Gene replacement and retrieval with recombinant M13mp bacteriophages

Author:

Blum P1,Holzschu D1,Kwan H S1,Riggs D1,Artz S1

Affiliation:

1. Department of Microbiology, University of California, Davis 95616.

Abstract

We have developed an allele exchange system for shuttling sequences of DNA to and from their original chromosomal loci. Cloned segments of the histidine operon of Salmonella typhimurium and the lactose operon of Escherichia coli served as target sequences and were used to develop the system. Replacement and retrieval of target sequences used the phage M13mp vectors and proceeded through an M13 lysogen intermediate. The intermediates and products of allele exchange were characterized by genetic and hybridization analyses. Several unique properties of M13 lysogens were exploited to devise positive selections to detect integration and excision. These positive selections were used to manipulate phenotypically silent alleles.

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

Reference39 articles.

1. Artz S. W. and D. Holzschu. 1983. Histidine biosynthesis and its regulation p. 379-404. In K. Herrmann and R. Somerville (ed.) Amino acid biosynthesis and genetic regulation. Addison-Wesley Reading Mass.

2. Use of M13mp phages to study gene regulation, structure and function: cloning and recombinational analysis of genes of the Salmonella typhimurium histidine operon;Artz S. W.;Gene,1983

3. Sequence homology requirements for intermolecular recombination in mammalian cells;Ayares D.;Proc. Natl. Acad. Sci. USA,1986

4. DNA sequence changes of mutations in the histidine operon control region that decrease attenuation;Barnes W. M.;J. Mol. Biol.,1983

5. Effects of bacteriophage fl gene III protein on the host cell membrane;Boeke J. D.;Mol. Gen. Genet.,1982

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