Briones Victorino, Muegge Kathrin
Laboratory of Cancer Prevention, SAIC- Frederick, Inc., NCI-Frederick, Frederick, MD 21701, USA.
Biochim Biophys Acta. 2012 Jul;1819(7):757-62. doi: 10.1016/j.bbagrm.2012.02.013. Epub 2012 Feb 22.
Methylation regulates DNA by altering chromatin and limiting accessibility of transcription factors and RNA polymerase. In this way, DNA methylation controls gene expression and plays a role in ES cell regulation, tissue differentiation and the development of the organism. In abnormal circumstances methylation can also induce diseases and promote cancer progression. Chromatin remodeling proteins such as the SNF2 family member Lsh regulates genome-wide cytosine methylation patterns during mammalian development. Lsh promotes methylation by targeting and repressing repeat sequences that are imbedded in heterochromatin. Lsh also regulates cytosine methylation at unique loci. Alterations in histone modifications (such as H3K4me3, histone acetylation, H3K27me3 and H2Aub) can be associated with DNA methylation changes making Lsh-mediated cytosine methylation part of a larger epigenetic network defining gene expression and cellular differentiation during development. This article is part of a Special Issue entitled: Chromatin in time and space.
甲基化通过改变染色质并限制转录因子和RNA聚合酶的可及性来调控DNA。通过这种方式,DNA甲基化控制基因表达,并在胚胎干细胞调控、组织分化和生物体发育中发挥作用。在异常情况下,甲基化也可诱发疾病并促进癌症进展。染色质重塑蛋白,如SNF2家族成员Lsh,在哺乳动物发育过程中调节全基因组胞嘧啶甲基化模式。Lsh通过靶向并抑制嵌入异染色质的重复序列来促进甲基化。Lsh还调节独特位点的胞嘧啶甲基化。组蛋白修饰(如H3K4me3、组蛋白乙酰化、H3K27me3和H2Aub)的改变可能与DNA甲基化变化相关,使得Lsh介导的胞嘧啶甲基化成为在发育过程中定义基因表达和细胞分化的更大表观遗传网络的一部分。本文是名为“时空染色质”的特刊的一部分。