Subramanian Vidya, Fields Paul A, Boyer Laurie A
Department of Biology, Massachusetts Institute of Technology 77 Massachusetts Avenue, Cambridge, MA 02139 USA.
F1000Prime Rep. 2015 Jan 5;7:01. doi: 10.12703/P7-01. eCollection 2015.
The replacement of nucleosomal H2A with the histone variant H2A.Z is critical for regulating DNA-mediated processes across eukaryotes and for early development of multicellular organisms. How this variant performs these seemingly diverse roles has remained largely enigmatic. Here, we discuss recent mechanistic insights that have begun to reveal how H2A.Z functions as a molecular rheostat for gene control. We focus on specific examples in metazoans as a model for understanding how H2A.Z integrates information from histone post-translational modifications, other histone variants, and transcription factors (TFs) to regulate proper induction of gene expression programs in response to cellular cues. Finally, we propose a general model of how H2A.Z incorporation regulates chromatin states in diverse processes.
用组蛋白变体H2A.Z替换核小体中的H2A,对于调控真核生物中DNA介导的过程以及多细胞生物的早期发育至关重要。这种变体如何履行这些看似多样的功能,在很大程度上仍然是个谜。在这里,我们讨论了最近的一些机制性见解,这些见解已开始揭示H2A.Z如何作为基因控制的分子变阻器发挥作用。我们重点关注后生动物中的具体例子,以此作为一个模型来理解H2A.Z如何整合来自组蛋白翻译后修饰、其他组蛋白变体和转录因子(TFs)的信息,以响应细胞信号来调控基因表达程序的正确诱导。最后,我们提出了一个关于H2A.Z掺入如何在不同过程中调节染色质状态的通用模型。