Trading places: How do DNA polymerases switch during translesion DNA synthesis?

被引:322
作者
Friedberg, EC [1 ]
Lehmann, AR
Fuchs, RPP
机构
[1] Univ Texas, SW Med Ctr, Dept Pathol, Lab Mol Pathol, Dallas, TX 75390 USA
[2] Univ Sussex, Genome Damage & Stabil Ctr, Brighton BN1 9RQ, E Sussex, England
[3] Ecole Super BIotechnol Strasbourg, CNRS, UPR 9003, F-67400 Strasbourg, France
关键词
D O I
10.1016/j.molcel.2005.03.032
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The replicative bypass of base damage in DNA (translesion DNA synthesis [TLS]) is a ubiquitous mechanism for relieving arrested DNA replication. The process requires multiple polymerase switching events during which the high-fidelity DNA polymerase in the replication machinery arrested at the primer terminus is replaced by one or more polymerases that are specialized for TLS. When replicative bypass is fully completed, the primer terminus is once again occupied by high-fidelity polymerases in the replicative machinery. This review addresses recent advances in our understanding of DNA polymerase switching during TLS in bacteria such as E. coli and in lower and higher eukaryotes.
引用
收藏
页码:499 / 505
页数:7
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