School of Biomedical Sciences, The University of Queensland, Queensland, Australia.
Institute for Molecular Bioscience, The University of Queensland, Queensland, Australia.
Sci Rep. 2017 Dec 15;7(1):17619. doi: 10.1038/s41598-017-17854-5.
Male infertility is a major and growing problem and, in most cases, the specific root cause is unknown. Here we show that the transcription factor SOX30 plays a critical role in mouse spermatogenesis. Sox30-null mice are healthy and females are fertile, but males are sterile. In the absence of Sox30 meiosis initiates normally in both sexes but, in males, germ cell development arrests during the post-meiotic round spermatid period. In the mutant testis, acrosome and axoneme development are aberrant, multinucleated germ cells (symplasts) form and round spermatids unable to process beyond step 3 of spermiogenesis. No elongated spermatids nor spermatozoa are produced. Thus, Sox30 represents a rare example of a gene for which loss of function results in a complete arrest of spermatogenesis at the onset of spermiogenesis. Our results suggest that SOX30 mutations may underlie some instances of unexplained non-obstructive azoospermia in humans.
男性不育是一个主要且日益严重的问题,在大多数情况下,特定的根本原因尚不清楚。在这里,我们表明转录因子 SOX30 在小鼠精子发生中起着关键作用。 Sox30 基因敲除小鼠健康,雌性可育,但雄性不育。在 Sox30 基因缺失的情况下,减数分裂在两性中正常启动,但在雄性中,生殖细胞发育在减数分裂后圆形精子细胞阶段停滞。在突变睾丸中,顶体和轴丝发育异常,形成多核生殖细胞(合胞体),圆形精子细胞无法进一步发育到精子发生的第 3 步。没有伸长的精子细胞或精子产生。因此,Sox30 代表了一个罕见的例子,即功能丧失导致精子发生在精子发生开始时完全停滞。我们的结果表明,SOX30 突变可能是人类某些不明原因的非阻塞性无精子症的基础。