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The fin-to-limb transition as the re-organization of a Turing pattern
A Turing mechanism implemented by BMP, SOX9 and WNT has been proposed to control mouse digit patterning. However, its generality and contribution to the morphological diversity of fins and limbs has not been explored. Here we provide evidence that the skeletal patterning of the catshark Scyliorhinus...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4879262/ https://www.ncbi.nlm.nih.gov/pubmed/27211489 http://dx.doi.org/10.1038/ncomms11582 |
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author | Onimaru, Koh Marcon, Luciano Musy, Marco Tanaka, Mikiko Sharpe, James |
author_facet | Onimaru, Koh Marcon, Luciano Musy, Marco Tanaka, Mikiko Sharpe, James |
author_sort | Onimaru, Koh |
collection | PubMed |
description | A Turing mechanism implemented by BMP, SOX9 and WNT has been proposed to control mouse digit patterning. However, its generality and contribution to the morphological diversity of fins and limbs has not been explored. Here we provide evidence that the skeletal patterning of the catshark Scyliorhinus canicula pectoral fin is likely driven by a deeply conserved Bmp–Sox9–Wnt Turing network. In catshark fins, the distal nodular elements arise from a periodic spot pattern of Sox9 expression, in contrast to the stripe pattern in mouse digit patterning. However, our computer model shows that the Bmp–Sox9–Wnt network with altered spatial modulation can explain the Sox9 expression in catshark fins. Finally, experimental perturbation of Bmp or Wnt signalling in catshark embryos produces skeletal alterations which match in silico predictions. Together, our results suggest that the broad morphological diversity of the distal fin and limb elements arose from the spatial re-organization of a deeply conserved Turing mechanism. |
format | Online Article Text |
id | pubmed-4879262 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48792622016-06-02 The fin-to-limb transition as the re-organization of a Turing pattern Onimaru, Koh Marcon, Luciano Musy, Marco Tanaka, Mikiko Sharpe, James Nat Commun Article A Turing mechanism implemented by BMP, SOX9 and WNT has been proposed to control mouse digit patterning. However, its generality and contribution to the morphological diversity of fins and limbs has not been explored. Here we provide evidence that the skeletal patterning of the catshark Scyliorhinus canicula pectoral fin is likely driven by a deeply conserved Bmp–Sox9–Wnt Turing network. In catshark fins, the distal nodular elements arise from a periodic spot pattern of Sox9 expression, in contrast to the stripe pattern in mouse digit patterning. However, our computer model shows that the Bmp–Sox9–Wnt network with altered spatial modulation can explain the Sox9 expression in catshark fins. Finally, experimental perturbation of Bmp or Wnt signalling in catshark embryos produces skeletal alterations which match in silico predictions. Together, our results suggest that the broad morphological diversity of the distal fin and limb elements arose from the spatial re-organization of a deeply conserved Turing mechanism. Nature Publishing Group 2016-05-23 /pmc/articles/PMC4879262/ /pubmed/27211489 http://dx.doi.org/10.1038/ncomms11582 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Onimaru, Koh Marcon, Luciano Musy, Marco Tanaka, Mikiko Sharpe, James The fin-to-limb transition as the re-organization of a Turing pattern |
title | The fin-to-limb transition as the re-organization of a Turing pattern |
title_full | The fin-to-limb transition as the re-organization of a Turing pattern |
title_fullStr | The fin-to-limb transition as the re-organization of a Turing pattern |
title_full_unstemmed | The fin-to-limb transition as the re-organization of a Turing pattern |
title_short | The fin-to-limb transition as the re-organization of a Turing pattern |
title_sort | fin-to-limb transition as the re-organization of a turing pattern |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4879262/ https://www.ncbi.nlm.nih.gov/pubmed/27211489 http://dx.doi.org/10.1038/ncomms11582 |
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