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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...

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Autores principales: Onimaru, Koh, Marcon, Luciano, Musy, Marco, Tanaka, Mikiko, Sharpe, James
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
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.
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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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