Cargando…

CFAP70 Is a Novel Axoneme-Binding Protein That Localizes at the Base of the Outer Dynein Arm and Regulates Ciliary Motility

In the present study, we characterized CFAP70, a candidate of cilia-related protein in mice. As this protein has a cluster of tetratricopeptide repeat (TPR) domains like many components of the intraflagellar transport (IFT) complex, we investigated the domain functions of particular interest in cili...

Descripción completa

Detalles Bibliográficos
Autores principales: Shamoto, Noritoshi, Narita, Keishi, Kubo, Tomohiro, Oda, Toshiyuki, Takeda, Sen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6162463/
https://www.ncbi.nlm.nih.gov/pubmed/30158508
http://dx.doi.org/10.3390/cells7090124
_version_ 1783359152295247872
author Shamoto, Noritoshi
Narita, Keishi
Kubo, Tomohiro
Oda, Toshiyuki
Takeda, Sen
author_facet Shamoto, Noritoshi
Narita, Keishi
Kubo, Tomohiro
Oda, Toshiyuki
Takeda, Sen
author_sort Shamoto, Noritoshi
collection PubMed
description In the present study, we characterized CFAP70, a candidate of cilia-related protein in mice. As this protein has a cluster of tetratricopeptide repeat (TPR) domains like many components of the intraflagellar transport (IFT) complex, we investigated the domain functions of particular interest in ciliary targeting and/or localization. RT-PCR and immunohistochemistry of various mouse tissues demonstrated the association of CFAP70 with motile cilia and flagella. A stepwise extraction of proteins from swine tracheal cilia showed that CFAP70 bound tightly to the ciliary axoneme. Fluorescence microscopy of the cultured ependyma expressing fragments of CFAP70 demonstrated that the N-terminus rather than the C-terminus with the TPR domains was more important for the ciliary localization. When CFAP70 was knocked down in cultured mouse ependyma, reductions in cilia beating frequency were observed. Consistent with these observations, a Chlamydomonas mutant lacking the CFAP70 homolog, FAP70, showed defects in outer dynein arm (ODA) activity and a reduction in flagellar motility. Cryo-electron tomography revealed that the N-terminus of FAP70 resided stably at the base of the ODA. These results demonstrated that CFAP70 is a novel regulatory component of the ODA in motile cilia and flagella, and that the N-terminus is important for its ciliary localization.
format Online
Article
Text
id pubmed-6162463
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-61624632018-10-02 CFAP70 Is a Novel Axoneme-Binding Protein That Localizes at the Base of the Outer Dynein Arm and Regulates Ciliary Motility Shamoto, Noritoshi Narita, Keishi Kubo, Tomohiro Oda, Toshiyuki Takeda, Sen Cells Article In the present study, we characterized CFAP70, a candidate of cilia-related protein in mice. As this protein has a cluster of tetratricopeptide repeat (TPR) domains like many components of the intraflagellar transport (IFT) complex, we investigated the domain functions of particular interest in ciliary targeting and/or localization. RT-PCR and immunohistochemistry of various mouse tissues demonstrated the association of CFAP70 with motile cilia and flagella. A stepwise extraction of proteins from swine tracheal cilia showed that CFAP70 bound tightly to the ciliary axoneme. Fluorescence microscopy of the cultured ependyma expressing fragments of CFAP70 demonstrated that the N-terminus rather than the C-terminus with the TPR domains was more important for the ciliary localization. When CFAP70 was knocked down in cultured mouse ependyma, reductions in cilia beating frequency were observed. Consistent with these observations, a Chlamydomonas mutant lacking the CFAP70 homolog, FAP70, showed defects in outer dynein arm (ODA) activity and a reduction in flagellar motility. Cryo-electron tomography revealed that the N-terminus of FAP70 resided stably at the base of the ODA. These results demonstrated that CFAP70 is a novel regulatory component of the ODA in motile cilia and flagella, and that the N-terminus is important for its ciliary localization. MDPI 2018-08-29 /pmc/articles/PMC6162463/ /pubmed/30158508 http://dx.doi.org/10.3390/cells7090124 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Shamoto, Noritoshi
Narita, Keishi
Kubo, Tomohiro
Oda, Toshiyuki
Takeda, Sen
CFAP70 Is a Novel Axoneme-Binding Protein That Localizes at the Base of the Outer Dynein Arm and Regulates Ciliary Motility
title CFAP70 Is a Novel Axoneme-Binding Protein That Localizes at the Base of the Outer Dynein Arm and Regulates Ciliary Motility
title_full CFAP70 Is a Novel Axoneme-Binding Protein That Localizes at the Base of the Outer Dynein Arm and Regulates Ciliary Motility
title_fullStr CFAP70 Is a Novel Axoneme-Binding Protein That Localizes at the Base of the Outer Dynein Arm and Regulates Ciliary Motility
title_full_unstemmed CFAP70 Is a Novel Axoneme-Binding Protein That Localizes at the Base of the Outer Dynein Arm and Regulates Ciliary Motility
title_short CFAP70 Is a Novel Axoneme-Binding Protein That Localizes at the Base of the Outer Dynein Arm and Regulates Ciliary Motility
title_sort cfap70 is a novel axoneme-binding protein that localizes at the base of the outer dynein arm and regulates ciliary motility
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6162463/
https://www.ncbi.nlm.nih.gov/pubmed/30158508
http://dx.doi.org/10.3390/cells7090124
work_keys_str_mv AT shamotonoritoshi cfap70isanovelaxonemebindingproteinthatlocalizesatthebaseoftheouterdyneinarmandregulatesciliarymotility
AT naritakeishi cfap70isanovelaxonemebindingproteinthatlocalizesatthebaseoftheouterdyneinarmandregulatesciliarymotility
AT kubotomohiro cfap70isanovelaxonemebindingproteinthatlocalizesatthebaseoftheouterdyneinarmandregulatesciliarymotility
AT odatoshiyuki cfap70isanovelaxonemebindingproteinthatlocalizesatthebaseoftheouterdyneinarmandregulatesciliarymotility
AT takedasen cfap70isanovelaxonemebindingproteinthatlocalizesatthebaseoftheouterdyneinarmandregulatesciliarymotility