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本文引用的文献

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Loss of histone H3.3 results in DNA replication defects and altered origin dynamics in .组蛋白 H3.3 的缺失导致. 中的 DNA 复制缺陷和起始原点动力学改变。
Genome Res. 2020 Dec;30(12):1740-1751. doi: 10.1101/gr.260794.120. Epub 2020 Nov 10.
2
Two HIRA-dependent pathways mediate H3.3 de novo deposition and recycling during transcription.两个依赖于 HIRA 的途径介导了转录过程中 H3.3 的从头沉积和回收。
Nat Struct Mol Biol. 2020 Nov;27(11):1057-1068. doi: 10.1038/s41594-020-0492-7. Epub 2020 Sep 7.
3
SUMOylated PRC1 controls histone H3.3 deposition and genome integrity of embryonic heterochromatin.SUMOylated PRC1 控制组蛋白 H3.3 的沉积和胚胎异染色质的基因组完整性。
EMBO J. 2020 Jul 1;39(13):e103697. doi: 10.15252/embj.2019103697. Epub 2020 May 12.
4
Similar yet critically different: the distribution, dynamics and function of histone variants.相似却又截然不同:组蛋白变体的分布、动态变化及功能
J Exp Bot. 2020 Aug 17;71(17):5191-5204. doi: 10.1093/jxb/eraa230.
5
Histone H4 variant, H4G, drives ribosomal RNA transcription and breast cancer cell proliferation by loosening nucleolar chromatin structure.组蛋白H4变体H4G通过松弛核仁染色质结构驱动核糖体RNA转录和乳腺癌细胞增殖。
J Cell Physiol. 2020 Dec;235(12):9601-9608. doi: 10.1002/jcp.29770. Epub 2020 May 9.
6
The regulation and functions of DNA and RNA G-quadruplexes.DNA 和 RNA G-四链体的调控和功能。
Nat Rev Mol Cell Biol. 2020 Aug;21(8):459-474. doi: 10.1038/s41580-020-0236-x. Epub 2020 Apr 20.
7
Short Histone H2A Variants: Small in Stature but not in Function.短型组蛋白 H2A 变体:个头虽小,但功能不减。
Cells. 2020 Apr 2;9(4):867. doi: 10.3390/cells9040867.
8
Histone variant H3.3 residue S31 is essential for Xenopus gastrulation regardless of the deposition pathway.组蛋白变体 H3.3 残基 S31 对于 Xenopus 原肠胚形成是必需的,而与沉积途径无关。
Nat Commun. 2020 Mar 9;11(1):1256. doi: 10.1038/s41467-020-15084-4.
9
Lysine 4 of histone H3.3 is required for embryonic stem cell differentiation, histone enrichment at regulatory regions and transcription accuracy.组蛋白 H3.3 的赖氨酸 4 对于胚胎干细胞分化、组蛋白在调控区域的富集和转录准确性是必需的。
Nat Genet. 2020 Mar;52(3):273-282. doi: 10.1038/s41588-020-0586-5. Epub 2020 Mar 5.
10
Histone H3K27 acetylation is dispensable for enhancer activity in mouse embryonic stem cells.组蛋白H3K27乙酰化对于小鼠胚胎干细胞中的增强子活性而言并非必需。
Genome Biol. 2020 Feb 21;21(1):45. doi: 10.1186/s13059-020-01957-w.

组蛋白变体在精细调节染色质结构和功能中的作用。

The roles of histone variants in fine-tuning chromatin organization and function.

机构信息

Green Center for Reproductive Biology Sciences, Department of Obstetrics and Gynecology, Children's Research Institute, University of Texas Southwestern Medical Center, Dallas, TX, USA.

出版信息

Nat Rev Mol Cell Biol. 2020 Sep;21(9):522-541. doi: 10.1038/s41580-020-0262-8. Epub 2020 Jul 14.

DOI:10.1038/s41580-020-0262-8
PMID:32665685
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8245300/
Abstract

Histones serve to both package and organize DNA within the nucleus. In addition to histone post-translational modification and chromatin remodelling complexes, histone variants contribute to the complexity of epigenetic regulation of the genome. Histone variants are characterized by a distinct protein sequence and a selection of designated chaperone systems and chromatin remodelling complexes that regulate their localization in the genome. In addition, histone variants can be enriched with specific post-translational modifications, which in turn can provide a scaffold for recruitment of variant-specific interacting proteins to chromatin. Thus, through these properties, histone variants have the capacity to endow specific regions of chromatin with unique character and function in a regulated manner. In this Review, we provide an overview of recent advances in our understanding of the contribution of histone variants to chromatin function in mammalian systems. First, we discuss new molecular insights into chaperone-mediated histone variant deposition. Next, we discuss mechanisms by which histone variants influence chromatin properties such as nucleosome stability and the local chromatin environment both through histone variant sequence-specific effects and through their role in recruiting different chromatin-associated complexes. Finally, we focus on histone variant function in the context of both embryonic development and human disease, specifically developmental syndromes and cancer.

摘要

组蛋白在细胞核内既能包装又能组织 DNA。除了组蛋白的翻译后修饰和染色质重塑复合物之外,组蛋白变体也有助于基因组表观遗传调控的复杂性。组蛋白变体的特点是独特的蛋白质序列以及一系列指定的伴侣蛋白系统和染色质重塑复合物,这些系统和复合物调节它们在基因组中的定位。此外,组蛋白变体可以富集特定的翻译后修饰,这些修饰反过来又可以为变体特异性相互作用蛋白募集到染色质提供支架。因此,通过这些特性,组蛋白变体能够以受调控的方式赋予染色质的特定区域独特的特征和功能。在这篇综述中,我们概述了近年来在理解组蛋白变体对哺乳动物系统染色质功能的贡献方面的最新进展。首先,我们讨论了伴侣蛋白介导的组蛋白变体沉积的新分子见解。接下来,我们讨论了组蛋白变体如何通过组蛋白变体序列特异性效应以及通过招募不同的染色质相关复合物来影响染色质特性(如核小体稳定性和局部染色质环境)的机制。最后,我们重点关注组蛋白变体在胚胎发育和人类疾病(特别是发育综合征和癌症)背景下的功能。