Department of Biochemistry, Emory University School of Medicine, 1510 Clifton Road, Atlanta, Georgia 30322, USA.
Biochemistry. 2010 Apr 13;49(14):2999-3008. doi: 10.1021/bi100213t.
One of the most fundamental questions in the control of gene expression in mammals is how epigenetic methylation patterns of DNA and histones are established, erased, and recognized. This central process in controlling metazoan gene expression includes coordinated covalent modifications of DNA and its associated histones. This review focuses on recent developments in characterizing the functional links between the methylation status of the DNA and of two particularly important histone marks. Mammalian DNA methylation is intricately connected to the presence of unmodified lysine 4 and methylated lysine 9 residues in histone H3. An interconnected network of methyltransferases, demethylases, and accessory proteins is responsible for changing or maintaining the modification status of specific regions of chromatin. The structural and functional interactions among members of this network are critical to processes that include imprinting and differentiation, dysregulation of which is associated with disorders ranging from inflammation to cancer.
哺乳动物中基因表达调控最基本的问题之一是 DNA 和组蛋白的表观遗传甲基化模式是如何建立、消除和识别的。这个控制后生动物基因表达的核心过程包括 DNA 及其相关组蛋白的共价修饰的协调。本综述重点介绍了近年来在描述 DNA 甲基化状态与两种特别重要的组蛋白标记之间功能联系方面的最新进展。哺乳动物 DNA 甲基化与组蛋白 H3 中未修饰的赖氨酸 4 和甲基化的赖氨酸 9 残基的存在密切相关。甲基转移酶、去甲基酶和辅助蛋白的相互关联网络负责改变或维持染色质特定区域的修饰状态。该网络成员之间的结构和功能相互作用对于包括印迹和分化在内的过程至关重要,这些过程的失调与从炎症到癌症等各种疾病有关。