首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >A promoter polymorphism in the interferon alpha-2 gene is associated with the clinical presentation of hepatitis B.
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A promoter polymorphism in the interferon alpha-2 gene is associated with the clinical presentation of hepatitis B.

机译:干扰素α-2基因的启动子多态性与乙型肝炎的临床表现有关。

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摘要

Cytokine gene polymorphisms influence the severity of infectious diseases of viral and parasitic origin. Interferon alpha (IFN-alpha) is known to be involved in the defence against hepatitis B. The promoter of the IFN-alpha-2 gene was investigated for mutations in 344 hepatitis B virus (HBV)-infected Vietnamese patients and 293 uninfected Vietnamese. We found a deletion in the promoter, which was present significantly more frequently in HBV-infected patients than in control individuals; 20% of the healthy, whereas 35% of the HBV-infected cohort carries this deletion (P<0.001). Reporter gene assays showed that a construct with the deletion had a lower level of transcription in comparison to the wild type (P=0.011). These findings indicate that the deletion in the promoter of the IFN-alpha-2 gene reduces the transcription of this gene in vitro. This reduction could explain the individually different interferon levels in humans and could also be one cause of susceptibility to hepatitis B.
机译:细胞因子基因多态性影响病毒和寄生虫源性传染病的严重程度。已知干扰素α(IFN-α)参与了对乙型肝炎的防御。针对344例感染了乙肝病毒(HBV)的越南患者和293例未感染的越南人,研究了IFN-alpha-2基因的启动子的突变。我们发现启动子中有一个缺失,该缺失在感染HBV的患者中比在对照组中更为常见。 20%的健康人群,而35%的HBV感染人群携带这种缺失(P <0.001)。报告基因分析表明,与野生型相比,具有缺失的构建体的转录水平较低(P = 0.011)。这些发现表明,IFN-α-2基因的启动子中的缺失在体外降低了该基因的转录。这种减少可能解释了人类体内不同的干扰素水平,也可能是对乙型肝炎易感性的原因之一。

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