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Allelic association and functional studies of promoter polymorphism in the leukotriene C4 synthase gene (LTC4S) in asthma

机译:哮喘患者白三烯C4合酶基因(LTC4S)启动子多态性的等位关联和功能研究

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摘要

>Background: LTC4 synthase is essential for the production of cysteinyl leukotrienes (Cys-LT), critical mediators in asthma. We have identified a novel promoter polymorphism at position -1072 (G/A) and a -444 (A/C) polymorphism has previously been reported. The role of these polymorphisms in the genetic susceptibility to asthma was examined. >Methods: To test for genetic association with asthma phenotypes, 341 white families (two asthmatic siblings) and 184 non-asthmatic control subjects were genotyped. Genetic association was assessed using case control and transmission disequilibrium test (TDT) analyses. LTC4S promoter luciferase constructs and transiently transfected human HeLa and KU812F cells were generated to determine the functional role of these polymorphisms on basal transcription. >Results: No associations were observed in case control analyses (–1072 A, q=0.09; -444 C, q=0.29); the TDT identified a borderline association between the -444 C allele and bronchial responsiveness to methacholine (p=0.065). Asthmatic children with the -444 C allele had a lower mean basal forced expiratory volume in 1 second (97.4 v 92.7% predicted, p=0.005). LTC4S promoter luciferase analyses provided no evidence for a functional role of either polymorphism in determining basal transcription. >Conclusion: This study does not support a role for these polymorphisms in genetic susceptibility to asthma but provides evidence to suggest a role in determining lung function parameters.
机译:>背景:LTC4合酶对于生产半胱氨酸白三烯(Cys-LT)(哮喘的关键介质)至关重要。我们已经在位置-1072(G / A)和-444(A / C)多态性中发现了一种新颖的启动子多态性,以前已有报道。研究了这些多态性在哮喘遗传易感性中的作用。 >方法:为检验与哮喘表型的遗传相关性,对341个白人家庭(两个哮喘兄弟姐妹)和184个非哮喘控制对象进行了基因分型。使用病例对照和传播不平衡测试(TDT)分析评估遗传关联。生成LTC4S启动子荧光素酶构建体和瞬时转染的人HeLa和KU812F细胞,以确定这些多态性对基础转录的功能作用。 >结果:在病例对照分析中未发现关联(–1072 A,q = 0.09; -444 C,q = 0.29); TDT鉴定了-444 C等位基因与支气管对乙酰甲胆碱的反应之间的临界关联(p = 0.065)。患有-444 C等位基因的哮喘儿童在1秒钟内具有较低的平均基础强迫呼气量(预测的97.4 v 92.7%,p = 0.005)。 LTC4S启动子荧光素酶分析未提供任何证据表明任一多态性在确定基础转录中的功能性作用。 >结论:该研究不支持这些多态性在哮喘遗传易感性中的作用,但提供了证据表明其在确定肺功能参数中的作用。

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