Wellcome Centre for Cell Biology, School of Biological Sciences, University of Edinburgh, Edinburgh EH9 3BF, UK.
Chan-Zuckerberg BioHub, San Francisco, California 94158, USA.
Nat Rev Mol Cell Biol. 2018 Apr;19(4):229-244. doi: 10.1038/nrm.2017.119. Epub 2017 Dec 13.
Heterochromatin is a key architectural feature of eukaryotic chromosomes, which endows particular genomic domains with specific functional properties. The capacity of heterochromatin to restrain the activity of mobile elements, isolate DNA repair in repetitive regions and ensure accurate chromosome segregation is crucial for maintaining genomic stability. Nucleosomes at heterochromatin regions display histone post-translational modifications that contribute to developmental regulation by restricting lineage-specific gene expression. The mechanisms of heterochromatin establishment and of heterochromatin maintenance are separable and involve the ability of sequence-specific factors bound to nascent transcripts to recruit chromatin-modifying enzymes. Heterochromatin can spread along the chromatin from nucleation sites. The propensity of heterochromatin to promote its own spreading and inheritance is counteracted by inhibitory factors. Because of its importance for chromosome function, heterochromatin has key roles in the pathogenesis of various human diseases. In this Review, we discuss conserved principles of heterochromatin formation and function using selected examples from studies of a range of eukaryotes, from yeast to human, with an emphasis on insights obtained from unicellular model organisms.
异染色质是真核染色体的一个关键结构特征,赋予特定基因组区域特定的功能特性。异染色质抑制转座元件活性、隔离重复区域的 DNA 修复并确保染色体正确分离的能力对维持基因组稳定性至关重要。异染色质区域的核小体显示出组蛋白的翻译后修饰,通过限制谱系特异性基因表达来参与发育调控。异染色质的建立和维持机制是可分离的,涉及与新生转录本结合的序列特异性因子招募染色质修饰酶的能力。异染色质可以从起始位点沿着染色质扩散。异染色质促进自身扩散和遗传的倾向受到抑制因子的拮抗。由于其对染色体功能的重要性,异染色质在各种人类疾病的发病机制中起着关键作用。在这篇综述中,我们使用从酵母到人类等各种真核生物的研究中的选定例子,讨论了异染色质形成和功能的保守原则,重点介绍了从单细胞模式生物中获得的见解。