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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2021
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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. |
format | Online Article Text |
id | pubmed-8741273 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
record_format | MEDLINE/PubMed |
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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