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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...

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Autores principales: Li, Zheng-Zheng, Zhao, Wen-Long, Wang, Gui-Shuan, Gu, Ni-Hao, Sun, Fei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2020
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.
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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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