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DNA polymerases are error-prone at RecA-mediated recombination intermediates
被引:17
|作者:
Pomerantz, Richard T.
[1
]
Goodman, Myron F.
[2
]
O'Donnell, Michael E.
[3
]
机构:
[1] Temple Univ, Sch Med, Fels Inst Canc Res, Dept Biochem, Philadelphia, PA 19122 USA
[2] Univ So Calif, Dept Biol Sci, Los Angeles, CA 90089 USA
[3] Rockefeller Univ, Howard Hughes Med Inst, New York, NY 10021 USA
来源:
基金:
美国国家卫生研究院;
关键词:
DNA replication;
homologous recombination;
double-strand break repair;
stress-induced mutagenesis;
adaptive mutagenesis;
break-induced replication;
STRESS-INDUCED MUTAGENESIS;
BREAK-INDUCED REPLICATION;
ESCHERICHIA-COLI;
KINETIC MECHANISM;
ADAPTIVE MUTATION;
HIGH-FIDELITY;
REPAIR;
BACTERIA;
DINB;
SWITCH;
D O I:
10.4161/cc.25691
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Genetic studies have suggested that Y-family translesion DNA polymerase IV (DinB) performs error-prone recombination-directed replication (RDR) under conditions of stress due to its ability to promote mutations during double-strand break (DSB) repair in growth-limited E. coli cells. In recent studies we have demonstrated that pol IV is preferentially recruited to D-loop recombination intermediates at stress-induced concentrations and is highly mutagenic during RDR in vitro. These findings verify longstanding genetic data that have implicated pol IV in promoting stress-induced mutagenesis at D-loops. In this Extra View, we demonstrate the surprising finding that A-family pol I, which normally exhibits high-fidelity DNA synthesis, is highly error-prone at D-loops like pol IV. These findings indicate that DNA polymerases are intrinsically error-prone at RecA-mediated D-loops and suggest that auxiliary factors are necessary for suppressing mutations during RDR in non-stressed proliferating cells.
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页码:2558 / 2563
页数:6
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