Nucleic acid amplification procedure using RNA and DNA composite primers

• US 7,939,258 B2
• Filed: 09/07/2006
• Issued: 05/10/2011
• Est. Priority Date: 09/07/2005
• Status: Active Grant

• Current Assignee: NuGEN Technologies, Inc. (Tecan Group AG)
• Original Assignee: NuGEN Technologies, Inc. (Tecan Group AG)
• Inventors: Kurn, Nurith, Wang, Shenglong
• Primary Examiner(s): Staples; Mark
• Application Number:
  US12/091,843
• Publication Number:
  US 20090130721A1
• Time in Patent Office: 1,706 Days
• Field of Search: None
• US Class Current: 435/6.12
• 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]

Abstract

The invention provides methods for amplification of polynucleotide sequences using primers containing single-stranded RNA. The methods employ use of an enzyme capable of cleaving single-stranded RNA, such as RNase I, to degrade a first RNA-containing primer prior to addition of a second RNA-containing primer. The invention also provides compositions and kits for practicing the amplification methods, as well as methods which use the amplification products.

Claims

1. A method for amplification of a polynucleotide template, comprising:

(a) extending a first primer hybridized to the polynucleotide template with at least one enzyme comprising a DNA polymerase activity, wherein the first primer is a single-stranded composite primer comprising an RNA portion and a 3′

DNA portion, whereby a first complex comprising a first primer extension product and the template polynucleotide is produced;

(b) extending a second primer hybridized to the first primer extension product to produce a second complex comprising the first primer extension product and a second primer extension product wherein the second complex comprises a double-stranded RNA-DNA heteroduplex at one end;

(c) incubating a reaction mixture comprising;

(i) the second complex comprising the first primer extension product and the second primer extension product wherein the second complex comprises a double-stranded RNA-DNA heteroduplex at one end;

(ii) unhybridized first primer; and

(iii) an enzyme that is capable of cleaving single-stranded RNA, whereby the single-stranded RNA portion of excess unhybridized first primer is cleaved prior to amplification;

(d) inactivating the enzyme that is capable of cleaving single-stranded RNA;

(e) cleaving RNA from the double-stranded RNA-DNA heteroduplex with at least one enzyme that is capable of cleaving RNA from a double-stranded RNA-DNA heteroduplex;

(f) introducing a composite amplification primer wherein the composite amplification primer hybridizes to the second primer extension product, and wherein the composite amplification primer comprises an RNA portion and a 3′

DNA portion; and

(g) extending the composite amplification primer hybridized to the second primer extension product with at least one enzyme comprising DNA-dependent DNA polymerase activity, whereby the first primer extension product is displaced, RNA is cleaved from the composite amplification primer and another composite amplification primer hybridizes such that primer extension and strand displacement are repeated, and whereby multiple copies of a polynucleotide amplification product are generated.

2. The method of claim 1, wherein the RNA portion of the first primer is 5′

with respect to the 3′

DNA portion.

3. The method of claim 2, wherein the 5′

RNA portion of the first primer is adjacent to the 3′

DNA portion.

4. The method of claim 1, wherein the first primer is hybridizable to a multiplicity of template polynucleotide sites.

5. The method of claim 1, wherein the RNA portion of the composite amplification primer is 5′

with respect to the 3′

DNA portion.

6. The method of claim 5, wherein the 5′

RNA portion of the composite amplification primer is adjacent to the 3′

DNA portion.

7. The method of claim 1, wherein the template polynucleotide is DNA.

8. The method of claim 1, wherein the template polynucleotide is RNA.

9. The method of claim 1, wherein the first primer comprises at least two different primers.

10. The method of claim 1, wherein the first primer comprises a random sequence.

11. The method of claim 1, wherein the at least one enzyme that cleaves RNA from a double-stranded RNA-DNA hybrid is RNase H.

12. The method of claim 1, wherein the enzyme capable of cleaving single-stranded RNA is RNase I.

13. The method of claim 12, wherein said inactivating said RNase I comprises inactivation by heat.

14. The method of claim 1, wherein step (g) comprises extension of said composite amplification primer in the presence of a non-canonical nucleotide.

15. The method of claim 14, wherein the non-canonical nucleotide is dUTP.

16. The method of claim 1, wherein step (g) comprises extension of said composite amplification primer in the presence of a labeled nucleotide.

17. The method of claim 1, wherein step (g) comprises extension of said composite amplification primer in the presence of a labeled nucleotide terminator.

18. The method of claim 1, wherein said multiple copies of a polynucleotide amplification product are contacted with an enzyme that is capable of cleaving single-stranded RNA, wherein RNA from the composite amplification primer is cleaved.

19. The method of claim 18, wherein the enzyme that is capable of cleaving single-stranded RNA is RNase I.

20. A method for amplification of a polynucleotide template comprising:

(a) providing a reaction mixture comprising;

(i) a complex comprising a first primer extension product and a second primer extension product wherein the complex comprises a double-stranded RNA-DNA heteroduplex at one end, wherein the first primer extension product is complementary to the template, and wherein the second primer extension product is complementary to the first primer extension product; and

(ii) unhybridized first primer that is a single-stranded composite primer comprising an RNA portion and a 3′

DNA portion wherein the 3′

DNA portion of the first primer is hybridizable to the polynucleotide template;

(b) contacting the reaction mixture with an enzyme that is capable of cleaving single-stranded RNA whereby the single-stranded RNA portion of the excess unhybridized first primer is cleaved prior to amplification;

(c) inactivating the enzyme capable of cleaving single-stranded RNA; and

(d) performing amplification on the complex.

21. The method of claim 20 wherein the amplification is carried out with a composite primer comprising a 5′

-RNA portion.

22. The method of claim 21 further comprising

(e) incubating the products of the amplification with an enzyme capable of cleaving single-stranded RNA.