Nucleic acid amplification procedure using RNA and DNA composite primers

• US 8,852,867 B2
• Filed: 05/09/2011
• Issued: 10/07/2014
• Est. Priority Date: 09/07/2005
• Status: Expired due to Fees

• Current Assignee: NuGEN Technologies, Inc. (Tecan Group AG)
• Original Assignee: NuGEN Technologies, Inc. (Tecan Group AG)
• Inventors: Kurn, Nurith, Wang, Shenglong
• Primary Examiner(s): Horlick, Kenneth R.
• Assistant Examiner(s): Tung, Joyce
• Application Number:
  US13/103,865
• Publication Number:
  US 20120045797A1
• Time in Patent Office: 1,247 Days
• Field of Search: 435/6.12, 435/91.2
• 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 amplifying a polynucleotide sequence complementary to a target polynucleotide sequence, comprising:

(a) extending a composite amplification primer in a complex comprising (i) a polynucleotide template comprising the target sequence, wherein the polynucleotide template comprising the target sequence is DNA; and

(ii) the composite amplification primer, wherein the composite amplification primer comprises an RNA portion and a 3′

DNA portion, wherein the composite amplification primer is hybridized to the polynucleotide template;

(b) cleaving the RNA portion of the annealed composite amplification primer with an enzyme that cleaves RNA from an RNA/DNA hybrid such that another composite amplification primer hybridizes to the template and repeats primer extension and strand displacement,

whereby multiple copies of a primer extension product comprising sequence complementary to the target sequence are produced; and

(c) incubating the multiple copies of the primer extension product comprising sequence complementary to the target sequence with an enzyme that is capable of cleaving single-stranded RNA, wherein residual single-stranded RNA from the composite amplification primer in the primer extension product comprising sequence complementary to the target sequence is cleaved.

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

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

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

with respect to the 3′

DNA portion.

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

2. A method of generating multiple copies of a polynucleotide sequence complementary to an RNA sequence of interest, the method comprising:

(a) extending a composite amplification primer in a complex comprising;

(i) a complex of first and second primer extension products, wherein the first primer extension product is produced by extension of a first primer hybridized to a target RNA with at least one enzyme comprising RNA-dependent DNA polymerase activity, wherein the first primer is a composite primer comprising an RNA portion and a 3′

DNA portion, wherein the second primer extension product is generated by extension of a second primer hybridized to the first primer extension product, wherein the second primer is different from the first primer, and wherein RNA from the complex of first and second primer extension products is cleaved with at least one enzyme that cleaves RNA from an RNA/DNA hybrid; and

(ii) a composite amplification primer, the composite amplification primer comprising an RNA portion and a 3′

DNA portion, wherein the composite amplification primer is hybridized to the second primer extension product;

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, whereby multiple copies of a primer extension product comprising polynucleotide sequence complementary to the RNA sequence of interest are generated; and

(b) contacting the multiple copies of the primer extension product comprising sequence complementary to the RNA sequence of interest with an enzyme that is capable of cleaving single-stranded RNA, wherein residual single-stranded RNA from the composite primer in the primer extension product comprising sequence complementary to the RNA sequence of interest is cleaved.

4. The method of claim 2, wherein the enzyme capable of cleaving single-stranded RNA is RNase I.

6. The method of claim 2, wherein the first primer is hybridizable to a multiplicity of template polynucleotide sites.

8. The method of claim 2, wherein the RNA portion of the composite amplification primer is 5′

with respect to the 3′

DNA portion.

10. The method of claim 2, wherein the at least one enzyme that cleaves RNA from a double-stranded RNA-DNA hybrid is RNase H.