Suppr超能文献

遗传高血压发病期和维持期全基因组基因表达差异的荟萃分析。

Meta-analysis of genome-wide gene expression differences in onset and maintenance phases of genetic hypertension.

机构信息

Basic & Clinical Genomics Laboratory, School of Medical Sciences and Bosch Institute, University of Sydney, Sydney, New South Wales, Australia.

出版信息

Hypertension. 2010 Aug;56(2):319-24. doi: 10.1161/HYPERTENSIONAHA.110.155366. Epub 2010 Jun 28.

Abstract

Gene expression differences accompany both the onset and established phases of hypertension. By an integrated genome-transcriptome approach we performed a meta-analysis of data from 74 microarray experiments available on public databases to identify genes with altered expression in the kidney, adrenal, heart, and artery of spontaneously hypertensive and Lyon hypertensive rats. To identify genes responsible for the onset of hypertension we used a statistical approach that sought to eliminate expression differences that occur during maturation unrelated to hypertension. Based on this adjusted fold-difference statistic, we found 36 genes for which the expression differed between the prehypertensive phase and established hypertension. Genes having possible relevance to hypertension onset included Actn2, Ankrd1, ApoE, Cd36, Csrp3, Me1, Myl3, Nppa, Nppb, Pln, Postn, Spp1, Slc21a4, Slc22a2, Thbs4, and Tnni3. In established hypertension 102 genes exhibited altered expression after Bonferroni correction (P<0.05). These included Atp5o, Ech1, Fabp3, Gnb3, Ldhb, Myh6, Lpl, Pkkaca, Vegfb, Vcam1, and reduced nicotinamide-adenine dinucleotide dehydrogenases. Among the genes identified, there was an overrepresentation of gene ontology terms involved in energy production, fatty acid and lipid metabolism, oxidation, and transport. These could contribute to increases in reactive oxygen species. Our meta-analysis has revealed many new genes for which the expression is altered in hypertension, so pointing to novel potential causative, maintenance, and responsive mechanisms and pathways.

摘要

基因表达的差异伴随着高血压的发生和确立阶段。通过综合基因组-转录组方法,我们对公共数据库中 74 个微阵列实验的数据进行了荟萃分析,以鉴定在自发性高血压和 Lyon 高血压大鼠的肾脏、肾上腺、心脏和动脉中表达改变的基因。为了鉴定与高血压发生相关的基因,我们使用了一种统计方法,旨在消除与高血压无关的成熟过程中发生的表达差异。基于这种调整后的倍数差异统计,我们发现了 36 个基因,它们在高血压前期和高血压期之间的表达存在差异。与高血压发生可能相关的基因包括 Actn2、Ankrd1、ApoE、Cd36、Csrp3、Me1、Myl3、Nppa、Nppb、Pln、Postn、Spp1、Slc21a4、Slc22a2、Thbs4 和 Tnni3。在已确立的高血压中,102 个基因在经过 Bonferroni 校正后表现出改变的表达(P<0.05)。这些基因包括 Atp5o、Ech1、Fabp3、Gnb3、Ldhb、Myh6、Lpl、Pkkaca、Vegfb、Vcam1 和减少的烟酰胺腺嘌呤二核苷酸脱氢酶。在所鉴定的基因中,有一个与能量产生、脂肪酸和脂质代谢、氧化和运输相关的基因本体术语的过表达。这可能导致活性氧的增加。我们的荟萃分析揭示了许多新的基因,它们在高血压中表达改变,因此指向新的潜在的因果、维持和反应性机制和途径。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验