The interleukin-10-1082 G/A polymorphism: allele frequency in different populations and functional significance.

L E N Rees, N A P Wood, K M Gillespie, K N Lai, K Gaston, P W Mathieson
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Abstract

Genotypic variation in the human interleukin-10 (IL-10) promoter may account for marked inter-individual variation in IL-10 production and may influence susceptibility to autoimmune diseases. The G/A polymorphism at position -1082 has been linked to high/low IL-10 producer status. We directly tested the functional significance of this polymorphism using DNA-binding assays and reporter gene assays, examined allele frequencies in two geographically distinct populations and assessed intra- and inter-individual variation in IL-10 production in vitro according to genotype. Functional analyses showed that the -1082 region contains a putative ETS-like transcription factor-binding site, and nuclear factors from a monocyte cell line bind to this region. Transient transfection studies in an Epstein-Barr virus-transformed B cell line indicated that the -1082 A allele confers a two fold increase in transcriptional activity of the IL-10 promoter compared to the G allele. There was marked inter-individual variation in IL-10 production by peripheral blood mononuclear cells in vitro, with no consistent effect of genotype.

白细胞介素-10-1082 G/A 多态性:不同人群中的等位基因频率及其功能意义。
人类白细胞介素-10(IL-10)启动子的基因型变异可能是导致IL-10产生的明显个体间差异的原因,并可能影响对自身免疫性疾病的易感性。位于 -1082 位的 G/A 多态性与高/低 IL-10 生成状态有关。我们使用 DNA 结合试验和报告基因试验直接检测了该多态性的功能意义,研究了两个不同地域人群的等位基因频率,并根据基因型评估了体外 IL-10 生产的个体内和个体间差异。功能分析显示,-1082区域包含一个假定的ETS类转录因子结合位点,单核细胞系的核因子与该区域结合。在Epstein-Barr病毒转化的B细胞系中进行的瞬时转染研究表明,与G等位基因相比,-1082 A等位基因可使IL-10启动子的转录活性增加两倍。外周血单核细胞在体外产生IL-10的过程中存在明显的个体差异,基因型没有一致的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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