Hinojos Cruz A, Boerwinkle Eric, Fornage Myriam, Doris Peter A
Institute for Molecular Medicine, University of Texas Health Science Center, Houston, TX 77030, USA.
Hypertension. 2005 Apr;45(4):698-704. doi: 10.1161/01.HYP.0000156498.78896.37. Epub 2005 Feb 14.
Allelic expression in genes has become recognized as a heritable trait by which phenotypes are generated. We have examined gene expression in the rat kidney using genome-wide microarray technology (Affymetrix). Gene expression was determined across 4 rat strains, 3 hypertensive spontaneously hypertensive rat (SHR) substrains (SHR-A3, SHR-B2, and SHR-C), and a normotensive strain (Wistar-Kyoto [WKY]). Expression measurements were made in multiple animals from all strains at 4 time points (4 weeks, 8 weeks, 12 weeks, and 18 weeks of age), covering the prehypertensive period in SHR (4 weeks), and the period of rapidly rising blood pressure (8 and 12 weeks) and of sustained hypertension (18 weeks). Regression analysis revealed a close relationship across all strains during the first 3 time points, after which SHR-A3 became a substantial outlier. SHR-B2 and SHR-C demonstrated a very close relationship in gene expression at all times but also showed increased differences compared with the other strains at 18 weeks of age. We identified genes that were consistently different in expression, comparing all SHR substrains at each time point with WKY. The resulting list of genes was compared with blood pressure quantitative trait loci reported for SHR to refine a number of genes consistently differentially expressed between SHR substrains and WKY, persistently differentially expressed across multiple time points, and located in SHR blood pressure-determinative regions of the genome. Genealogical relationships and SHR substrain intercrosses suggest that genes responsible for heritable hypertension in SHR are shared across SHR substrains. The present approach identifies a number of genes that may influence blood pressure in SHR by virtue of allelic effects on gene expression.
基因中的等位基因表达已被视为一种可遗传的性状,通过它可产生表型。我们使用全基因组微阵列技术(Affymetrix)检测了大鼠肾脏中的基因表达。在4种大鼠品系、3种高血压自发性高血压大鼠(SHR)亚品系(SHR - A3、SHR - B2和SHR - C)以及一种正常血压品系(Wistar - Kyoto [WKY])中测定了基因表达。在所有品系的多只动物中,于4个时间点(4周龄、8周龄、12周龄和18周龄)进行表达测量,涵盖了SHR的高血压前期(4周)、血压快速上升期(8周和12周)以及持续性高血压期(18周)。回归分析显示,在前3个时间点所有品系之间存在密切关系,此后SHR - A3成为一个显著的异常值。SHR - B2和SHR - C在所有时间点的基因表达都显示出非常密切的关系,但在18周龄时与其他品系相比也表现出更大的差异。我们通过将每个时间点的所有SHR亚品系与WKY进行比较,确定了表达始终存在差异的基因。将所得基因列表与已报道的SHR血压数量性状基因座进行比较,以筛选出在SHR亚品系和WKY之间始终差异表达、在多个时间点持续差异表达且位于SHR基因组血压决定区域的一些基因。系谱关系和SHR亚品系杂交表明,SHR中导致遗传性高血压的基因在SHR亚品系中是共享的。本方法鉴定出了一些可能通过对基因表达的等位基因效应影响SHR血压的基因。