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Single-cell transcriptomic analysis of zebrafish cranial neural crest reveals spatiotemporal regulation of lineage decisions during development

Neural crest (NC) cells migrate throughout vertebrate embryos to give rise to a huge variety of cell types, but when and where lineages emerge and their regulation remain unclear. We have performed single-cell RNA sequencing (RNA-seq) of cranial NC cells from the first pharyngeal arch in zebrafish o...

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Autores principales: Tatarakis, David, Cang, Zixuan, Wu, Xiaojun, Sharma, Praveer P., Karikomi, Matthew, MacLean, Adam L., Nie, Qing, Schilling, Thomas F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8741273/
https://www.ncbi.nlm.nih.gov/pubmed/34936864
http://dx.doi.org/10.1016/j.celrep.2021.110140
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author Tatarakis, David
Cang, Zixuan
Wu, Xiaojun
Sharma, Praveer P.
Karikomi, Matthew
MacLean, Adam L.
Nie, Qing
Schilling, Thomas F.
author_facet Tatarakis, David
Cang, Zixuan
Wu, Xiaojun
Sharma, Praveer P.
Karikomi, Matthew
MacLean, Adam L.
Nie, Qing
Schilling, Thomas F.
author_sort Tatarakis, David
collection PubMed
description Neural crest (NC) cells migrate throughout vertebrate embryos to give rise to a huge variety of cell types, but when and where lineages emerge and their regulation remain unclear. We have performed single-cell RNA sequencing (RNA-seq) of cranial NC cells from the first pharyngeal arch in zebrafish over several stages during migration. Computational analysis combining pseudotime and real-time data reveals that these NC cells first adopt a transitional state, becoming specified mid-migration, with the first lineage decisions being skeletal and pigment, followed by neural and glial progenitors. In addition, by computationally integrating these data with RNA-seq data from a transgenic Wnt reporter line, we identify gene cohorts with similar temporal responses to Wnts during migration and show that one, Atp6ap2, is required for melanocyte differentiation. Together, our results show that cranial NC cell lineages arise progressively and uncover a series of spatially restricted cell interactions likely to regulate such cell-fate decisions.
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spelling pubmed-87412732022-01-07 Single-cell transcriptomic analysis of zebrafish cranial neural crest reveals spatiotemporal regulation of lineage decisions during development Tatarakis, David Cang, Zixuan Wu, Xiaojun Sharma, Praveer P. Karikomi, Matthew MacLean, Adam L. Nie, Qing Schilling, Thomas F. Cell Rep Article Neural crest (NC) cells migrate throughout vertebrate embryos to give rise to a huge variety of cell types, but when and where lineages emerge and their regulation remain unclear. We have performed single-cell RNA sequencing (RNA-seq) of cranial NC cells from the first pharyngeal arch in zebrafish over several stages during migration. Computational analysis combining pseudotime and real-time data reveals that these NC cells first adopt a transitional state, becoming specified mid-migration, with the first lineage decisions being skeletal and pigment, followed by neural and glial progenitors. In addition, by computationally integrating these data with RNA-seq data from a transgenic Wnt reporter line, we identify gene cohorts with similar temporal responses to Wnts during migration and show that one, Atp6ap2, is required for melanocyte differentiation. Together, our results show that cranial NC cell lineages arise progressively and uncover a series of spatially restricted cell interactions likely to regulate such cell-fate decisions. 2021-12-21 /pmc/articles/PMC8741273/ /pubmed/34936864 http://dx.doi.org/10.1016/j.celrep.2021.110140 Text en https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ).
spellingShingle Article
Tatarakis, David
Cang, Zixuan
Wu, Xiaojun
Sharma, Praveer P.
Karikomi, Matthew
MacLean, Adam L.
Nie, Qing
Schilling, Thomas F.
Single-cell transcriptomic analysis of zebrafish cranial neural crest reveals spatiotemporal regulation of lineage decisions during development
title Single-cell transcriptomic analysis of zebrafish cranial neural crest reveals spatiotemporal regulation of lineage decisions during development
title_full Single-cell transcriptomic analysis of zebrafish cranial neural crest reveals spatiotemporal regulation of lineage decisions during development
title_fullStr Single-cell transcriptomic analysis of zebrafish cranial neural crest reveals spatiotemporal regulation of lineage decisions during development
title_full_unstemmed Single-cell transcriptomic analysis of zebrafish cranial neural crest reveals spatiotemporal regulation of lineage decisions during development
title_short Single-cell transcriptomic analysis of zebrafish cranial neural crest reveals spatiotemporal regulation of lineage decisions during development
title_sort single-cell transcriptomic analysis of zebrafish cranial neural crest reveals spatiotemporal regulation of lineage decisions during development
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8741273/
https://www.ncbi.nlm.nih.gov/pubmed/34936864
http://dx.doi.org/10.1016/j.celrep.2021.110140
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