Institute of Reproductive Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, People's Republic of China.
College of Animal Science and Technology, Northwest A&F University, Yangling, People's Republic of China.
Reprod Biol Endocrinol. 2019 Nov 23;17(1):98. doi: 10.1186/s12958-019-0542-3.
Ovol2, a mouse homolog of Drosophila ovo, was identified as a zinc finger transcription factor predominantly expressed in testis. However, the function of Ovol2 in postnatal male germ cell development remains enigmatic. Here, we firstly examined the mRNA and protein levels of Ovol2 in developing mouse testes by RT-qPCR and western blot and found that both mRNA and protein of Ovol2 are continually expressed in postnatal developing testes from postnatal day 0 (P0) testes to adult testes (P56) and exhibits its higher level at adult testis. Further testicular immuno-staining revealed that OVOL2 is highly expressed in the spermatogonia, spermatocytes and round spermatids. Interestingly, our conditional ovol2 knockout mouse model show that loss of ovol2 in embryonic germ cells does not affect fecundity in mice. Our data also show that Ovol1 may have compensated for the loss of Ovol2 functions in germ cells. Overall, our data indicate that ovol2 is dispensable for germ cell development and spermatogenesis.
Ovol2 是果蝇 ovo 的小鼠同源物,被鉴定为一种主要在睾丸中表达的锌指转录因子。然而,Ovol2 在出生后雄性生殖细胞发育中的功能仍然是个谜。在这里,我们首先通过 RT-qPCR 和 Western blot 检测了发育中的小鼠睾丸中 Ovol2 的 mRNA 和蛋白水平,发现 Ovol2 的 mRNA 和蛋白均在出生后(P0)睾丸到成年(P56)睾丸的发育过程中持续表达,并在成年睾丸中表达水平更高。进一步的睾丸免疫染色显示,OVOL2 在精原细胞、精母细胞和圆形精子中高度表达。有趣的是,我们的条件性 ovol2 敲除小鼠模型表明,胚胎生殖细胞中 ovol2 的缺失并不影响小鼠的生育能力。我们的数据还表明,Ovol1 可能补偿了生殖细胞中 Ovol2 功能的缺失。总的来说,我们的数据表明 ovol2 对于生殖细胞发育和精子发生是可有可无的。