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Characterization of a common susceptibility locus for asthma-related traits

机译:哮喘相关性状常见易感基因座的表征

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Susceptibility to asthma depends on variation at an unknown number of genetic loci. To identify susceptibility genes on chromosome 7p, we adopted a hierarchical genotyping design, leading to the identification of a 133-kilobase risk-conferring segment containing two genes. One of these coded for an orphan G protein coupled receptor named GPRA ( G protein - coupled receptor for asthma susceptibility), which showed distinct distribution of protein isoforms between bronchial biopsies from healthy and asthmatic individuals. In three cohorts from Finland and Canada, single nucleotide polymorphism - tagged haplotypes associated with high serum immunoglobulin E or asthma. The murine ortholog of GPRA was up-regulated in a mouse model of ovalbumin-induced inflammation. Together, these data implicate GPRA in the pathogenesis of atopy and asthma.
机译:哮喘的易感性取决于未知基因位点的变异。为了鉴定7p号染色体上的易感基因,我们采用了分级基因分型设计,从而鉴定了一个包含两个基因的133碱基的风险赋予片段。其中一个编码孤儿G蛋白偶联受体GPRA(G蛋白偶联哮喘易感性受体),该受体在健康人和哮喘患者的支气管活检组织中显示出不同的蛋白同工型分布。在来自芬兰和加拿大的三个队列中,单核苷酸多态性标记的单倍型与高血清免疫球蛋白E或哮喘相关。 GPRA的鼠直系同源基因在卵清蛋白诱导的炎症小鼠模型中上调。总之,这些数据暗示GPRA与特应性疾病和哮喘有关。

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