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CatSperζ regulates the structural continuity of sperm Ca(2+) signaling domains and is required for normal fertility
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 qua...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5362262/ https://www.ncbi.nlm.nih.gov/pubmed/28226241 http://dx.doi.org/10.7554/eLife.23082 |
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author | Chung, Jean-Ju Miki, Kiyoshi Kim, Doory Shim, Sang-Hee Shi, Huanan F Hwang, Jae Yeon Cai, Xinjiang Iseri, Yusuf Zhuang, Xiaowei Clapham, David E |
author_facet | Chung, Jean-Ju Miki, Kiyoshi Kim, Doory Shim, Sang-Hee Shi, Huanan F Hwang, Jae Yeon Cai, Xinjiang Iseri, Yusuf Zhuang, Xiaowei Clapham, David E |
author_sort | Chung, Jean-Ju |
collection | PubMed |
description | 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: http://dx.doi.org/10.7554/eLife.23082.001 |
format | Online Article Text |
id | pubmed-5362262 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-53622622017-03-24 CatSperζ regulates the structural continuity of sperm Ca(2+) signaling domains and is required for normal fertility Chung, Jean-Ju Miki, Kiyoshi Kim, Doory Shim, Sang-Hee Shi, Huanan F Hwang, Jae Yeon Cai, Xinjiang Iseri, Yusuf Zhuang, Xiaowei Clapham, David E eLife Biophysics and Structural Biology 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: http://dx.doi.org/10.7554/eLife.23082.001 eLife Sciences Publications, Ltd 2017-02-23 /pmc/articles/PMC5362262/ /pubmed/28226241 http://dx.doi.org/10.7554/eLife.23082 Text en © 2017, Chung et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Biophysics and Structural Biology Chung, Jean-Ju Miki, Kiyoshi Kim, Doory Shim, Sang-Hee Shi, Huanan F Hwang, Jae Yeon Cai, Xinjiang Iseri, Yusuf Zhuang, Xiaowei Clapham, David E CatSperζ regulates the structural continuity of sperm Ca(2+) signaling domains and is required for normal fertility |
title | CatSperζ regulates the structural continuity of sperm Ca(2+) signaling domains and is required for normal fertility |
title_full | CatSperζ regulates the structural continuity of sperm Ca(2+) signaling domains and is required for normal fertility |
title_fullStr | CatSperζ regulates the structural continuity of sperm Ca(2+) signaling domains and is required for normal fertility |
title_full_unstemmed | CatSperζ regulates the structural continuity of sperm Ca(2+) signaling domains and is required for normal fertility |
title_short | CatSperζ regulates the structural continuity of sperm Ca(2+) signaling domains and is required for normal fertility |
title_sort | catsperζ regulates the structural continuity of sperm ca(2+) signaling domains and is required for normal fertility |
topic | Biophysics and Structural Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5362262/ https://www.ncbi.nlm.nih.gov/pubmed/28226241 http://dx.doi.org/10.7554/eLife.23082 |
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