Emilsson L, Saetre P, Jazin E
Department of Evolution, Genomics and Systematics, Uppsala University, Norbyvagen 18D, 75236 Uppsala, Sweden.
Neurobiol Dis. 2006 Mar;21(3):618-25. doi: 10.1016/j.nbd.2005.09.004. Epub 2005 Oct 27.
We combined global and high-resolution strategies to find genes with altered mRNA expression levels in one of the largest collection of brain autopsies from Alzheimer's patients and controls ever studied. Our global analysis involved microarray hybridizations of large pools of samples obtained from 114 individuals, using two independent sets of microarrays. Ten genes selected from the microarray experiments were quantified on each individual separately using real-time RT-PCR. This high-resolution analysis accounted for systematic differences in age, postmortem interval, brain pH, and reference gene expression, and it estimated the effect of disease on mRNA levels, on top of the effect of all other variables. Differential expression was confirmed for eight out of ten genes. Among them, Type B inositol 1,4,5-trisphosphate 3-kinase (ITPKB), and regulator of G protein signaling 4 (RGS4) showed highly altered expression levels in patients (P values < 0.0001). Our results point towards increased inositol triphospate (IP3)-mediated calcium signaling in Alzheimer's disease.
我们结合了全局和高分辨率策略,在有史以来研究的最大规模的阿尔茨海默病患者和对照脑尸检样本集中寻找mRNA表达水平发生改变的基因。我们的全局分析涉及使用两组独立的微阵列,对从114名个体获得的大量样本进行微阵列杂交。从微阵列实验中选出的10个基因,分别使用实时逆转录聚合酶链反应(RT-PCR)对每个个体进行定量分析。这种高分辨率分析考虑了年龄、死后间隔时间、脑pH值和参照基因表达的系统差异,并在所有其他变量的影响之上,估计了疾病对mRNA水平的影响。10个基因中有8个的差异表达得到了证实。其中,B型肌醇1,4,5-三磷酸3-激酶(ITPKB)和G蛋白信号调节因子4(RGS4)在患者中表现出高度改变的表达水平(P值<0.0001)。我们的结果表明,阿尔茨海默病中肌醇三磷酸(IP3)介导的钙信号传导增强。