Department of Pharmaceutical Chemistry, University of California San Francisco, San Francisco, CA, 94158, USA.
Department of Biochemistry and Biophysics, University of California San Francisco, San Francisco, CA, 94158, USA.
Curr Opin Cell Biol. 2020 Jun;64:90-96. doi: 10.1016/j.ceb.2020.03.004. Epub 2020 May 17.
A large portion of the eukaryotic genome is packed into heterochromatin, a versatile platform that is essential to maintain genome stability. Often associated with a compact and transcriptionally repressed chromatin state, heterochromatin was earlier considered a static and locked compartment. However, cumulative findings over the last 17 years have suggested that heterochromatin displays dynamics at different timescales and size scales. These dynamics are thought to be essential for the regulation of heterochromatin. This review illustrates how the key principles underlying heterochromatin structure and function have evolved along the years and summarizes the discoveries that have led to the continuous revision of these principles. Using heterochromatin protein 1-mediated heterochromatin as a context, we discuss a novel paradigm for heterochromatin organization based on two emerging concepts, phase separation and nucleosome structural plasticity. We also examine the broader implications of this paradigm for chromatin organization and regulation beyond heterochromatin.
真核生物基因组的很大一部分被包装成异染色质,这是一个多功能的平台,对于维持基因组稳定性至关重要。异染色质通常与紧凑和转录抑制的染色质状态相关联,早期被认为是一个静态和锁定的隔室。然而,过去 17 年来的累积发现表明,异染色质在不同的时间尺度和大小尺度上表现出动力学。这些动力学被认为是调节异染色质所必需的。本综述说明了异染色质结构和功能的关键原则是如何随着时间的推移而演变的,并总结了导致这些原则不断修正的发现。我们使用异染色质蛋白 1 介导的异染色质作为背景,讨论了基于两个新兴概念,相分离和核小体结构可塑性的异染色质组织的新范例。我们还研究了这个范例对染色质组织和调控超越异染色质的更广泛影响。