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本文引用的文献

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Epigenetic regulation: methylation of histone and non-histone proteins.表观遗传调控:组蛋白和非组蛋白的甲基化
Sci China C Life Sci. 2009 Apr;52(4):311-22. doi: 10.1007/s11427-009-0054-z. Epub 2009 Apr 21.
2
Regulation of Set9-mediated H4K20 methylation by a PWWP domain protein.一个含PWWP结构域蛋白对Set9介导的H4K20甲基化的调控
Mol Cell. 2009 Feb 27;33(4):428-37. doi: 10.1016/j.molcel.2009.02.002.
3
Monomethylation of histone H4-lysine 20 is involved in chromosome structure and stability and is essential for mouse development.组蛋白H4赖氨酸20的单甲基化参与染色体结构和稳定性的维持,对小鼠发育至关重要。
Mol Cell Biol. 2009 Apr;29(8):2278-95. doi: 10.1128/MCB.01768-08. Epub 2009 Feb 17.
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Structural origins for the product specificity of SET domain protein methyltransferases.SET结构域蛋白甲基转移酶产物特异性的结构起源
Proc Natl Acad Sci U S A. 2008 Dec 30;105(52):20659-64. doi: 10.1073/pnas.0806712105. Epub 2008 Dec 16.
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Monomethylation of lysine 20 on histone H4 facilitates chromatin maturation.组蛋白H4赖氨酸20位点的单甲基化促进染色质成熟。
Mol Cell Biol. 2009 Jan;29(1):57-67. doi: 10.1128/MCB.00989-08. Epub 2008 Nov 10.
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Di-methyl H4 lysine 20 targets the checkpoint protein Crb2 to sites of DNA damage.二甲基化的组蛋白H4赖氨酸20将检查点蛋白Crb2靶向到DNA损伤位点。
J Biol Chem. 2008 Nov 28;283(48):33168-74. doi: 10.1074/jbc.M806857200. Epub 2008 Sep 29.
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The effect of H3K79 dimethylation and H4K20 trimethylation on nucleosome and chromatin structure.组蛋白H3赖氨酸79二甲基化和组蛋白H4赖氨酸20三甲基化对核小体及染色质结构的影响。
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A chromatin-wide transition to H4K20 monomethylation impairs genome integrity and programmed DNA rearrangements in the mouse.在小鼠中,全染色质向H4K20单甲基化的转变会损害基因组完整性和程序性DNA重排。
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Functional characterization of the Drosophila Hmt4-20/Suv4-20 histone methyltransferase.果蝇Hmt4-20/Suv4-20组蛋白甲基转移酶的功能特性
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程度决定一切:组蛋白H4赖氨酸20甲基化的多功能性

Degrees make all the difference: the multifunctionality of histone H4 lysine 20 methylation.

作者信息

Wang Yu, Jia Songtao

机构信息

Department of Biological Sciences, Columbia University, New York, NY 10027, USA.

出版信息

Epigenetics. 2009 Jul 1;4(5):273-6. doi: 10.4161/epi.4.5.9212. Epub 2009 Jul 5.

DOI:10.4161/epi.4.5.9212
PMID:19571682
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5116398/
Abstract

Residue and degree-specific methylation of histone lysines along with other epigenetic modifications organizes chromatin into distinct domains and regulates almost every aspect of DNA metabolism. Identification of histone methyltransferases and demethylases, as well as proteins that recognize methylated lysines, has clarified the role of each methylation event in regulating different biological pathways. Methylation of histone H4 lysine 20 (H4K20me) plays critical roles in diverse cellular processes such as gene expression, cell cycle progression and DNA damage repair, with each of the three degrees of methylation (mono-, di- and tri-methylation) making a unique contribution. Here we discuss recent studies of H4K20me that have greatly improved our understanding of the regulation and function of this fascinating histone modification.

摘要

组蛋白赖氨酸的残基特异性和程度特异性甲基化,连同其他表观遗传修饰,将染色质组织成不同的结构域,并调节DNA代谢的几乎每个方面。组蛋白甲基转移酶、去甲基酶以及识别甲基化赖氨酸的蛋白质的鉴定,阐明了每个甲基化事件在调节不同生物学途径中的作用。组蛋白H4赖氨酸20(H4K20me)的甲基化在多种细胞过程中发挥关键作用,如基因表达、细胞周期进程和DNA损伤修复,三种甲基化程度(单甲基化、二甲基化和三甲基化)各自都有独特贡献。在这里,我们讨论了关于H4K20me的最新研究,这些研究极大地增进了我们对这种迷人的组蛋白修饰的调控和功能的理解。