人腺苷A2B受体基因的单核苷酸多态性分析:哮喘患者和正常人的snp患病率

Gino van Heeke, Rachael Seamons, Jean-Yves Metais, John R. Fozard, Stephen Goff, Amanda Wheatley, Jane Dewar, Ian P. Hall
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引用次数: 3

摘要

腺苷A2B受体存在于人肺肥大细胞中,被认为介导哮喘患者对腺苷反应的支气管收缩。因此,它代表了哮喘和过敏性鼻炎的一个有吸引力的治疗靶点。由于药物靶点的遗传变异可能影响个体对治疗的反应,我们分析了腺苷A2B受体基因的多态性及其在高加索人群中的流行程度。发现A2B受体基因的编码区以及基因的内含子-外显子边界没有遗传变异。在该基因的启动子区发现了3个单核苷酸多态性,其中一个产生了BamHI限制性片段长度多态性。三种单核苷酸多态性在未选择人群中的流行率为5%。在英国40名哮喘患者和40名非哮喘患者中调查了BamHI多态性的流行情况:在哮喘患者中未观察到BamHI变体的过量。数据表明,药物反应的任何变异性可能不是由于A2B受体蛋白的直接结构变化。此外,A2B受体基因组位点的多态性不太可能导致人群患哮喘的风险。
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Single Nucleotide Polymorphism analysis of the human adenosine A2B receptor gene: prevalence of SNPs in asthmatics and normal subjects

The adenosine A2B receptor is found on human lung mast cells and is believed to mediate the bronchoconstriction in response to adenosine characteristic of asthmatics. As such it represents an attractive therapeutic target for asthma and allergic rhinitis. As genetic variability in drug targets may affect an individual's response to treatment, the adenosine A2B receptor gene was analyzed for polymorphisms and their prevalence defined in a Caucasian population. The coding region of the A2B receptor gene as well as the intron-exon boundaries of the gene were found to be free of genetic variation. Three single nucleotide polymorphisms were identified in the promoter region of the gene, one of which created a BamHI restriction fragment length polymorphism. The prevalence of the three single nucleotide polymorphisms in an unselected population was <5%. The prevalence of the BamHI polymorphism was investigated in a British population of 40 asthmatics and 40 non-asthmatics: no excess of the BamHI variant was observed in asthmatic subjects. The data indicates that any variability in drug response would likely not be due to direct structural variation of the A2B receptor protein. Further, polymorphism at the A2B receptor genomic locus is unlikely to contribute to the population risk of developing asthma.

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