Genomics and Epigenetics Division, Garvan Institute of Medical Research, Sydney 2010, New South Wales, Australia.
St Vincent's Clinical School, Faculty of Medicine, University of New South Wales, Sydney 2010, New South Wales, Australia.
Essays Biochem. 2019 Dec 20;63(6):707-715. doi: 10.1042/EBC20190030.
DNA methylation involves the addition of a methyl group to the fifth carbon of the pyrimidine cytosine ring (5-methylcytosine, 5mC). 5mC is widespread in vertebrate genomes where it is predominantly found within CpG dinucleotides. In mammals, 5mC participates in long-term silencing processes such as X-chromosome inactivation, genomic imprinting, somatic silencing of germline genes, and silencing of repetitive DNA elements. The evidence for 5mC as a dynamic gene-regulatory mechanism is mostly limited to specific examples, and is far from being completely understood. Recent work from diverse model systems suggests that 5mC might not always act as a dominant repressive mechanism and that hypermethylated promoters and enhancers can be permissive to transcription in vivo and in vitro. In this review, we discuss the links between 5mC and enhancer activity, and evaluate the role of this biochemical mechanism in various biological contexts.
DNA 甲基化涉及将一个甲基基团添加到嘧啶胞嘧啶环的第五个碳原子上(5-甲基胞嘧啶,5mC)。5mC 在脊椎动物基因组中广泛存在,主要存在于 CpG 二核苷酸中。在哺乳动物中,5mC 参与长期沉默过程,如 X 染色体失活、基因组印迹、生殖细胞基因的体细胞沉默和重复 DNA 元件的沉默。5mC 作为一种动态基因调控机制的证据主要局限于特定的例子,而且远未完全理解。来自不同模式系统的最近的工作表明,5mC 可能并不总是作为一种主要的抑制机制,并且超甲基化的启动子和增强子在体内和体外都可以允许转录。在这篇综述中,我们讨论了 5mC 与增强子活性之间的联系,并评估了这种生化机制在各种生物学背景下的作用。