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1
Histone H4K20 Demethylation by Two hHR23 Proteins.两个 hHR23 蛋白对组蛋白 H4K20 的去甲基化作用。
Cell Rep. 2020 Mar 24;30(12):4152-4164.e6. doi: 10.1016/j.celrep.2020.03.001.
2
H2A.Z facilitates licensing and activation of early replication origins.H2A.Z 促进早期复制起始点的许可和激活。
Nature. 2020 Jan;577(7791):576-581. doi: 10.1038/s41586-019-1877-9. Epub 2019 Dec 25.
3
The SMYD3 methyltransferase promotes myogenesis by activating the myogenin regulatory network.SMYD3 甲基转移酶通过激活肌生成素调控网络促进成肌生成。
Sci Rep. 2019 Nov 21;9(1):17298. doi: 10.1038/s41598-019-53577-5.
4
The Suv420h histone methyltransferases regulate PPAR-γ and energy expenditure in response to environmental stimuli.Suv420h 组蛋白甲基转移酶可响应环境刺激调节 PPAR-γ 和能量消耗。
Sci Adv. 2019 Apr 17;5(4):eaav1472. doi: 10.1126/sciadv.aav1472. eCollection 2019 Apr.
5
miR-29a contributes to breast cancer cells epithelial-mesenchymal transition, migration, and invasion via down-regulating histone H4K20 trimethylation through directly targeting SUV420H2.miR-29a 通过直接靶向 SUV420H2 下调组蛋白 H4K20 三甲基化,从而促进乳腺癌细胞上皮-间充质转化、迁移和侵袭。
Cell Death Dis. 2019 Feb 21;10(3):176. doi: 10.1038/s41419-019-1437-0.
6
Histone H4K20 methylation mediated chromatin compaction threshold ensures genome integrity by limiting DNA replication licensing.组蛋白 H4K20 甲基化介导的染色质紧缩阈值通过限制 DNA 复制许可来确保基因组完整性。
Nat Commun. 2018 Sep 12;9(1):3704. doi: 10.1038/s41467-018-06066-8.
7
The histone demethylase Phf2 acts as a molecular checkpoint to prevent NAFLD progression during obesity.组蛋白去甲基化酶 Phf2 作为一个分子检测点,可防止肥胖期间 NAFLD 的进展。
Nat Commun. 2018 May 29;9(1):2092. doi: 10.1038/s41467-018-04361-y.
8
Suv4-20h1 promotes G1 to S phase transition by downregulating p21 expression in chronic myeloid leukemia K562 cells.Suv4-20h1通过下调慢性髓性白血病K562细胞中的p21表达来促进G1期到S期的转变。
Oncol Lett. 2018 May;15(5):6123-6130. doi: 10.3892/ol.2018.8092. Epub 2018 Feb 21.
9
Dynamic Control of Chromosome Topology and Gene Expression by a Chromatin Modification.染色质修饰对染色体拓扑结构和基因表达的动态调控
Cold Spring Harb Symp Quant Biol. 2017;82:279-291. doi: 10.1101/sqb.2017.82.034439. Epub 2018 Feb 22.
10
Phf8 histone demethylase deficiency causes cognitive impairments through the mTOR pathway.PHF8组蛋白去甲基化酶缺乏通过mTOR途径导致认知障碍。
Nat Commun. 2018 Jan 9;9(1):114. doi: 10.1038/s41467-017-02531-y.

组蛋白 H4 赖氨酸 20 的甲基化:领域现状的批判性分析。

Methylation of histone 4's lysine 20: a critical analysis of the state of the field.

机构信息

Molecular Biology Interdepartmental Program, University of California, Los Angeles, California.

Department of Molecular, Cell, and Developmental Biology, University of California, Los Angeles, California.

出版信息

Physiol Genomics. 2021 Jan 1;53(1):22-32. doi: 10.1152/physiolgenomics.00128.2020. Epub 2020 Nov 16.

DOI:10.1152/physiolgenomics.00128.2020
PMID:33197229
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7847046/
Abstract

Chromatin is a highly dynamic structure whose plasticity is achieved through multiple processes including the posttranslational modification of histone tails. Histone modifications function through the recruitment of nonhistone proteins to chromatin and thus have the potential to influence many fundamental biological processes. Here, we focus on the function and regulation of lysine 20 of histone H4 (H4K20) methylation in multiple biological processes including DNA repair, cell cycle regulation, and DNA replication. The purpose of this review is to highlight recent studies that elucidate the functions associated with each of the methylation states of H4K20, their modifying enzymes, and their protein readers. Based on our current knowledge of H4K20 methylation, we critically analyze the data supporting these functions and outline questions for future research.

摘要

染色质是一种高度动态的结构,其可塑性通过多种过程实现,包括组蛋白尾巴的翻译后修饰。组蛋白修饰通过招募非组蛋白蛋白到染色质上来发挥作用,因此有可能影响许多基本的生物学过程。在这里,我们专注于组蛋白 H4 赖氨酸 20(H4K20)甲基化在多种生物学过程中的功能和调节,包括 DNA 修复、细胞周期调控和 DNA 复制。本文的目的是强调最近的研究,这些研究阐明了与 H4K20 的每种甲基化状态、其修饰酶及其蛋白读取器相关的功能。基于我们目前对 H4K20 甲基化的了解,我们批判性地分析了支持这些功能的数据,并概述了未来研究的问题。