Hoffman P L, Saba L M, Flink S, Grahame N J, Kechris K, Tabakoff B
Department of Pharmacology, University of Colorado School of Medicine, Aurora, CO.
Genes Brain Behav. 2014 Nov;13(8):743-57. doi: 10.1111/gbb.12175. Epub 2014 Sep 29.
Numerous selective breeding experiments have been performed with rodents, in an attempt to understand the genetic basis for innate differences in preference for alcohol consumption. Quantitative trait locus (QTL) analysis has been used to determine regions of the genome that are associated with the behavioral difference in alcohol preference/consumption. Recent work suggests that differences in gene expression represent a major genetic basis for complex traits. Therefore, the QTLs are likely to harbor regulatory regions (eQTLs) for the differentially expressed genes that are associated with the trait. In this study, we examined brain gene expression differences over generations of selection of the third replicate lines of high and low alcohol-preferring (HAP3 and LAP3) mice, and determined regions of the genome that control the expression of these differentially expressed genes (de eQTLs). We also determined eQTL regions (rv eQTLs) for genes that showed a decrease in variance of expression levels over the course of selection. We postulated that de eQTLs that overlap with rv eQTLs, and also with phenotypic QTLs, represent genomic regions that are affected by the process of selection. These overlapping regions controlled the expression of candidate genes (that displayed differential expression and reduced variance of expression) for the predisposition to differences in alcohol consumption by the HAP3/LAP3 mice.
为了理解对酒精消费偏好的先天差异的遗传基础,人们对啮齿动物进行了大量选择性育种实验。数量性状基因座(QTL)分析已被用于确定基因组中与酒精偏好/消费行为差异相关的区域。最近的研究表明,基因表达差异是复杂性状的主要遗传基础。因此,QTL可能包含与该性状相关的差异表达基因的调控区域(eQTL)。在本研究中,我们检查了高酒精偏好(HAP3)和低酒精偏好(LAP3)小鼠第三代重复品系在多代选择过程中的脑基因表达差异,并确定了控制这些差异表达基因(de eQTL)表达的基因组区域。我们还确定了在选择过程中表达水平方差降低的基因的eQTL区域(rv eQTL)。我们推测,与rv eQTL以及表型QTL重叠的de eQTL代表了受选择过程影响的基因组区域。这些重叠区域控制了HAP3/LAP3小鼠酒精消费差异易感性的候选基因(显示差异表达和表达方差降低)的表达。