A CUG-initiated CATSPERθ functions in the CatSper channel assembly and serves as a checkpoint for flagellar trafficking

Author:

Huang Xiaofang1ORCID,Miyata Haruhiko2ORCID,Wang Huafeng1ORCID,Mori Giulia3ORCID,Iida-Norita Rie2ORCID,Ikawa Masahito2ORCID,Percudani Riccardo3ORCID,Chung Jean-Ju14ORCID

Affiliation:

1. Department of Cellular and Molecular Physiology, Yale School of Medicine, Yale University, New Haven, CT 06510

2. Research Institute for Microbial Diseases, Osaka University, Suita 565-0871, Japan

3. Department of Chemistry, Life sciences, and Environmental Sustainability, University of Parma, Parma 43124, Italy

4. Department of Obstetrics, Gynecology and Reproductive Sciences, Yale School of Medicine, Yale University, New Haven, CT 06510

Abstract

Calcium signaling is critical for successful fertilization. In spermatozoa, calcium influx into the sperm flagella mediated by the sperm-specific CatSper calcium channel is necessary for hyperactivated motility and male fertility. CatSper is a macromolecular complex and is repeatedly arranged in zigzag rows within four linear nanodomains along the sperm flagella. Here, we report that the Tmem249 -encoded transmembrane (TM) domain–containing protein, CATSPERθ is essential for the CatSper channel assembly during sperm tail formation. CATSPERθ facilitates the channel assembly by serving as a scaffold for a pore-forming subunit CATSPER4. CATSPERθ is specifically localized at the interface of a CatSper dimer and can self-interact, suggesting its potential role in CatSper dimer formation. Male mice lacking CATSPERθ are infertile because the sperm lack the entire CatSper channel from sperm flagella, rendering sperm unable to hyperactivate, regardless of their normal expression in the testis. In contrast, genetic abrogation of any of the other CatSper TM subunits results in loss of CATSPERθ protein in the spermatid cells during spermatogenesis. CATSPERθ might act as a checkpoint for the properly assembled CatSper channel complex to traffic to sperm flagella. This study provides insights into the CatSper channel assembly and elucidates the physiological role of CATSPERθ in sperm motility and male fertility.

Funder

HHS | NIH | Eunice Kennedy Shriver National Institute of Child Health and Human Development

MEXT | Japan Society for the Promotion of Science

the Italian Ministry for Education, University and Research (MIUR) PRIN grant

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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