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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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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. |
format | Online Article Text |
id | pubmed-8748784 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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