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Microarray analysis of differentially expressed genes in placental tissue of pre-eclampsia: up-regulation of obesity-related genes.

机译:子痫前期胎盘组织中差异表达基因的微阵列分析:肥胖相关基因的上调。

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Susceptibility genes present in both mother and fetus most likely contribute to the risk of pre-eclampsia. Placental biopsies were therefore investigated by high-density DNA microarray analysis to determine genes differentially regulated within chorionic villous tissue in pre-eclampsia and normal pregnancy. The pooled RNAs of pre-eclamptic and normotensive subjects were hybridized to the HuGeneFL array representing sequences from approximately 5600 full-length human cDNAs. The differentially expressed genes that were detected could be categorized into nine groups: adhesion molecules, obesity-related genes, transcription factors/signalling molecules, immunological factors, neuromediators, oncogenic factors, protease inhibitors, hormones and growth factor-binding proteins. Among those, the obesity-related genes included putative candidate genes associated with the pathogenesis of pre-eclampsia. One of the most up-regulated transcripts was the obese gene (43.6-fold change), and this was reflected by elevated leptin protein levels. In the case of feto-maternal contribution of polymorphic genes to pre-eclampsia, expression analysis of placental tissue has lead to numerous target genes waiting for large scale genetic linkage analyses.
机译:母亲和胎儿中都存在的易感基因很可能导致先兆子痫的风险。因此,通过高密度DNA微阵列分析研究胎盘活检,以确定先兆子痫和正常妊娠在绒毛膜绒毛组织内差异调节的基因。将先兆子痫和血压正常者的合并RNA与代表约5600个全长人cDNA序列的HuGeneFL阵列杂交。检测到的差异表达基因可分为九类:粘附分子,肥胖相关基因,转录因子/信号分子,免疫学因子,神经介质,致癌因子,蛋白酶抑制剂,激素和生长因子结合蛋白。其中,与肥胖相关的基因包括与先兆子痫的发病机理相关的推定候选基因。肥胖基因(上调幅度为43.6倍)是上调程度最高的转录本之一,瘦素蛋白水平升高反映了这一点。在胎儿-母亲多态性基因对先兆子痫的贡献的情况下,胎盘组织的表达分析已导致众多靶基因等待大规模遗传连锁分析。

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