Cargando…
The cilia and flagella associated protein CFAP52 orchestrated with CFAP45 is required for sperm motility in mice
Asthenozoospermia characterized by decreased sperm motility is a major cause of male infertility, but the majority of the etiology remains unknown. Here, we showed that the cilia and flagella associated protein 52 (Cfap52) gene was predominantly expressed in testis and its deletion in a Cfap52 knock...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Biochemistry and Molecular Biology
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10319328/ https://www.ncbi.nlm.nih.gov/pubmed/37236356 http://dx.doi.org/10.1016/j.jbc.2023.104858 |
_version_ | 1785068226445574144 |
---|---|
author | Wu, Bingbing Li, Rachel Ma, Shuang Ma, Yanjie Fan, Lijun Gong, Chunxiu Liu, Chao Sun, Ling Yuan, Li |
author_facet | Wu, Bingbing Li, Rachel Ma, Shuang Ma, Yanjie Fan, Lijun Gong, Chunxiu Liu, Chao Sun, Ling Yuan, Li |
author_sort | Wu, Bingbing |
collection | PubMed |
description | Asthenozoospermia characterized by decreased sperm motility is a major cause of male infertility, but the majority of the etiology remains unknown. Here, we showed that the cilia and flagella associated protein 52 (Cfap52) gene was predominantly expressed in testis and its deletion in a Cfap52 knockout mouse model resulted in decreased sperm motility and male infertility. Cfap52 knockout also led to the disorganization of the midpiece–principal piece junction of the sperm tail but had no effect on the axoneme ultrastructure in spermatozoa. Furthermore, we found that CFAP52 interacted with the cilia and flagella associated protein 45 (CFAP45) and knockout of Cfap52 decreased the expression level of CFAP45 in sperm flagellum, which further disrupted the microtubule sliding produced by dynein ATPase. Together, our studies demonstrate that CFAP52 plays an essential role in sperm motility by interacting with CFAP45 in sperm flagellum, providing insights into the potential pathogenesis of the infertility of the human CFAP52 mutations. |
format | Online Article Text |
id | pubmed-10319328 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-103193282023-07-05 The cilia and flagella associated protein CFAP52 orchestrated with CFAP45 is required for sperm motility in mice Wu, Bingbing Li, Rachel Ma, Shuang Ma, Yanjie Fan, Lijun Gong, Chunxiu Liu, Chao Sun, Ling Yuan, Li J Biol Chem Research Article Asthenozoospermia characterized by decreased sperm motility is a major cause of male infertility, but the majority of the etiology remains unknown. Here, we showed that the cilia and flagella associated protein 52 (Cfap52) gene was predominantly expressed in testis and its deletion in a Cfap52 knockout mouse model resulted in decreased sperm motility and male infertility. Cfap52 knockout also led to the disorganization of the midpiece–principal piece junction of the sperm tail but had no effect on the axoneme ultrastructure in spermatozoa. Furthermore, we found that CFAP52 interacted with the cilia and flagella associated protein 45 (CFAP45) and knockout of Cfap52 decreased the expression level of CFAP45 in sperm flagellum, which further disrupted the microtubule sliding produced by dynein ATPase. Together, our studies demonstrate that CFAP52 plays an essential role in sperm motility by interacting with CFAP45 in sperm flagellum, providing insights into the potential pathogenesis of the infertility of the human CFAP52 mutations. American Society for Biochemistry and Molecular Biology 2023-05-24 /pmc/articles/PMC10319328/ /pubmed/37236356 http://dx.doi.org/10.1016/j.jbc.2023.104858 Text en © 2023 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Research Article Wu, Bingbing Li, Rachel Ma, Shuang Ma, Yanjie Fan, Lijun Gong, Chunxiu Liu, Chao Sun, Ling Yuan, Li The cilia and flagella associated protein CFAP52 orchestrated with CFAP45 is required for sperm motility in mice |
title | The cilia and flagella associated protein CFAP52 orchestrated with CFAP45 is required for sperm motility in mice |
title_full | The cilia and flagella associated protein CFAP52 orchestrated with CFAP45 is required for sperm motility in mice |
title_fullStr | The cilia and flagella associated protein CFAP52 orchestrated with CFAP45 is required for sperm motility in mice |
title_full_unstemmed | The cilia and flagella associated protein CFAP52 orchestrated with CFAP45 is required for sperm motility in mice |
title_short | The cilia and flagella associated protein CFAP52 orchestrated with CFAP45 is required for sperm motility in mice |
title_sort | cilia and flagella associated protein cfap52 orchestrated with cfap45 is required for sperm motility in mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10319328/ https://www.ncbi.nlm.nih.gov/pubmed/37236356 http://dx.doi.org/10.1016/j.jbc.2023.104858 |
work_keys_str_mv | AT wubingbing theciliaandflagellaassociatedproteincfap52orchestratedwithcfap45isrequiredforspermmotilityinmice AT lirachel theciliaandflagellaassociatedproteincfap52orchestratedwithcfap45isrequiredforspermmotilityinmice AT mashuang theciliaandflagellaassociatedproteincfap52orchestratedwithcfap45isrequiredforspermmotilityinmice AT mayanjie theciliaandflagellaassociatedproteincfap52orchestratedwithcfap45isrequiredforspermmotilityinmice AT fanlijun theciliaandflagellaassociatedproteincfap52orchestratedwithcfap45isrequiredforspermmotilityinmice AT gongchunxiu theciliaandflagellaassociatedproteincfap52orchestratedwithcfap45isrequiredforspermmotilityinmice AT liuchao theciliaandflagellaassociatedproteincfap52orchestratedwithcfap45isrequiredforspermmotilityinmice AT sunling theciliaandflagellaassociatedproteincfap52orchestratedwithcfap45isrequiredforspermmotilityinmice AT yuanli theciliaandflagellaassociatedproteincfap52orchestratedwithcfap45isrequiredforspermmotilityinmice AT wubingbing ciliaandflagellaassociatedproteincfap52orchestratedwithcfap45isrequiredforspermmotilityinmice AT lirachel ciliaandflagellaassociatedproteincfap52orchestratedwithcfap45isrequiredforspermmotilityinmice AT mashuang ciliaandflagellaassociatedproteincfap52orchestratedwithcfap45isrequiredforspermmotilityinmice AT mayanjie ciliaandflagellaassociatedproteincfap52orchestratedwithcfap45isrequiredforspermmotilityinmice AT fanlijun ciliaandflagellaassociatedproteincfap52orchestratedwithcfap45isrequiredforspermmotilityinmice AT gongchunxiu ciliaandflagellaassociatedproteincfap52orchestratedwithcfap45isrequiredforspermmotilityinmice AT liuchao ciliaandflagellaassociatedproteincfap52orchestratedwithcfap45isrequiredforspermmotilityinmice AT sunling ciliaandflagellaassociatedproteincfap52orchestratedwithcfap45isrequiredforspermmotilityinmice AT yuanli ciliaandflagellaassociatedproteincfap52orchestratedwithcfap45isrequiredforspermmotilityinmice |