人上皮细胞黏附分子shRNA表达载体的构建及鉴定
投稿时间:2015-10-09  修订日期:2015-10-09  点此下载全文
引用本文:张敏娜,庄英杰.人上皮细胞黏附分子shRNA表达载体的构建及鉴定[J].医学研究杂志,2016,45(4):29-31
DOI: 10.11969/j.issn.1673-548X.2016.04.009
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作者单位E-mail
张敏娜 100039 北京, 中国人民解放军第302医院感染性疾病诊疗与研究中心  
庄英杰 100039 北京, 中国人民解放军第302医院感染控制科 Yingjiezhuang@sina.com 
基金项目:国家自然科学基金资助项目(81372248)
中文摘要:目的 以人上皮细胞黏附分子(epithelial cell adhesion molecule,EpCAM)基因为靶基因,构建shRNA重组表达载体。方法 根据GenBank中EpCAM序列(BC014785.1)的mRNA设计4组shRNA序列,插入pSGU6/GFP/Neo载体,构建重组载体,转化至Top10感受态细胞,经卡那霉素筛选并挑取阳性克隆,进行PCR鉴定及DNA测序分析。结果 PCR鉴定及DNA测序结果显示重组载体EpCAM-pSGU6/GFP/Neo-shRNA构建成功。结论 成功构建了干扰人EpCAM基因的重组表达载体,为研究EpCAM分子的生物学功能打下基础。
中文关键词:上皮细胞黏附分子  RNA干扰  短发夹RNA
 
Construction of ShRNA Eukaryotic Recombinant Plasmid Targeting Human EpCAM
Abstract:Objective To construct the recombinant eukaryotic vector expressing short hairpin RNA(shRNA) section targeting human EpCAM gene. Methods According to the sequence of human EpCAM mRNA (GenBank ID:BC014785.1), four groups of shRNA sequence were designed and cloned into pSGU6/GFP/Neo vector to construct the recombinant plasmids, which were transformed into Top10 competent cells, screened by kanamycin.The positive clones were selected, and the extracted plasmids were identifed by PCR analysis and gene sequencing. Results PCR analysis and DNA sequencing results showed that the eukayotic expression vector of EpCAM-pSGU6/GFP/Neo-shRNA were successfully constructed. Conclusion The eukaryotic expression vector expressing shRNA targetin human EpCAM is successfully constructed, which provide a foundation for further study on the function of EpCAM.
keywords:Epithelia cell adhesion molecule  RNA interference  Short hairpin RNA
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