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作 者:袁慧星[1] 王涛[1] 饶可[1] 李明超[1] 李路[1] 詹鹰[1] 刘继红[1]
机构地区:[1]华中科技大学同济医学院附属同济医院泌尿外科,武汉430030
出 处:《临床泌尿外科杂志》2010年第12期942-944,共3页Journal of Clinical Urology
基 金:国家自然科学基金资助项目(编号30872574)
摘 要:目的:构建编码诱导型一氧化氮合酶(iNOS)启动子的shRNA质粒表达载体,为利用基因激活技术治疗勃起功能障碍的研究做准备。方法:根据大鼠iNOS启动子序列设计并合成shRNA寡核苷酸片段,退火形成双链并克隆进入载体pDC316-EGFP-U6,构建重组质粒,并进行PCR鉴定以及测序分析。结果:PCR鉴定以及测序证实重组质粒构建成功。结论:成功构建了靶向iNOS基因的shRNA质粒表达载体,为进一步探索勃起功能障碍基因治疗奠定了基础。Objective:To construct a plasmid expression vector coding for the short hairpin RNA(shRNA) targeting iNOS promoter,for the use of gene activation in the treatment of erctile dysfunction in preparation. Methods:According to rat iNOS promoter sequence, were designed and synthesized shRNA oligonucleotides, annealed to form double-stranded and cloned into the vector Pdc316-EGFP-U6, recombinant plasmid, for PCR identification and sequencing. Results:PCR identification and sequencing showed that the recombinant plasmid was successfully con- structed. Conclusions:Tbe plasmid expression vectors coding for shRNA targeting iNOS promoter have been constructed successfuUy,established a favourable foundation for further explore gene therapy of erectile dysfunction.
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