Mechanisms for Maintaining Eukaryotic Replisome Progression in the Presence of DNA Damage

被引:9
|
作者
Guilliam, Thomas A. [1 ]
机构
[1] Med Res Council Lab Mol Biol, Div Prot & Nucle Acid Chem, Cambridge, England
基金
英国医学研究理事会; 英国惠康基金;
关键词
DNA replication; replisome; DNA damage tolerance; translesion synthesis; repriming; recoupling; replication fork; CELL NUCLEAR ANTIGEN; REPLICATION FORK REVERSAL; PROTEIN CROSS-LINK; CRYO-EM STRUCTURE; TRANSLESION SYNTHESIS; POLYMERASE-DELTA; CMG HELICASE; HUMAN PRIMPOL; MCM2-7; HELICASE; STRANDED-DNA;
D O I
10.3389/fmolb.2021.712971
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 eukaryotic replisome coordinates template unwinding and nascent-strand synthesis to drive DNA replication fork progression and complete efficient genome duplication. During its advancement along the parental template, each replisome may encounter an array of obstacles including damaged and structured DNA that impede its progression and threaten genome stability. A number of mechanisms exist to permit replisomes to overcome such obstacles, maintain their progression, and prevent fork collapse. A combination of recent advances in structural, biochemical, and single-molecule approaches have illuminated the architecture of the replisome during unperturbed replication, rationalised the impact of impediments to fork progression, and enhanced our understanding of DNA damage tolerance mechanisms and their regulation. This review focusses on these studies to provide an updated overview of the mechanisms that support replisomes to maintain their progression on an imperfect template.
引用
收藏
页数:19
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