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

被引:40
作者
Guo, Yan
Xiong, Dong-Hai
Yang, Tie-Lin
Guo, Yan-Fang
Recker, Robert R.
Deng, Hong-Wen
机构
[1] Univ Missouri, Sch Med, Dept Orthoped Surg, Kansas City, MO 64108 USA
[2] Xi An Jiao Tong Univ, Minist Educ, Key Lab Biomed Informat Engn, Xian 710049, Peoples R China
[3] Xi An Jiao Tong Univ, Inst Mol Genet, Sch Life Sci & Technol, Xian 710049, Peoples R China
[4] Creighton Univ, Osteoporosis Res Ctr, Omaha, NE 68131 USA
[5] Creighton Univ, Dept Biomed Sci, Omaha, NE 68131 USA
[6] Hunan Normal Univ, Coll Life Sci, Lab Mol & State Genet, Changsha 410081, Hunan, Peoples R China
关键词
D O I
10.1093/hmg/ddl155
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
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.
引用
收藏
页码:2401 / 2408
页数:8
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