Target-dependent reactions using structure-bridging oligonucleotides

• US 6,355,437 B1
• Filed: 10/02/2000
• Issued: 03/12/2002
• Est. Priority Date: 09/19/1997
• Status: Expired due to Term

• Current Assignee: Gen-Probe Incorporated (Hologic Incorporated)
• Original Assignee: Third Wave Technologies Incorporated (Hologic Incorporated)
• Inventors: Neri, Bruce, Fors, Lance, Dong, Fang, Lyamichev, Victor, Brow, Mary Ann D.
• Primary Examiner(s): WHISENANT, ETHAN C
• Application Number:
  US09/677,218
• Time in Patent Office: 526 Days
• Field of Search: 435/6, 536/23.1, 536/24.3, 935/76, 935/77, 935/78
• US Class Current: 506/9
• CPC Class Codes: C12Q 1/6816 characterised by the detection means C12Q1/6804 takes precedence
• CPC Class Codes: C12Q 1/701 Specific hybridization probes
• CPC Class Codes: C12Q 2521/301 Endonuclease
• CPC Class Codes: C12Q 2525/161 incorporating target specific and non-target specific sites
• CPC Class Codes: C12Q 2525/301 Hairpin oligonucleotides

Abstract

The present invention relates to methods and compositions for analyzing nucleic acids. In particular, the present invention provides methods and compositions for the detection and characterization of nucleic acid sequences and sequence changes. The methods of the present invention permit the detection and/or identification of genetic polymorphism such as those associated with human disease and permit the identification of pathogens (e.g., viral and bacterial strain identification).

Claims

1. A method for detecting the presence of a target nucleic acid in a sample, comprising:

a) providing;

i) a sample suspected of containing a target nucleic acid, said target nucleic acid comprising first and second non-contiguous single-stranded regions separated by an intervening region, said intervening region comprising a first double-stranded portion and a second double-stranded portion separated by a connecting single-stranded portion; and

ii) a bridging oligonucleotide comprising a first portion complementary to said first non-contiguous single-stranded region of said target nucleic acid and a second portion complementary to said second non-contiguous single-stranded region of said target nucleic acid;

b) mixing said sample and said bridging oligonucleotide under conditions such that, when said target nucleic acid is present in said sample, said bridging oligonucleotide hybridizes to said target nucleic acid to form an oligonucleotide/target complex; and

c) detecting said oligonucleotide/target complex, thereby detecting the presence of said target nucleic acid in said sample.

2. The method of claim 1, wherein said target nucleic acid is DNA.

3. The method of claim 2, wherein said DNA is viral DNA.

4. The method of claim 3, wherein said virus is selected from the group consisting of Parvoviridae, Papovaviridae, Adenoviridae, Hepadnaviridae, Herpesviridae, Iridoviridae, and Poxviridae.

5. The method of claim 1, wherein said target nucleic acid is RNA.

6. The method of claim 5, wherein said RNA is viral RNA.

7. The method of claim 6, wherein said virus is selected from the group consisting of Picornaviridae, Caliciviridae, Reoviridae, Togaviridae, Flaviviridae, Orthomyxoviridae, Paramyxoviridae, Arenaviridae, Rhabdoviridae, Coronaviridae, Bunyaviridae, and Retroviridae.

8. The method of claim 1, wherein said sample comprises a tissue sample.

9. The method of claim 1, wherein said sample comprises a clinical sample.

10. The method of claim 1, wherein said sample comprises a patient sample.