摘要
目的:采用双荧光素酶报告基因系统分析CYP3A4*1G多态性对CYP3A4基因转录活性的影响。方法:构建含CYP3A4*1G突变位点的荧光素酶基因表达载体,用Lipofectamine 2000转染HepG2细胞,化学发光法检测荧光素酶活性。结果:应用双荧光素酶报告基因系统检测显示,pGL3-promoter-A质粒转染后荧光素酶活性显著高于pGL3-promoter-G(P=0.022<0.05)。结论:CYP3A4*1G能够增强荧光素酶基因的表达,可能增强CYP3A4基因的转录活性。
Objective: To analyze the effects of CYP3A4 * 1G polymorphism on the transcriptional activity of the CYP3A4 gene by the dual luciferase reporter assay system. Methods: The luciferase gene plasmids containing the CYP3A4 * 1G mutated sites was constructed by genetic engineering. The human hepatoma cell line, HepG2, was used for transfection with the plasmid constructs by li- pofectamine 2000. Results: The results of the dual luciferase reporter assay system indicated that the IVS10 + 12A construct showed higher luciferase activity than the IVS10 + 12G construct (P =0. 022). Conclusion: The CYP3A4 * 1G is able to enhance the expression of the luciferase gene, which implies that it may enhance the transcriptional activity of CYP3A4 gene.
出处
《河南医学研究》
CAS
2014年第7期4-7,共4页
Henan Medical Research
基金
国家自然科学基金项目(81302796)
河南省医学科技攻关计划项目(201203148)