Liu Qing-Rong, Drgon Tomas, Walther Donna, Johnson Catherine, Poleskaya Oxanna, Hess Judith, Uhl George R
Molecular Neurobiology Branch, National Institute on Drug Abuse Intramural Research Program, National Institutes of Health, Box 5180, Baltimore, MD 21224, USA.
Proc Natl Acad Sci U S A. 2005 Aug 16;102(33):11864-9. doi: 10.1073/pnas.0500329102. Epub 2005 Aug 9.
Association genome scanning is of increasing interest for identifying the chromosomal regions that contain gene variants that contribute to vulnerability to complex disorders, including addictions. To improve the power and feasibility of this approach, we have validated "10k" microarray-based allelic frequency assessments in pooled DNA samples and have used this approach to seek allelic frequency differences between heavy poly-substance abusers and well characterized control individuals. Thirty-eight loci contain SNPs that display robust allele frequency differences between abusers and controls in both European- and African-American samples. These loci identify an alcohol/acetaldehyde dehydrogenase gene cluster and genes implicated in cellular signaling, gene regulation, development, "cell adhesion," and Mendelian disorders. The results converge with previous linkage and association results for addictions. Pooled association genome scanning provides a useful tool for elucidating molecular genetic underpinnings of complex disorders and identifies both previously understood and previously unanticipated mechanisms for addiction vulnerability.
关联基因组扫描对于识别包含导致对包括成瘾在内的复杂疾病易感性的基因变异的染色体区域越来越受关注。为了提高这种方法的效能和可行性,我们已经在混合DNA样本中验证了基于“10k”微阵列的等位基因频率评估,并已使用这种方法来寻找重度多物质滥用者与特征明确的对照个体之间的等位基因频率差异。在欧洲裔和非裔美国人样本中,有38个位点包含的单核苷酸多态性(SNP)在滥用者和对照者之间显示出显著的等位基因频率差异。这些位点鉴定出一个酒精/乙醛脱氢酶基因簇以及与细胞信号传导、基因调控、发育、“细胞黏附”和孟德尔疾病相关的基因。这些结果与先前关于成瘾的连锁和关联研究结果一致。混合关联基因组扫描为阐明复杂疾病的分子遗传基础提供了一个有用的工具,并识别出了成瘾易感性的先前已知和先前未知的机制。