首页> 外文期刊>European journal of human genetics: EJHG >Indication of linkage and genetic heterogeneity for asthma and atopy on chromosomes 8p and 12q in 107 French EGEA families.
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Indication of linkage and genetic heterogeneity for asthma and atopy on chromosomes 8p and 12q in 107 French EGEA families.

机译:在107个法国EGEA家庭的8p和12q染色体上显示哮喘和特应性的联系和遗传异质性。

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Using the sample of 107 families with at least two asthmatic siblings, as part of the EGEA study, we have investigated linkage to asthma (or atopy) and genetic heterogeneity according to the presence/absence of atopy (or asthma) using two approaches: (1) the triangle test statistic (TTS), which considers the identical by descent (IBD) distribution among affected sib-pairs discordant for another associated phenotype (eg asthmatic sib-pairs discordant for atopy) and (2) the predivided sample test (PST), which compares the IBD distribution of marker alleles between affected sib-pairs concordant and discordant for the associated phenotype. Two regions, 8p and 12q, already reported to be linked to both asthma and atopy, were examined here. A total of 20 asthmatic sib-pairs discordant for atopy and 24 atopic pairs discordant for asthma were analyzed by both TTS and PST methods and 83 pairs with atopic asthma by PST. Some evidence for linkage was observed for two markers in the 8p23.3-p23.2 region; D8S504 forasthma with genetic heterogeneity according to the presence/absence of atopy and D8S503 for atopy with genetic heterogeneity according to the presence/absence of asthma. In the 12q14.2-q21.33 region, there was also some evidence of linkage to two markers, D12S83 and D12S95, for atopy and asthma, respectively, with genetic heterogeneity according to the presence/absence of the associated trait. Provided the small distance between the two markers on either 8p (16 cM) or 12q (21 cM), it is unclear whether one or two genetic factors are involved in either region.
机译:作为EGEA研究的一部分,我们使用了107个至少有两个哮喘兄弟姐妹的家庭的样本,我们使用两种方法根据是否存在特应性(或哮喘)调查了与哮喘(或特应性)的联系以及遗传异质性: 1)三角检验统计量(TTS),它考虑了与另一个相关表型不一致的受影响同胞对之间同系下降(IBD)分布(例如,与特应性不一致的哮喘同胞对)和(2)预先抽样的样本检验(PST) ),比较了相关表型的受影响同胞对和不同胞对之间标记等位基因的IBD分布。在这里检查了两个区域8p和12q,它们已经被报告与哮喘和特应性疾病有关。通过TTS和PST方法分析了总共20对异位性哮喘的同胞对和24个哮喘异位对,通过PST分析了83对异位性哮喘。在8p23.3-p23.2区域观察到两个标记存在连锁的证据;根据特应性的存在/不存在,D8S504具有遗传异质性哮喘;根据哮喘的存在/不存在,D8S503用于具有遗传异质性异位性哮喘。在12q14.2-q21.33区域,也有证据表明,特应性和哮喘分别与两个标记D12S83和D12S95连锁,并根据是否存在相关性状具有遗传异质性。如果在8p(16 cM)或12q(21 cM)上两个标记之间的距离很小,则不清楚在任一区域中是否涉及一个或两个遗传因子。

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