METHOD FOR INSERTING GENETIC MATERIAL INTO GENOMIC DNA

• US 20140377870A1
• Filed: 08/29/2014
• Published: 12/25/2014
• Est. Priority Date: 06/08/2010
• Status: Abandoned Application

• Current Assignee: Arizona Board of Regents (University of Arizona)
• Original Assignee: Arizona Board of Regents (University of Arizona)
• Inventors: JACOBS, Bertram, Langland, Jeffrey, Jancovich, James, Kibler, Karen, White, Stacy, Conwell, Kip
• Application Number:
  US14/473,219
• Publication Number:
  US 20140377870A1
• Time in Patent Office: Days
• US Class Current: 435/456
• CPC Class Codes: C12N 15/70 Vectors or expression systems specially adapted for E. coli
• CPC Class Codes: C12N 15/79 Vectors or expression systems specially adapted for eukaryotic hosts
• CPC Class Codes: C12N 15/80 for fungi
• CPC Class Codes: C12N 15/82 for plant cells , e.g. plant artificial chromosomes (PACs)
• CPC Class Codes: C12N 15/85 for animal cells
• CPC Class Codes: C12N 15/86 Viral vectors
• CPC Class Codes: C12N 15/907 in mammalian cells
• CPC Class Codes: C12N 2710/24143 viral genome or elements thereof as genetic vector
• CPC Class Codes: C12N 2800/40 Systems of functionally co-operating vectors

Abstract

The present invention provides reagents and methods for improved homologous recombination.

Claims

1. A method for homologous recombination, comprising

(a) expressing in a host cell a first nucleic acid encoding a coumermycin dimerization domain of E. coli gyrase B fused to a catalytic domain of mammalian dsRNA dependent protein kinase, PKR (GyrB-PKR), wherein the first nucleic acid is operatively linked to nucleic acid control sequences, and wherein the first nucleic acid is present on a first nucleic acid construct that further comprises:

(i) a first homologous recombination site flanking the first nucleic acid; and

(ii) a second homologous recombination site flanking the first nucleic acid;

wherein the first homologous recombination site and the second homologous recombination site are not capable of recombining with each other;

(b) expressing in the host cell a second expression vector comprising a gene of interest flanked by the first homologous recombination site and the second homologous recombination site, wherein the gene of interest is operatively linked to nucleic acid control sequences; and

(c) culturing the cells in medium comprising coumermycin under conditions suitable to cause host cell death if homologous recombination between the first expression vector and the second expression vector has not occurred.

2. The method of claim 1, wherein the first nucleic acid construct comprises a first expression vector.

3. The method of claim 1, wherein the first nucleic acid construct is stably integrated into the host cell genome.

4. The method of claim 1, wherein the first nucleic acid encodes the GyrB-PKR of SEQ ID NO:

4.

5. The method of claim 1, wherein the first nucleic acid construct further comprises a second nucleic acid encoding a second selection marker, wherein the first homologous recombination site and the second homologous recombination site flank the second nucleic acid.

6. The method of claim 3, wherein the second selection marker is a positive selection marker.

7. The method of claim 3, wherein the second selection marker is a negative selection marker.

8. The method of claim 1, wherein the first nucleic acid construct is a DNA construct and the second expression vector is a DNA vector.

9. The method of claim 1, wherein the first nucleic acid construct comprises a first expression vector.

10. The method of claim 9, wherein the first expression vector and the second expression vector are plasmid expression vectors.

11. The method of claim 9, wherein the first expression vector is a viral expression vector.