ATM基因siRNA真核表达载体的构建及其对转染宫颈癌细胞株ATM表达的抑制作用  

Construction of eukaryotic expression plasmid expressing siRNA targeting ATM gene and its inhibitory effect on ATM expression in transfected human cervical carcinoma cells

作　　者：魏莉[1] 辛晓燕[1] 王健[1] 雷迎锋[2] 薛小平[2] 

机构地区：[1]第四军医大学西京医院妇产科 [2]第四军医大学基础部微生物学教研室,陕西西安710033

出　　处：《第四军医大学学报》2005年第5期393-396,共4页Journal of the Fourth Military Medical University

摘　　要：目的:研究特异性siRNA对宫颈癌ATM基因的阻 抑效果以及用RNAi效应对宫颈癌做基因治疗的可行性. 方法:构建可表达人ATM基因siRNA的重组真核表达质粒 pSuppressorNeo ATM,电穿孔法转染Siha宫颈癌细胞株.应用 RT PCR,Westernblot,流式细胞术、免疫荧光法等方法检测转 染的宫颈癌细胞中ATM基因的表达水平.结果:RT PCR, Western blot均表明瞬时转染pSuppressorNeo ATM的宫颈癌 细胞中ATM基因的表达受到明显抑制,流式细胞术、免疫荧 光法检测表明ATM蛋白含量明显下降.结论:pSuppressor Neo ATM质粒构建成功,瞬时转染宫颈癌细胞后可以明显抑 制ATM基因的表达.AIM: To study inhibitory effect of siRNA on ATM expression in human cervical carcinoma cells and to determine the feasibility of RNAi application in gene-therapy of cervical cancer. METHODS: Hairpin siRNA templates were designed based on ATM gene sequence and mRNA structure and was cloned into pSuppressor vector. Siha cells were transfected by pSuppressor-ATM with electroporation and the non-transfected cells and non-specific siRNA transfected cells were used as controls. The inhibitory effect of ATM mRNA was detected by semi-quantitative RT-PCR and Western-blot, and the inhibitory effect of ATM protein expression was detected by FCM and immunofluorescency. RESULTS: Semi-quantitative RT-PCR, Western-blot, FCM and immunofluorescency all revealed a potent inhibition of the expression of ATM in the transfected Siha cells. CONCLUSION: The plasmid vector was successfully constructed. Transient transfection can significantly decrease the ATM level in transfected cells.

关 键 词：ATM基因 RNA干扰 宫颈癌 转染 

分 类 号：R969.4[医药卫生—药理学]