IP Library Granted Patent US 8,785,157
Granted Patent B2
US 8,785,157 · App. 13/208,985 · Granted Jul 22, 2014

Method for using ref protein as a targeted reca-dependent nuclease

Inventors: Michael M. Cox (Oregon, WI); Marielle C. Eichhorn-Gruenig (Berlin, DE); James L. Keck (Monona, WI)
Assignee: Wisconsin Alumni Research Foundation
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Quick Facts
Patent No.
US 8,785,157
App. No.
13/208,985
Granted
Jul 22, 2014
Kind
B2
Abstract

Kits and a method for cleaving double-stranded DNA using Ref and RecA protein and variants thereof at a site having a DNA sequence homologous to the sequence on a single-stranded DNA targeting fragment are disclosed.

Claims (14)

1. A method of cleaving a duplex DNA molecule at any target defined nucleotide sequence, comprising the steps of:

(a) assembling a complex of a single-stranded DNA targeting fragment comprising a nucleotide sequence homologous to a target nucleotide sequence of a duplex DNA molecule with a RecA protein comprising: (i) the amino acid sequence of SEQ ID NO:1; (ii) the amino acid sequence of SEQ ID NO:1 wherein lysine is substituted for glutamic acid at amino acid residue 38, or (iii) an amino acid sequence that has at least 90% sequence identity to SEQ ID NO:1, wherein the RecA functionality is retained;

(b) contacting the complex that is assembled in step (a) with the duplex DNA molecule; and

(c) contacting a Ref protein comprising: (i) SEQ ID NO:2, or (ii) an amino acid sequence that has at least 90% sequence identity to SEQ ID NO:2, wherein the Ref functionality is retained with the duplex DNA molecule;

wherein both strands of the targeted duplex DNA molecule are cleaved within the sequences defined by homology to the single-stranded DNA used as the targeting fragment.

2. The method of claim 1 , wherein the RecA protein used in step 1(a) is a RecA protein comprising the amino acid sequence of SEQ ID NO:1 or a RecA protein comprising the amino acid sequence of SEQ ID NO:1 wherein lysine is substituted for glutamic acid at amino acid residue 38.

3. The method of claim 1 , wherein the Ref protein used in step 1(c) is a Ref protein comprising the amino acid sequence of SEQ ID NO:2.

4. The method of claim 1 , wherein the Ref protein comprising an amino acid sequence that has at least 90% sequence identity to SEQ ID NO:2 that is used in step 1(c) comprises a ββα-metal core fold motif having the amino acid sequence of amino acid residues 112-123 of SEQ ID NO:2, and further comprises two metal binding motifs, one such motif C-terminal to the ββα-metal core fold motif and comprising the amino acid sequence of amino acid residues 96-99 of SEQ ID NO:2, and one such motif N-terminal to the ββα-metal core fold motif and comprising the amino acid sequence of amino acid residues 130-133 of SEQ ID NO:2.

5. The method of claim 1 , wherein the single-stranded DNA targeting fragment is from 30-1,000 nucleotides in length.

6. The method of claim 5 , wherein the single-stranded DNA targeting fragment is from 90-1,000 nucleotides in length.

7. The method of claim 5 , wherein the nucleotide sequence on the single-stranded DNA targeting fragment that is homologous to the target nucleotide sequence is from 60-150 nucleotides in length.

8. The method of claim 1 , wherein one or more of steps 1(a), 1(b), and 1(c) occur within a solution comprising a divalent metal ion.

9. The method of claim 8 , wherein the divalent metal ion is Mg 2+ or Mn 2+ .

10. The method of claim 9 , wherein the divalent metal ion is Mg 2+ .

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 26, 2013
From: COX, MICHAEL; EICHHORN-GRUENIG, MARIELLE; KECK, JAMES
To: WISCONSIN ALUMNI RESEARCH FOUNDATION
Reel/Frame 029876/0219 →
CONFIRMATORY LICENSE Recorded Sep 2, 2011
From: WISCONSIN ALUMNI RESEARCH FOUNDATION
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 026848/0829 →
Continuity (2)
Provisional Application 61373453 · Aug 13, 2010
Related Publication 20120088276A1 · Apr 12, 2012