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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2018
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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. |
format | Online Article Text |
id | pubmed-5935068 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
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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