靶向hTERT 人工miRNA 表达框架的构建及其对HepG2 细胞端粒酶活性的抑制作用
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彭剑雄, Email: jxpeng@csu.edu.cn

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中南大学本科生自由探索计划项目资助(2282014bks193)。


Construction of artificial miRNA expression cassettes targeting hTERT and their inhibitory effects on telomerase activity in HepG2 cells
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    摘要:

    目的:构建针对hTERT基因的人工miRNA表达框架,并验证其对HepG2细胞端粒酶活性的抑制作用。 方法:应用融合PCR技术针对不同位点设计并构建3个靶向hTERT的人工miRNA表达框架,对各表达框架鉴定后,将其单独或两种共转染HepG2细胞,采用TRAP-银染法和TRAP-二聚体蝎形探针荧光定量PCR法检测细胞端粒酶活性。 结果:3个针对hTERT基因的人工miRNA表达框架均成功构建,单独或共转染HepG2细胞后,HepG2细胞的端粒酶活性均被不同程度的抑制,且两种表达框架共转染的抑制作用明显大于单独转染,差异均有统计学意义(均P<0.05)。 结论:靶向hTERT基因的人工miRNA表达框架能有效而特异抑制HepG2细胞端粒酶活性,多位点联合抑制是一种有效的实验方案。

    Abstract:

    Objective: To construct the artificial miRNA expression cassettes targeting hTERT gene and validate their inhibitory effect on telomerase activity in HepG2 cells. Methods: Three artificial miRNA expression cassettes targeting different sites of hTERT gene were designed and constructed by overlap extension PCR method. After identification, the cassettes were transfected alone or co-transfected into HepG2 cells, and then the telomerase activities in HepG2 cells were detected by TRAP-silver staining and TRAP-duplex scorpion probe fluorescence quantitative PCR. Results: The three artificial miRNA expression cassettes targeting hTERT gene were all successfully constructed, and after they were transfected alone or co-transfected into the HepG2 cells, the telomerase activities in HepG2 cells were inhibited to different degrees, and the inhibitory effect of co-transfection with two miRNA expression cassettes was significantly stronger than those of any lone transfection. All the differences reached statistical significance (all P<0.05). Conclusion: The artificial miRNA expression cassettes targeting hTERT gene can effectively inhibit telomerase activity in HepG2 cells, and combined inhibition is an effective experimental program.

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徐慧,龚霞,赵丹丹,范张玲,彭剑雄.靶向hTERT 人工miRNA 表达框架的构建及其对HepG2 细胞端粒酶活性的抑制作用[J].中国普通外科杂志,2014,23(12):1647-1651.
DOI:10.7659/j. issn.1005-6947.2014.12.009

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  • 收稿日期:2014-10-30
  • 最后修改日期:2014-11-25
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  • 在线发布日期: 2014-12-15