Kimpel Mark W, Strother Wendy N, McClintick Jeanette N, Carr Lucinda G, Liang Tiebing, Edenberg Howard J, McBride William J
Department of Psychiatry, Indiana University School of Medicine, Indianapolis, IN 46202-4887, USA.
Alcohol. 2007 Mar;41(2):95-132. doi: 10.1016/j.alcohol.2007.03.003.
The objective of this study was to determine if there are innate differences in gene expression in selected CNS regions between inbred alcohol-preferring (iP) and -non-preferring (iNP) rats. Gene expression was determined in the nucleus accumbens (ACB), amygdala (AMYG), frontal cortex (FC), caudate-putamen (CPU), and hippocampus (HIPP) of alcohol-naïve adult male iP and iNP rats, using Affymetrix Rat Genome U34A microarrays (n = 6/strain). Using Linear Modeling for Microarray Analysis with a false discovery rate threshold of 0.1, there were 16 genes with differential expression in the ACB, 54 in the AMYG, 8 in the FC, 24 in the CPU, and 21 in the HIPP. When examining the main effect of strain across regions, 296 genes were differentially expressed. Although the relatively small number of genes found significant within individual regions precluded a powerful analysis for over-represented Gene Ontology categories, the much larger list resulting from the main effect of strain analysis produced 17 over-represented categories (P < .05), including axon guidance, gliogenesis, negative regulation of programmed cell death, regulation of programmed cell death, regulation of synapse structure function, and transmission of nerve impulse. Co-citation analysis and graphing of significant genes revealed a network involved in the neuropeptide Y (NPY) transmitter system. Correlation of all significant genes with those located within previously established rat alcohol QTLs revealed that of the total of 313 significant genes, 71 are located within such QTLs. The many regional and overall gene expression differences between the iP and iNP rat lines may contribute to the divergent alcohol drinking phenotypes of these rats.
本研究的目的是确定在近交系嗜酒(iP)和非嗜酒(iNP)大鼠的特定中枢神经系统区域中,基因表达是否存在先天性差异。使用Affymetrix大鼠基因组U34A微阵列(每个品系n = 6),测定了未接触过酒精的成年雄性iP和iNP大鼠伏隔核(ACB)、杏仁核(AMYG)、额叶皮质(FC)、尾状核-壳核(CPU)和海马体(HIPP)中的基因表达。使用微阵列分析的线性模型,错误发现率阈值为0.1,结果显示ACB中有16个基因差异表达,AMYG中有54个,FC中有8个,CPU中有24个,HIPP中有21个。在检查跨区域品系的主要效应时,有296个基因差异表达。尽管在各个区域内发现的显著基因数量相对较少,无法对过度富集的基因本体类别进行有力分析,但品系分析主要效应产生的大得多的列表产生了17个过度富集的类别(P <.05),包括轴突导向、神经胶质生成、程序性细胞死亡的负调控、程序性细胞死亡的调控、突触结构功能的调控和神经冲动传递。对显著基因的共引用分析和绘图揭示了一个涉及神经肽Y(NPY)递质系统的网络。所有显著基因与先前建立的大鼠酒精数量性状基因座(QTL)内的基因的相关性显示,在总共313个显著基因中,有71个位于此类QTL内。iP和iNP大鼠品系之间许多区域和整体的基因表达差异可能导致了这些大鼠不同的饮酒表型。