Qureshi Irfan A, Mehler Mark F
Roslyn and Leslie Goldstein Laboratory for Stem Cell Biology and Regenerative Medicine; Institute for Brain Disorders and Neural Regeneration; Departments of Neurology, Neuroscience, Psychiatry and Behavioral Sciences and Rose F. Kennedy Center for Research on Intellectual and Developmental Disabilities, Albert Einstein College of Medicine, Bronx, NY, United States.
Roslyn and Leslie Goldstein Laboratory for Stem Cell Biology and Regenerative Medicine; Institute for Brain Disorders and Neural Regeneration; Departments of Neurology, Neuroscience, Psychiatry and Behavioral Sciences; Rose F. Kennedy Center for Research on Intellectual and Developmental Disabilities; Einstein Cancer Center; Ruth L. and David S. Gottesman Stem Cell Institute; and Center for Epigenomics and Institute for Aging Research, Albert Einstein College of Medicine, Bronx, NY, United States.
Handb Clin Neurol. 2018;147:43-58. doi: 10.1016/B978-0-444-63233-3.00005-1.
Epigenetic mechanisms act as control systems for modulating genomic structure and activity in response to evolving profiles of cell-extrinsic, cell-cell, and cell-intrinsic signals. These dynamic processes are responsible for mediating cell- and tissue-specific gene expression and function and gene-gene and gene-environmental interactions. The major epigenetic mechanisms include DNA methylation and hydroxymethylation; histone protein posttranslational modifications, nucleosome remodeling/repositioning, and higher-order chromatin reorganization; noncoding RNA regulation; and RNA editing. These mechanisms are intimately involved in executing fundamental genomic programs, including gene transcription, posttranscriptional RNA processing and transport, translation, X-chromosome inactivation, genomic imprinting, retrotransposon regulation, DNA replication, and DNA repair and the maintenance of genomic stability. For the nervous system, epigenetics offers a novel and robust framework for explaining how brain development and aging occur, neural cellular diversity is generated, synaptic and neural network connectivity and plasticity are mediated, and complex cognitive and behavioral phenotypes are inherited transgenerationally. Epigenetic factors and processes are, not surprisingly, implicated in nervous system disease pathophysiology through several emerging paradigms - mutations and genetic variation in genes encoding epigenetic factors; impairments in epigenetic factor expression, localization, and function; epigenetic mechanisms modulating disease-associated factors and pathways; and the presence of deregulated epigenetic profiles in central and peripheral tissues.
表观遗传机制作为控制系统,可根据细胞外、细胞间和细胞内信号不断变化的特征来调节基因组结构和活性。这些动态过程负责介导细胞和组织特异性的基因表达与功能以及基因-基因和基因-环境相互作用。主要的表观遗传机制包括DNA甲基化和羟甲基化;组蛋白的翻译后修饰、核小体重塑/重新定位以及高阶染色质重组;非编码RNA调控;以及RNA编辑。这些机制密切参与执行基本的基因组程序,包括基因转录、转录后RNA加工与转运、翻译、X染色体失活、基因组印记、逆转座子调控、DNA复制、DNA修复以及基因组稳定性的维持。对于神经系统而言,表观遗传学提供了一个新颖且强大的框架,用于解释大脑发育和衰老如何发生、神经细胞多样性如何产生、突触和神经网络连接性与可塑性如何介导,以及复杂的认知和行为表型如何跨代遗传。毫不奇怪,表观遗传因素和过程通过几种新出现的模式参与神经系统疾病的病理生理学——编码表观遗传因素的基因突变和遗传变异;表观遗传因素表达、定位和功能的受损;调节疾病相关因素和途径的表观遗传机制;以及中枢和外周组织中失调的表观遗传谱的存在。