摘要
目的构建携带Smac基因、人前列腺特异性抗原(PSA)增强子(PSAE)/PSA启动子(PSAP)调控的前列腺特异性真核表达载体。方法切除含Smac基因的真核表达载体pcDNA3.1-Smac内部的人巨细胞病毒/T7启动子序列,替换为在前列腺组织特异性表达的PSAE、PSAP调控序列。构建的质粒经双酶切凝胶电泳及测序鉴定。结果成功构建携带Smac基因人PSAE-PSAP调控的前列腺特异性真核表达载体pcDNA3-PSAE-PSAP-Smac质粒。结论新构建的载体为前列腺癌的靶向基因治疗奠定了基础。
Objective To construct the expression vector carrying Smac gene driven by human prostate-specific antigen enhancer/promoter(PSAE/PSAP). Methods CMV and T7 promoters were deleted from eukaryotic expression vector pc DNA3. 1-Smac and replaced by human prostate-specific antigen enhancer/promoter. After restriction digestion and agarose electrophoresis of the recombinant vector, the new plasmid was confirmed by DNA sequencing. Results The eukaryotic expression vector pcDNA3-PSAE-PSAP-Smac was constructed successfully. Conclesion The new recombinant vector plays a basic role in prostate cancer-targeted gene therapy.
出处
《华中医学杂志》
CAS
2007年第1期11-12,F0004,共3页
Central China Medical Journal
基金
国家自然科学基金资助课题(No.30271301)