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应用依赖随机化末端连接物聚合酶链反应技术研究重铬酸钾对大鼠肺p53基因DNA损伤
引用本文:熊开容,张治位,衡正昌.应用依赖随机化末端连接物聚合酶链反应技术研究重铬酸钾对大鼠肺p53基因DNA损伤[J].卫生研究,2003,32(3):189-191.
作者姓名:熊开容  张治位  衡正昌
作者单位:四川大学华西公共卫生学院,成都,610041
基金项目:国家自然科学基金资助项目 (No .39670 62 6)
摘    要:应用依赖随机化末端连接物PCR(RandomizedTerminalLinker-dependentPCR ,RDPCR)技术于体内试验的研究 ,从而检测特定基因的DNA损伤。腹腔注射重铬酸钾染毒大鼠 ,提取肺组织基因组DNA ,经p5 3基因外显子 7特异性引物P1重复直线延伸后与接头 (Linker)连接 ,用基因特异性引物P2和连接物引物经PCR扩增 ,电泳、转印 ,再与地高辛标记的探针杂交后显色。结果显示 ,在 2 0 .0mg kg和 40 .0mg kg剂量下 ,出现了两条清晰的杂交带 ,表明重铬酸钾可引起大鼠肺p5 3基因外显子 7的DNA损伤 ,且有两个损伤位点。此结果有助于进一步探讨六价铬化合物的致突变机制 ,同时也拓展了RDPCR技术在毒理学领域的应用

关 键 词:连接物聚合酶链反应  DNA损伤  体内试验  p53基因  重铬酸钾
文章编号:1000-8020(2003)03-0189-03
修稿时间:2002年7月26日

Applying randomized terminal linker-dependent PCR to detect the DNA damage of p53 gene in rat
Xiong Kairong,Zhang Zhiwei,Heng Zhengchang School of Public Health,Huaxi School of Public Health,Sichuan University,Chengdu ,China.Applying randomized terminal linker-dependent PCR to detect the DNA damage of p53 gene in rat[J].Journal of Hygiene Research,2003,32(3):189-191.
Authors:Xiong Kairong  Zhang Zhiwei  Heng Zhengchang School of Public Health  Huaxi School of Public Health  Sichuan University  Chengdu  China
Institution:School of Public Health, Huaxi School of Public Health, Sichuan University, Chengdu 610041, China.
Abstract:In order to use the technique of Randomized Terminal Linker-dependent PCR(RDPCR) to detect DNA lesions of specific gene in vivo, rats were administered with potassium dichromate by i.p.injection and genomic DNA of lung were extracted. Single-stranded products were made by repeated primer extension, these products were ligated to a linker and thus amplified by primer P2 and PL. The final PCR products were detected by electrophoresis and Southern hybridization with DIG-labeled probe. The results showed that two hybridization bands for extron 7 of p53 gene were found with doseage of 20.0 mg/kg and 40.0 mg/kg indicating the DNA lesions of extron 7 of p53 gene, by potassium dichromate and there were two DNA lesion cites. The findings from this study provide evidences both for further investigation of mutational mechanism of hexavalent chromium and expansion on using RDPCR in toxicology.
Keywords:RDPCR  DNA damage  in vivo  p53 gene  potassium dichromate
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