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Lifelong single-cell profiling of cranial neural crest diversification in zebrafish

The cranial neural crest generates a huge diversity of derivatives, including the bulk of connective and skeletal tissues of the vertebrate head. How neural crest cells acquire such extraordinary lineage potential remains unresolved. By integrating single-cell transcriptome and chromatin accessibili...

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Autores principales: Fabian, Peter, Tseng, Kuo-Chang, Thiruppathy, Mathi, Arata, Claire, Chen, Hung-Jhen, Smeeton, Joanna, Nelson, Nellie, Crump, J. Gage
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8748784/
https://www.ncbi.nlm.nih.gov/pubmed/35013168
http://dx.doi.org/10.1038/s41467-021-27594-w
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author Fabian, Peter
Tseng, Kuo-Chang
Thiruppathy, Mathi
Arata, Claire
Chen, Hung-Jhen
Smeeton, Joanna
Nelson, Nellie
Crump, J. Gage
author_facet Fabian, Peter
Tseng, Kuo-Chang
Thiruppathy, Mathi
Arata, Claire
Chen, Hung-Jhen
Smeeton, Joanna
Nelson, Nellie
Crump, J. Gage
author_sort Fabian, Peter
collection PubMed
description The cranial neural crest generates a huge diversity of derivatives, including the bulk of connective and skeletal tissues of the vertebrate head. How neural crest cells acquire such extraordinary lineage potential remains unresolved. By integrating single-cell transcriptome and chromatin accessibility profiles of cranial neural crest-derived cells across the zebrafish lifetime, we observe progressive and region-specific establishment of enhancer accessibility for distinct fates. Neural crest-derived cells rapidly diversify into specialized progenitors, including multipotent skeletal progenitors, stromal cells with a regenerative signature, fibroblasts with a unique metabolic signature linked to skeletal integrity, and gill-specific progenitors generating cell types for respiration. By retrogradely mapping the emergence of lineage-specific chromatin accessibility, we identify a wealth of candidate lineage-priming factors, including a Gata3 regulatory circuit for respiratory cell fates. Rather than multilineage potential being established during cranial neural crest specification, our findings support progressive and region-specific chromatin remodeling underlying acquisition of diverse potential.
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spelling pubmed-87487842022-01-20 Lifelong single-cell profiling of cranial neural crest diversification in zebrafish Fabian, Peter Tseng, Kuo-Chang Thiruppathy, Mathi Arata, Claire Chen, Hung-Jhen Smeeton, Joanna Nelson, Nellie Crump, J. Gage Nat Commun Article The cranial neural crest generates a huge diversity of derivatives, including the bulk of connective and skeletal tissues of the vertebrate head. How neural crest cells acquire such extraordinary lineage potential remains unresolved. By integrating single-cell transcriptome and chromatin accessibility profiles of cranial neural crest-derived cells across the zebrafish lifetime, we observe progressive and region-specific establishment of enhancer accessibility for distinct fates. Neural crest-derived cells rapidly diversify into specialized progenitors, including multipotent skeletal progenitors, stromal cells with a regenerative signature, fibroblasts with a unique metabolic signature linked to skeletal integrity, and gill-specific progenitors generating cell types for respiration. By retrogradely mapping the emergence of lineage-specific chromatin accessibility, we identify a wealth of candidate lineage-priming factors, including a Gata3 regulatory circuit for respiratory cell fates. Rather than multilineage potential being established during cranial neural crest specification, our findings support progressive and region-specific chromatin remodeling underlying acquisition of diverse potential. Nature Publishing Group UK 2022-01-10 /pmc/articles/PMC8748784/ /pubmed/35013168 http://dx.doi.org/10.1038/s41467-021-27594-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Fabian, Peter
Tseng, Kuo-Chang
Thiruppathy, Mathi
Arata, Claire
Chen, Hung-Jhen
Smeeton, Joanna
Nelson, Nellie
Crump, J. Gage
Lifelong single-cell profiling of cranial neural crest diversification in zebrafish
title Lifelong single-cell profiling of cranial neural crest diversification in zebrafish
title_full Lifelong single-cell profiling of cranial neural crest diversification in zebrafish
title_fullStr Lifelong single-cell profiling of cranial neural crest diversification in zebrafish
title_full_unstemmed Lifelong single-cell profiling of cranial neural crest diversification in zebrafish
title_short Lifelong single-cell profiling of cranial neural crest diversification in zebrafish
title_sort lifelong single-cell profiling of cranial neural crest diversification in zebrafish
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8748784/
https://www.ncbi.nlm.nih.gov/pubmed/35013168
http://dx.doi.org/10.1038/s41467-021-27594-w
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