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Journal of Bacteriology, January 2000, p. 463-468, Vol. 182, No. 2
Department of Pharmacology and Molecular
Toxicology, University of Massachusetts Medical School, Worcester,
Massachusetts 01655
Received 20 July 1999/Accepted 29 October 1999
Double mutants of Escherichia coli dam (DNA adenine
methyltransferase) strains with ruvA, ruvB, or
ruvC could not be constructed, whereas dam
derivatives with recD, recF, recJ,
and recR were viable. The ruv gene products are
required for Holliday junction translocation and resolution of
recombination intermediates. A dam recG (Holliday junction
translocation) mutant strain was isolated but at a very much lower
frequency than expected. The inviability of a dam lexA (Ind
0021-9193/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Recombination Is Essential for Viability of an
Escherichia coli dam (DNA Adenine Methyltransferase)
Mutant
) host was abrogated by the simultaneous presence of
plasmids encoding both recA and ruvAB. This
result indicates that of more than 20 SOS genes, only recA
and ruvAB need to be derepressed to allow for
dam mutant survival. The presence of mutS or
mutL mutations allowed the construction of dam
lexA (Ind
) derivatives. The requirement for
recA, recB, recC, ruvA,
ruvB, ruvC, and possibly recG gene
expression indicates that recombination is essential for viability of
dam bacteria probably to repair DNA double-strand breaks.
The effect of mutS and mutL mutations indicates
that DNA mismatch repair is the ultimate source of most of these DNA
breaks. The requirement for recombination also suggests an explanation
for the sensitivity of dam cells to certain DNA-damaging agents.
*
Mailing address: Department of Pharmacology and
Molecular Toxicology, University of Massachusetts Medical School, 55 Lake Ave., Worcester, MA 01655. Phone: (508) 856-3330. Fax: (508)
856-3036. E-mail: martin.marinus{at}umassmed.edu.
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