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Transcriptomic profiling of tissue environments critical for post-embryonic patterning and morphogenesis of zebrafish skin

Pigment patterns and skin appendages are prominent features of vertebrate skin. In zebrafish, regularly patterned pigment stripes and an array of calcified scales form simultaneously in the skin during post-embryonic development. Understanding the mechanisms that regulate stripe patterning and scale...

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Autores principales: Aman, Andrew J, Saunders, Lauren M, Carr, August A, Srivatasan, Sanjay, Eberhard, Colten, Carrington, Blake, Watkins-Chow, Dawn, Pavan, William J, Trapnell, Cole, Parichy, David M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10495112/
https://www.ncbi.nlm.nih.gov/pubmed/37695017
http://dx.doi.org/10.7554/eLife.86670
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author Aman, Andrew J
Saunders, Lauren M
Carr, August A
Srivatasan, Sanjay
Eberhard, Colten
Carrington, Blake
Watkins-Chow, Dawn
Pavan, William J
Trapnell, Cole
Parichy, David M
author_facet Aman, Andrew J
Saunders, Lauren M
Carr, August A
Srivatasan, Sanjay
Eberhard, Colten
Carrington, Blake
Watkins-Chow, Dawn
Pavan, William J
Trapnell, Cole
Parichy, David M
author_sort Aman, Andrew J
collection PubMed
description Pigment patterns and skin appendages are prominent features of vertebrate skin. In zebrafish, regularly patterned pigment stripes and an array of calcified scales form simultaneously in the skin during post-embryonic development. Understanding the mechanisms that regulate stripe patterning and scale morphogenesis may lead to the discovery of fundamental mechanisms that govern the development of animal form. To learn about cell types and signaling interactions that govern skin patterning and morphogenesis, we generated and analyzed single-cell transcriptomes of skin from wild-type fish as well as fish having genetic or transgenically induced defects in squamation or pigmentation. These data reveal a previously undescribed population of epidermal cells that express transcripts encoding enamel matrix proteins, suggest hormonal control of epithelial–mesenchymal signaling, clarify the signaling network that governs scale papillae development, and identify a critical role for the hypodermis in supporting pigment cell development. Additionally, these comprehensive single-cell transcriptomic data representing skin phenotypes of biomedical relevance should provide a useful resource for accelerating the discovery of mechanisms that govern skin development and homeostasis.
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spelling pubmed-104951122023-09-12 Transcriptomic profiling of tissue environments critical for post-embryonic patterning and morphogenesis of zebrafish skin Aman, Andrew J Saunders, Lauren M Carr, August A Srivatasan, Sanjay Eberhard, Colten Carrington, Blake Watkins-Chow, Dawn Pavan, William J Trapnell, Cole Parichy, David M eLife Developmental Biology Pigment patterns and skin appendages are prominent features of vertebrate skin. In zebrafish, regularly patterned pigment stripes and an array of calcified scales form simultaneously in the skin during post-embryonic development. Understanding the mechanisms that regulate stripe patterning and scale morphogenesis may lead to the discovery of fundamental mechanisms that govern the development of animal form. To learn about cell types and signaling interactions that govern skin patterning and morphogenesis, we generated and analyzed single-cell transcriptomes of skin from wild-type fish as well as fish having genetic or transgenically induced defects in squamation or pigmentation. These data reveal a previously undescribed population of epidermal cells that express transcripts encoding enamel matrix proteins, suggest hormonal control of epithelial–mesenchymal signaling, clarify the signaling network that governs scale papillae development, and identify a critical role for the hypodermis in supporting pigment cell development. Additionally, these comprehensive single-cell transcriptomic data representing skin phenotypes of biomedical relevance should provide a useful resource for accelerating the discovery of mechanisms that govern skin development and homeostasis. eLife Sciences Publications, Ltd 2023-09-11 /pmc/articles/PMC10495112/ /pubmed/37695017 http://dx.doi.org/10.7554/eLife.86670 Text en https://creativecommons.org/publicdomain/zero/1.0/This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication (https://creativecommons.org/publicdomain/zero/1.0/) .
spellingShingle Developmental Biology
Aman, Andrew J
Saunders, Lauren M
Carr, August A
Srivatasan, Sanjay
Eberhard, Colten
Carrington, Blake
Watkins-Chow, Dawn
Pavan, William J
Trapnell, Cole
Parichy, David M
Transcriptomic profiling of tissue environments critical for post-embryonic patterning and morphogenesis of zebrafish skin
title Transcriptomic profiling of tissue environments critical for post-embryonic patterning and morphogenesis of zebrafish skin
title_full Transcriptomic profiling of tissue environments critical for post-embryonic patterning and morphogenesis of zebrafish skin
title_fullStr Transcriptomic profiling of tissue environments critical for post-embryonic patterning and morphogenesis of zebrafish skin
title_full_unstemmed Transcriptomic profiling of tissue environments critical for post-embryonic patterning and morphogenesis of zebrafish skin
title_short Transcriptomic profiling of tissue environments critical for post-embryonic patterning and morphogenesis of zebrafish skin
title_sort transcriptomic profiling of tissue environments critical for post-embryonic patterning and morphogenesis of zebrafish skin
topic Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10495112/
https://www.ncbi.nlm.nih.gov/pubmed/37695017
http://dx.doi.org/10.7554/eLife.86670
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