Research Institute for Microbial Diseases, Osaka University, 565-0871 Osaka, Japan.
Graduate School of Pharmaceutical Sciences, Osaka University, 565-0871 Osaka, Japan.
Proc Natl Acad Sci U S A. 2020 May 26;117(21):11493-11502. doi: 10.1073/pnas.1922650117. Epub 2020 May 11.
Sperm-oocyte membrane fusion is one of the most important events for fertilization. So far, IZUMO1 and Fertilization Influencing Membrane Protein (FIMP) on the sperm membrane and CD9 and JUNO (IZUMO1R/FOLR4) on the oocyte membrane have been identified as fusion-required proteins. However, the molecular mechanisms for sperm-oocyte fusion are still unclear. Here, we show that testis-enriched genes, sperm-oocyte fusion required 1 (//), transmembrane protein 95 (), and sperm acrosome associated 6 (), encode sperm proteins required for sperm-oocyte fusion in mice. These knockout (KO) spermatozoa carry IZUMO1 but cannot fuse with the oocyte plasma membrane, leading to male sterility. Transgenic mice which expressed mouse , and rescued the sterility of , , and KO males, respectively. SOF1 and SPACA6 remain in acrosome-reacted spermatozoa, and SPACA6 translocates to the equatorial segment of these spermatozoa. The coexpression of SOF1, TMEM95, and SPACA6 in IZUMO1-expressing cultured cells did not enhance their ability to adhere to the oocyte membrane or allow them to fuse with oocytes. SOF1, TMEM95, and SPACA6 may function cooperatively with IZUMO1 and/or unknown fusogens in sperm-oocyte fusion.
精卵膜融合是受精过程中最重要的事件之一。到目前为止,已经鉴定出精子膜上的 IZUMO1 和受精影响膜蛋白 (FIMP) 以及卵母细胞膜上的 CD9 和 JUNO (IZUMO1R/FOLR4) 是融合所需的蛋白。然而,精卵融合的分子机制尚不清楚。在这里,我们表明富含睾丸的基因、精子-卵融合必需 1 (//)、跨膜蛋白 95 () 和精子顶体相关 6 () 编码了小鼠精卵融合所需的精子蛋白。这些敲除 (KO) 精子携带 IZUMO1,但不能与卵母细胞质膜融合,导致雄性不育。表达小鼠 //、和 的转基因小鼠分别挽救了 //、和 KO 雄性的不育。SOF1 和 SPACA6 仍留在顶体反应的精子中,SPACA6 向这些精子的赤道段移位。SOF1、TMEM95 和 SPACA6 在表达 IZUMO1 的培养细胞中的共表达并没有增强它们与卵母细胞膜的粘附能力或允许它们与卵母细胞融合。SOF1、TMEM95 和 SPACA6 可能与 IZUMO1 和/或精子-卵融合中的未知融合因子协同作用。