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TLR4 -2242 T→C variant increases transcriptional activity of its promoter

TLR4 -2242 T→C variant increases transcriptional activity of its promoter
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摘要 Objective:To investigate the effects of -2242,-1892 and -1837 single nucleotide polymorphisms(SNPs) on toll-like receptor 4(TLR4) promoter activity.Methods:Polymerase chain reaction(PCR) and site direct mutation technology were used to construct TLR4 basic promoter and -2242C,-1892A and -1837G mutate promoter plasmids.Dual-Luciferase Reporter assay system was used to detect the activity of constructed promoter following human embryonic kidney(HEK) 293 cells were transiently cotransfected with the constructed plasmids and the control plasmid pRL-CMV.Results:In HEK293 cells,the activity of -2242C mutate promoter was higher than -2242T promoter,and there was no significant difference when both -1892A and -1837G mutate promoter compared with -1892G and -1837A promoter,respectively.Conclusion:It is implied that -2242T→C base variation can enhance the activity of TLR4 promoter,while -1892 and -1837 SNPs have no effect on TLR4 promoter activity. Objective: To investigate the effects of-2242, 1892 and -1837 single nucleotide polymorphisms (SNPs) on toll-like receptor 4 (TLR4) promoter activity. Methods: Polymerase chain reaction (PCR) and site direct mutation technology were used to construct TLR4 basic promoter and -2242C, -1892A and -1837G mutate promoter plasmids. Dual-Luciferase Reporter assay system was used to detect the activity of constructed promoter following human embryonic kidney (HEK) 293 cells were transiently cotransfected with the constructed plasmids and the control plasmid pRL-CMV. Results: In HEK293 cells, the activity of-2242C mutate promoter was higher than -2242T promoter, and there was no significant difference when both -1892A and -1837G mutate promoter compared with -1892G and -1837A promoter, respectively. Conclusion: It is implied that -2242T→C base variation can enhance the activity of TLR4 promoter, while -1892 and -1837 SNPs have no effect on TLR4 promoter activity.
出处 《Journal of Medical Colleges of PLA(China)》 CAS 2009年第2期69-75,共7页 中国人民解放军军医大学学报(英文版)
基金 Supported by the Major State Basic Research Development Program of China (2005CB522602) the National Funds for Outstanding Youth Scientists (30325040)
关键词 Toll-like receptor 4 PROMOTER Single nucleotide polymorphisms Toll样受体4 启动子活性 转录活性 G突变 HEK293细胞 单核苷酸多态性 启动子变异 聚合酶链反应
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