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高度保守的NANOS2蛋白:睾丸特异性表达及其对人类男性生殖的意义。

The highly conserved NANOS2 protein: testis-specific expression and significance for the human male reproduction.

作者信息

Kusz K M, Tomczyk L, Sajek M, Spik A, Latos-Bielenska A, Jedrzejczak P, Pawelczyk L, Jaruzelska J

机构信息

Institute of Human Genetics Polish Academy of Sciences, Poznan, Poland.

出版信息

Mol Hum Reprod. 2009 Mar;15(3):165-71. doi: 10.1093/molehr/gap003. Epub 2009 Jan 23.

Abstract

The highly conserved Nanos gene was found to encode a translational repressor necessary for germ-cell development in lower organisms. The mammalian homologue, Nanos2, was recently found to be expressed in the mouse germ cells. Since its disruption caused infertility exclusively in males, we sought to study the significance of this gene in human male reproduction. Here, we describe for the first time the expression pattern of the NANOS2 gene in human tissues and show that it is testis specific. We found that NANOS2 protein is present in prenatal germ cells and at later stages in spermatogenesis. To elucidate the role of NANOS2 in human germ-line development, we screened this gene for mutations in 214 males with isolated sterility and spermatogenic abnormalities. We identified two heterozygous variants, each in a different oligospermic patient, the second allele being the wild-type. The influence of the first variant, a missense mutation H68Q on the sterility phenotype, was not obvious since it was accompanied by a microdeletion within the AZF region of the Y chromosome. The second variant contained a silent mutation, H109H. Although both mutations were situated within the most conserved RNA-binding domain and were absent in 400 fertile males, it is not obvious that they cause male infertility.

摘要

人们发现高度保守的Nanos基因编码一种对低等生物生殖细胞发育所必需的翻译抑制因子。最近发现哺乳动物的同源物Nanos2在小鼠生殖细胞中表达。由于其缺失仅导致雄性不育,我们试图研究该基因在人类男性生殖中的意义。在此,我们首次描述了NANOS2基因在人体组织中的表达模式,并表明它具有睾丸特异性。我们发现NANOS2蛋白存在于产前生殖细胞以及精子发生的后期阶段。为了阐明NANOS2在人类种系发育中的作用,我们在214例患有孤立性不育和生精异常的男性中筛查了该基因的突变。我们鉴定出两个杂合变体,分别存在于不同的少精子症患者中,另一个等位基因为野生型。第一个变体是错义突变H68Q,由于它伴有Y染色体AZF区域内的微缺失,其对不育表型的影响并不明显。第二个变体包含一个沉默突变H109H。尽管这两个突变都位于最保守的RNA结合域内,且在400名可育男性中不存在,但尚不清楚它们是否会导致男性不育。

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