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Polymorphisms of estrogen-biosynthesis genes CYP17 and CYP19 may influence age at menarche: a genetic association study in Caucasian females

机译:雌激素-生物合成基因CYP17和CYP19的多态性可能影响初潮的年龄:一项针对白人女性的遗传关联研究

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摘要

Variation in age at menarche (AAM) is known to be substantially influenced by genetic factors, but the true causal genes remain largely unidentified. Because the increased amplitude of estrogen exposure of tissues initiates the onset of menarche, the genes involved in estrogen biosynthesis are natural candidate genes underlying AAM. Our study aimed to identify whether the CYP17 and CYP19, the two key genes involved in the biosynthesis of estrogen, are associated with AAM variation in 1048 females from 354 Caucasian nuclear families. We genotyped 38 SNPs and established the linkage disequilibrium blocks and haplotype structures that covered the full transcript length of those two genes. Family-based and population-based statistical analyses were used to test for associations with all of the single SNPs and haplotypes. Both methods consistently detected significant associations for five SNPs of CYP19 with AAM. Haplotype analyses corroborated our single-SNP results by showing that the haplotypes in block 1 were highly significant to AAM in population-based analyses. However, we could not find any association of CYP17 with AAM. Our study is the first to suggest the important effect of CYP19 on AAM variation in Caucasian females. It will be valuable to replicate and confirm these findings in other independent studies, aiming at eventually finding the hidden genetic mechanisms underlying the variation in AAM.
机译:已知初潮年龄的变化(AAM)受遗传因素的影响很大,但真正的因果基因在很大程度上仍未确定。由于组织中雌激素暴露幅度的增加引发了初潮的发生,因此参与雌激素生物合成的基因是AAM的天然候选基因。我们的研究旨在确定CYP17和CYP19这两个参与雌激素生物合成的关键基因是否与354个白种人核心家庭的1048名女性的AAM变异有关。我们对38个SNPs进行了基因分型,并建立了覆盖这两个基因全部转录长度的连锁不平衡区和单倍型结构。基于家庭和基于人口的统计分析用于测试与所有单个SNP和单倍型的关联。两种方法均一致地检测到CYP19的5个SNP与AAM的显着关联。单倍型分析通过显示在基于人群的分析中,区块1中的单倍型对AAM非常重要,从而证实了我们的单SNP结果。但是,我们找不到CYP17与AAM的任何关联。我们的研究首次提出CY​​P19对白种女性AAM变异的重要影响。在其他独立研究中复制和确认这些发现将是有价值的,目的是最终找到AAM变异背后的隐藏遗传机制。

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