Methods and compositions for generation of multiple copies of nucleic acid sequences and methods of detection thereof

• US 8,334,116 B2
• Filed: 06/02/2010
• Issued: 12/18/2012
• Est. Priority Date: 12/13/2000
• Status: Expired due to Fees

• Current Assignee: NuGEN Technologies, Inc. (Tecan Group AG)
• Original Assignee: NuGEN Technologies, Inc. (Tecan Group AG)
• Inventors: Kurn, Nurith
• Primary Examiner(s): Mummert, Stephanie K
• Application Number:
  US12/792,702
• Publication Number:
  US 20100311066A1
• Time in Patent Office: 930 Days
• Field of Search: None
• US Class Current: 435/91.2
• CPC Class Codes: C12Q 1/6823 Release of bound markers
• CPC Class Codes: C12Q 1/6827 for detection of mutation or polymorphism
• CPC Class Codes: C12Q 1/6853 using modified primers or templates
• CPC Class Codes: C12Q 1/6869 Methods for sequencing
• CPC Class Codes: C12Q 2521/301 Endonuclease
• CPC Class Codes: C12Q 2525/121 incorporating both deoxyribonucleotides and ribonucleotides
• CPC Class Codes: C12Q 2525/186 incorporating a non-extendable or blocking moiety
• CPC Class Codes: C12Q 2527/101 Temperature
• CPC Class Codes: C12Q 2531/119 Strand displacement amplification [SDA]
• CPC Class Codes: C12Q 2533/101 Primer extension
• CPC Class Codes: C12Q 2533/107 Probe or oligonucleotide ligation
• CPC Class Codes: C12Q 2535/125 Allele specific primer extension

Abstract

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.

Claims

1. A kit, comprising:

(i) a composite primer comprising a 3′

DNA portion and an RNA portion that is 5′

to the 3′

DNA portion, wherein the 3′

DNA portion comprises a 3′

most nucleotide, such that the 3′

most nucleotide of the 3′

DNA portion of the primer hybridizes from about 1 nucleotide to about 10 nucleotides from a sequence of interest;

(ii) one or more terminator deoxyribonucleotide triphosphates; and

(iii) at least one but not all four types of deoxyribonucleotide triphosphates.

2. The kit of claim 1, further comprising a DNA polymerase.

3. A kit, comprising:

(i) a composite primer comprising a 3′

DNA portion and an RNA portion that is 5′

to the 3′

DNA portion, wherein the 3′

DNA portion comprises a 3′

most nucleotide, such that the 3′

most nucleotide of the 3′

DNA portion of the primer hybridizes from about 1 nucleotide to about 10 nucleotides from a sequence of interest;

(ii) one or more terminator deoxyribonucleotide triphosphates; and

(iii) a DNA polymerase, wherein said DNA polymerase does not comprise strand displacement activity.

4. A kit, comprising:

(i) a composite primer comprising a 3′

DNA portion and an RNA portion that is 5′

to the 3′

DNA portion, wherein the 3′

DNA portion comprises a 3′

most nucleotide, such that the 3′

most nucleotide of the 3′

DNA portion of the primer hybridizes from about 1 nucleotide to about 10 nucleotides from a sequence of interest;

(ii) one or more terminator deoxyribonucleotide triphosphates; and

(iii) an enzyme that cleaves RNA from an RNA/DNA hybrid.

5. The kit of claim 4, wherein said composite primer is capable of hybridizing to a sequence on a target polynucleotide such that its hybridization to the target polynucleotide is favored over that of a primer extension product generated by limited extension of said composite primer hybridized to said target polynucleotide and cleavage of RNA from the limited primer extension product.

6. A reaction mixture for generating multiple copies of sequence of interest, said reaction mixture comprising:

(a) a target polynucleotide;

(b) a composite primer that hybridizes to said target polynucleotide, said composite primer comprising an RNA portion and a 3′

DNA portion, said RNA portion is 5′

to the 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 about 1 nucleotide to about 10 nucleotides from a sequence of interest;

(c) a DNA polymerase; and

(d) an enzyme that cleaves RNA from an RNA/DNA hybrid,

wherein when said reaction mixture is incubated under conditions that permit primer hybridization, primer extension and RNA cleavage, 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, whereby multiple copies are generated.

7. The reaction mixture of claim 6, further comprising one or more terminator deoxyribonucleotide triphosphates.

8. The reaction mixture of claim 6, further comprising at least one but not all four types of deoxyribonucleotide triphosphates.

9. The reaction mixture of claim 6, wherein said composite primer is capable of hybridizing to a sequence on the target polynucleotide such that its hybridization to the target polynucleotide is favored over that of a primer extension product generated by limited extension of said composite primer hybridized to the target polynucleotide and cleavage of RNA from the limited primer extension product.

10. The reaction mixture of claim 6, wherein the 3′

DNA portion has 7 to 18 nucleotides.