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对一大群不育男性的编码类固醇生成因子 1 的 NR5A1 基因进行全面序列分析。

Comprehensive sequence analysis of the NR5A1 gene encoding steroidogenic factor 1 in a large group of infertile males.

机构信息

Institute of Human Genetics, University of Münster, Münster, Germany.

出版信息

Eur J Hum Genet. 2013 Sep;21(9):1012-5. doi: 10.1038/ejhg.2012.290. Epub 2013 Jan 9.

Abstract

The steroidogenic factor 1 (SF1) protein, encoded by the NR5A1 gene, plays a central role in gonadal development and steroidogenesis. Mutations in NR5A1 were first described in patients with primary adrenal insufficiency and 46,XY disorders of sexual development and later also in men with hypospadias, bilateral anorchia and micropenis and women with primary ovarian insufficiency. Recently, heterozygous missense mutations were found in 4% of infertile men with unexplained reduced sperm counts living in France, but all mutation carriers were of non-Caucasian ancestry. Therefore, we performed a comprehensive NR5A1 sequence analysis in 488 well-characterised predominantly Caucasian patients with azoo- or severe oligozoospermia. Two-hundred-thirty-seven men with normal semen parameters were sequenced as controls. In addition to several synonymous variants of unclear pathogenicity, three heterozygous missense mutations predicted to be damaging to SF1 protein function were identified. The andrological phenotype in infertile but otherwise healthy mutation carriers seems variable. In conclusion, mutations altering SF1 protein function and causing spermatogenic failure are also found in men of German origin, but the prevalence seems markedly lower than in other populations.

摘要

类固醇生成因子 1(SF1)蛋白由 NR5A1 基因编码,在性腺发育和类固醇生成中起核心作用。NR5A1 基因突变首先在原发性肾上腺功能不全和 46,XY 性发育障碍患者中描述,后来也在患有尿道下裂、双侧无睾症和小阴茎以及原发性卵巢功能不全的女性中发现。最近,在法国居住的不明原因精子计数减少的 4%不育男性中发现了杂合错义突变,但所有突变携带者均非白种人血统。因此,我们对 488 名特征明确的、主要为白种人、无精子症或严重少精子症患者进行了全面的 NR5A1 序列分析。237 名精液参数正常的男性作为对照进行测序。除了一些致病性不明的同义变体外,还鉴定出了三种预测会破坏 SF1 蛋白功能的杂合错义突变。在不育但其他方面健康的突变携带者中,男性的表型似乎是可变的。总之,在德国男性中也发现了改变 SF1 蛋白功能并导致精子发生失败的突变,但患病率似乎明显低于其他人群。

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本文引用的文献

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Steroidogenic factor-1 (SF-1, NR5A1) and human disease.类固醇生成因子-1(SF-1,NR5A1)与人类疾病。
Mol Cell Endocrinol. 2011 Apr 10;336(1-2):198-205. doi: 10.1016/j.mce.2010.11.006. Epub 2010 Nov 13.
4
Clinical Review#: State of the art for genetic testing of infertile men.临床评论#:男性不育基因检测的最新技术。
J Clin Endocrinol Metab. 2010 Mar;95(3):1013-24. doi: 10.1210/jc.2009-1925. Epub 2010 Jan 20.
5
Male infertility caused by spermiogenic defects: lessons from gene knockouts.精子发生缺陷导致的男性不育:基因敲除研究的启示
Mol Cell Endocrinol. 2009 Jul 10;306(1-2):24-32. doi: 10.1016/j.mce.2009.03.003. Epub 2009 Mar 20.
6
Genetics of spermatogenic failure.生精障碍的遗传学
Sex Dev. 2008;2(4-5):251-9. doi: 10.1159/000152041. Epub 2008 Nov 5.
7
Gene polymorphisms/mutations relevant to abnormal spermatogenesis.与精子发生异常相关的基因多态性/突变
Reprod Biomed Online. 2008 Apr;16(4):504-13. doi: 10.1016/s1472-6483(10)60457-9.
10
Male infertility: role of genetic background.男性不育:遗传背景的作用
Reprod Biomed Online. 2007 Jun;14(6):734-45. doi: 10.1016/s1472-6483(10)60677-3.

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