Affiliation:
1. Departmento de Biotecnología Microbiana, Centro Nacional de Biotecnología, CSIC
2. Max-Planck-Institut für Molekulare Genetik, Berlin, Germany
3. Departamento de Biología Molecular, Universidad Autónoma de Madrid, Madrid, Spain
Abstract
ABSTRACT
Bacillus subtilis
mutants classified within the ε (
ruvA
, Δ
ruvB
, Δ
recU
, and
recD
) and η (Δ
recG
) epistatic groups, in an otherwise
rec
+
background, render cells impaired in chromosomal segregation. A less-pronounced segregation defect in Δ
recA
and Δ
sms
(Δ
radA
) cells was observed. The repair deficiency of
addAB
, Δ
recO
, Δ
recR
,
recH
, Δ
recS
, and Δ
subA
cells did not correlate with a chromosomal segregation defect. The sensitivity of ε epistatic group mutants to DNA-damaging agents correlates with ongoing DNA replication at the time of exposure to the agents. The Δ
sms
(Δ
radA
) and Δ
subA
mutations partially suppress the DNA repair defect in
ruvA
and
recD
cells and the segregation defect in
ruvA
and Δ
recG
cells. The Δ
sms
(Δ
radA
) and Δ
subA
mutations partially suppress the DNA repair defect of Δ
recU
cells but do not suppress the segregation defect in these cells. The Δ
recA
mutation suppresses the segregation defect but does not suppress the DNA repair defect in Δ
recU
cells. These results result suggest that (i) the RuvAB and RecG branch migrating DNA helicases, the RecU Holliday junction (HJ) resolvase, and RecD bias HJ resolution towards noncrossovers and that (ii) Sms (RadA) and SubA proteins might play a role in the stabilization and or processing of HJ intermediates.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
55 articles.
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