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酒精相关电生理表型的连锁分析:微卫星与单核苷酸多态性的全基因组扫描比较。

Linkage analysis of alcoholism-related electrophysiological phenotypes: genome scans with microsatellites compared to single-nucleotide polymorphisms.

机构信息

Department of Epidemiology and Biostatistics, Case Western Reserve University, Cleveland, OH, USA.

出版信息

BMC Genet. 2005 Dec 30;6 Suppl 1(Suppl 1):S156. doi: 10.1186/1471-2156-6-S1-S156.

Abstract

P300 amplitude is an electrophysiological quantitative trait that is correlated with both alcoholism and smoking status. Using the Collaborative Study on the Genetics of Alcoholism data, we performed model-free linkage analysis to investigate the relationship between alcoholism, P300 amplitude, and habitual smoking. We also analyzed the effect of parent-of-origin on alcoholism, and utilized both microsatellites (MS) markers and single-nucleotide polymorphisms (SNPs). We found significant evidence of linkage for alcoholism to chromosome 10; inclusion of P300 amplitude as a covariate provided additional evidence of linkage to chromosome 12. This same region on chromosome 12 showed some evidence for a parent-of-origin effect. We found evidence of linkage for the P300 phenotype to chromosome 7 in non-smokers, and to chromosome 17 in alcoholics. The effects of alcoholism and habitual smoking on P300 amplitude appear to have separate genetic determinants. Overall, there were few differences between MS and SNP genome scans. The use of covariates and parent-of-origin effects allowed detection of linkage not seen otherwise.

摘要

P300 振幅是一种与酗酒和吸烟状况相关的电生理定量特征。利用酒精中毒遗传学合作研究的数据,我们进行了无模型连锁分析,以研究酗酒、P300 振幅和习惯性吸烟之间的关系。我们还分析了父本或母本来源对酗酒的影响,并同时利用微卫星(MS)标记和单核苷酸多态性(SNP)进行了分析。我们发现酗酒与 10 号染色体之间存在显著的连锁证据;将 P300 振幅作为协变量包含在内,为 12 号染色体的连锁提供了额外的证据。在 12 号染色体的同一区域,存在着父本或母本来源效应的一些证据。我们发现非吸烟者的 P300 表型与 7 号染色体存在连锁,而酗酒者则与 17 号染色体存在连锁。酗酒和习惯性吸烟对 P300 振幅的影响似乎有独立的遗传决定因素。总的来说,MS 和 SNP 基因组扫描之间的差异很少。使用协变量和父本或母本来源效应可以检测到其他方法无法检测到的连锁。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5571/1866778/ab772b67d96e/1471-2156-6-S1-S156-1.jpg

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