cDNA基因芯片技术分析三聚氰胺肾毒性的相关基因表达  

Gene Expression Studies of Melamine-related Renal Toxicity Based on cDNA Microarray

作　　者：时美[1] 范雪梅[1] 李雪[2] 王铮[3] 王义明[2] 罗国安[1,2] 

机构地区：[1]华东理工大学药学院,上海200237 [2]清华大学中药现代化研究中心,北京100084 [3]南开大学药学院,天津300071

出　　处：《高等学校化学学报》2010年第4期684-689,共6页Chemical Journal of Chinese Universities

基　　金：国家"九七三"计划项目(批准号:2007CB714505);国家"十一五"科技支撑项目(批准号:2006BAI08BO4-01);教育部博士点基金(批准号:20080031012)资助

摘　　要：利用基因芯片技术筛查不同剂量的三聚氰胺干预大鼠肾脏的差异表达基因,并对筛查的差异基因进行生物信息学分析,推测三聚氰胺肾毒性的分子作用机制.结果表明,高剂量三聚氰胺干预的大鼠肾脏差异表达基因数多于低剂量干预的肾脏差异表达基因,并且涉及到更多重要的分子功能和代谢途径,表明三聚氰胺肾毒性具有剂量依赖性,相比低剂量而言,高剂量三聚氰胺干预对肾脏的危害更为严重.Nowadays,microarray technology has been used in toxicogenomics more and more often.In this paper,we applied it into the renal toxicity research of melamine,which is an intermediate of resin in chemical industry.The experimental,through microarray and bioinformatics,was designed to find the differences between two cases in which the rats independently intervened by high and low doses melamine,and then to interpret the molecular mechanism of renal toxicity.The result indicated that the number of differentially expressed genes intervened by high dose of melamine were more than that by low dose of melamine.Besides,the differential expressed genes interfered by high dose melamine have been proved to have close connection with some important pathways as follow：valine,leucine and isoleucine degradation,citrate metabolism,glutathione metabolism,fatty acid metabolism,and the molecular function such as mental binding,lyase activ-ity,ligase activity,symporter activity,glutathione transferase activity,monooxygenase activity.Our research show the toxicity in kidney intervened by melamine,and demonstrated the special advantage of microarray technology in toxicogenomics.

关 键 词：三聚氰胺 基因芯片 肾毒性 肾结石 

分 类 号：O657[理学—分析化学]