| First Author | Chen H | Year | 2022 |
| Journal | Front Cell Dev Biol | Volume | 10 |
| Pages | 850052 | PubMed ID | 35547809 |
| Mgi Jnum | J:324492 | Mgi Id | MGI:7277953 |
| Doi | 10.3389/fcell.2022.850052 | Citation | Chen H, et al. (2022) Homozygous Loss of Septin12, but not its Haploinsufficiency, Leads to Male Infertility and Fertilization Failure. Front Cell Dev Biol 10:850052 |
| abstractText | The SEPTIN12 gene has been associated with male infertility. Male Septin12 (+/-) chimera mice were infertile, supporting the prevailing view that SEPTIN12 haploinsufficiency causes male infertility. In this study, we identified a heterozygous mutation on SEPTIN12, c.72C>A (p.Cys24Ter) in the male partner of a patient couple, who had a previous fertilization failure (FF) after intracytoplasmic sperm injection (ICSI) and became pregnant after ICSI together with artificial oocyte activation (AOA). To investigate the role of SEPTIN12 in FF and oocyte activation, we constructed Septin12 knockout mice. Surprisingly, Septin12 (-/-) male mice, but not Septin12 (+/-) male mice, are infertile, and have reduced sperm counts and abnormal sperm morphology. Importantly, AOA treatment enhances the 2-cell embryo rate of ICSI embryos injected with Septin12 (-/-) sperm, indicating that FF caused by male Septin12 deficiency is overcome by AOA. Mechanistically, loss of PLCzeta around the acrosome might be the reason for FF of Septin12 (-/-) sperm. Taken together, our data indicated that homozygous knockout of Septin12, but not Septin12 haploinsufficiency, leads to male infertility and FF. |
