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酒精使用障碍病理生理学中DNA、组蛋白和RNA甲基化机制的进展。

Advances in DNA, histone, and RNA methylation mechanisms in the pathophysiology of alcohol use disorder.

作者信息

Cruise Tara M, Kotlo Kumar, Malovic Emir, Pandey Subhash C

机构信息

Center for Alcohol Research in Epigenetics, Department of Psychiatry, University of Illinois at Chicago, Chicago, IL, United States.

Jesse Brown Veterans Affairs Medical Center, Chicago, IL, United States.

出版信息

Adv Drug Alcohol Res. 2023 Feb 15;3:10871. doi: 10.3389/adar.2023.10871. eCollection 2023.

Abstract

Alcohol use disorder (AUD) has a complex, multifactorial etiology involving dysregulation across several brain regions and peripheral organs. Acute and chronic alcohol consumption cause epigenetic modifications in these systems, which underlie changes in gene expression and subsequently, the emergence of pathophysiological phenotypes associated with AUD. One such epigenetic mechanism is methylation, which can occur on DNA, histones, and RNA. Methylation relies on one carbon metabolism to generate methyl groups, which can then be transferred to acceptor substrates. While DNA methylation of particular genes generally represses transcription, methylation of histones and RNA can have bidirectional effects on gene expression. This review summarizes one carbon metabolism and the mechanisms behind methylation of DNA, histones, and RNA. We discuss the field's findings regarding alcohol's global and gene-specific effects on methylation in the brain and liver and the resulting phenotypes characteristic of AUD.

摘要

酒精使用障碍(AUD)具有复杂的多因素病因,涉及多个脑区和外周器官的调节异常。急性和慢性酒精摄入会导致这些系统发生表观遗传修饰,这些修饰是基因表达变化的基础,进而导致与AUD相关的病理生理表型的出现。一种这样的表观遗传机制是甲基化,它可以发生在DNA、组蛋白和RNA上。甲基化依赖于一碳代谢来生成甲基基团,然后这些甲基基团可以转移到受体底物上。虽然特定基因的DNA甲基化通常会抑制转录,但组蛋白和RNA的甲基化对基因表达可以产生双向影响。本综述总结了一碳代谢以及DNA、组蛋白和RNA甲基化背后的机制。我们讨论了该领域关于酒精对大脑和肝脏甲基化的整体和基因特异性影响以及由此产生的AUD特征性表型的研究结果。

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