Klose Robert J, Zhang Yi
Howard Hughes Medical Institute, Department of Biochemistry and Biophysics, Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599-7295, USA.
Nat Rev Mol Cell Biol. 2007 Apr;8(4):307-18. doi: 10.1038/nrm2143. Epub 2007 Mar 7.
Histone methylation has important roles in regulating transcription, genome integrity and epigenetic inheritance. Historically, methylated histone arginine and lysine residues have been considered static modifications because of the low levels of methyl-group turnover in chromatin. The recent identification of enzymes that antagonize or remove histone methylation has changed this view and now the dynamic nature of these modifications is being appreciated. Here, we examine the enzymatic and structural basis for the mechanisms that these enzymes use to counteract histone methylation and provide insights into their substrate specificity and biological function.
组蛋白甲基化在调控转录、基因组完整性和表观遗传继承中发挥着重要作用。从历史上看,由于染色质中甲基基团周转水平较低,甲基化的组蛋白精氨酸和赖氨酸残基一直被视为静态修饰。最近对拮抗或去除组蛋白甲基化的酶的鉴定改变了这一观点,现在人们开始认识到这些修饰的动态性质。在这里,我们研究了这些酶用于抵消组蛋白甲基化的机制的酶学和结构基础,并深入了解它们的底物特异性和生物学功能。