大鼠野生型钾通道亚基Kir2.3基因真核表达载体的构建及其在PC12细胞中的表达

    Construction of rat Kir2.3 eukaryotic expression vector and its expression in PC12 cells

    • 摘要: 目的:克隆大鼠野生型钾通道亚基基因Kir2.3并构建真核表达载体pcDNA3-flag/Kir2.3,观察其在大鼠嗜铬细胞瘤(PC12)细胞中的表达。方法:从成年大鼠纹状体中提取总RNA,用RT-PCR方法获得大鼠野生型Kir2.3基因的全长cDNA,经限制性内切酶双酶切后,克隆至真核表达载体pcDNA3-flag质粒中。Kir2.3基因测序结果与基因库登录序列比对,序列正确的重组质粒用脂质体转染PC12细胞,Western blot和荧光显微镜观察基因表达情况。结果:Kir2.3基因测序结果与基因库登录序列比对显示完全一致。Western blot证实pcDNA3-flag/Kir2.3转染PC12细胞24 h后有Kir2.3的过表达,且至少持续72 h。结论:成功构建了大鼠野生型Kir2.3基因的真核表达载体,获得了瞬时表达大鼠野生型Kir2.3基因的PC12细胞克隆,为进一步研究Kir2.3的生物学功能以及Kir2.3在帕金森病发病机制中的作用奠定了良好的基础。

       

      Abstract: Objective: To construct the eukaryotic expression vector of rat potassium channels subunit gene Kir2.3,and to detect its expression in rat adrenal pheochromocytoma cells(PC12).Methods: The total RNA was extracted from the striatum of adult rat brain.The full length cDNA encoding Kir2.3 gene was obtained using the RT-PCR method and subcloned to eukaryotic expression vector pcDNA3-flag by restriction enzymes.The sequence of Kir2.3 gene was confirmed by blasting to Genbank.The recombinant plasmids were transfected into PC12 cells by lipofectamin method.The expression of Kir2.3 gene in PC12 cells was assayed by Western blot and fluorescence microscopy.Results: The sequence of Kir2.3 gene was correct by blasting to Genbank.Western Blot showed that Kir2.3 gene was overexpressed for at least 72 h,which was detected at beginning of 24 h after pcDNA3-flag/Kir2.3 plasmids were transfected into PC12 cells.Conclusions: The eukaryotic expression plasmid pcDNA3-flag/Kir2.3 was successfully constructed and expressed in the dopaminergic like cells-PC12 cells.

       

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