Genetics and Developmental Biology Department, Institut Curie, Paris Sciences Lettres University, INSERM, CNRS, Paris, France.
Nat Rev Mol Cell Biol. 2019 Oct;20(10):590-607. doi: 10.1038/s41580-019-0159-6. Epub 2019 Aug 9.
DNA methylation is of paramount importance for mammalian embryonic development. DNA methylation has numerous functions: it is implicated in the repression of transposons and genes, but is also associated with actively transcribed gene bodies and, in some cases, with gene activation per se. In recent years, sensitive technologies have been developed that allow the interrogation of DNA methylation patterns from a small number of cells. The use of these technologies has greatly improved our knowledge of DNA methylation dynamics and heterogeneity in embryos and in specific tissues. Combined with genetic analyses, it is increasingly apparent that regulation of DNA methylation erasure and (re-)establishment varies considerably between different developmental stages. In this Review, we discuss the mechanisms and functions of DNA methylation and demethylation in both mice and humans at CpG-rich promoters, gene bodies and transposable elements. We highlight the dynamic erasure and re-establishment of DNA methylation in embryonic, germline and somatic cell development. Finally, we provide insights into DNA methylation gained from studying genetic diseases.
DNA 甲基化对哺乳动物胚胎发育至关重要。DNA 甲基化具有多种功能:它涉及转座子和基因的抑制,但也与活跃转录的基因体有关,在某些情况下,与基因激活本身有关。近年来,开发了一些敏感的技术,可以从小数目的细胞中检测 DNA 甲基化模式。这些技术的使用极大地提高了我们对胚胎和特定组织中 DNA 甲基化动态和异质性的认识。结合遗传分析,越来越明显的是,DNA 甲基化的消除和(重新)建立的调控在不同的发育阶段有很大的差异。在这篇综述中,我们讨论了在富含 CpG 的启动子、基因体和转座元件中,DNA 甲基化和去甲基化在小鼠和人类中的机制和功能。我们强调了胚胎、生殖系和体细胞发育中 DNA 甲基化的动态消除和重新建立。最后,我们从研究遗传疾病中获得了对 DNA 甲基化的深入了解。