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An interdigit signalling centre instructs coordinate phalanx-joint formation governed by 5′Hoxd–Gli3 antagonism
The number of phalanges and joints are key features of digit ‘identity' and are central to limb functionality and evolutionary adaptation. Prior chick work indicated that digit phalanges and their associated joints arise in a different manner than the more sparsely jointed long bones, and their...
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/PMC5059757/ https://www.ncbi.nlm.nih.gov/pubmed/27713395 http://dx.doi.org/10.1038/ncomms12903 |
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author | Huang, Bau-Lin Trofka, Anna Furusawa, Aki Norrie, Jacqueline L. Rabinowitz, Adam H. Vokes, Steven A. Mark Taketo, M. Zakany, Jozsef Mackem, Susan |
author_facet | Huang, Bau-Lin Trofka, Anna Furusawa, Aki Norrie, Jacqueline L. Rabinowitz, Adam H. Vokes, Steven A. Mark Taketo, M. Zakany, Jozsef Mackem, Susan |
author_sort | Huang, Bau-Lin |
collection | PubMed |
description | The number of phalanges and joints are key features of digit ‘identity' and are central to limb functionality and evolutionary adaptation. Prior chick work indicated that digit phalanges and their associated joints arise in a different manner than the more sparsely jointed long bones, and their identity is regulated by differential signalling from adjacent interdigits. Currently, there is no genetic evidence for this model, and the molecular mechanisms governing digit joint specification remain poorly understood. Using genetic approaches in mouse, here we show that functional 5′Hoxd–Gli3 antagonism acts indirectly, through Bmp signalling from the interdigital mesenchyme, to regulate specification of joint progenitors, which arise in conjunction with phalangeal precursors at the digit tip. Phalanx number, although co-regulated, can be uncoupled from joint specification. We propose that 5′Hoxd genes and Gli3 are part of an interdigital signalling centre that sets net Bmp signalling levels from different interdigits to coordinately regulate phalanx and joint formation. |
format | Online Article Text |
id | pubmed-5059757 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50597572016-10-26 An interdigit signalling centre instructs coordinate phalanx-joint formation governed by 5′Hoxd–Gli3 antagonism Huang, Bau-Lin Trofka, Anna Furusawa, Aki Norrie, Jacqueline L. Rabinowitz, Adam H. Vokes, Steven A. Mark Taketo, M. Zakany, Jozsef Mackem, Susan Nat Commun Article The number of phalanges and joints are key features of digit ‘identity' and are central to limb functionality and evolutionary adaptation. Prior chick work indicated that digit phalanges and their associated joints arise in a different manner than the more sparsely jointed long bones, and their identity is regulated by differential signalling from adjacent interdigits. Currently, there is no genetic evidence for this model, and the molecular mechanisms governing digit joint specification remain poorly understood. Using genetic approaches in mouse, here we show that functional 5′Hoxd–Gli3 antagonism acts indirectly, through Bmp signalling from the interdigital mesenchyme, to regulate specification of joint progenitors, which arise in conjunction with phalangeal precursors at the digit tip. Phalanx number, although co-regulated, can be uncoupled from joint specification. We propose that 5′Hoxd genes and Gli3 are part of an interdigital signalling centre that sets net Bmp signalling levels from different interdigits to coordinately regulate phalanx and joint formation. Nature Publishing Group 2016-10-07 /pmc/articles/PMC5059757/ /pubmed/27713395 http://dx.doi.org/10.1038/ncomms12903 Text en Copyright © 2016, The Author(s) 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 Huang, Bau-Lin Trofka, Anna Furusawa, Aki Norrie, Jacqueline L. Rabinowitz, Adam H. Vokes, Steven A. Mark Taketo, M. Zakany, Jozsef Mackem, Susan An interdigit signalling centre instructs coordinate phalanx-joint formation governed by 5′Hoxd–Gli3 antagonism |
title | An interdigit signalling centre instructs coordinate phalanx-joint formation governed by 5′Hoxd–Gli3 antagonism |
title_full | An interdigit signalling centre instructs coordinate phalanx-joint formation governed by 5′Hoxd–Gli3 antagonism |
title_fullStr | An interdigit signalling centre instructs coordinate phalanx-joint formation governed by 5′Hoxd–Gli3 antagonism |
title_full_unstemmed | An interdigit signalling centre instructs coordinate phalanx-joint formation governed by 5′Hoxd–Gli3 antagonism |
title_short | An interdigit signalling centre instructs coordinate phalanx-joint formation governed by 5′Hoxd–Gli3 antagonism |
title_sort | interdigit signalling centre instructs coordinate phalanx-joint formation governed by 5′hoxd–gli3 antagonism |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5059757/ https://www.ncbi.nlm.nih.gov/pubmed/27713395 http://dx.doi.org/10.1038/ncomms12903 |
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