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染色质状态的复制偶联遗传

Replication-coupled inheritance of chromatin states.

作者信息

Song Aoqun, Wang Yunting, Liu Cuifang, Yu Juan, Zhang Zixu, Lan Liting, Lin Haiyan, Zhao Jicheng, Li Guohong

机构信息

New Cornerstone Science Laboratory, Frontier Science Center for Immunology and Metabolism, Hubei Key Laboratory of Cell Homeostasis, College of Life Sciences, Taikang Center for Life and Medical Sciences, Wuhan University, Wuhan, 430072, China.

National Laboratory of Biomacromolecules, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, China.

出版信息

Cell Insight. 2024 Aug 23;3(6):100195. doi: 10.1016/j.cellin.2024.100195. eCollection 2024 Dec.

DOI:10.1016/j.cellin.2024.100195
PMID:39391004
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11462216/
Abstract

During the development of eukaryote, faithful inheritance of chromatin states is central to the maintenance of cell fate. DNA replication poses a significant challenge for chromatin state inheritance because every nucleosome in the genome is disrupted as the replication fork passes. It has been found that many factors including DNA polymerases, histone chaperones, as well as, RNA Pol II and histone modifying enzymes coordinate spatially and temporally to maintain the epigenome during this progress. In this review, we provide a summary of the detailed mechanisms of replication-coupled nucleosome assembly and post-replication chromatin maturation, highlight the inheritance of chromatin states and epigenome during these processes, and discuss the future directions and challenges in this field.

摘要

在真核生物的发育过程中,染色质状态的忠实遗传对于细胞命运的维持至关重要。DNA复制对染色质状态的遗传构成了重大挑战,因为当复制叉通过时,基因组中的每个核小体都会被破坏。已经发现,包括DNA聚合酶、组蛋白伴侣以及RNA聚合酶II和组蛋白修饰酶在内的许多因子在空间和时间上协同作用,以在这一过程中维持表观基因组。在本综述中,我们总结了复制偶联核小体组装和复制后染色质成熟的详细机制,强调了这些过程中染色质状态和表观基因组的遗传,并讨论了该领域的未来方向和挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2206/11462216/91161b094803/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2206/11462216/db78e15f1504/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2206/11462216/91161b094803/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2206/11462216/db78e15f1504/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2206/11462216/91161b094803/gr2.jpg

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1
Replication-coupled inheritance of chromatin states.染色质状态的复制偶联遗传
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本文引用的文献

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Structure of a histone hexamer bound by the chaperone domains of SPT16 and MCM2.由SPT16和MCM2的伴侣结构域结合的组蛋白六聚体的结构。
Sci China Life Sci. 2024 Jun;67(6):1305-1307. doi: 10.1007/s11427-024-2560-8. Epub 2024 Mar 7.
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Parental histone transfer caught at the replication fork.组蛋白从亲代到子代的转移发生在复制叉处。
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RNA polymerase II promotes the organization of chromatin following DNA replication.RNA 聚合酶 II 促进 DNA 复制后染色质的组织。
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Specialized replication of heterochromatin domains ensures self-templated chromatin assembly and epigenetic inheritance.染色质结构域的特异性复制确保了自我模板化的染色质组装和表观遗传遗传。
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The N-terminus of Spt16 anchors FACT to MCM2-7 for parental histone recycling.Spt16 的 N 端将 FACT 锚定到 MCM2-7 上,以进行亲本组蛋白的回收。
Nucleic Acids Res. 2023 Nov 27;51(21):11549-11567. doi: 10.1093/nar/gkad846.
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Symmetric inheritance of parental histones contributes to safeguarding the fate of mouse embryonic stem cells during differentiation.亲本组蛋白的对称遗传有助于在分化过程中保护小鼠胚胎干细胞的命运。
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Symmetric inheritance of parental histones governs epigenome maintenance and embryonic stem cell identity.双亲组蛋白的对称遗传控制着表观基因组的维持和胚胎干细胞的身份。
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