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组蛋白变体表观遗传作用背后的结构决定因素

The Structural Determinants behind the Epigenetic Role of Histone Variants.

作者信息

Cheema Manjinder S, Ausió Juan

机构信息

Department of Biochemistry and Microbiology, University of Victoria, Victoria, BC V8W-3P6, Canada.

出版信息

Genes (Basel). 2015 Jul 23;6(3):685-713. doi: 10.3390/genes6030685.

Abstract

Histone variants are an important part of the histone contribution to chromatin epigenetics. In this review, we describe how the known structural differences of these variants from their canonical histone counterparts impart a chromatin signature ultimately responsible for their epigenetic contribution. In terms of the core histones, H2A histone variants are major players while H3 variant CenH3, with a controversial role in the nucleosome conformation, remains the genuine epigenetic histone variant. Linker histone variants (histone H1 family) haven't often been studied for their role in epigenetics. However, the micro-heterogeneity of the somatic canonical forms of linker histones appears to play an important role in maintaining the cell-differentiated states, while the cell cycle independent linker histone variants are involved in development. A picture starts to emerge in which histone H2A variants, in addition to their individual specific contributions to the nucleosome structure and dynamics, globally impair the accessibility of linker histones to defined chromatin locations and may have important consequences for determining different states of chromatin metabolism.

摘要

组蛋白变体是组蛋白对染色质表观遗传学贡献的重要组成部分。在本综述中,我们描述了这些变体与其经典组蛋白对应物已知的结构差异如何赋予染色质特征,最终导致其表观遗传学贡献。就核心组蛋白而言,H2A组蛋白变体是主要参与者,而H3变体CenH3在核小体构象中具有争议性作用,仍是真正的表观遗传组蛋白变体。连接组蛋白变体(组蛋白H1家族)在表观遗传学中的作用鲜少被研究。然而,连接组蛋白体细胞经典形式的微异质性似乎在维持细胞分化状态中起重要作用,而不依赖细胞周期的连接组蛋白变体则参与发育过程。一幅图景开始浮现,即H2A组蛋白变体除了对核小体结构和动力学有各自特定贡献外,还会整体损害连接组蛋白与特定染色质位置的结合能力,这可能对决定染色质代谢的不同状态产生重要影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31dc/4584325/f029c72b27bd/genes-06-00685-g001.jpg

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