靶向β-catenin的shRNA真核表达质粒的构建及鉴定
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江苏省卫生厅社会发展基金资助项目(J200624)


Construction of eukaryotic vector expressing shRNA of β-catenin
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    摘要:

    目的:针对β-连环蛋白(β-catenin)基因的不同部位,构建靶向β-catenin的shRNA真核表达质粒,鉴定并筛选出最佳抑制效率的表达质粒-方法:针对β-catenin基因的不同部位设计3对短发卡RNA(shRNA)的寡核苷酸片段,克隆到真核表达载体pGPU6中,构建靶向β-catenin的shRNA真核表达质粒pGPU6-β-catenin-shRNA-1-2-3-利用脂质体转染人胃癌细胞株AGS,Western blot法检测并筛选最佳抑制效率的shRNA表达质粒-结果:3个靶向β-catenin的shRNA真核表达质粒pGPU6-β-catenin-shRNA-1-2-3经限制性酶切和测序确实基因插入正确,Western blot法证实pGPU6-β-catenin-shRNA-3明显降低细胞内β-catenin蛋白的表达-结论:成功构建了靶向β-catenin的shRNA真核表达质粒pGPU6-β-catenin-shRNA -1-2-3,并筛选出最佳抑制效率的表达质粒,为进一步研究Wnt/β-catenin信号通路在胃癌中的作用奠定了基础-

    Abstract:

    Objective:To construct short hairpin RNA(shRNA) eukaryotic expression vectors selectively silencing β-catenin gene. Methods:Three oligonucleotides targeting of β-catenin gene were synthesized and cloned into eukaryotic expression plasmids pGPU6. Three combinant plasmids pGPU6-β-catenin-shRNA -1,2,3 were transfected into AGS cells by lipofectamine reagent. The gene silencing efficiency was measured by Western blotting. Results:Three shRNA expression vectors were confirmed by restricted endonuclease analysis and partial nucleotide sequencing. pGPU6-β-catenin-shRNA-3 knocked down the expression of β-catenin protein dramatically by Western blot. Conclusion:The eukaryotic vectors expressing shRNA of β-catenin were constructed successfully. The results of this study lay the foundation for further studying on the role of Wnt/β-catenin signaling pathway in gastric cancer.

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姜 红,亢 健,丁永斌,夏建国.靶向β-catenin的shRNA真核表达质粒的构建及鉴定[J].南京医科大学学报(自然科学版),2009,29(1):12-16

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  • 收稿日期:2008-10-07
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