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组蛋白H4赖氨酸20三甲基化:染色质结构与疾病中的关键表观遗传调控因子

Histone 4 lysine 20 tri-methylation: a key epigenetic regulator in chromatin structure and disease.

作者信息

Agredo Alejandra, Kasinski Andrea L

机构信息

Department of Biological Sciences, Purdue University, West Lafayette, IN, United States.

Purdue Life Sciences Interdisciplinary Program (PULSe), Purdue University, West Lafayette, IN, United States.

出版信息

Front Genet. 2023 Aug 21;14:1243395. doi: 10.3389/fgene.2023.1243395. eCollection 2023.

Abstract

Chromatin is a vital and dynamic structure that is carefully regulated to maintain proper cell homeostasis. A great deal of this regulation is dependent on histone proteins which have the ability to be dynamically modified on their tails via various post-translational modifications (PTMs). While multiple histone PTMs are studied and often work in concert to facilitate gene expression, here we focus on the tri-methylation of histone H4 on lysine 20 (H4K20me3) and its function in chromatin structure, cell cycle, DNA repair, and development. The recent studies evaluated in this review have shed light on how H4K20me3 is established and regulated by various interacting partners and how H4K20me3 and the proteins that interact with this PTM are involved in various diseases. Through analyzing the current literature on H4K20me3 function and regulation, we aim to summarize this knowledge and highlights gaps that remain in the field.

摘要

染色质是一种至关重要且动态变化的结构,受到精细调控以维持细胞内环境的稳态。这种调控在很大程度上依赖于组蛋白,这些组蛋白能够通过各种翻译后修饰(PTM)在其尾部进行动态修饰。虽然多种组蛋白PTM已被研究,并且它们常常协同作用以促进基因表达,但在此我们聚焦于组蛋白H4赖氨酸20位点的三甲基化(H4K20me3)及其在染色质结构、细胞周期、DNA修复和发育中的功能。本综述中评估的近期研究揭示了H4K20me3是如何由各种相互作用的伙伴建立和调控的,以及H4K20me3和与这种PTM相互作用的蛋白质如何参与各种疾病。通过分析关于H4K20me3功能和调控的现有文献,我们旨在总结这些知识并突出该领域仍存在的空白。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6287/10475950/0330d7f5c0a2/fgene-14-1243395-g001.jpg

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