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PMID: 8510642 Published · ppublish English Journal Article

Genetic recombination in Bacillus subtilis 168: effect of recN, recF, recH and addAB mutations on DNA repair and recombination.

Molecular & general genetics : MGG ·Vol. 239 ·No. 1-2 ·1993-05-00 ·Pages 129-36

Alonso JC, Stiege AC, Lüder G

Abstract

A recN- (recN1) strain of Bacillus subtilis was constructed. The effects of this and recF, recH and addAB mutations on recombination proficiency were tested. Mutations in the recN, recF, recH and addAB genes, when present in an otherwise Rec+ B. subtilis strain, did not affect genetic exchange. Strains carrying different combinations of mutations in these genes were constructed and examined for their sensitivity to 4-nitroquinoline-1-oxide (4NQO) and recombination proficiency. The recH mutation did not affect the 4NQO sensitivity of recN and recF cells and it only marginally affected that of addA addB cells. However, it reduced genetic recombination in these cells 10(2)- to 10(4)-fold. The addA addB mutations increased the 4NQO sensitivity of recF and recN cells, but completely blocked genetic recombination of recF cells and marginally affected recombination in recN cells. The recN mutation did not affect the recombinational capacity of recF cells. These data indicate that the recN gene product is required for DNA repair and recombination and that the recF, recH and addAB genes provide overlapping activities that compensate for the effects of single mutants proficiency. We proposed that the recF, recH, recB and addA gene products define four different epistatic groups.

Related Genes
MeSH Terms
Bacillus subtilis/genetics Bacterial Proteins/genetics DNA Repair DNA Restriction Enzymes DNA, Bacterial/genetics DNA-Binding Proteins/genetics Genes, Bacterial Genetic Markers Mutation Recombination, Genetic
Chemicals
Bacterial Proteins DNA, Bacterial DNA-Binding Proteins Genetic Markers recF protein, Bacteria DNA Restriction Enzymes RecN protein, Bacteria
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Alonso J C
Max-Planck-Institut für molekulare Genetik, Berlin, Germany.
Stiege A C
Lüder G
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34 references, click to expand
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Article Info
Journal
Molecular & general genetics : MGG
Abbr.
Mol Gen Genet
ISSN
0026-8925
Published
1993-05-00
Pages
129-36
Language
English
Region
Germany
NLM ID
0125036
Subset
IM
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