Lu Lin-Yu, Yu Xiaochun
a Key Laboratory of Reproductive Genetics; Ministry of Education and Women's Reproductive Health Laboratory of Zhejiang Province; Women's Hospital; School of Medicine; Zhejiang University ; Hangzhou , Zhejiang , China.
b Institute of Translational Medicine; Zhejiang University ; Hangzhou , Zhejiang , China.
Cell Cycle. 2015;14(21):3454-60. doi: 10.1080/15384101.2015.1093701.
DNA damage response is required for male fertility. DNA damage repair mediates recombination between homologous chromosomes in meiotic prophase, which is essential for proper chromosome segregation during meiotic division. Interestingly, some DNA damage response proteins are also required for the survival of premeiotic germ cells, but their roles in these cells are still unclear. CHFR was recently shown to participate in DNA damage response, but it remains to be established if CHFR is required for male fertility. In this study, we characterized Chfr knockout male mice and found that around 30% of them were infertile. The onset of spermatogenesis was delayed and there was significant increase in apoptosis in premeiotic germ cells. This resulted in complete loss of germ cells in testes in 3 months and azoospermia in these mice. We further demonstrated that ATM activation was compromised in the testes of these mice. Therefore, CHFR is important for the survival of male premeiotic germ cells, which is likely through maintaining genomic stability in spermatogonial stem cells.
DNA损伤反应是雄性生育所必需的。DNA损伤修复介导减数分裂前期同源染色体之间的重组,这对于减数分裂期间染色体的正确分离至关重要。有趣的是,一些DNA损伤反应蛋白对于减数分裂前生殖细胞的存活也是必需的,但其在这些细胞中的作用仍不清楚。CHFR最近被证明参与DNA损伤反应,但CHFR是否为雄性生育所必需仍有待确定。在本研究中,我们对Chfr基因敲除雄性小鼠进行了表征,发现约30%的小鼠不育。精子发生起始延迟,减数分裂前生殖细胞凋亡显著增加。这导致这些小鼠在3个月内睾丸中的生殖细胞完全丧失,出现无精子症。我们进一步证明这些小鼠睾丸中的ATM激活受损。因此,CHFR对雄性减数分裂前生殖细胞的存活很重要,这可能是通过维持精原干细胞中的基因组稳定性来实现的。