Central Laboratory, Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing Maternal and Child Health Care Hospital, Beijing, China.
Department of Pharmacy, Heze University, Heze, Shandong, China.
Biol Reprod. 2022 Aug 9;107(2):619-634. doi: 10.1093/biolre/ioac069.
During spermiogenesis, the formation of the mitochondrial sheath is critical for male fertility. The molecular processes that govern the development of the mitochondrial sheath remain unknown. Whether TBC1D21 serves as a GTPase-activating protein (GAP) for GTP hydrolysis in the testis is unclear, despite recent findings indicating that it collaborates with numerous proteins to regulate the formation of the mitochondrial sheath. To thoroughly examine the property of TBC1D21 in spermiogenesis, we applied the CRISPR/Cas9 technology to generate the Tbc1d21-/- mice, Tbc1d21D125A R128K mice with mutation in the GAP catalytic residues (IxxDxxR), and Tbc1d21-3xFlag mice. Male Tbc1d21-/- mice were infertile due to the curved spermatozoa flagella. In vitro fertilization is ineffective for Tbc1d21-/- sperm, although healthy offspring were obtained by intracytoplasmic sperm injection. Electron microscopy revealed aberrant ultrastructural changes in the mitochondrial sheath. Thirty-four Rab vectors were constructed followed by co-immunoprecipitation, which identified RAB13 as a novel TBC1D21 binding protein. Interestingly, infertility was not observed in Tbc1d21D125A R128K mice harboring the catalytic residue, suggesting that TBC1D21 is not a typical GAP for Rab-GTP hydrolysis. Moreover, TBC1D21 was expressed in the sperm mitochondrial sheath in Tbc1d21-3xFlag mice. Immunoprecipitation-mass spectrometry demonstrated the interactions of TBC1D21 with ACTB, TPM3, SPATA19, and VDAC3 to regulate the architecture of the sperm midpiece. The collective findings suggest that TBC1D21 is a scaffold protein required for the organization and stabilization of the mitochondrial sheath morphology.
在精子发生过程中,线粒体鞘的形成对于雄性生育力至关重要。指导线粒体鞘发育的分子过程尚不清楚。尽管最近的研究发现 TBC1D21 与许多蛋白质合作来调节线粒体鞘的形成,但它是否作为 GTP 水解的 GTP 酶激活蛋白(GAP)在睾丸中发挥作用尚不清楚。为了彻底研究 TBC1D21 在精子发生中的特性,我们应用 CRISPR/Cas9 技术生成 Tbc1d21-/- 小鼠、突变 GAP 催化残基(IxxDxxR)的 Tbc1d21D125A R128K 小鼠和 Tbc1d21-3xFlag 小鼠。由于弯曲的精子鞭毛,雄性 Tbc1d21-/- 小鼠不育。尽管通过胞质内精子注射获得了健康的后代,但 Tbc1d21-/- 精子的体外受精无效。电子显微镜显示线粒体鞘的异常超微结构变化。构建了 34 个 Rab 载体,随后进行共免疫沉淀,鉴定出 RAB13 是一种新型 TBC1D21 结合蛋白。有趣的是,携带催化残基的 Tbc1d21D125A R128K 小鼠并未观察到不育,这表明 TBC1D21 不是 Rab-GTP 水解的典型 GAP。此外,在 Tbc1d21-3xFlag 小鼠的精子线粒体鞘中表达了 TBC1D21。免疫沉淀-质谱分析表明 TBC1D21 与 ACTB、TPM3、SPATA19 和 VDAC3 相互作用,调节精子中段的结构。这些发现表明 TBC1D21 是一种支架蛋白,需要其组织和稳定线粒体鞘形态。