Malerba G, Lindgren C M, Xumerle L, Kiviluoma P, Trabetti E, Laitinen T, Galavotti R, Pescollderungg L, Boner A L, Kere J, Pignatti P F
Department of Mother and Child, Biology and Genetics, University of Verona, Verona, Italy.
Clin Exp Allergy. 2007 Jan;37(1):83-9. doi: 10.1111/j.1365-2222.2006.02615.x.
Several genome scans have reported linkage of markers on chromosome 7p with asthma and related phenotypes in different populations. A fine mapping in Finnish and French-Canadian populations has associated the GPR154 gene (also known as G-protein-coupled receptor for asthma susceptibility, GPRA) with elevated IgE or asthma.
To confirm chromosome 7p linkage and candidate gene association in Italian families with atopic asthma.
In a two-phase approach, we first performed a linkage analysis of chromosome 7, and then a family-based association study on the GPR154 gene for allergic asthma phenotypes in the Italian population.
The screening of 117 families with 19 microsatellite markers showed potential linkage for elevated IgE (P<0.002 at 22 cM from p-ter), asthma (P<0.005 at 44 cM), or atopy (P<0.005 at 54 cM). In the second phase of the present study, candidate gene GPR154, which is located in the phase one-linked region, was investigated in 211 families with seven single nucleotide polymorphisms (SNPs) that tag most haplotype variability, by the pedigree disequilibrium test. Elevated IgE levels were associated with two GPR154 gene SNPs (SNP 546333, P=0.0046; rs740 347, P=0.006), and with haplotypes in the global test (P=0.013). Haplotype analysis performed in nuclear families having at least 1 asthmatic parent showed a significant association with asthma (P=0.0173), atopy (P=0.0058), SPT (P=0.0025), and bronchial hyper reactivity (P=0.0163).
These results support a susceptibility locus for asthma and related phenotypes on chromosome 7, and are in agreement with recent reports suggesting that a common susceptibility factor for atopic manifestations in asthma is likely conferred by the locus containing the GPR154 gene.
多项全基因组扫描报告称,7号染色体短臂上的标记与不同人群中的哮喘及相关表型存在连锁关系。在芬兰和法裔加拿大人群中进行的精细定位研究已将GPR154基因(也称为哮喘易感性G蛋白偶联受体,GPRA)与IgE升高或哮喘联系起来。
在患有特应性哮喘的意大利家庭中确认7号染色体短臂的连锁关系及候选基因关联。
采用两阶段方法,我们首先对7号染色体进行连锁分析,然后针对意大利人群中过敏性哮喘表型对GPR154基因进行基于家系的关联研究。
对117个家庭的19个微卫星标记进行筛查显示,IgE升高(距短臂末端22厘摩处,P<0.002)、哮喘(44厘摩处,P<0.005)或特应性(54厘摩处,P<0.005)存在潜在连锁关系。在本研究的第二阶段,通过家系不平衡检验,在211个家庭中对位于第一阶段连锁区域的候选基因GPR154进行了研究,该基因有7个单核苷酸多态性(SNP),可标记大多数单倍型变异。IgE水平升高与两个GPR154基因SNP(SNP 546333,P=0.0046;rs740347,P=0.006)以及整体检验中的单倍型相关(P=;0.013)。在至少有1名哮喘患者的核心家庭中进行的单倍型分析显示,与哮喘(P=0.0173)、特应性(P=0.0058)、皮肤点刺试验(SPT)(P=0.0025)和支气管高反应性(P=0.0163)存在显著关联。
这些结果支持7号染色体上存在哮喘及相关表型的易感基因座,并且与最近的报告一致,即哮喘中特应性表现的常见易感因素可能由包含GPR154基因的基因座赋予。