Cleavage agents

• US 6,090,606 A
• Filed: 12/02/1996
• Issued: 07/18/2000
• Est. Priority Date: 01/24/1996
• Status: Expired due to Term

• Current Assignee: Gen-Probe Incorporated (Hologic Incorporated)
• Original Assignee: Third Wave Technologies Incorporated (Hologic Incorporated)
• Inventors: Lyamichev, Victor I., Kaiser, Michael W., Lyamicheva, Natasha
• Primary Examiner(s): Jones, W. Gary
• Assistant Examiner(s): SHOEMAKER, DEBRA GUNNERSEN
• Application Number:
  US08/758,314
• Time in Patent Office: 1,324 Days
• Field of Search: 435/320.1, 435/199, 435/325, 536/23.1, 536/23.2, 536/23.5, 536/23.7, 536/24.3, 536/24.31, 935/6
• US Class Current: 435/199
• CPC Class Codes: C12N 9/22 Ribonucleases RNAses, DNAses catalytic nucleic acids C12N15/113
• CPC Class Codes: C12Q 1/6823 Release of bound markers
• CPC Class Codes: C12Q 1/683 involving restriction enzymes, e.g. restriction fragment length polymorphism [RFLP]
• CPC Class Codes: C12Q 2561/109 Invader technology

Abstract

The present invention relates to means for the detection and characterization of nucleic acid sequences, as well as variations in nucleic acid sequences. The present invention also relates to improved cleavage means for the detection and characterization of nucleic acid sequences. Structure-specific nucleases derived from a variety of thermostabe organisms are provided. These structure-specific nucleases are used to cleave target-dependent cleavage structures, thereby indicating the presence of specific nucleic acid sequences or specific variations thereof.

Claims

1. A thermostable structure-specific nuclease having an amino acid sequence selected from the group consisting of SEQ ID NOS:

102, 107, 130 and 132.

2. The nuclease of claim 1, wherein said nuclease is encoded by a DNA sequence selected from the group consisting of SEQ ID NO:

101, 106, 129 and 131.

3. A recombinant DNA vector comprising DNA having a nucleotide sequence encoding a structure-specific nuclease, said nucleotide sequence selected from the group consisting of SEQ ID NO:

101, 106, 129 and 131.

4. A host cell transformed with the recombinant vector of claim 3.

5. The host cell of claim 4, wherein said host cell is an Escherichia coli cell.

6. A purified Pyrococcus woesii FEN-1 endonuclease, wherein said Pyrococcus woesii FEN-1 endonuclease is encoded by the plasmid pTrc99-PWFEN-1 (ACTT 207094).

7. The purified endonuclease of claim 6, wherein said endonuclease has a molecular weight of about 38.7 kilodaltons.

8. An isolated oligonucleotide comprising at least a portion of the plasmid pTrc99-PWFEN-1 (ACTT 207094), said portion encoding Pyrococcus woesii FEN-1 endonuclease.

9. The isolated oligonucleotide of claim 8, wherein said oligonucleotide encoding said endonuclease is operably linked to a heterologous promoter.

10. The isolated oligonucleotide of claim 9, wherein said heterologous promoter is an inducible promoter.

11. The isolated oligonucleotide of claim 10, wherein said inducible promoter is selected from the group consisting of the λ

-P_L promoter, the tac promoter, the trp promoter and the trc promoter.

12. A recombinant DNA vector comprising an isolated oligonucleotide, said oligonucleotide comprising at least a portion of the plasmid pTrc99-PWFEN-1 (ACTT 207094), said portion encoding Pyrococcus woesii FEN-1 endonuclease.

13. A host cell transformed with the recombinant vector of claim 12.

14. The host cell of claim 13, wherein said host cell is an Escherichia coli cell.

15. An isolated oligonucleotide comprising a gene encoding a Pyrococcus woesii FEN-1 endonuclease having a molecular weight of about 38.7 kilodaltons, wherein said Pyrococcus woesii FEN-1 endonuclease comprises the plasmid pTrc-99FWFEN-1 (ACTT 207094).

16. The isolated oligonucleotide of claim 15, wherein said gene encoding a Pyrococcus woseii FEN-1 endonuclease is operably linked to a heterologous promoter.

17. The isolated oligonucleotide of claim 16, wherein said heterologous promoter is an inducible promoter.

18. The isolated oligonucleotide of claim 17, wherein said inducible promoter is selected from the group consisting of the λ

-P_L promoter, the tac promoter, the trp promoter and the trc promoter.

19. A recombinant DNA vector comprising DNA having a nucleotide sequence encoding a Pyrococcus woesii FEN-1 endonuclease having a molecular weight of about 38.7 kilodaltons, and wherein said Pyrococcus woesii FEN-1 endonuclease comprises the plasmid pTrc-99FWFEN-1 (ACTT 207094).

20. A host cell transformed with the recombinant vector of claim 19.

21. The host cell of claim 20, wherein said host cell is an Escherichia coli cell.

22. An isolated oligonucleotide encoding Pyrococcus woesii FEN-1 endonuclease, said oligonucleotide comprising a sequence fully complementary to at least 15 consecutive nucleotides of a sequence selected from the group consisting of SEQ ID NOS:

116-119.

23. A recombinant DNA vector comprising the isolated oligonucleotide of claim 22.

24. A host cell transformed with the recombinant vector of claim 23.