The composition of claim 19, wherein the plurality of target nucleic acid sequences comprises mitochondrial DNA.

30. The composition of claim 19, wherein the plurality of target nucleic acid sequences comprises one or more forensic markers.

31. The composition of claim 19, wherein the reaction composition comprises one set of primers.

32. A method of amplifying a plurality of target nucleic acid sequences comprising:

forming a reaction composition comprising (a) a plurality of target nucleic acid sequences comprising a first position and a second position, (b) at least one set of primers, and (c) at least one DNA polymerase;

incubating the reaction composition under amplification conditions wherein one or more of the plurality of target nucleic acid sequences are amplified to form amplification products;

wherein at least one of the at least one set of primers comprises a plurality of primers, wherein each primer of the plurality of primers comprises at least one designed portion and at least one random portion;

wherein the at least one set of primers produces a first amplification product comprising the first position and a second amplification product comprising the second position;

wherein the amount of first amplification product produced with the at least one set of primers is greater than the amount of first amplification product produced with random primers incubated under the amplification conditions with the plurality of target nucleic acid sequences and the at least one polymerase; and

wherein the amount of second amplification product produced with the at least one set of primers is greater than the amount of second amplification product produced with random primers incubated under the amplification conditions with the plurality of target nucleic acid sequences and the at least one polymerase.

33. The method of claim 32, wherein the first position comprises a telomere region.

34. The method of claim 32, wherein the first position comprises a centromere region.

35. The method of claim 32, wherein the first set of primers comprises primers of the sequence N₃T₄N₃ (SEQ ID NO:

5).

36. A method of determining similarity between a plurality of target nucleic acid sequences from one or more sources and one or more reference sequences comprising:

forming a reaction composition comprising (a) a plurality of target nucleic acid sequences from one or more sources, (b) at least one set of primers, and (c) at least one DNA polymerase;

incubating the reaction composition under conditions wherein one or more of the plurality of target nucleic acid sequences are amplified to form amplification products;

wherein at least one of the at least one set of primers comprises a plurality of primers, wherein each primer of the plurality of primers comprises at least one designed portion and at least one random portion;

wherein one of the at least one designed portions consists of two nucleotides at the 5′

portion of the primer;

comparing sequence information of the amplification products with sequence information of the one or more reference sequences to identify similarities and differences between the sequence information of the amplification products and the sequence information of the one or more reference sequences;

wherein each of the one or more reference sequences comprises a plurality of nucleic acid sequences;

determining the similarity between a plurality of target nucleic acid sequences from one or more sources and the one or more reference sequences based on the identified similarities and differences.

37. The method of claim 36, wherein the comparing sequence information of the amplification products with the sequence information of the one or more reference sequences comprises comparing the sequence of the amplification products at a given nucleic acid polymorphic site to the sequence of the one or more reference sequences at the given nucleic acid polymorphic site.

38. The method of claim 37, wherein the nucleic acid polymorphic site comprises a single nucleotide polymorphism.

39. The method of claim 36, further comprising determining whether one or more of the plurality of target nucleic acid sequences is the same as one of the one or more reference sequences.

40. A method of amplifying a plurality of target nucleic acid sequences comprising:

forming a reaction composition comprising (a) a plurality of target nucleic acid sequences, (b) at least one set of primers, and (c) at least one DNA polymerase;

incubating the reaction composition under conditions wherein one or more of the plurality of target nucleic acid sequences are amplified;

wherein at least one of the at least one set of primers comprises a plurality of primers, wherein each primer of the plurality of primers comprises at least one designed portion and at least one random portion;

wherein one of the at least one designed portions comprises the 5′

portion of the primer.

41. A method of amplifying a plurality of target nucleic acid sequences comprising:

forming a reaction composition comprising (a) a plurality of target nucleic acid sequences, (b) at least one set of primers, and (c) at least one DNA polymerase;

incubating the reaction composition under conditions wherein one or more of the plurality of target nucleic acid sequences are amplified;

wherein at least one of the at least one set of primers comprises a plurality of primers, wherein each primer of the plurality of primers comprises at least one designed portion and at least one random portion;

wherein one of the at least one designed portions comprises the 3′

portion of the primer.

42. A method of amplifying a plurality of target nucleic acid sequences comprising:

forming a reaction composition comprising (a) a plurality of target nucleic acid sequences, (b) at least one set of primers, and (c) at least one DNA polymerase;

incubating the reaction composition under conditions wherein one or more of the plurality of target nucleic acid sequences are amplified;

wherein at least one of the at least one set of primers comprises a plurality of primers, wherein each primer of the plurality of primers comprises at least one designed portion and at least one random portion;

wherein at least one of the at least one designed portions is not a constant portion.