Leicester Institute for Structural and Chemical Biology, Department of Molecular and Cell Biology, University of Leicester, Leicester, LE1 9HN, UK.
Leicester Institute for Structural and Chemical Biology, Department of Molecular and Cell Biology, University of Leicester, Leicester, LE1 9HN, UK.
Curr Opin Struct Biol. 2021 Dec;71:156-163. doi: 10.1016/j.sbi.2021.06.012. Epub 2021 Jul 22.
Eukaryotic genomes are segregated into active euchromatic and repressed heterochromatic compartments. Gene regulatory networks, chromosomal structures, and genome integrity rely on the timely and locus-specific establishment of active and silent states to protect the genome and provide the basis for cell division and specification of cellular identity. Here, we focus on the mechanisms and molecular machinery that establish heterochromatin in Schizosaccharomyces pombe and compare it with Saccharomyces cerevisiae and the mammalian polycomb system. We present recent structural and mechanistic evidence, which suggests that histone acetylation protects active transcription by disrupting the positive feedback loops used by the heterochromatin machinery and that H2A and H3 monoubiquitination actively drives heterochromatin, whereas H2B monoubiquitination mobilizes the defenses to quench heterochromatin.
真核基因组被分隔成活跃的常染色质和受抑制的异染色质区室。基因调控网络、染色体结构和基因组完整性依赖于活性和沉默状态的及时和位置特异性建立,以保护基因组并为细胞分裂和细胞身份的特化提供基础。在这里,我们专注于在酿酒酵母和哺乳动物多梳系统中建立异染色质的机制和分子机制。我们提出了最近的结构和机制证据,表明组蛋白乙酰化通过破坏异染色质机制使用的正反馈环来保护活性转录,并且 H2A 和 H3 单泛素化主动驱动异染色质,而 H2B 单泛素化调动防御机制来抑制异染色质。