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Conserved gene signalling and a derived patterning mechanism underlie the development of avian footpad scales
BACKGROUND: Vertebrates possess a diverse range of integumentary epithelial appendages, including scales, feathers and hair. These structures share extensive early developmental homology, as they mostly originate from a conserved anatomical placode. In the context of avian epithelial appendages, fea...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6693258/ https://www.ncbi.nlm.nih.gov/pubmed/31428299 http://dx.doi.org/10.1186/s13227-019-0130-9 |
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author | Cooper, Rory L. Lloyd, Victoria J. Di-Poï, Nicolas Fletcher, Alexander G. Barrett, Paul M. Fraser, Gareth J. |
author_facet | Cooper, Rory L. Lloyd, Victoria J. Di-Poï, Nicolas Fletcher, Alexander G. Barrett, Paul M. Fraser, Gareth J. |
author_sort | Cooper, Rory L. |
collection | PubMed |
description | BACKGROUND: Vertebrates possess a diverse range of integumentary epithelial appendages, including scales, feathers and hair. These structures share extensive early developmental homology, as they mostly originate from a conserved anatomical placode. In the context of avian epithelial appendages, feathers and scutate scales are known to develop from an anatomical placode. However, our understanding of avian reticulate (footpad) scale development remains unclear. RESULTS: Here, we demonstrate that reticulate scales develop from restricted circular domains of thickened epithelium, with localised conserved gene expression in both the epithelium and underlying mesenchyme. These domains constitute either anatomical placodes, or circular initiatory fields (comparable to the avian feather tract). Subsequent patterning of reticulate scales is consistent with reaction–diffusion (RD) simulation, whereby this primary domain subdivides into smaller secondary units, which produce individual scales. In contrast, the footpad scales of a squamate model (the bearded dragon, Pogona vitticeps) develop synchronously across the ventral footpad surface. CONCLUSIONS: Widely conserved gene signalling underlies the initial development of avian reticulate scales. However, their subsequent patterning is distinct from the footpad scale patterning of a squamate model, and the feather and scutate scale patterning of birds. Therefore, we suggest reticulate scales are a comparatively derived epithelial appendage, patterned through a modified RD system. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13227-019-0130-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6693258 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-66932582019-08-19 Conserved gene signalling and a derived patterning mechanism underlie the development of avian footpad scales Cooper, Rory L. Lloyd, Victoria J. Di-Poï, Nicolas Fletcher, Alexander G. Barrett, Paul M. Fraser, Gareth J. EvoDevo Research BACKGROUND: Vertebrates possess a diverse range of integumentary epithelial appendages, including scales, feathers and hair. These structures share extensive early developmental homology, as they mostly originate from a conserved anatomical placode. In the context of avian epithelial appendages, feathers and scutate scales are known to develop from an anatomical placode. However, our understanding of avian reticulate (footpad) scale development remains unclear. RESULTS: Here, we demonstrate that reticulate scales develop from restricted circular domains of thickened epithelium, with localised conserved gene expression in both the epithelium and underlying mesenchyme. These domains constitute either anatomical placodes, or circular initiatory fields (comparable to the avian feather tract). Subsequent patterning of reticulate scales is consistent with reaction–diffusion (RD) simulation, whereby this primary domain subdivides into smaller secondary units, which produce individual scales. In contrast, the footpad scales of a squamate model (the bearded dragon, Pogona vitticeps) develop synchronously across the ventral footpad surface. CONCLUSIONS: Widely conserved gene signalling underlies the initial development of avian reticulate scales. However, their subsequent patterning is distinct from the footpad scale patterning of a squamate model, and the feather and scutate scale patterning of birds. Therefore, we suggest reticulate scales are a comparatively derived epithelial appendage, patterned through a modified RD system. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13227-019-0130-9) contains supplementary material, which is available to authorized users. BioMed Central 2019-08-13 /pmc/articles/PMC6693258/ /pubmed/31428299 http://dx.doi.org/10.1186/s13227-019-0130-9 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Cooper, Rory L. Lloyd, Victoria J. Di-Poï, Nicolas Fletcher, Alexander G. Barrett, Paul M. Fraser, Gareth J. Conserved gene signalling and a derived patterning mechanism underlie the development of avian footpad scales |
title | Conserved gene signalling and a derived patterning mechanism underlie the development of avian footpad scales |
title_full | Conserved gene signalling and a derived patterning mechanism underlie the development of avian footpad scales |
title_fullStr | Conserved gene signalling and a derived patterning mechanism underlie the development of avian footpad scales |
title_full_unstemmed | Conserved gene signalling and a derived patterning mechanism underlie the development of avian footpad scales |
title_short | Conserved gene signalling and a derived patterning mechanism underlie the development of avian footpad scales |
title_sort | conserved gene signalling and a derived patterning mechanism underlie the development of avian footpad scales |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6693258/ https://www.ncbi.nlm.nih.gov/pubmed/31428299 http://dx.doi.org/10.1186/s13227-019-0130-9 |
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