首页> 外文期刊>The Journal of Allergy and Clinical Immunology >Fine mapping and positional candidate studies on chromosome 5p13 identify multiple asthma susceptibility loci.
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Fine mapping and positional candidate studies on chromosome 5p13 identify multiple asthma susceptibility loci.

机译:在5p13染色体上的精细作图和位置候选研究确定了多个哮喘易感基因座。

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摘要

BACKGROUND: Genome-wide linkage scans to identify asthma susceptibility loci have revealed many linked regions, including a broad region on chromosome 5p. OBJECTIVE: To identify a 5p-linked asthma or bronchial hyperresponsiveness (BHR) locus. METHODS: We performed fine mapping and positional candidate studies of this region in the Hutterites and an outbred case-control sample from Germany by genotyping 89 single nucleotide polymorphisms (SNPs) in 22 genes. SNP and haplotype analyses were performed. RESULTS: Three genes in a distal region (zinc finger RNA binding protein [ZFR], natriuretic peptide receptor C, and a disintegrin and metalloproteinase domain with thrombospondin type 1 motif [ADAMTS12]) were associated with BHR, whereas 4 genes in a proximal region (prolactin receptor, IL-7 receptor [IL7R], leukemia inhibitory factor receptor [LIFR], and prostaglandin E4 receptor [PTGER4]) were associated with asthma symptoms in the Hutterites. Furthermore, nearly the entire original linkage signal in the Hutterites was generated by individuals who had the risk-associated alleles in ZFR3, natriuretic peptide receptor C, ADAMTS12, LIFR, and PTGER4. Variation in ADAMTS12, IL7R, and PTGER4 were also associated with asthma in the outbred Germans, and the frequencies of long-range haplotypes composed of SNPs at ZFR, ADAMTS12, IL7R, LIFR, and PTGER4 were significantly different between both the German and Hutterite cases and controls. There is little linkage disequilbrium between alleles in these 2 regions in either population. CONCLUSION: These results suggest that a broad region on 5p, separated by >9 Mb, harbors at least 2 and possibly 5 asthma or BHR susceptibility loci. These findings are consistent with the hypothesis that regions providing evidence for linkage in multiple populations may, in fact, house more than 1 susceptibility locus, as appears to be the case for the linked region on 5p. CLINICAL IMPLICATIONS: Identifying asthma or BHR genes could lead to novel therapeutic approaches.
机译:背景:全基因组连锁扫描以鉴定哮喘易感基因座揭示了许多连锁区域,包括5p染色体上的一个宽区域。目的:确定5p连锁性哮喘或支气管高反应性(BHR)基因座。方法:我们通过对22个基因中的89个单核苷酸多态性(SNP)进行基因分型,对哈特族人和来自德国的近交病例对照样品中的该区域进行了精细定位和候选位置研究。进行SNP和单倍型分析。结果:远端区域中的三个基因(锌指RNA结合蛋白[ZFR],利钠肽受体C以及具有血小板反应蛋白1型基序的整合素和金属蛋白酶结构域[ADAMTS12])与BHR相关,而近端区域中有4个基因(催乳素受体,IL-7受体[IL7R],白血病抑制因子受体[LIFR]和前列腺素E4受体[PTGER4])与Hutterites的哮喘症状相关。此外,Hutterites中几乎所有的原始连锁信号都是由在ZFR3,利钠肽受体C,ADAMTS12,LIFR和PTGER4中具有风险相关等位基因的个体产生的。远亲德国人中ADAMTS12,IL7R和PTGER4的变异也与哮喘有关,德国和Hutterite病例在ZFR,ADAMTS12,IL7R,LIFR和PTGER4处由SNP组成的远程单倍型的频率也存在显着差异和控件。在这两个人群中,这两个区域的等位基因之间几乎没有连锁不平衡。结论:这些结果表明5p上的一个宽广区域,由> 9 Mb隔开,具有至少2个甚至5个哮喘或BHR易感基因座。这些发现与这样的假设相一致,即提供多族群连锁证据的区域实际上可能容纳1个以上的易感基因座,就像5p上的连锁区域就是这种情况。临床意义:鉴定哮喘或BHR基因可能导致新的治疗方法。

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