首页 | 官方网站   微博 | 高级检索  
     

Construction of Smac gene-carrying and human uroplakin Ib promoter-Regulated Genetic Vector and its Expression
作者姓名:Zhongxing Zhang  Fuqing Zeng  Guiyi Liao  Xianghui Yue
作者单位:Department of Urology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China
摘    要:Objective: To construct an eukaryotic expression vector that contains Smac gene, which is regulated by human Uroplakin Ib (UpIb) promoter. Methods: For the directionality of Smac expression in the transitional cell carcinoma of bladder, internal CMV and T7 promoter sequences in eukaryotic expression vector pcDNA3.1-Smac were replaced with UpIb promoter to construct a new plasmid. The plasmid DNA was identified by gel electrophoresis after being double digested at respective sites, and then the sequence was analyzed. The expression of Smac mRNA and protein in BIU87 cell line were detected after the transfection by using the newly constructed vector. Results: The Smac gene-carrying and UpIb promoter-regulated eukaryotic expression vector pcDNA3-UpIb-promoter-Smac was successfully constructed. The expression of Smac mRNA was approximately increased by 2.1 times and the expression of Smac protein was increased in about 71% BIU87 cells. Conclusion: The new vector can be effectively expressed in bladder cancer cells and be of great significance for bladder cancer-targeted gene therapy.

关 键 词:遗传因子  真核表达  催化剂  病理机制
收稿时间:2006-02-05

Construction of Smac gene-carrying and human uroplakin Ib promoter-Regulated Genetic Vector and its Expression
Zhongxing Zhang,Fuqing Zeng,Guiyi Liao,Xianghui Yue.Construction of Smac gene-carrying and human uroplakin Ib promoter-Regulated Genetic Vector and its Expression[J].Acta Universitatis Medicinalis Nanjing,2006,20(5):275-278.
Authors:Zhongxing Zhang  Fuqing Zeng  Guiyi Liao  Xianghui Yue
Abstract:Objective: To construct an eukaryotic expression vector that contains Smac gene, which is regulated by human Uroplakin Ib (UpIb) promoter. Methods: For the directionality of Smac expression in the transitional cell carcinoma of bladder, internal CMV and T7 promoter sequences in eukaryotic expression vector pcDNA3.1-Smac were replaced with UpIb promoter to construct a new plasmid. The plasmid DNA was identified by gel electrophoresis after being double digested at respective sites, and then the sequence was analyzed. The expression of Smac mRNA and protein in BIU87 cell line were detected after the transfection by using the newly constructed vector. Results: The Smac gene-carrying and UpIb promoter-regulated eukaryotic expression vector pcDNA3-UpIb-promoter-Smac was successfully constructed. The expression of Smac mRNA was approximately increased by 2.1 times and the expression of Smac protein was increased in about 71% BIU87 cells. Conclusion: The new vector can be effectively expressed in bladder cancer cells and be of great significance for bladder cancer-targeted gene therapy.
Keywords:Smac  Uroplakin Ib  promoter  eukaryotic expression vector
本文献已被 CNKI 维普 万方数据 等数据库收录!
点击此处可从《南京医科大学学报》浏览原始摘要信息
点击此处可从《南京医科大学学报》下载全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司    京ICP备09084417号-23

京公网安备 11010802026262号