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Fine Mapping and Positional Candidate Studies Identify HLA-G as an Asthma Susceptibility Gene on Chromosome 6p21

机译:精细定位和位置候选研究确定HLA-G是6p21染色体上的哮喘易感基因

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摘要

Asthma affects nearly 14 million people worldwide and has been steadily increasing in frequency for the past 50 years. Although environmental factors clearly influence the onset, progression, and severity of this disease, family and twin studies indicate that genetic variation also influences susceptibility. Linkage of asthma and related phenotypes to chromosome 6p21 has been reported in seven genome screens, making it the most replicated region of the genome. However, because many genes with individually small effects are likely to contribute to risk, identification of asthma susceptibility loci has been challenging. In this study, we present evidence from four independent samples in support of HLA-G as a novel asthma and bronchial hyperresponsiveness susceptibility gene in the human leukocyte antigen region on chromosome 6p21, and we speculate that this gene might contribute to risk for other inflammatory diseases that show linkage to this region.
机译:哮喘影响着全球近1400万人,并且在过去50年中,哮喘的发病率一直在稳步上升。尽管环境因素明显影响该疾病的发作,进展和严重程度,但家庭和双胞胎研究表明遗传变异也影响易感性。哮喘和相关表型与6p21染色体的关联已在七个基因组筛选中被报道,使其成为基因组中复制最多的区域。然而,由于许多影响较小的基因可能会增加患病风险,因此哮喘易感基因座的鉴定一直具有挑战性。在这项研究中,我们提供了来自四个独立样本的证据,这些证据支持HLA-G作为6p21染色体上人类白细胞抗原区域中的一种新型哮喘和支气管高反应性易感基因,并且我们推测该基因可能与其他炎症性疾病的风险有关表明与该地区的联系。

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