Kanemori Yoshinori, Koga Yoshitaka, Sudo Mai, Kang Woojin, Kashiwabara Shin-Ichi, Ikawa Masahito, Hasuwa Hidetoshi, Nagashima Kiyoshi, Ishikawa Yu, Ogonuki Narumi, Ogura Atsuo, Baba Tadashi
Faculty of Life and Environmental Sciences, University of Tsukuba, Tsukuba Science City, Ibaraki 305-8572, Japan; PhD Program in Human Biology, School of Integrative and Global Majors, University of Tsukuba, Tsukuba Science City, Ibaraki 305-8572, Japan;
Faculty of Life and Environmental Sciences, University of Tsukuba, Tsukuba Science City, Ibaraki 305-8572, Japan;
Proc Natl Acad Sci U S A. 2016 Jun 28;113(26):E3696-705. doi: 10.1073/pnas.1522333113. Epub 2016 Jun 14.
Proper biogenesis of a sperm-specific organelle, the acrosome, is essential for gamete interaction. An acrosomal matrix protein, ACRBP, is known as a proacrosin-binding protein. In mice, two forms of ACRBP, wild-type ACRBP-W and variant ACRBP-V5, are generated by pre-mRNA alternative splicing of Acrbp Here, we demonstrate the functional roles of these two ACRBP proteins. ACRBP-null male mice lacking both proteins showed a severely reduced fertility, because of malformation of the acrosome. Notably, ACRBP-null spermatids failed to form a large acrosomal granule, leading to the fragmented structure of the acrosome. The acrosome malformation was rescued by transgenic expression of ACRBP-V5 in ACRBP-null spermatids. Moreover, exogenously expressed ACRBP-W blocked autoactivation of proacrosin in the acrosome. Thus, ACRBP-V5 functions in the formation and configuration of the acrosomal granule during early spermiogenesis. The major function of ACRBP-W is to retain the inactive status of proacrosin in the acrosome until acrosomal exocytosis.
精子特异性细胞器顶体的正常生物合成对于配子相互作用至关重要。顶体基质蛋白ACRBP是一种已知的前顶体蛋白酶结合蛋白。在小鼠中,Acrbp的前体mRNA可变剪接产生了两种形式的ACRBP,即野生型ACRBP-W和变体ACRBP-V5。在此,我们展示了这两种ACRBP蛋白的功能作用。缺乏这两种蛋白的ACRBP基因敲除雄性小鼠由于顶体畸形,生育能力严重下降。值得注意的是,ACRBP基因敲除的精子细胞未能形成大的顶体颗粒,导致顶体结构破碎。在ACRBP基因敲除的精子细胞中通过转基因表达ACRBP-V5挽救了顶体畸形。此外,外源表达的ACRBP-W可阻断顶体中前顶体蛋白酶的自激活。因此,ACRBP-V5在精子发生早期的顶体颗粒形成和构型中发挥作用。ACRBP-W的主要功能是在顶体胞吐之前保持顶体中前顶体蛋白酶的无活性状态。