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作 者:张永新[1] 李子健[1] 闫洁[1] 张幼怡[1]
机构地区:[1]北京大学第三医院血管医学研究所,分子心血管学教育部重点实验室,北京100191
出 处:《中国病理生理杂志》2009年第11期2081-2087,共7页Chinese Journal of Pathophysiology
基 金:国家重点基础研究发展规划项目计划(973计划)资助(No.2006CB503806);教育部科学技术研究重大资助项目(No.307001);国家自然科学基金资助项目(No.30821001)
摘 要:目的:利用心肌肥大病理过程中基因表达谱的变化,构建基因/蛋白质调控网络。方法:以苯肾上腺素诱导新生大鼠心肌细胞肥大为模型,在分析肥大心肌细胞基因表达谱变化的基础上,进一步利用Pathwaystudio和Agilent Literature Search软件结合文献挖掘方法,构建基因/蛋白质相互作用网络。结果:构建的网络包含450个相互作用的基因/蛋白质(节点)以及592个它们之间相互作用的关系(边)。拓扑分析表明该网络具有无尺度特性,同时分析确定14个基因/蛋白质是网络的关键节点。通过GO(gene ontology)分析,发现在苯肾上腺素诱导新生大鼠心肌细胞肥大的过程中,与物质代谢、细胞信号转导及细胞骨架等密切相关的基因可能发挥了重要作用。结论:构建基因/蛋白质网络为研究心肌肥大的分子机制提供了有用的信息和方法。AIM : To construct a genomic regulatory network based on gene expression profiling of hypertrophic cardiomyocytes induced by phenylephrine in neonatal rats. METHODS: Cultured neonatal hypertrophic cardiomyocytes were induced by phenylephedrine. The gene expression profiles of these cells were assessed by using a cDNA microarray, and the microarray data were further analyzed by Pathwaystudio and Agilent Literature Search software. RESULTS: A genes/proteins interaction network was constructed with 450 nodes and 592 edges by analyzing the gene expression in hypertrophic cardiomyocytes and literature mining. The network belongs to scale - free network by topological analysis, and 14 genes/proteins as key nodes, including PTPN11, TRAF6, HSPA8, VIM, RPS6KA3, PTHRP, GRB2 and PI3K, were predicted. Based on GO analysis, the genes/proteins associated with metabolism, signal transduction and cytoskeleton may play important roles in the process of cardiomyocytes hypertrophy induced by phenylephedrine in neonatal rat. CONCLUSION: The genomic regulalory network based on gene expression profiling and literature mining may provide integrated clue to elaborate hypotheses about the evolution of cardiomyocyte hypertrophy.
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