Single-molecule insight into stalled replication fork rescue in Escherichia coli

被引:17
作者
Bianco, Piero R. [1 ]
Lu, Yue [1 ]
机构
[1] Univ Nebraska Med Ctr, Coll Pharm, Dept Pharmaceut Sci, Omaha, NE 68198 USA
基金
美国国家卫生研究院;
关键词
DNA-STRAND EXCHANGE; TRANSLOCATING RECBCD ENZYME; RECOMBINATION HOTSPOT-CHI; HOT-SPOT CHI; RECA PROTEIN; BINDING-PROTEIN; HOLLIDAY-JUNCTIONS; HOMOLOGOUS RECOMBINATION; CRYSTAL-STRUCTURE; HELICASE ACTIVITY;
D O I
10.1093/nar/gkab142
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
DNA replication forks stall at least once per cell cycle in Escherichia coli. DNA replication must be restarted if the cell is to survive. Restart is amulti-step process requiring the sequential action of several proteins whose actions are dictated by the nature of the impediment to fork progression. When fork progress is impeded, the sequential actions of SSB, RecG and the RuvABC complex are required for rescue. In contrast, when a template discontinuity results in the forked DNA breaking apart, the actions of the RecBCD pathway enzymes are required to resurrect the fork so that replication can resume. In this review, we focus primarily on the significant insight gained from single-molecule studies of individual proteins, protein complexes, and also, partially reconstituted regression and RecBCD pathways. This insight is related to the bulk-phase biochemical data to provide a comprehensive review of each protein or protein complex as it relates to stalled DNA replication fork rescue.
引用
收藏
页码:4220 / 4238
页数:19
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