Kurz Thorsten, Hoffjan Sabine, Hayes M Geoffrey, Schneider Dan, Nicolae Raluca, Heinzmann Andrea, Jerkic Sylvija P, Parry Rod, Cox Nancy J, Deichmann Klaus A, Ober Carole
Department of Human Genetics, University of Chicago, 920 East 58th Street, Chicago, IL 60637, USA.
J Allergy Clin Immunol. 2006 Aug;118(2):396-402. doi: 10.1016/j.jaci.2006.04.036. Epub 2006 Jun 9.
Genome-wide linkage scans to identify asthma susceptibility loci have revealed many linked regions, including a broad region on chromosome 5p.
To identify a 5p-linked asthma or bronchial hyperresponsiveness (BHR) locus.
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.
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.
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.
Identifying asthma or BHR genes could lead to novel therapeutic approaches.
全基因组连锁扫描以识别哮喘易感基因座已揭示出许多连锁区域,包括5号染色体短臂上的一个广泛区域。
识别一个与5号染色体短臂连锁的哮喘或支气管高反应性(BHR)基因座。
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,在哈特派人群以及一个来自德国的非近亲病例对照样本中对该区域进行精细定位和位置候选研究。进行了SNP和单倍型分析。
在一个远端区域的三个基因(锌指RNA结合蛋白[ZFR]、利钠肽受体C以及含血小板反应蛋白基序的解聚素和金属蛋白酶结构域[ADAMTS12])与BHR相关,而在近端区域的四个基因(催乳素受体、白细胞介素7受体[IL7R]、白血病抑制因子受体[LIFR]以及前列腺素E4受体[PTGER4])与哈特派人群中的哮喘症状相关。此外,哈特派人群中几乎所有原始连锁信号均由在ZFR3、利钠肽受体C、ADAMTS12、LIFR和PTGER4中携带风险相关等位基因的个体产生。ADAMTS12、IL7R和PTGER4的变异在非近亲的德国人中也与哮喘相关,并且由ZFR、ADAMTS12、IL7R、LIFR和PTGER4处的SNP组成的长程单倍型频率在德国人和哈特派人群的病例与对照之间存在显著差异。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。
这些结果表明,5号染色体短臂上一个跨度超过9 Mb的广泛区域至少含有2个,可能多达5个哮喘或BHR易感基因座。这些发现与以下假设一致,即在多个群体中提供连锁证据的区域实际上可能包含不止1个易感基因座,5号染色体短臂上的连锁区域似乎就是这种情况。
识别哮喘或BHR基因可能会带来新的治疗方法。