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Interferon-gamma receptor 1 promoter polymorphisms: population distribution and functional implications.

机译:干扰素-γ受体1启动子多态性:人口分布和功能的影响。

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Different polymorphisms have been described in the minimal promoter region (MPR) of the interferon-gamma receptor 1 (IFNGR1), a molecule that plays a critical role in mycobacterial control. We sequenced the IFNGR1 MPR from African American, Caucasian and Korean controls, and from mycobacteria-infected patients. Six different single nucleotide polymorphisms (SNPs) were detected in the IFNGR1 MPR. The three ethnic groups showed different SNP distribution patterns, but no significant differences were detected between mycobacterial cases and controls. Two polymorphisms were found in all populations (G-611A, T-56C). We cloned the four allelic variants (var) of haplotype G-611A/T-56C into a luciferase reporter vector and determined their promoter activity. Polymorphisms at position -611 had a stronger effect on the promoter activity than those at position -56, and constructs carrying G-611 produced a stronger promoter activity than -611A constructs. The IFNGR1 MPR is a polymorphic region with at least two SNPs influencing its activity, but these are not associated with increased mycobacterial susceptibility.
机译:在干扰素-γ受体1(IFNGR1)的最小启动子区域(MPR)中已描述了不同的多态性,该分子在分枝杆菌控制中起着至关重要的作用。我们对非洲裔美国人,白种人和韩国人对照以及分枝杆菌感染患者的IFNGR1 MPR进行了测序。在IFNGR1 MPR中检测到六个不同的单核苷酸多态性(SNP)。这三个族裔显示出不同的SNP分布模式,但在分枝杆菌病例和对照组之间没有发现显着差异。在所有人群中均发现了两个多态性(G-611A,T-56C)。我们将单倍型G-611A / T-56C的四个等位基因变体(var)克隆到荧光素酶报告载体中,并确定了它们的启动子活性。 -611位的多态性比-56位的多态性对启动子活性的影响更大,带有G-611的构建体比-611A的多态性具有更强的启动子活性。 IFNGR1 MPR是一个多态性区域,具有至少两个影响其活性的SNP,但这些与分枝杆菌敏感性增加无关。

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