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多能性与疾病中的组蛋白变体。

Histone variants in pluripotency and disease.

机构信息

Howard Hughes Medical Institute, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.

出版信息

Development. 2013 Jun;140(12):2513-24. doi: 10.1242/dev.091439.

Abstract

Most histones are assembled into nucleosomes during replication to package genomic DNA. However, several variant histones are deposited independently of replication at particular regions of chromosomes. Such histone variants include cenH3, which forms the nucleosomal foundation for the centromere, and H3.3, which replaces histones that are lost during dynamic processes that disrupt nucleosomes. Furthermore, various H2A variants participate in DNA repair, gene regulation and other processes that are, as yet, not fully understood. Here, we review recent studies that have implicated histone variants in maintaining pluripotency and as causal factors in cancer and other diseases.

摘要

大多数组蛋白在复制过程中组装成核小体,以包装基因组 DNA。然而,有几种变体组蛋白在染色体的特定区域独立于复制而沉积。这些组蛋白变体包括 cenH3,它为着丝粒形成核小体的基础,以及 H3.3,它取代在破坏核小体的动态过程中丢失的组蛋白。此外,各种 H2A 变体参与 DNA 修复、基因调控和其他尚未完全理解的过程。在这里,我们回顾了最近的研究,这些研究表明组蛋白变体在维持多能性以及在癌症和其他疾病中的因果因素。

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