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Novel regulatory SNPs in the promoter region of the TNFRSF18 gene in a Gabonese population

机译:在加蓬人口中TNFRSF18基因启动子区域的新型调节性SNP。

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Parasites are accountable for driving diversity within immune gene families. We identified and investigated regulatory single nucleotide polymorphisms (SNPs) in the promoter regions of the tumor necrosis factor receptor superfamily member 18 (TNFRSF18) gene by direct sequencing in a group of male Gabonese individuals exposed to a wide array of parasitic diseases such as malaria, filariasis and schistosomiasis. Two new promoter variants were identified in 40 individuals. Both novel variants were heterozygous and were linked to SNP #rs3753344 (C/T), which has been described. One of the SNP variants (ss2080581728) was close to the general transcription factor site, the TATA box. We further validated these new promoter variants for their allelic gene expression using transient transfection assays. One new promoter variant with two base changes (C/T - ss2080581728/rs3753344) displayed an altered expression of the marker gene. Both novel variants remained less active at the non-induced state in comparison to the major allele. The allele frequencies observed in this study were consistent with data for other African populations. The detection and analysis of these human immune gene polymorphisms contribute to a better understanding of the interaction between host-parasite and expression of Treg activity.
机译:寄生虫负责驱动免疫基因家族内的多样性。我们通过直接测序在一组暴露于多种寄生虫病(例如疟疾)的男性加蓬人中确定并调查了肿瘤坏死因子受体超家族成员18(TNFRSF18)基因的启动子区域中的调节性单核苷酸多态性(SNP)。丝虫病和血吸虫病。在40个个体中鉴定出两个新的启动子变体。这两个新的变体都是杂合的,并与已描述的SNP#rs3753344(C / T)相关。 SNP变体之一(ss2080581728)靠近通用转录因子位点TATA框。我们使用瞬时转染测定进一步验证了这些新的启动子变体的等位基因表达。一个具有两个碱基改变的新启动子变体(C / T-ss2080581728 / rs3753344)显示了标记基因表达的改变。与主要等位基因相比,这两个新的变体在非诱导状态下的活性都较低。在这项研究中观察到的等位基因频率与其他非洲人群的数据一致。这些人类免疫基因多态性的检测和分析有助于更好地理解宿主寄生虫与Treg活性表达之间的相互作用。

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