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Lack of association between the GRP78 polymorphisms in the promoter and 3' UTR and susceptibility to chronic HBV infection in a Chinese Han population

机译:在中国汉族人群中,启动子和3'UTR的GRP78多态性与慢性HBV感染易感性之间缺乏关联

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Background Hepatitis B virus (HBV) infection causes large amount of unfolding or false-folding protein accumulation in the endoplasmic reticulum (ER), which in turn induces the expression of glucose-regulated protein 78 (GRP78). The aim in the present study was to analyse the potential association between GRP78 single-nucleotide polymorphisms (SNPs) and the risk of HBV infection. Methods The associations between seven common GRP78 polymorphisms in the promoter (rs391957, rs17840762, rs17840761, rs11355458) and in the 3' untranslated region (UTR) (rs16927997, rs1140763, rs12009) and possible risk of chronic HBV infection were assessed in a case-control study. 496 cases and 539 individually matched healthy controls were genotyped. Results Overall, no associations were observed in genotypic analyses. In addition, haplotypes and diplotypes combining those SNPs in the promoter or in the 3' UTR in high linkage disequilibrium (LD) were also not associated with HBV risk. Conclusion These observations do not support a role for GRP78 polymorphisms in HBV infection in a predominantly Chinese Han population.
机译:背景乙型肝炎病毒(HBV)感染导致内质网(ER)中大量未折叠或错误折叠的蛋白积聚,进而诱导葡萄糖调节蛋白78(GRP78)的表达。本研究的目的是分析GRP78单核苷酸多态性(SNP)与HBV感染风险之间的潜在关联。方法在以下情况下,评估了启动子(rs391957,rs17840762,rs17840761,rs11355458)和3'非翻译区(UTR)(rs16927997,rs1140763,rs12009)的七个常见GRP78多态性之间的关联以及可能的慢性HBV感染风险对照研究。对496例病例和539例个体匹配的健康对照者进行基因分型。结果总体而言,在基因型分析中未发现任何关联。此外,高启动不平衡(LD)中启动子或3'UTR中那些SNP结合的单倍型和双倍型也与HBV风险无关。结论这些观察结果不支持GRP78基因多态性在以中国汉族为主的HBV感染中的作用。

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