Yoshimura Takuji, Toyoda Shuichi, Kuramochi-Miyagawa Satomi, Miyazaki Tatsushi, Miyazaki Satsuki, Tashiro Fumi, Yamato Eiji, Nakano Toru, Miyazaki Jun-Ichi
Supply Center of Inbred Animals of Osaka University, 2-2 Yamadaoka, Suita, Osaka 565-0871, Japan.
Dev Biol. 2009 Nov 1;335(1):216-27. doi: 10.1016/j.ydbio.2009.09.003. Epub 2009 Sep 6.
We recently reported that the Gtsf1/Cue110 gene, a member of the evolutionarily conserved UPF0224 family, is expressed predominantly in male germ cells, and that the GTSF1/CUE110 protein is localized to the cytoplasm of these cells in the adult testis. Here, to analyze the roles of the Gtsf1/Cue110 gene in spermatogenesis, we produced Gtsf1/Cue110-null mice by gene targeting. The Gtsf1/Cue110-null mice grew normally and appeared healthy; however, the males were sterile due to massive apoptotic death of their germ cells after postnatal day 14. In contrast, the null females were fertile. Detailed analyses revealed that the Gtsf1/Cue110-null male meiocytes ceased meiotic progression before the zygotene stage. Thus, the Gtsf1/Cue110 gene is essential for spermatogenesis beyond the early meiotic phase. Furthermore, the loss of the Gtsf1/Cue110 gene caused increased transcription of the long interspersed nucleotide element (Line-1) and the intracisternal A-particle (IAP) retrotransposons, accompanied by demethylation of their promoter regions. These observations indicate that Gtsf1/Cue110 is required for spermatogenesis and involved in retrotransposon suppression in male germ cells.
我们最近报道,进化上保守的UPF0224家族成员Gtsf1/Cue110基因主要在雄性生殖细胞中表达,并且GTSF1/CUE110蛋白在成年睾丸中定位于这些细胞的细胞质。在此,为了分析Gtsf1/Cue110基因在精子发生中的作用,我们通过基因靶向产生了Gtsf1/Cue110基因敲除小鼠。Gtsf1/Cue110基因敲除小鼠生长正常且外观健康;然而,雄性小鼠由于出生后第14天其生殖细胞大量凋亡死亡而不育。相比之下,基因敲除雌性小鼠是可育的。详细分析表明,Gtsf1/Cue110基因敲除雄性减数分裂细胞在偶线期之前停止减数分裂进程。因此,Gtsf1/Cue110基因对于减数分裂早期之后的精子发生至关重要。此外,Gtsf1/Cue110基因的缺失导致长散在核苷酸元件(Line-1)和胞内A颗粒(IAP)逆转录转座子的转录增加,同时伴随着其启动子区域的去甲基化。这些观察结果表明,Gtsf1/Cue110是精子发生所必需的,并且参与雄性生殖细胞中逆转录转座子的抑制。