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PMID: 2955904 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Mismatch repair and recombination in E. coli.

Cell ·Vol. 50 ·No. 4 ·1987-08-14 ·Pages 621-6

Jones M, Wagner R, Radman M

Abstract

The involvement of the E. coli methyl-directed and very short patch (vsp) mismatch repair systems in bacteriophage lambda recombination has been studied. Genetic crosses and heteroduplex transfection experiments were performed using lambda phages with sequenced mutations in the cl gene. The results indicate that methyl-directed repair does operate during bacteriophage lambda recombination but generally does not contribute to the formation of recombinants involving close markers. Vsp repair apparently acts during bacteriophage lambda recombination to produce recombinants involving close markers because its action does not involve extensive excision tracts. Marker-specific hyperrecombination and the apparent clustering of genetic exchanges in bacteriophage lambda recombination can be accounted for by the action of the vsp repair system.

MeSH Terms
Bacteriophage lambda/genetics Base Composition Crosses, Genetic DNA Repair DNA, Viral/genetics,metabolism DNA-Binding Proteins Escherichia coli/metabolism Genes, Viral Methylation Recombination, Genetic Repressor Proteins/genetics Transfection Viral Proteins Viral Regulatory and Accessory Proteins
Chemicals
DNA, Viral DNA-Binding Proteins Repressor Proteins Viral Proteins Viral Regulatory and Accessory Proteins phage repressor proteins
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Jones M
Wagner R
Radman M
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1987-08-14
Pages
621-6
Language
English
Region
United States
NLM ID
0413066
Subset
IM
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