Application of DNA microarrays to study human alcoholism

被引:49
作者
Lewohl, JM
Dodd, PR
Mayfield, RD
Harris, RA
机构
[1] Univ Texas, Waggoner Ctr Alcohol & Addict Res, Austin, TX 78712 USA
[2] Univ Queensland, Dept Biochem, St Lucia, Qld, Australia
关键词
gene expression; gene chip; myelin; frontal cortex;
D O I
10.1159/000054010
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
An emerging idea is that long-term alcohol abuse results in changes in gene expression in the brain and that these changes are responsible at least partly for alcohol tolerance, dependence and neurotoxicity, The overall goal of our research is to identify genes which are differentia[ly expressed in the brains of well-characterized human alcoholics as compared with non-alcoholics. This should identify as-yet-unknown alcohol-responsive genes, and may well confirm changes in the expression of genes which have been delineated in animal models of alcohol abuse. Cases were carefully selected and samples pooled on the basis of relevant criteria; differential expression was monitored by microarray hybridization. The inherent diversity of human alcoholics can be exploited to identify genes associated with specific pathological processes, as well as to assess the effects of concomitant disease, severity of brain damage, drinking behavior, and factors such as gender and smoking history. initial results show selective changes in gene expression in alcoholics; of particular importance is a coordinated reduction in genes coding for myelin components, Copyright (C) 2001 National Science Council, ROC and S. Karger AG, Basel.
引用
收藏
页码:28 / 36
页数:9
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