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The microtubule affinity regulating kinase MARK4 promotes axoneme extension during early ciliogenesis

Despite the critical contributions of cilia to embryonic development and human health, key regulators of cilia formation await identification. In this paper, a functional RNA interference–based screen linked 30 novel protein kinases with ciliogenesis. Of them, we have studied the role of the microtu...

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Autores principales: Kuhns, Stefanie, Schmidt, Kerstin N., Reymann, Jürgen, Gilbert, Daniel F., Neuner, Annett, Hub, Birgit, Carvalho, Ricardo, Wiedemann, Philipp, Zentgraf, Hanswalter, Erfle, Holger, Klingmüller, Ursula, Boutros, Michael, Pereira, Gislene
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3575539/
https://www.ncbi.nlm.nih.gov/pubmed/23400999
http://dx.doi.org/10.1083/jcb.201206013
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author Kuhns, Stefanie
Schmidt, Kerstin N.
Reymann, Jürgen
Gilbert, Daniel F.
Neuner, Annett
Hub, Birgit
Carvalho, Ricardo
Wiedemann, Philipp
Zentgraf, Hanswalter
Erfle, Holger
Klingmüller, Ursula
Boutros, Michael
Pereira, Gislene
author_facet Kuhns, Stefanie
Schmidt, Kerstin N.
Reymann, Jürgen
Gilbert, Daniel F.
Neuner, Annett
Hub, Birgit
Carvalho, Ricardo
Wiedemann, Philipp
Zentgraf, Hanswalter
Erfle, Holger
Klingmüller, Ursula
Boutros, Michael
Pereira, Gislene
author_sort Kuhns, Stefanie
collection PubMed
description Despite the critical contributions of cilia to embryonic development and human health, key regulators of cilia formation await identification. In this paper, a functional RNA interference–based screen linked 30 novel protein kinases with ciliogenesis. Of them, we have studied the role of the microtubule (MT)-associated protein/MT affinity regulating kinase 4 (MARK4) in depth. MARK4 associated with the basal body and ciliary axoneme in human and murine cell lines. Ultrastructural and functional analyses established that MARK4 kinase activity was required for initiation of axoneme extension. We identified the mother centriolar protein ODF2 as an interaction partner of MARK4 and showed that ODF2 localization to the centriole partially depended on MARK4. Our data indicated that, upon MARK4 or ODF2 knockdown, the ciliary program arrested before the complete removal of the CP110–Cep97 inhibitory complex from the mother centriole, suggesting that these proteins act at this level of axonemal extension. We propose that MARK4 is a critical positive regulator of early steps in ciliogenesis.
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spelling pubmed-35755392013-08-18 The microtubule affinity regulating kinase MARK4 promotes axoneme extension during early ciliogenesis Kuhns, Stefanie Schmidt, Kerstin N. Reymann, Jürgen Gilbert, Daniel F. Neuner, Annett Hub, Birgit Carvalho, Ricardo Wiedemann, Philipp Zentgraf, Hanswalter Erfle, Holger Klingmüller, Ursula Boutros, Michael Pereira, Gislene J Cell Biol Research Articles Despite the critical contributions of cilia to embryonic development and human health, key regulators of cilia formation await identification. In this paper, a functional RNA interference–based screen linked 30 novel protein kinases with ciliogenesis. Of them, we have studied the role of the microtubule (MT)-associated protein/MT affinity regulating kinase 4 (MARK4) in depth. MARK4 associated with the basal body and ciliary axoneme in human and murine cell lines. Ultrastructural and functional analyses established that MARK4 kinase activity was required for initiation of axoneme extension. We identified the mother centriolar protein ODF2 as an interaction partner of MARK4 and showed that ODF2 localization to the centriole partially depended on MARK4. Our data indicated that, upon MARK4 or ODF2 knockdown, the ciliary program arrested before the complete removal of the CP110–Cep97 inhibitory complex from the mother centriole, suggesting that these proteins act at this level of axonemal extension. We propose that MARK4 is a critical positive regulator of early steps in ciliogenesis. The Rockefeller University Press 2013-02-18 /pmc/articles/PMC3575539/ /pubmed/23400999 http://dx.doi.org/10.1083/jcb.201206013 Text en © 2013 Kuhns et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Research Articles
Kuhns, Stefanie
Schmidt, Kerstin N.
Reymann, Jürgen
Gilbert, Daniel F.
Neuner, Annett
Hub, Birgit
Carvalho, Ricardo
Wiedemann, Philipp
Zentgraf, Hanswalter
Erfle, Holger
Klingmüller, Ursula
Boutros, Michael
Pereira, Gislene
The microtubule affinity regulating kinase MARK4 promotes axoneme extension during early ciliogenesis
title The microtubule affinity regulating kinase MARK4 promotes axoneme extension during early ciliogenesis
title_full The microtubule affinity regulating kinase MARK4 promotes axoneme extension during early ciliogenesis
title_fullStr The microtubule affinity regulating kinase MARK4 promotes axoneme extension during early ciliogenesis
title_full_unstemmed The microtubule affinity regulating kinase MARK4 promotes axoneme extension during early ciliogenesis
title_short The microtubule affinity regulating kinase MARK4 promotes axoneme extension during early ciliogenesis
title_sort microtubule affinity regulating kinase mark4 promotes axoneme extension during early ciliogenesis
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3575539/
https://www.ncbi.nlm.nih.gov/pubmed/23400999
http://dx.doi.org/10.1083/jcb.201206013
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