Lee Han-Teo, Oh Sanghyeon, Ro Du Hyun, Yoo Hyerin, Kwon Yoo-Wook
Department of Molecular Medicine and Biopharmaceutical Sciences, Graduate School of Convergence Science, Seoul National University, Seoul, Korea.
Interdisciplinary Program in Stem Cell Biology, Graduate School of Medicine, Seoul National University, Seoul, Korea.
J Lipid Atheroscler. 2020 Sep;9(3):419-434. doi: 10.12997/jla.2020.9.3.419. Epub 2020 Sep 21.
Atherosclerosis, which is the most common chronic disease of the coronary artery, constitutes a vascular pathology induced by inflammation and plaque accumulation within arterial vessel walls. Both DNA methylation and histone modifications are epigenetic changes relevant for atherosclerosis. Recent studies have shown that the DNA methylation and histone modification systems are closely interrelated and mechanically dependent on each other. Herein, we explore the functional linkage between these systems, with a particular emphasis on several recent findings suggesting that histone acetylation can help in targeting DNA methylation and that DNA methylation may control gene expression during atherosclerosis.
动脉粥样硬化是冠状动脉最常见的慢性疾病,是一种由动脉血管壁内炎症和斑块积聚引起的血管病变。DNA甲基化和组蛋白修饰都是与动脉粥样硬化相关的表观遗传变化。最近的研究表明,DNA甲基化和组蛋白修饰系统密切相关且在机制上相互依赖。在此,我们探讨这些系统之间的功能联系,特别强调最近的几项研究结果,这些结果表明组蛋白乙酰化有助于靶向DNA甲基化,并且DNA甲基化可能在动脉粥样硬化过程中控制基因表达。