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首页> 外文期刊>Psychiatric genetics >Hardy-Weinberg disequilibrium identified genotyping error of the serotonin transporter (SLC6A4) promoter polymorphism.
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Hardy-Weinberg disequilibrium identified genotyping error of the serotonin transporter (SLC6A4) promoter polymorphism.

机译:Hardy-Weinberg不平衡确定了5-羟色胺转运蛋白(SLC6A4)启动子多态性的基因分型错误。

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摘要

We analyzed the putative functional promoter polymorphism of the serotonin transporter (5-HTTLPR) in two large autism spectrum disorder samples and a control sample. A Hardy-Weinberg disequilibrium was detected for 5-HTTLPR in the unaffected founders of both autism spectrum disorder samples and control samples. When we lowered the total magnesium concentration in the polymerase chain reaction below levels reported in previously published studies, we observed a shift in relative allele frequencies and restoration of the Hardy-Weinberg equilibrium. Our data suggest that higher magnesium concentrations caused allele-dependent, non-random genotyping errors. Genotyping data obtained from the 2 mM magnesium protocol increased the significance of linkage and gave suggestive (P=0.06) association with autism spectrum disorder, whereas the corrected genotypes of 5-HTTLPR provide no linkage information beyond the results we have previously published and no evidence of association with autism spectrum disorder. Wepresent details regarding appropriate polymerase chain reaction conditions for the accurate genotyping of this polymorphism.
机译:我们分析了血清白蛋白转运蛋白(5-HTTLPR)的假定功能启动子多态性在两个大的自闭症谱系障碍样本和一个对照样本中。在自闭症谱系障碍样本和对照样本的未受影响的创建者中检测到5-HTTLPR的Hardy-Weinberg不平衡。当我们将聚合酶链反应中的总镁浓度降低到先前发表的研究报告中所报道的水平以下时,我们观察到相对等位基因频率发生了变化,并且Hardy-Weinberg平衡得以恢复。我们的数据表明,较高的镁浓度会导致等位基因依赖性,非随机基因分型错误。从2 mM镁方案获得的基因分型数据增加了连锁的重要性,并提示与自闭症谱系障碍相关(P = 0.06),而更正的5-HTTLPR基因型除了我们先前发表的结果外,没有提供连锁信息,也没有证据与自闭症谱系障碍的关系。我们提供了有关适当的聚合酶链反应条件的详细信息,以便对该多态性进行准确的基因分型。

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