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CPAP is required for cilia formation in neuronal cells

The primary cilium is a microtubule-based structure protruded from the basal body analogous to the centriole. CPAP (centrosomal P4.1-associated protein) has previously been reported to be a cell cycle-regulated protein that controls centriole length. Mutations in CPAP cause primary microcephaly (MCP...

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Detalles Bibliográficos
Autores principales: Wu, Kuo-Sheng, Tang, Tang K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3509446/
https://www.ncbi.nlm.nih.gov/pubmed/23213448
http://dx.doi.org/10.1242/bio.20121388
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author Wu, Kuo-Sheng
Tang, Tang K.
author_facet Wu, Kuo-Sheng
Tang, Tang K.
author_sort Wu, Kuo-Sheng
collection PubMed
description The primary cilium is a microtubule-based structure protruded from the basal body analogous to the centriole. CPAP (centrosomal P4.1-associated protein) has previously been reported to be a cell cycle-regulated protein that controls centriole length. Mutations in CPAP cause primary microcephaly (MCPH) in humans. Here, using a cell-based system that we established to monitor cilia formation in neuronal CAD (Cath.a-differentiated) cells and hippocampal neurons, we found that CPAP is required for cilia biogenesis. Overexpression of wild-type CPAP promoted cilia formation and induced longer cilia. In contrast, an exogenously expressed CPAP-377EE mutant that lacks tubulin-dimer binding significantly inhibited cilia formation and caused cilia shortening. Furthermore, depletion of CPAP inhibited ciliogenesis and such effect was effectively rescued by expression of wild-type CPAP, but not by the CPAP-377EE mutant. Taken together, our results suggest that CPAP is a positive regulator of ciliogenesis whose intrinsic tubulin-dimer binding activity is required for cilia formation in neuronal cells.
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spelling pubmed-35094462012-12-04 CPAP is required for cilia formation in neuronal cells Wu, Kuo-Sheng Tang, Tang K. Biol Open Research Article The primary cilium is a microtubule-based structure protruded from the basal body analogous to the centriole. CPAP (centrosomal P4.1-associated protein) has previously been reported to be a cell cycle-regulated protein that controls centriole length. Mutations in CPAP cause primary microcephaly (MCPH) in humans. Here, using a cell-based system that we established to monitor cilia formation in neuronal CAD (Cath.a-differentiated) cells and hippocampal neurons, we found that CPAP is required for cilia biogenesis. Overexpression of wild-type CPAP promoted cilia formation and induced longer cilia. In contrast, an exogenously expressed CPAP-377EE mutant that lacks tubulin-dimer binding significantly inhibited cilia formation and caused cilia shortening. Furthermore, depletion of CPAP inhibited ciliogenesis and such effect was effectively rescued by expression of wild-type CPAP, but not by the CPAP-377EE mutant. Taken together, our results suggest that CPAP is a positive regulator of ciliogenesis whose intrinsic tubulin-dimer binding activity is required for cilia formation in neuronal cells. The Company of Biologists 2012-04-24 /pmc/articles/PMC3509446/ /pubmed/23213448 http://dx.doi.org/10.1242/bio.20121388 Text en © 2012. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by-nc-sa/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial Share Alike License (http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Research Article
Wu, Kuo-Sheng
Tang, Tang K.
CPAP is required for cilia formation in neuronal cells
title CPAP is required for cilia formation in neuronal cells
title_full CPAP is required for cilia formation in neuronal cells
title_fullStr CPAP is required for cilia formation in neuronal cells
title_full_unstemmed CPAP is required for cilia formation in neuronal cells
title_short CPAP is required for cilia formation in neuronal cells
title_sort cpap is required for cilia formation in neuronal cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3509446/
https://www.ncbi.nlm.nih.gov/pubmed/23213448
http://dx.doi.org/10.1242/bio.20121388
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