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Differential promoter activities of functional haplotypes in the 5′-flanking region of human Sulfotransferase 1A1

机译:人类磺基转移酶1A1 5'侧翼区功能性单倍型的启动子活性的差异。

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摘要

Previously, we reported five common single nucleotide polymorphisms (SNPs), -624G>C, -396G>A, -358A>C, -341C>G, and -294T>C, and six common haplotypes (CGACT, GAACT, GGAGC, GGACC, CAACT, and GAACC) in the 5′-flanking region of the SULT1A1 gene that were associated with altered enzymatic activity. In the present study, we performed in vitro assays to determine the functional impact of these genetic variations on the promoter activity. Dual luciferase reporter assays revealed that these SNPs are located in a negative regulatory fragment of the SULT1A1 gene. Further experiments demonstrated that these SNPs and haplotypes affected promoter activities of SULT1A1. Electrophoretic mobility shift assays showed distinctive binding patterns for the SNPs -396G>A and -294T>C, due to differential binding affinities of the G/A alleles and the T/C alleles to nuclear proteins extracted from the liver carcinoma cell lines, HepG2 and Huh7.
机译:先前,我们报道了五个常见的单核苷酸多态性(SNP),分别为-624G> C,-396G> A,-358A> C,-341C> G和-294T> C,以及六个常见的单倍型(CGACT,GAACT,GGAGC, SULT1A1基因5'侧翼区域中的GGACC,CAACT和GAACC),这些区域与酶活性的改变有关。在本研究中,我们进行了体外测定,以确定这些遗传变异对启动子活性的功能影响。双重荧光素酶报告基因测定表明,这些SNP位于SULT1A1基因的负调控片段中。进一步的实验表明,这些SNP和单倍型会影响SULT1A1的启动子活性。电泳迁移率迁移分析显示SNP -396G> A和-294T> C具有独特的结合模式,这是由于G / A等位基因和T / C等位基因与从肝癌细胞系HepG2提取的核蛋白的结合亲和力不同和呵呵。

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