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sbcB15 and Δ sbcB Mutations Activate Two Types of RecF Recombination Pathways in Escherichia coli
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ABSTRACT
Escherichia coli
cells with mutations in
recBC
genes are defective for the main RecBCD pathway of recombination and have severe reductions in conjugational and transductional recombination, as well as in recombinational repair of double-stranded DNA breaks. This phenotype can be corrected by suppressor mutations in
sbcB
and
sbcC
(
D
) genes, which activate an alternative RecF pathway of recombination. It was previously suggested that
sbcB15
and Δ
sbcB
mutations, both of which inactivate exonuclease I, are equally efficient in suppressing the
recBC
phenotype. In the present work we reexamined the effects of
sbcB15
and Δ
sbcB
mutations on DNA repair after UV and γ irradiation, on conjugational recombination, and on the viability of
recBC
(
sbcC
) cells. We found that the
sbcB15
mutation is a stronger
recBC
suppressor than Δ
sbcB
, suggesting that some unspecified activity of the mutant SbcB15 protein may be favorable for recombination in the RecF pathway. We also showed that the
xonA2
mutation, a member of another class of ExoI mutations, had the same effect on recombination as Δ
sbcB
, suggesting that it is an
sbcB
null mutation. In addition, we demonstrated that recombination in a
recBC sbcB15 sbcC
mutant is less affected by
recF
and
recQ
mutations than recombination in
recBC
Δ
sbcB sbcC
and
recBC xonA2 sbcC
strains is, indicating that SbcB15 alleviates the requirement for the RecFOR complex and RecQ helicase in recombination processes. Our results suggest that two types of
sbcB
-sensitive RecF pathways can be distinguished in
E. coli
, one that is activated by the
sbcB15
mutation and one that is activated by
sbcB
null mutations. Possible roles of SbcB15 in recombination reactions in the RecF pathway are discussed.
American Society for Microbiology
Title: sbcB15
and Δ
sbcB
Mutations Activate Two Types of RecF Recombination Pathways in
Escherichia coli
Description:
ABSTRACT
Escherichia coli
cells with mutations in
recBC
genes are defective for the main RecBCD pathway of recombination and have severe reductions in conjugational and transductional recombination, as well as in recombinational repair of double-stranded DNA breaks.
This phenotype can be corrected by suppressor mutations in
sbcB
and
sbcC
(
D
) genes, which activate an alternative RecF pathway of recombination.
It was previously suggested that
sbcB15
and Δ
sbcB
mutations, both of which inactivate exonuclease I, are equally efficient in suppressing the
recBC
phenotype.
In the present work we reexamined the effects of
sbcB15
and Δ
sbcB
mutations on DNA repair after UV and γ irradiation, on conjugational recombination, and on the viability of
recBC
(
sbcC
) cells.
We found that the
sbcB15
mutation is a stronger
recBC
suppressor than Δ
sbcB
, suggesting that some unspecified activity of the mutant SbcB15 protein may be favorable for recombination in the RecF pathway.
We also showed that the
xonA2
mutation, a member of another class of ExoI mutations, had the same effect on recombination as Δ
sbcB
, suggesting that it is an
sbcB
null mutation.
In addition, we demonstrated that recombination in a
recBC sbcB15 sbcC
mutant is less affected by
recF
and
recQ
mutations than recombination in
recBC
Δ
sbcB sbcC
and
recBC xonA2 sbcC
strains is, indicating that SbcB15 alleviates the requirement for the RecFOR complex and RecQ helicase in recombination processes.
Our results suggest that two types of
sbcB
-sensitive RecF pathways can be distinguished in
E.
coli
, one that is activated by the
sbcB15
mutation and one that is activated by
sbcB
null mutations.
Possible roles of SbcB15 in recombination reactions in the RecF pathway are discussed.
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