Processes for quantitative or qualitative detection of single-stranded nucleic acids

• US 8,247,179 B2
• Filed: 10/15/2009
• Issued: 08/21/2012
• Est. Priority Date: 03/12/2002
• Status: Expired due to Term

• Current Assignee: Enzo Life Sciences Incorporated (Enzo Biochem Incorporated)
• Original Assignee: Enzo Life Sciences Incorporated (Enzo Biochem Incorporated)
• Inventors: Rabbani, Elazar, Stavrianopoulos, Jannis G., Donegan, James J., Coleman, Jack, Liu, Dakai
• Primary Examiner(s): Chunduru, Prabha
• Application Number:
  US12/580,053
• Publication Number:
  US 20100184042A1
• Time in Patent Office: 1,041 Days
• Field of Search: 435/6, 435/91.2, 536/22.1, 536/24.33
• US Class Current: 435/6.12
• CPC Class Codes: C12Q 1/6818 involving interaction of two or more labels, e.g. resonant energy transfer
• CPC Class Codes: C12Q 1/6834 Enzymatic or biochemical coupling of nucleic acids to a solid phase
• 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 1/686 Polymerase chain reaction [PCR]
• CPC Class Codes: C12Q 2533/101 Primer extension
• CPC Class Codes: C12Q 2561/113 Real time assay
• CPC Class Codes: C12Q 2565/101 Interaction between at least two labels
• CPC Class Codes: G01N 21/64 Fluorescence; Phosphorescence
• CPC Class Codes: G01N 21/6486 Measuring fluorescence of biological material, e.g. DNA, RNA, cells G01N21/6428 takes precedence

Abstract

This invention provides for compositions for use in real time nucleic acid detection processes. Such real time nucleic acid detection processes are carried out with energy transfer elements attached to nucleic acid primers, nucleotides, nucleic acid probes or nucleic acid binding agents. Real time nucleic acid detection allows for the qualitative or quantitative detection or determination of single-stranded or double-stranded nucleic acids of interest in a sample. Other processes are provided by this invention including processes for removing a portion of a homopolymeric sequence, e.g., poly A sequence or tail, from an analyte or library of analytes. Compositions useful in carrying out such removal processes are also described and provided.

Claims

1. A process for detecting qualitatively or quantitatively the presence of a single-stranded or double-stranded nucleic acid of interest in a sample, said process comprising the steps of:

(a) providing

(i) a composition of matter comprising at least two parts;

a first part comprising at least one first nucleic acid primer that comprises

(A) at least one first energy transfer element; and

(B) a nucleic acid sequence that is complementary to a nucleotide sequence in at least a portion of said nucleic acid of interest; and

a second part comprising at least one second nucleic acid primer that comprises;

(A′

) at least one second energy transfer element; and

(B′

) a nucleic acid sequence that is identical to a nucleotide sequence in at least a portion of said nucleic acid of interest;

wherein

said first nucleic acid primer does not comprise said second energy transfer element, and wherein said second nucleic acid primer does not comprise said first energy transfer element,

said first energy transfer element is an energy transfer donor and said second energy transfer element is an energy transfer acceptor, or said first energy transfer element is an energy transfer acceptor and said second energy transfer element is an energy transfer donor, and

neither the first nucleic acid primer nor the second nucleic acid primer is fixed or immobilized to a solid support;

(ii) a sample suspected of containing said nucleic acid of interest; and

(iii) reagents for carrying out nucleic acid strand extension;

(b) forming a reaction mixture comprising (i), (ii) and (iii) above;

(c) contacting under hybridization conditions said first nucleic acid primer with one strand of said nucleic acid of interest and contacting under hybridization conditions said second nucleic acid primer with the complementary strand of said nucleic acid of interest if present;

(d) extending said first nucleic acid primer and said second nucleic acid primer to form a first primer-extended nucleic acid sequence and a second primer-extended nucleic acid sequence if said complementary strand is present;

(e) separating said first primer-extended nucleic acid sequence from said nucleic acid of interest and separating said second primer-extended nucleic acid sequence from said complementary strand of said nucleic acid of interest if present;

(f) contacting under hybridization conditions said first nucleic acid primer with said nucleic acid of interest or said second primer-extended nucleic acid sequence from step (e), and contacting under hybridization conditions said second nucleic acid primer with said first primer-extended nucleic acid sequence from step (e); and

(g) detecting the presence or quantity of said nucleic acid of interest by detecting energy transfer between said first and second energy transfer elements.

2. The process of claim 1, wherein said complementary strand of the nucleic acid of interest is present.

3. The process of claim 1, wherein after said contacting step (f), said process further comprises repeating said extending step (d).

4. The process of claim 3, said process further comprising the step (e′

) of separating said first primer-extended nucleic acid sequence from said second primer-extended nucleic acid sequence, and repeating step (f) thereafter.

5. The process of claim 4, wherein steps (d), (e′

) and (f) are repeated.

6. The process of claim 5, wherein said detecting step (g) is carried out at specific intervals during or after said extending step (d), said separating step (e′

), or said contacting step (f).

7. The process of claim 4, wherein in the providing step (a), said reagents (iii) comprise DNA polymerase, DNA ligase, or both.

8. The process of claim 7, wherein said DNA polymerase, DNA ligase, or both, are thermostable.

9. The process of claim 1, wherein said separating step is carried out by thermal denaturation or strand displacement.

10. The process of claims 1, wherein said nucleic acid of interest has been rendered single stranded before or during said reaction mixture forming step (b).

11. The process of claim 1, wherein in said providing step (a), said first nucleic acid primer comprises more than one first energy transfer element.

12. The process of claim 1, wherein in said providing step (a), said second nucleic acid primer comprises more than one second energy transfer element.

13. The process of claim 1, wherein in said providing step (a), more than one first nucleic acid primer, or more than one second nucleic acid primer, or both, are provided.

14. The process of claim 1, wherein in said providing step (a), said first energy transfer element and said second energy transfer element independently comprise fluorescein, fluorescein isothiocyanate (FITC), 6-carboxyfluorescein (6-FAM), naphthofluorescein, rhodamine, rhodamine 6G, rhodamine X, rhodol, sulforhodamine 101, tetramethylrhodamine (TAMRA), tetramethylrhodamineisothiocyanate (TRITC), 4,7-dichlororhodamine, eosin, eosinisothiocyanate (EITC), dansyl, hydroxycoumarin, methoxycoumarin or p-(Dimethyl aminophenylazo) benzoic acid (DABCYL), cyanine dyes, or derivatives of any of the foregoing.

15. The process of claim 1, wherein said first energy transfer element or said second energy transfer element comprises Cy3 or Cy5.

16. The process of claim 1, wherein any or all of said steps are carried out in a closed container system.

17. The process of claim 16, wherein said closed container system comprises an illumination source and a detection device or unit.

18. The process of claim 1, wherein in the providing step (a), said reagents (iii) comprise DNA polymerase.

19. The process of claim 1, wherein in the providing step (a), said reagents (iii) comprise DNA ligase.