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Intraflagellar transport is deeply integrated in hedgehog signaling

The vertebrate hedgehog pathway is organized in primary cilia, and hedgehog components relocate into or out of cilia during signaling. Defects in intraflagellar transport (IFT) typically disrupt ciliary assembly and attenuate hedgehog signaling. Determining whether IFT drives the movement of hedgeho...

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Detalles Bibliográficos
Autores principales: Eguether, Thibaut, Cordelieres, Fabrice P., Pazour, Gregory J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5935068/
https://www.ncbi.nlm.nih.gov/pubmed/29540531
http://dx.doi.org/10.1091/mbc.E17-10-0600
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author Eguether, Thibaut
Cordelieres, Fabrice P.
Pazour, Gregory J.
author_facet Eguether, Thibaut
Cordelieres, Fabrice P.
Pazour, Gregory J.
author_sort Eguether, Thibaut
collection PubMed
description The vertebrate hedgehog pathway is organized in primary cilia, and hedgehog components relocate into or out of cilia during signaling. Defects in intraflagellar transport (IFT) typically disrupt ciliary assembly and attenuate hedgehog signaling. Determining whether IFT drives the movement of hedgehog components is difficult due to the requirement of IFT for building cilia. Unlike most IFT proteins, IFT27 is dispensable for cilia formation but affects hedgehog signaling similarly to other IFTs, allowing us to examine its role in the dynamics of signaling. Activating signaling at points along the pathway in Ift27 mutant cells showed that IFT is extensively involved in the pathway. Similar analysis of Bbs mutant cells showed that BBS proteins participate at many levels of signaling but are not needed to concentrate Gli transcription factors at the ciliary tip. Our analysis showed that smoothened delivery to cilia does not require IFT27, but the role of other IFTs is not known. Using a rapamycin-induced dimerization system to sequester IFT-B proteins at the mitochondria in cells with fully formed cilia did not affect the delivery of Smo to cilia, suggesting that this membrane protein may not require IFT-B for delivery.
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spelling pubmed-59350682018-07-30 Intraflagellar transport is deeply integrated in hedgehog signaling Eguether, Thibaut Cordelieres, Fabrice P. Pazour, Gregory J. Mol Biol Cell Articles The vertebrate hedgehog pathway is organized in primary cilia, and hedgehog components relocate into or out of cilia during signaling. Defects in intraflagellar transport (IFT) typically disrupt ciliary assembly and attenuate hedgehog signaling. Determining whether IFT drives the movement of hedgehog components is difficult due to the requirement of IFT for building cilia. Unlike most IFT proteins, IFT27 is dispensable for cilia formation but affects hedgehog signaling similarly to other IFTs, allowing us to examine its role in the dynamics of signaling. Activating signaling at points along the pathway in Ift27 mutant cells showed that IFT is extensively involved in the pathway. Similar analysis of Bbs mutant cells showed that BBS proteins participate at many levels of signaling but are not needed to concentrate Gli transcription factors at the ciliary tip. Our analysis showed that smoothened delivery to cilia does not require IFT27, but the role of other IFTs is not known. Using a rapamycin-induced dimerization system to sequester IFT-B proteins at the mitochondria in cells with fully formed cilia did not affect the delivery of Smo to cilia, suggesting that this membrane protein may not require IFT-B for delivery. The American Society for Cell Biology 2018-05-15 /pmc/articles/PMC5935068/ /pubmed/29540531 http://dx.doi.org/10.1091/mbc.E17-10-0600 Text en © 2018 Eguether et al. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. http://creativecommons.org/licenses/by-nc-sa/3.0/ This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License.
spellingShingle Articles
Eguether, Thibaut
Cordelieres, Fabrice P.
Pazour, Gregory J.
Intraflagellar transport is deeply integrated in hedgehog signaling
title Intraflagellar transport is deeply integrated in hedgehog signaling
title_full Intraflagellar transport is deeply integrated in hedgehog signaling
title_fullStr Intraflagellar transport is deeply integrated in hedgehog signaling
title_full_unstemmed Intraflagellar transport is deeply integrated in hedgehog signaling
title_short Intraflagellar transport is deeply integrated in hedgehog signaling
title_sort intraflagellar transport is deeply integrated in hedgehog signaling
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5935068/
https://www.ncbi.nlm.nih.gov/pubmed/29540531
http://dx.doi.org/10.1091/mbc.E17-10-0600
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