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休眠起始点对基因组稳定性的贡献:从细胞生物学到人类遗传学

The contribution of dormant origins to genome stability: from cell biology to human genetics.

作者信息

Alver Robert C, Chadha Gaganmeet Singh, Blow J Julian

机构信息

Centre for Gene Regulation & Expression, College of Life Sciences, University of Dundee, Dow Street, Dundee DD1 5EH, UK.

Centre for Gene Regulation & Expression, College of Life Sciences, University of Dundee, Dow Street, Dundee DD1 5EH, UK.

出版信息

DNA Repair (Amst). 2014 Jul;19(100):182-9. doi: 10.1016/j.dnarep.2014.03.012. Epub 2014 Apr 24.

DOI:10.1016/j.dnarep.2014.03.012
PMID:24767947
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4065331/
Abstract

The ability of a eukaryotic cell to precisely and accurately replicate its DNA is crucial to maintain genome stability. Here we describe our current understanding of the process by which origins are licensed for DNA replication and review recent work suggesting that fork stalling has exerted a strong selective pressure on the positioning of licensed origins. In light of this, we discuss the complex and disparate phenotypes observed in mouse models and humans patients that arise due to defects in replication licensing proteins.

摘要

真核细胞精确且准确地复制其DNA的能力对于维持基因组稳定性至关重要。在此,我们描述了目前对DNA复制起始点获得许可的过程的理解,并回顾了近期的研究工作,这些工作表明复制叉停滞对已获得许可的起始点的定位施加了强大的选择压力。鉴于此,我们讨论了在小鼠模型和人类患者中由于复制许可蛋白缺陷而观察到的复杂且不同的表型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3fcb/4065331/2e451de6f85e/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3fcb/4065331/e551dec46823/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3fcb/4065331/f7f1dc1a2c61/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3fcb/4065331/ba2163a97a87/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3fcb/4065331/2e451de6f85e/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3fcb/4065331/e551dec46823/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3fcb/4065331/f7f1dc1a2c61/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3fcb/4065331/ba2163a97a87/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3fcb/4065331/2e451de6f85e/gr4.jpg

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引用本文的文献

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本文引用的文献

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ATR prohibits replication catastrophe by preventing global exhaustion of RPA.ATR 通过防止 RPA 的全球耗竭来阻止复制灾难。
Cell. 2013 Nov 21;155(5):1088-103. doi: 10.1016/j.cell.2013.10.043.
2
Multi-step loading of human minichromosome maintenance proteins in live human cells.活细胞中人源微小染色体维持蛋白的多步加载。
J Biol Chem. 2013 Dec 13;288(50):35852-67. doi: 10.1074/jbc.M113.474825. Epub 2013 Oct 24.
3
A Meier-Gorlin syndrome mutation in a conserved C-terminal helix of Orc6 impedes origin recognition complex formation.
ORC缺陷细胞中的特定起始点选择和过量功能性MCM2-7装载
Nucleic Acids Res. 2025 Jun 6;53(11). doi: 10.1093/nar/gkaf518.
4
Embryonic genome instability upon DNA replication timing program emergence.胚胎基因组在 DNA 复制时间程序出现时的不稳定性。
Nature. 2024 Sep;633(8030):686-694. doi: 10.1038/s41586-024-07841-y. Epub 2024 Aug 28.
5
Embryonic stem cells maintain high origin activity and slow forks to coordinate replication with cell cycle progression.胚胎干细胞保持着较高的起始活性,并减缓叉的速度,以协调复制与细胞周期进程。
EMBO Rep. 2024 Sep;25(9):3757-3776. doi: 10.1038/s44319-024-00207-5. Epub 2024 Jul 25.
6
APC/C prevents a noncanonical order of cyclin/CDK activity to maintain CDK4/6 inhibitor-induced arrest.后期促进复合物/细胞周期体(APC/C)可防止细胞周期蛋白/细胞周期蛋白依赖性激酶(cyclin/CDK)活性出现非经典顺序,以维持CDK4/6抑制剂诱导的细胞停滞。
Proc Natl Acad Sci U S A. 2024 Jul 23;121(30):e2319574121. doi: 10.1073/pnas.2319574121. Epub 2024 Jul 18.
7
DBF4, not DRF1, is the crucial regulator of CDC7 kinase at replication forks.在复制叉处,DBF4 而非 DRF1 是 CDC7 激酶的关键调节因子。
J Cell Biol. 2024 Aug 5;223(8). doi: 10.1083/jcb.202402144. Epub 2024 Jun 12.
8
RNF4 prevents genomic instability caused by chronic DNA under-replication.RNF4可防止由慢性DNA复制不足引起的基因组不稳定。
DNA Repair (Amst). 2024 Mar;135:103646. doi: 10.1016/j.dnarep.2024.103646. Epub 2024 Feb 7.
9
APC/C prevents non-canonical order of cyclin/CDK activity to maintain CDK4/6 inhibitor-induced arrest.后期促进复合物/细胞周期体(APC/C)可防止细胞周期蛋白/细胞周期蛋白依赖性激酶(cyclin/CDK)活性的非经典顺序,以维持CDK4/6抑制剂诱导的细胞停滞。
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10
Origins of DNA replication in eukaryotes.真核生物中 DNA 复制的起源。
Mol Cell. 2023 Feb 2;83(3):352-372. doi: 10.1016/j.molcel.2022.12.024. Epub 2023 Jan 13.
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