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The novel testicular enrichment protein Cfap58 is required for Notch-associated ciliogenesis
Cilia and flagella are critical organelles with conserved internal structures and diverse developmental and physiological processes according to cell type. Although the core components of structures are shared with thousands of associated proteins involved in cilia or flagella formation, we hypothes...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Portland Press Ltd.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6970087/ https://www.ncbi.nlm.nih.gov/pubmed/31904090 http://dx.doi.org/10.1042/BSR20192666 |
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author | Li, Zheng-Zheng Zhao, Wen-Long Wang, Gui-Shuan Gu, Ni-Hao Sun, Fei |
author_facet | Li, Zheng-Zheng Zhao, Wen-Long Wang, Gui-Shuan Gu, Ni-Hao Sun, Fei |
author_sort | Li, Zheng-Zheng |
collection | PubMed |
description | Cilia and flagella are critical organelles with conserved internal structures and diverse developmental and physiological processes according to cell type. Although the core components of structures are shared with thousands of associated proteins involved in cilia or flagella formation, we hypothesized that some unknown proteins, such as outer dense fiber 2 (Odf2/Cenexin) perform distinct functions in these organelles. In the present study, we identified several uncharacterized proteins through mass spectrometry interactome analysis of Odf2/Cenexin proteins. We further examined the expression patterns and functions of a protein named cilia and flagella associated protein 58 (Cfap58) in cultured astrocytes and sperm flagella. The results of a combination of biochemical analyses and drug administration studies reveal that Cfap58 is a testis-enrichment protein that exhibits similar localization to Odf2/Cenexin proteins and is required for the elongation of the primary cilium and sperm midpiece via modulation of the Notch signaling pathway. However, the cell cycle-related functions and localization of Odf2/Cenexin in the mother centriole were not altered in Cfap58 knockdown cells. These findings indicate that Cfap58 may be partially recruited by Odf2/Cenexin proteins and is indispensable for the cilia and flagellar assembly. These data provide us with a better understanding of ciliogenesis and flagellar elongation and may aid in identifying new targets for diseases caused by Notch-mediated ciliopathies and flagellar abnormalities. |
format | Online Article Text |
id | pubmed-6970087 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Portland Press Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-69700872020-01-24 The novel testicular enrichment protein Cfap58 is required for Notch-associated ciliogenesis Li, Zheng-Zheng Zhao, Wen-Long Wang, Gui-Shuan Gu, Ni-Hao Sun, Fei Biosci Rep Cell Cycle, Growth & Proliferation Cilia and flagella are critical organelles with conserved internal structures and diverse developmental and physiological processes according to cell type. Although the core components of structures are shared with thousands of associated proteins involved in cilia or flagella formation, we hypothesized that some unknown proteins, such as outer dense fiber 2 (Odf2/Cenexin) perform distinct functions in these organelles. In the present study, we identified several uncharacterized proteins through mass spectrometry interactome analysis of Odf2/Cenexin proteins. We further examined the expression patterns and functions of a protein named cilia and flagella associated protein 58 (Cfap58) in cultured astrocytes and sperm flagella. The results of a combination of biochemical analyses and drug administration studies reveal that Cfap58 is a testis-enrichment protein that exhibits similar localization to Odf2/Cenexin proteins and is required for the elongation of the primary cilium and sperm midpiece via modulation of the Notch signaling pathway. However, the cell cycle-related functions and localization of Odf2/Cenexin in the mother centriole were not altered in Cfap58 knockdown cells. These findings indicate that Cfap58 may be partially recruited by Odf2/Cenexin proteins and is indispensable for the cilia and flagellar assembly. These data provide us with a better understanding of ciliogenesis and flagellar elongation and may aid in identifying new targets for diseases caused by Notch-mediated ciliopathies and flagellar abnormalities. Portland Press Ltd. 2020-01-17 /pmc/articles/PMC6970087/ /pubmed/31904090 http://dx.doi.org/10.1042/BSR20192666 Text en © 2020 The Author(s). https://creativecommons.org/licenses/by/4.0/ This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY). |
spellingShingle | Cell Cycle, Growth & Proliferation Li, Zheng-Zheng Zhao, Wen-Long Wang, Gui-Shuan Gu, Ni-Hao Sun, Fei The novel testicular enrichment protein Cfap58 is required for Notch-associated ciliogenesis |
title | The novel testicular enrichment protein Cfap58 is required for Notch-associated ciliogenesis |
title_full | The novel testicular enrichment protein Cfap58 is required for Notch-associated ciliogenesis |
title_fullStr | The novel testicular enrichment protein Cfap58 is required for Notch-associated ciliogenesis |
title_full_unstemmed | The novel testicular enrichment protein Cfap58 is required for Notch-associated ciliogenesis |
title_short | The novel testicular enrichment protein Cfap58 is required for Notch-associated ciliogenesis |
title_sort | novel testicular enrichment protein cfap58 is required for notch-associated ciliogenesis |
topic | Cell Cycle, Growth & Proliferation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6970087/ https://www.ncbi.nlm.nih.gov/pubmed/31904090 http://dx.doi.org/10.1042/BSR20192666 |
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