连接体组蛋白:核小体结构特异性识别的新见解。

Amber R. Cutter, J. Hayes
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引用次数: 20

摘要

连接体组蛋白(h1)是后生动物染色质的主要组成部分,在体外和体内都具有多种功能,包括稳定DNA在核小体周围的包裹,促进高阶染色质结构的折叠和组装,影响DNA上的核小体间距,以及调节特定基因的表达。然而,H1如何与核小体结合并识别核小体表面独特结构特征的许多分子细节仍不清楚。许多混杂的研究不仅由于实验限制,而且由于使用了不同的连接蛋白异构体和核小体结构而变得复杂。这篇综述总结了几十年来的研究结果,得出了H1与核小体相关的几种模型,重点介绍了H1在染色质中相互作用的多种模式的最新进展,同时强调了剩余的问题。
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Linker histones: novel insights into structure-specific recognition of the nucleosome.
Linker histones (H1s) are a primary component of metazoan chromatin, fulfilling numerous functions, both in vitro and in vivo, including stabilizing the wrapping of DNA around the nucleosome, promoting folding and assembly of higher order chromatin structures, influencing nucleosome spacing on DNA, and regulating specific gene expression. However, many molecular details of how H1 binds to nucleosomes and recognizes unique structural features on the nucleosome surface remain undefined. Numerous, confounding studies are complicated not only by experimental limitations, but the use of different linker histone isoforms and nucleosome constructions. This review summarizes the decades of research that has resulted in several models of H1 association with nucleosomes, with a focus on recent advances that suggest multiple modes of H1 interaction in chromatin, while highlighting the remaining questions.
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