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A conserved role for Notch signaling in priming the cellular response to Shh through ciliary localisation of the key Shh transducer Smo
Notochord-derived Sonic Hedgehog (Shh) is essential for dorsoventral patterning of the overlying neural tube. Increasing concentration and duration of Shh signal induces progenitors to acquire progressively more ventral fates. We show that Notch signalling augments the response of neuroepithelial ce...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4510595/ https://www.ncbi.nlm.nih.gov/pubmed/25995356 http://dx.doi.org/10.1242/dev.125237 |
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author | Stasiulewicz, Magdalena Gray, Shona D. Mastromina, Ioanna Silva, Joana C. Björklund, Mia Seymour, Philip A. Booth, David Thompson, Calum Green, Richard J. Hall, Emma A. Serup, Palle Dale, J. Kim |
author_facet | Stasiulewicz, Magdalena Gray, Shona D. Mastromina, Ioanna Silva, Joana C. Björklund, Mia Seymour, Philip A. Booth, David Thompson, Calum Green, Richard J. Hall, Emma A. Serup, Palle Dale, J. Kim |
author_sort | Stasiulewicz, Magdalena |
collection | PubMed |
description | Notochord-derived Sonic Hedgehog (Shh) is essential for dorsoventral patterning of the overlying neural tube. Increasing concentration and duration of Shh signal induces progenitors to acquire progressively more ventral fates. We show that Notch signalling augments the response of neuroepithelial cells to Shh, leading to the induction of higher expression levels of the Shh target gene Ptch1 and subsequently induction of more ventral cell fates. Furthermore, we demonstrate that activated Notch1 leads to pronounced accumulation of Smoothened (Smo) within primary cilia and elevated levels of full-length Gli3. Finally, we show that Notch activity promotes longer primary cilia both in vitro and in vivo. Strikingly, these Notch-regulated effects are Shh independent. These data identify Notch signalling as a novel modulator of Shh signalling that acts mechanistically via regulation of ciliary localisation of key components of its transduction machinery. |
format | Online Article Text |
id | pubmed-4510595 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | The Company of Biologists |
record_format | MEDLINE/PubMed |
spelling | pubmed-45105952015-09-29 A conserved role for Notch signaling in priming the cellular response to Shh through ciliary localisation of the key Shh transducer Smo Stasiulewicz, Magdalena Gray, Shona D. Mastromina, Ioanna Silva, Joana C. Björklund, Mia Seymour, Philip A. Booth, David Thompson, Calum Green, Richard J. Hall, Emma A. Serup, Palle Dale, J. Kim Development Research Article Notochord-derived Sonic Hedgehog (Shh) is essential for dorsoventral patterning of the overlying neural tube. Increasing concentration and duration of Shh signal induces progenitors to acquire progressively more ventral fates. We show that Notch signalling augments the response of neuroepithelial cells to Shh, leading to the induction of higher expression levels of the Shh target gene Ptch1 and subsequently induction of more ventral cell fates. Furthermore, we demonstrate that activated Notch1 leads to pronounced accumulation of Smoothened (Smo) within primary cilia and elevated levels of full-length Gli3. Finally, we show that Notch activity promotes longer primary cilia both in vitro and in vivo. Strikingly, these Notch-regulated effects are Shh independent. These data identify Notch signalling as a novel modulator of Shh signalling that acts mechanistically via regulation of ciliary localisation of key components of its transduction machinery. The Company of Biologists 2015-07-01 /pmc/articles/PMC4510595/ /pubmed/25995356 http://dx.doi.org/10.1242/dev.125237 Text en © 2015. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article Stasiulewicz, Magdalena Gray, Shona D. Mastromina, Ioanna Silva, Joana C. Björklund, Mia Seymour, Philip A. Booth, David Thompson, Calum Green, Richard J. Hall, Emma A. Serup, Palle Dale, J. Kim A conserved role for Notch signaling in priming the cellular response to Shh through ciliary localisation of the key Shh transducer Smo |
title | A conserved role for Notch signaling in priming the cellular response to Shh through ciliary localisation of the key Shh transducer Smo |
title_full | A conserved role for Notch signaling in priming the cellular response to Shh through ciliary localisation of the key Shh transducer Smo |
title_fullStr | A conserved role for Notch signaling in priming the cellular response to Shh through ciliary localisation of the key Shh transducer Smo |
title_full_unstemmed | A conserved role for Notch signaling in priming the cellular response to Shh through ciliary localisation of the key Shh transducer Smo |
title_short | A conserved role for Notch signaling in priming the cellular response to Shh through ciliary localisation of the key Shh transducer Smo |
title_sort | conserved role for notch signaling in priming the cellular response to shh through ciliary localisation of the key shh transducer smo |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4510595/ https://www.ncbi.nlm.nih.gov/pubmed/25995356 http://dx.doi.org/10.1242/dev.125237 |
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