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CatSperζ regulates the structural continuity of sperm Ca2+ signaling domains and is required for normal fertility

机译:CatSperζ调节精子Ca2 +信号传导域的结构连续性是正常生育所必需的

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摘要

We report that the Gm7068 (CatSpere) and Tex40 (CatSperz) genes encode novel subunits of a 9-subunit CatSper ion channel complex. Targeted disruption of CatSperz reduces CatSper current and sperm rheotactic efficiency in mice, resulting in severe male subfertility. Normally distributed in linear quadrilateral nanodomains along the flagellum, the complex lacking CatSperζ is disrupted at ~0.8 μm intervals along the flagellum. This disruption renders the proximal flagellum inflexible and alters the 3D flagellar envelope, thus preventing sperm from reorienting against fluid flow in vitro and efficiently migrating in vivo. Ejaculated CatSperz-null sperm cells retrieved from the mated female uterus partially rescue in vitro fertilization (IVF) that failed with epididymal spermatozoa alone. Human CatSperε is quadrilaterally arranged along the flagella, similar to the CatSper complex in mouse sperm. We speculate that the newly identified CatSperζ subunit is a late evolutionary adaptation to maximize fertilization inside the mammalian female reproductive tract.>DOI:
机译:我们报告说,Gm7068(CatSpere)和Tex40(CatSperz)基因编码9个亚基CatSper离子通道复合物的新亚基。 CatSperz的靶向破坏会降低小鼠的CatSper电流和精子流变效率,导致严重的男性不育。沿着鞭毛通常分布在线性四边形纳米域中,缺少CatSperζ的复合物沿着鞭毛以〜0.8μm的间隔被破坏。这种破坏使近端鞭毛变得不灵活,并改变了3D鞭毛的包膜,从而防止了精子在体外针对流体流动重新定向并在体内有效迁移。从交配的雌性子宫中回收的射精的CatSperz-null精子细胞部分挽救了体外受精(IVF),而仅靠附睾的精子就失败了。人CatSperε沿着鞭毛四边形排列,类似于小鼠精子中的CatSper复合物。我们推测,新近鉴定出的CatSperζ亚基是晚期进化适应,可最大限度地提高哺乳动物雌性生殖道内的受精量。> DOI:

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