Petry Clive J, Ong Ken K, Michelmore Katherine F, Artigas Soraya, Wingate Dianne L, Balen Adam H, de Zegher Francis, Ibáñez Lourdes, Dunger David B
Department of Paediatrics, University of Cambridge, UK.
J Steroid Biochem Mol Biol. 2006 Mar;98(4-5):199-206. doi: 10.1016/j.jsbmb.2005.09.007. Epub 2006 Feb 10.
We recently reported association between a coding-region single nucleotide polymorphism (SNP50) in the aromatase gene that encodes a key enzyme in testosterone metabolism, with risk for the development of precocious pubarche and circulating testosterone concentrations in two independent female populations. We have now explored further association with variation in the promoter-region of the aromatase gene. We genotyped six promoter-region haplotype-tag SNPs in young women from Oxford, UK (n = 109), and in girls with precocious pubarche (n = 186) and controls (n = 71) from Barcelona, Spain. Aromatase distal promoter-region variation was associated with plasma testosterone concentrations in both Oxford (r(2) = 18.3%, p = 0.01) and Barcelona (r(2) = 8.5%, p = 0.03) females. These associations were independent of SNP50, but appeared to be dependent on different SNPs in Oxford (r(2) = 13.7%, p = 0.006 with SNPs 11 (p = 0.009), 28 (p = 0.02) and 39 (p = 0.06)) and Barcelona (r(2) = 5.9%, p = 0.002 with SNP43 (p = 0.002)) populations. Aromatase distal promoter-region variation was also associated with PCOS symptom score in Oxford women (r(2) = 14.5%, p = 0.048), but, unlike SNP50, was not associated with precocious pubarche risk in Barcelona girls. In conclusion, aromatase distal promoter-region variation appears to have functional consequences for plasma testosterone concentrations in females. The variable associations with androgen-related clinical features could possibly reflect the tissue-specific promoters of the aromatase gene.
我们最近报告了编码睾酮代谢关键酶的芳香化酶基因中的一个编码区单核苷酸多态性(SNP50)与青春期阴毛早现发生风险以及两个独立女性群体中循环睾酮浓度之间的关联。我们现在进一步探究了与芳香化酶基因启动子区变异的关联。我们对来自英国牛津的年轻女性(n = 109)以及来自西班牙巴塞罗那的青春期阴毛早现女孩(n = 186)和对照组(n = 71)中的六个启动子区单倍型标签SNP进行了基因分型。芳香化酶远端启动子区变异与牛津女性(r² = 18.3%,p = 0.01)和巴塞罗那女性(r² = 8.5%,p = 0.03)的血浆睾酮浓度均相关。这些关联独立于SNP50,但在牛津人群(与SNP11(p = 0.009)、28(p = 0.02)和39(p = 0.06)的r² = 13.7%,p = 0.006)和巴塞罗那人群(与SNP43(p = 0.002)的r² = 5.9%,p = 0.002)中似乎依赖于不同的SNP。芳香化酶远端启动子区变异也与牛津女性的多囊卵巢综合征症状评分相关(r² = 14.5%,p = 0.048),但与SNP50不同,在巴塞罗那女孩中与青春期阴毛早现风险无关。总之,芳香化酶远端启动子区变异似乎对女性血浆睾酮浓度具有功能影响。与雄激素相关临床特征的可变关联可能反映了芳香化酶基因的组织特异性启动子。