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新型组蛋白修饰类型及位点成为转录调控竞争中的参与者。

Novel types and sites of histone modifications emerge as players in the transcriptional regulation contest.

作者信息

Kebede Adam F, Schneider Robert, Daujat Sylvain

机构信息

Institut de Génétique et de Biologie Moléculaire et Cellulaire, CNRS UMR 7104 - Inserm U964, Université de Strasbourg, Illkirch, France.

出版信息

FEBS J. 2015 May;282(9):1658-74. doi: 10.1111/febs.13047. Epub 2014 Oct 7.

Abstract

N-terminal tails of histones are easily accessible outside of the nucleosomal core particle and post-translational modifications (PTMs) of these tails have been the focus of attention in the past 15-20 years. By recruiting (or excluding) specific readers, histone modifications can regulate chromatin dynamics and, by extension, DNA-dependent processes. However, until very recently, the direct impact of histone PTMs on nucleosome structure and thus on chromatin function has remained somewhat elusive. Recent findings of novel sites and types of histone PTMs located within the globular domain of histones and, in particular, on the lateral surface of the histone octamer have changed this. As a result of their structurally important location in close proximity to the DNA molecule, this new class of histone PTMs can have a direct impact on chromatin function. Depending on their precise position at the nucleosome lateral surface (e.g. near the DNA entry/exit sites or in the dyad region), histone PTMs can regulate nucleosome structure and/or stability differently. We review recent progress on how histone PTMs can influence DNA unwrapping and/or nucleosome disassembly and shed light on how these types of novel modifications contribute mechanistically to the regulation of transcriptional activity.

摘要

组蛋白的N端尾巴在核小体核心颗粒外部易于接近,在过去15至20年中,这些尾巴的翻译后修饰(PTMs)一直是关注的焦点。通过招募(或排除)特定的读取器,组蛋白修饰可以调节染色质动力学,进而调节依赖DNA的过程。然而,直到最近,组蛋白PTMs对核小体结构以及染色质功能的直接影响仍有些难以捉摸。最近在组蛋白球状结构域内,特别是在组蛋白八聚体侧面发现了新的组蛋白PTM位点和类型,这改变了这种情况。由于它们在结构上紧邻DNA分子的重要位置,这类新的组蛋白PTMs可以直接影响染色质功能。根据它们在核小体侧面的精确位置(例如靠近DNA进入/退出位点或在二分区域),组蛋白PTMs可以不同程度地调节核小体结构和/或稳定性。我们综述了组蛋白PTMs如何影响DNA解旋和/或核小体解体的最新进展,并阐明了这些新型修饰如何在机制上对转录活性的调节做出贡献。

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