Department of Medicine, Indiana University School of Medicine, Medical Research and Library Building, Indianapolis, IN 46202, USA.
Alcohol. 2010 Sep;44(6):477-85. doi: 10.1016/j.alcohol.2010.06.004. Epub 2010 Aug 12.
The high and low alcohol-drinking (HAD and LAD) rats were selectively bred for differences in alcohol intake. The HAD/LAD rats originated from the N/Nih heterogeneous stock developed from intercrossing eight inbred rat strains. The HAD×LAD F2 were genotyped, and a powerful analytical approach, using ancestral recombination and F2 recombination, was used to narrow a quantitative trait loci (QTL) for alcohol drinking to a 2-cM region on distal chromosome 10 that was in common in the HAD1/LAD1 and HAD2/LAD2 analyses. Quantitative real-time PCR was used to examine mRNA expression of six candidate genes (Crebbp, Trap1, Gnptg, Clcn7, Fahd1, and Mapk8ip3) located within the narrowed QTL region in the HAD1/LAD1 rats. Expression was examined in five brain regions, including the nucleus accumbens, amygdala, caudate putamen, hippocampus, and prefrontal cortex. All six genes showed differential expression in at least one brain region. Of the genes tested in this study, Crebbp and Mapk8ip3 may be the most promising candidates with regard to alcohol drinking.
高酒精和低酒精摄入(HAD 和 LAD)大鼠是通过对酒精摄入量的差异进行选择性繁殖而培育出来的。HAD/LAD 大鼠源自 N/Nih 异质品系,由 8 个近交系大鼠杂交而成。对 HAD×LAD F2 进行了基因分型,并采用祖先重组和 F2 重组的强大分析方法,将酒精摄入的数量性状基因座(QTL)缩小到第 10 号染色体远端的 2-cM 区域,该区域在 HAD1/LAD1 和 HAD2/LAD2 分析中是共同存在的。实时定量 PCR 用于检测位于 HAD1/LAD1 大鼠缩小的 QTL 区域内的六个候选基因(Crebbp、Trap1、Gnptg、Clcn7、Fahd1 和 Mapk8ip3)的 mRNA 表达。在包括伏隔核、杏仁核、尾壳核、海马和前额皮质在内的五个脑区检查了表达情况。所有六个基因在至少一个脑区都表现出差异表达。在本研究中测试的基因中,Crebbp 和 Mapk8ip3 可能是与饮酒最相关的最有希望的候选基因。