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发育、衰老和疾病中的组蛋白与非组蛋白可逆乙酰化作用

Histone and Non-histone Reversible Acetylation in Development, Aging, and Disease.

作者信息

Gunes Sezgin, Hekim Neslihan, Ergun Sercan, Alkan Elzem Nisa, Can Cansu

机构信息

Department of Medical Biology, Medical Faculty, Ondokuz Mayis University, Samsun, Türkiye.

Stem Cell Application and Research Center, Ondokuz Mayis University, Samsun, Türkiye.

出版信息

Results Probl Cell Differ. 2025;75:3-24. doi: 10.1007/978-3-031-91459-1_1.

DOI:10.1007/978-3-031-91459-1_1
PMID:40593205
Abstract

Post-translational modifications (PTM) involve chemical modifications of amino acid residues within histone and non-histone proteins and are chemically diverse. PTM plays a vital role in regulating the chromatin structure in the nucleus, thus gene regulation. Among the various PTM, reversible acetylation of histone non-histone proteins has fundamental functions in various cellular processes. In all organisms, histone acetylation of lysine residues is connected with transcription activation. Acetyltransferases and deacetylases are well-known enzymes in the acetylation of the histone and non-histone proteins. This chapter will review the latest progress in histone and non-histone reversible acetylation epigenetic alterations and mechanisms and summarize how they affect development, aging, and diseases.

摘要

翻译后修饰(PTM)涉及组蛋白和非组蛋白内氨基酸残基的化学修饰,且化学性质多样。PTM在调节细胞核内的染色质结构从而调控基因方面起着至关重要的作用。在各种PTM中,组蛋白和非组蛋白的可逆乙酰化在多种细胞过程中具有基本功能。在所有生物体中,赖氨酸残基的组蛋白乙酰化与转录激活相关。乙酰转移酶和去乙酰化酶是组蛋白和非组蛋白乙酰化过程中广为人知的酶。本章将综述组蛋白和非组蛋白可逆乙酰化表观遗传改变及机制的最新进展,并总结它们如何影响发育、衰老和疾病。

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本文引用的文献

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Role of histone deacetylases and their inhibitors in neurological diseases.组蛋白去乙酰化酶及其抑制剂在神经退行性疾病中的作用。
Pharmacol Res. 2024 Oct;208:107410. doi: 10.1016/j.phrs.2024.107410. Epub 2024 Sep 12.
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Structure of the human TIP60 complex.人源 TIP60 复合物的结构。
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KAT8 is upregulated and recruited to the promoter of Atg8 by FOXO to induce H4 acetylation for autophagy under 20-hydroxyecdysone regulation.KAT8 通过 FOXO 被上调并募集到 Atg8 的启动子上,以在 20-羟基蜕皮酮调节下诱导自噬的 H4 乙酰化。
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Persistent Acetylation of Histone H3 Lysine 56 Compromises the Activity of DNA Replication Origins.组蛋白 H3 赖氨酸 56 的持续乙酰化破坏 DNA 复制起始点的活性。
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Histone 4 lysine 5/12 acetylation enables developmental plasticity of Pristionchus mouth form.组蛋白 4 赖氨酸 5/12 乙酰化使秀丽隐杆线虫口型的发育可塑性成为可能。
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