Journal of Bacteriology, October 2001, p. 5772-5777, Vol. 183, No. 19
0021-9193/01/$04.00+0 DOI: 10.1128/JB.183.19.5772-5777.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
helD on DNA Repair
and Homologous Recombination
Department of Microbial Biotechnology, Centro Nacional de Biotecnología, CSIC, Campus Universidad Autónoma de Madrid, Cantoblanco, 28049 Madrid, Spain,1 and INRA-Génétique Microbienne, 78352 Jouy-en-Josas Cedex, France2
Received 18 April 2001/Accepted 9 July 2001
The B. subtilis
helD allele
rendered cells proficient in transformational recombination and
moderately sensitive to methyl methanesulfonate when present in an
otherwise Rec+ strain. The
helD allele
was introduced into rec-deficient strains representative
of the
(recF strain),
(addA addB),
(recH),
(
recU), and
(
recS) epistatic groups. The
helD
mutation increased the sensitivity to DNA-damaging agents of
addAB,
recU, and
recS cells, did not affect the survival of
recH cells, and decreased the sensitivity of
recF cells.
helD also partially suppressed the DNA repair phenotype of other mutations classified within the
epistatic group, namely the recL,
recO, and recR mutations. The
helD allele marginally reduced plasmid transformation (three- to sevenfold) of mutations classified within the
,
, and
epistatic groups. Altogether, these data indicate that the loss of
helicase IV might stabilize recombination repair intermediates formed
in the absence of recFLOR and render
recFLOR, addAB, and recH cells impaired in plasmid transformation.
| Appl. Environ. Microbiol. | Infect. Immun. | Eukaryot. Cell |
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