Eberhart C G, Maines J Z, Wasserman S A
Department of Biochemistry, Unvirsity of Texas Southwestern Medical Center, Dallas, 75235-9038, USA.
Nature. 1996 Jun 27;381(6585):783-5. doi: 10.1038/381783a0.
Infertility resulting from a severe defect in sperm production affects 2% of men worldwide. Of these men with azoospermia, the absence of sperm in semen, one in eight carry de novo deletions for a specific region of the Y chromosome. A candidate gene for the Y-chromosome azoospermia factor (AZF) has been identified and named Deleted in Azoospermia (DAZ). Here we describe the cloning and characterization of the Drosophila gene boule, which is a homologue of DAZ. The two genes encode closely related proteins that contain a predicted RNA-binding motif, and both loci are expressed exclusively in the testis. Loss of boule function results in azoospermia; meiotic divisions are blocked, although limited spermatid differentiation occurs. Histological examination of boule testes with cell-cycle markers indicates that the primary defect is at the meiotic G2/M transition. These results support the hypothesis that DAZ is the human AZF, and indicate that Boule and DAZ have an essential meiotic function in fly and human spermatogenesis.
精子生成严重缺陷导致的不育影响着全球2%的男性。在这些无精子症(即精液中没有精子)的男性中,八分之一的人在Y染色体的特定区域存在新生缺失。Y染色体无精子症因子(AZF)的一个候选基因已被鉴定出来,并命名为无精子症缺失基因(DAZ)。在此,我们描述了果蝇基因boule的克隆和特性,它是DAZ的同源物。这两个基因编码紧密相关的蛋白质,这些蛋白质含有一个预测的RNA结合基序,并且两个基因座都仅在睾丸中表达。boule功能缺失会导致无精子症;减数分裂被阻断,不过仍会发生有限的精子细胞分化。用细胞周期标记物对boule睾丸进行组织学检查表明,主要缺陷发生在减数分裂G2/M转换期。这些结果支持了DAZ是人类AZF的假说,并表明Boule和DAZ在果蝇和人类精子发生过程中具有重要的减数分裂功能。