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拓扑异构酶 IV 在大肠杆菌 DNA 复制过程中跟踪复制叉和 SeqA 复合物。

Topoisomerase IV tracks behind the replication fork and the SeqA complex during DNA replication in Escherichia coli.

机构信息

Department of Microbiology, Molecular Microbiology, Oslo University Hospital, P.O. Box 4950, 0424, Oslo, Norway.

Department of Clinical and Molecular Medicine, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology, Trondheim, Norway.

出版信息

Sci Rep. 2021 Jan 12;11(1):474. doi: 10.1038/s41598-020-80043-4.

DOI:10.1038/s41598-020-80043-4
PMID:33436807
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7803763/
Abstract

Topoisomerase IV (TopoIV) is a vital bacterial enzyme which disentangles newly replicated DNA and enables segregation of daughter chromosomes. In bacteria, DNA replication and segregation are concurrent processes. This means that TopoIV must continually remove inter-DNA linkages during replication. There exists a short time lag of about 10-20 min between replication and segregation in which the daughter chromosomes are intertwined. Exactly where TopoIV binds during the cell cycle has been the subject of much debate. We show here that TopoIV localizes to the origin proximal side of the fork trailing protein SeqA and follows the movement pattern of the replication machinery in the cell.

摘要

拓扑异构酶 IV(TopoIV)是一种重要的细菌酶,可解开新复制的 DNA 并促进子染色体的分离。在细菌中,DNA 复制和分离是同时进行的过程。这意味着 TopoIV 必须在复制过程中不断去除 DNA 之间的连接。在复制和分离之间存在大约 10-20 分钟的短暂时间差,在此期间,子染色体交织在一起。TopoIV 在细胞周期中的结合位置一直是争论的焦点。我们在这里表明,TopoIV 定位于分叉后尾随蛋白 SeqA 的原点近端侧,并遵循细胞中复制机制的运动模式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9c3/7803763/1d305a28d052/41598_2020_80043_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9c3/7803763/036599f38927/41598_2020_80043_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9c3/7803763/c77e0c804499/41598_2020_80043_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9c3/7803763/1d305a28d052/41598_2020_80043_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9c3/7803763/036599f38927/41598_2020_80043_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9c3/7803763/c77e0c804499/41598_2020_80043_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9c3/7803763/1d305a28d052/41598_2020_80043_Fig3_HTML.jpg

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Topoisomerase Inhibitors: Fluoroquinolone Mechanisms of Action and Resistance.拓扑异构酶抑制剂:氟喹诺酮类药物的作用机制与耐药性
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Lack of the H-NS Protein Results in Extended and Aberrantly Positioned DNA during Chromosome Replication and Segregation in Escherichia coli.
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Antibacterials with Novel Chemical Scaffolds in Clinical Development.处于临床开发阶段的具有新型化学骨架的抗菌药物。
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Temporospatial control of topoisomerases by essential cellular processes.细胞基本过程对拓扑异构酶的时空控制。
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Hypothesis: bacteria live on the edge of phase transitions with a cell cycle regulated by a water-clock.假说:细菌生活在相变的边缘,其细胞周期受水钟调控。
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10
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PLoS Genet. 2013;9(8):e1003673. doi: 10.1371/journal.pgen.1003673. Epub 2013 Aug 22.