Institute of Biochemistry, University of Giessen, Friedrichstrasse 24, 35392, Giessen, Germany.
Institute for Genetics, University of Giessen, Heinrich-Buff-Ring 58-62, 35392, Giessen, Germany.
Epigenetics Chromatin. 2019 Jun 14;12(1):37. doi: 10.1186/s13072-019-0274-9.
The histone variant H2A.Z is involved in several processes such as transcriptional control, DNA repair, regulation of centromeric heterochromatin and, not surprisingly, is implicated in diseases such as cancer. Here, we review the recent developments on H2A.Z focusing on its role in transcriptional activation and repression. H2A.Z, as a replication-independent histone, has been studied in several model organisms and inducible mammalian model systems. Its loading machinery and several modifying enzymes have been recently identified, and some of the long-standing discrepancies in transcriptional activation and/or repression are about to be resolved. The buffering functions of H2A.Z, as supported by genome-wide localization and analyzed in several dynamic systems, are an excellent example of transcriptional control. Posttranslational modifications such as acetylation and ubiquitination of H2A.Z, as well as its specific binding partners, are in our view central players in the control of gene expression. Understanding the key-mechanisms in either turnover or stabilization of H2A.Z-containing nucleosomes as well as defining the H2A.Z interactome will pave the way for therapeutic applications in the future.
组蛋白变体 H2A.Z 参与多个过程,如转录调控、DNA 修复、着丝粒异染色质的调控,并且不出所料,与癌症等疾病有关。在这里,我们回顾了 H2A.Z 的最新研究进展,重点介绍了它在转录激活和抑制中的作用。H2A.Z 作为一种与复制无关的组蛋白,已经在多个模式生物和可诱导的哺乳动物模型系统中进行了研究。其加载机制和几种修饰酶最近已经被鉴定出来,一些关于转录激活和/或抑制的长期存在的差异即将得到解决。H2A.Z 的缓冲功能得到了全基因组定位的支持,并在几个动态系统中进行了分析,这是转录控制的一个极好的例子。H2A.Z 的翻译后修饰,如乙酰化和泛素化,以及其特定的结合伙伴,是我们控制基因表达的核心因素。了解 H2A.Z 核小体的周转率或稳定性的关键机制,并定义 H2A.Z 的相互作用组,将为未来的治疗应用铺平道路。