Zhang Tianyi, Cooper Sarah, Brockdorff Neil
Developmental Epigenetics, Department of Biochemistry, University of Oxford, Oxford, UK.
Developmental Epigenetics, Department of Biochemistry, University of Oxford, Oxford, UK
EMBO Rep. 2015 Nov;16(11):1467-81. doi: 10.15252/embr.201540945. Epub 2015 Oct 15.
Histones are subject to a vast array of posttranslational modifications including acetylation, methylation, phosphorylation, and ubiquitylation. The writers of these modifications play important roles in normal development and their mutation or misregulation is linked with both genetic disorders and various cancers. Readers of these marks contain protein domains that allow their recruitment to chromatin. Interestingly, writers often contain domains which can read chromatin marks, allowing the reinforcement of modifications through a positive feedback loop or inhibition of their activity by other modifications. We discuss how such positive reinforcement can result in chromatin states that are robust and can be epigenetically maintained through cell division. We describe the implications of these regulatory systems in relation to modifications including H3K4me3, H3K79me3, and H3K36me3 that are associated with active genes and H3K27me3 and H3K9me3 that have been linked to transcriptional repression. We also review the crosstalk between active and repressive modifications, illustrated by the interplay between the Polycomb and Trithorax histone-modifying proteins, and discuss how this may be important in defining gene expression states during development.
组蛋白会经历大量的翻译后修饰,包括乙酰化、甲基化、磷酸化和泛素化。这些修饰的写入蛋白在正常发育中发挥重要作用,它们的突变或调控异常与遗传疾病和各种癌症都有关联。这些修饰标记的读取蛋白含有能使其被招募到染色质的蛋白质结构域。有趣的是,写入蛋白通常含有能读取染色质标记的结构域,这使得修饰能够通过正反馈回路得到加强,或者被其他修饰抑制其活性。我们讨论了这种正反馈如何导致染色质状态变得稳定,并且能够在细胞分裂过程中通过表观遗传得以维持。我们描述了这些调控系统与包括H3K4me3、H3K79me3和H3K36me3等与活跃基因相关的修饰以及与H3K27me3和H3K9me3等与转录抑制相关的修饰之间的关系。我们还回顾了激活和抑制性修饰之间的相互作用,以多梳蛋白和三胸蛋白组蛋白修饰蛋白之间的相互作用为例,并讨论了这在发育过程中定义基因表达状态方面可能有多重要。