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印度不育男性的雌激素受体β基因突变

Estrogen receptor beta gene mutations in Indian infertile men.

作者信息

Khattri A, Pandey R K, Gupta N J, Chakravarty B, Deenadayal M, Singh L, Thangaraj K

机构信息

Centre for Cellular and Molecular Biology, Uppal Road, Hyderabad 500 007, India.

出版信息

Mol Hum Reprod. 2009 Aug;15(8):513-20. doi: 10.1093/molehr/gap044. Epub 2009 Jun 9.

DOI:10.1093/molehr/gap044
PMID:19509112
Abstract

Recent studies suggest that estrogens play an important role in male fertility. Estrogen signaling is mediated by Estrogen Receptors (ERalpha and ERbeta). Association of ERbeta with male infertility has not been analyzed to date except for genotyping of known polymorphisms in two different studies, which yielded controversial interpretation. Hence, we performed sequencing of all the exons and untranslated regions of ERbeta gene in 300 infertile and 255 fertile control Indian men. We identified eight novel mutations and four known single nucleotide polymorphisms (SNPs). Of the eight novel mutations, four were non-synonymous, of which one was detected only in infertile men, whereas the other three mutations were detected only in fertile men. Using different bioinformatics tools, we predicted that non-synonymous mutations were benign and they neither altered the structure nor the function of the protein. Among synonymous novel mutations, one was detected in both fertile and infertile men, two were exclusive to infertile men and one was exclusive to fertile men. None of the known SNPs or novel mutations showed statistically significant difference between infertile and fertile men. Moreover, infertile men having ERbeta mutations had normal reproductive tract and serum hormone levels. Our results suggest that the SNPs and mutations in ERbeta gene are not a common cause of spermatogenesis failure in Indian men, although mutations specifically found in infertile men can affect transcription, translation or have synergic effect with other variants in causing infertility.

摘要

近期研究表明,雌激素在男性生育中发挥着重要作用。雌激素信号由雌激素受体(ERα和ERβ)介导。迄今为止,除了在两项不同研究中对已知多态性进行基因分型外,尚未对ERβ与男性不育的关联进行分析,而这两项研究得出了相互矛盾的解释。因此,我们对300名印度不育男性和255名可育对照男性的ERβ基因所有外显子和非翻译区进行了测序。我们鉴定出8个新突变和4个已知单核苷酸多态性(SNP)。在这8个新突变中,4个是非同义突变,其中1个仅在不育男性中检测到,而其他3个突变仅在可育男性中检测到。使用不同的生物信息学工具,我们预测非同义突变是良性的,它们既不改变蛋白质的结构也不改变其功能。在同义新突变中,1个在可育和不育男性中均检测到,2个仅在不育男性中出现,1个仅在可育男性中出现。已知的SNP或新突变在不育和可育男性之间均未显示出统计学上的显著差异。此外,携带ERβ突变的不育男性生殖道和血清激素水平正常。我们的结果表明,ERβ基因中的SNP和突变并非印度男性精子发生失败的常见原因,尽管在不育男性中特别发现的突变可能会影响转录、翻译或在导致不育方面与其他变异产生协同作用。

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