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S 期未完成的任务如何影响有丝分裂及其他过程。

How unfinished business from S-phase affects mitosis and beyond.

机构信息

Department of Cellular and Molecular Medicine, Nordea Center for Healthy Aging, Copenhagen N, Denmark.

出版信息

EMBO J. 2013 Oct 16;32(20):2661-71. doi: 10.1038/emboj.2013.211. Epub 2013 Sep 24.

DOI:10.1038/emboj.2013.211
PMID:24065128
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3801442/
Abstract

The eukaryotic cell cycle is conventionally viewed as comprising several discrete steps, each of which must be completed before the next one is initiated. However, emerging evidence suggests that incompletely replicated, or unresolved, chromosomes from S-phase can persist into mitosis, where they present a potential threat to the faithful segregation of sister chromatids. In this review, we provide an overview of the different classes of loci where this 'unfinished S-phase business' can lead to a variety of cytogenetically distinct DNA structures throughout the various steps of mitosis. Furthermore, we discuss the potential ways in which cells might not only tolerate this inevitable aspect of chromosome biology, but also exploit it to assist in the maintenance of genome stability.

摘要

真核细胞周期通常被认为包括几个离散的步骤,每个步骤必须在启动下一个步骤之前完成。然而,新出现的证据表明,来自 S 期的不完全复制或未解决的染色体可以持续到有丝分裂期,在那里它们对姐妹染色单体的忠实分离构成潜在威胁。在这篇综述中,我们概述了不同类别的基因座,在这些基因座中,“未完成的 S 期事务”可以导致有丝分裂的各个步骤中出现各种不同的细胞遗传学上不同的 DNA 结构。此外,我们还讨论了细胞不仅可以容忍这种不可避免的染色体生物学方面,还可以利用它来帮助维持基因组稳定性的潜在方法。

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本文引用的文献

1
ERCC1 and MUS81-EME1 promote sister chromatid separation by processing late replication intermediates at common fragile sites during mitosis.ERCC1 和 MUS81-EME1 在有丝分裂过程中通过处理共同脆弱位点的晚期复制中间体,促进姐妹染色单体分离。
Nat Cell Biol. 2013 Aug;15(8):1008-15. doi: 10.1038/ncb2793. Epub 2013 Jun 30.
2
MUS81 promotes common fragile site expression.MUS81 促进常见脆弱位点的表达。
Nat Cell Biol. 2013 Aug;15(8):1001-7. doi: 10.1038/ncb2773. Epub 2013 Jun 30.
3
Portrait of replication stress viewed from telomeres.从端粒角度看复制应激。
Cancer Sci. 2013 Jul;104(7):790-4. doi: 10.1111/cas.12165. Epub 2013 May 12.
4
Transcription-replication encounters, consequences and genomic instability.转录-复制冲突、后果和基因组不稳定性。
Nat Struct Mol Biol. 2013 Apr;20(4):412-8. doi: 10.1038/nsmb.2543.
5
DNA topoisomerase III localizes to centromeres and affects centromeric CENP-A levels in fission yeast.DNA 拓扑异构酶 III 定位于着丝粒,并影响裂殖酵母着丝粒 CENP-A 水平。
PLoS Genet. 2013;9(3):e1003371. doi: 10.1371/journal.pgen.1003371. Epub 2013 Mar 14.
6
Functions of the centromere and kinetochore in chromosome segregation.着丝粒和动粒在染色体分离中的功能。
Curr Opin Cell Biol. 2013 Jun;25(3):334-40. doi: 10.1016/j.ceb.2013.02.001. Epub 2013 Mar 13.
7
Impediments to replication fork movement: stabilisation, reactivation and genome instability.复制叉移动的障碍:稳定、重新激活与基因组不稳定
Chromosoma. 2013 Mar;122(1-2):33-45. doi: 10.1007/s00412-013-0398-9. Epub 2013 Feb 28.
8
Replication stress links structural and numerical cancer chromosomal instability.复制压力将结构和数量上的癌症染色体不稳定性联系起来。
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