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单分子视角下的大肠杆菌复制叉停滞挽救。

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

机构信息

Department of Pharmaceutical Sciences, College of Pharmacy, University of Nebraska Medical Center, Omaha, NE 68198-6025, USA.

出版信息

Nucleic Acids Res. 2021 May 7;49(8):4220-4238. doi: 10.1093/nar/gkab142.

Abstract

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 a multi-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.

摘要

在大肠杆菌中,DNA 复制叉至少会在每个细胞周期中停顿一次。如果细胞要存活,就必须重新启动 DNA 复制。重新启动是一个多步骤的过程,需要几个蛋白质的顺序作用,这些蛋白质的作用取决于阻碍叉前进的性质。当叉前进受阻时,需要 SSB、RecG 和 RuvABC 复合物的顺序作用来进行挽救。相比之下,当模板不连续性导致分叉的 DNA 断裂时,需要 RecBCD 途径酶的作用来复活叉,以便复制可以继续。在这篇综述中,我们主要关注从单个蛋白质、蛋白质复合物的单分子研究以及部分重建的回归和 RecBCD 途径中获得的重要见解。这些见解与批量生化数据相关联,为每个与停滞 DNA 复制叉挽救相关的蛋白质或蛋白质复合物提供了全面的综述。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea49/8096234/94a556e500c8/gkab142fig1.jpg

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