Gene expression profiling in the human alcoholic brain

NEUROPHARMACOLOGY

卷:122

Review

Warden, Anna S.^1,2  Mayfield, R. Dayne² 

[1] Univ Texas Austin, Inst Neurosci, 1 Univ Stn,C7000, Austin, TX 78712 USA

[2] Univ Texas Austin, Waggoner Ctr Alcohol & Addict Res, 2500 Speedway,A4800, Austin, TX 78712 USA

关键词: Gene expression;    Co-expression networks;    Transcriptional regulation;    RNA-seq;    Alcohol;   

DOI  :  10.1016/j.neuropharm.2017.02.017

来源: Elsevier

【 摘 要 】

Long-term alcohol use causes widespread changes in gene expression in the human brain. Aberrant gene expression changes likely contribute to the progression from occasional alcohol use to alcohol use disorder (including alcohol dependence). Transcriptome studies have identified individual gene candidates that are linked to alcohol-dependence phenotypes. The use of bioinformatics techniques to examine expression datasets has provided novel systems-level approaches to transcriptome profiling in human postmortem brain. These analytical advances, along with recent developments in next-generation sequencing technology, have been instrumental in detecting both known and novel coding and non-coding RNAs, alternative splicing events, and cell-type specific changes that may contribute to alcohol-related pathologies. This review offers an integrated perspective on alcohol-responsive transcriptional changes in the human brain underlying the regulatory gene networks that contribute to alcohol dependence. This article is part of the Special Issue entitled Alcoholism. (C) 2017 Elsevier Ltd. All rights reserved.

【 授权许可】

Free