Cargando…

Single-cell atlas of early chick development reveals gradual segregation of neural crest lineage from the neural plate border during neurulation

The epiblast of vertebrate embryos is comprised of neural and non-neural ectoderm, with the border territory at their intersection harboring neural crest and cranial placode progenitors. Here, we a generate single-cell atlas of the developing chick epiblast from late gastrulation through early neuru...

Descripción completa

Detalles Bibliográficos
Autores principales: Williams, Ruth M, Lukoseviciute, Martyna, Sauka-Spengler, Tatjana, Bronner, Marianne E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798042/
https://www.ncbi.nlm.nih.gov/pubmed/35088714
http://dx.doi.org/10.7554/eLife.74464
_version_ 1784641699985752064
author Williams, Ruth M
Lukoseviciute, Martyna
Sauka-Spengler, Tatjana
Bronner, Marianne E
author_facet Williams, Ruth M
Lukoseviciute, Martyna
Sauka-Spengler, Tatjana
Bronner, Marianne E
author_sort Williams, Ruth M
collection PubMed
description The epiblast of vertebrate embryos is comprised of neural and non-neural ectoderm, with the border territory at their intersection harboring neural crest and cranial placode progenitors. Here, we a generate single-cell atlas of the developing chick epiblast from late gastrulation through early neurulation stages to define transcriptional changes in the emerging ‘neural plate border’ as well as other regions of the epiblast. Focusing on the border territory, the results reveal gradual establishment of heterogeneous neural plate border signatures, including novel genes that we validate by fluorescent in situ hybridization. Developmental trajectory analysis infers that segregation of neural plate border lineages only commences at early neurulation, rather than at gastrulation as previously predicted. We find that cells expressing the prospective neural crest marker Pax7 contribute to multiple lineages, and a subset of premigratory neural crest cells shares a transcriptional signature with their border precursors. Together, our results suggest that cells at the neural plate border remain heterogeneous until early neurulation, at which time progenitors become progressively allocated toward defined neural crest and placode lineages. The data also can be mined to reveal changes throughout the developing epiblast.
format Online
Article
Text
id pubmed-8798042
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-87980422022-01-31 Single-cell atlas of early chick development reveals gradual segregation of neural crest lineage from the neural plate border during neurulation Williams, Ruth M Lukoseviciute, Martyna Sauka-Spengler, Tatjana Bronner, Marianne E eLife Developmental Biology The epiblast of vertebrate embryos is comprised of neural and non-neural ectoderm, with the border territory at their intersection harboring neural crest and cranial placode progenitors. Here, we a generate single-cell atlas of the developing chick epiblast from late gastrulation through early neurulation stages to define transcriptional changes in the emerging ‘neural plate border’ as well as other regions of the epiblast. Focusing on the border territory, the results reveal gradual establishment of heterogeneous neural plate border signatures, including novel genes that we validate by fluorescent in situ hybridization. Developmental trajectory analysis infers that segregation of neural plate border lineages only commences at early neurulation, rather than at gastrulation as previously predicted. We find that cells expressing the prospective neural crest marker Pax7 contribute to multiple lineages, and a subset of premigratory neural crest cells shares a transcriptional signature with their border precursors. Together, our results suggest that cells at the neural plate border remain heterogeneous until early neurulation, at which time progenitors become progressively allocated toward defined neural crest and placode lineages. The data also can be mined to reveal changes throughout the developing epiblast. eLife Sciences Publications, Ltd 2022-01-28 /pmc/articles/PMC8798042/ /pubmed/35088714 http://dx.doi.org/10.7554/eLife.74464 Text en © 2022, Williams et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Developmental Biology
Williams, Ruth M
Lukoseviciute, Martyna
Sauka-Spengler, Tatjana
Bronner, Marianne E
Single-cell atlas of early chick development reveals gradual segregation of neural crest lineage from the neural plate border during neurulation
title Single-cell atlas of early chick development reveals gradual segregation of neural crest lineage from the neural plate border during neurulation
title_full Single-cell atlas of early chick development reveals gradual segregation of neural crest lineage from the neural plate border during neurulation
title_fullStr Single-cell atlas of early chick development reveals gradual segregation of neural crest lineage from the neural plate border during neurulation
title_full_unstemmed Single-cell atlas of early chick development reveals gradual segregation of neural crest lineage from the neural plate border during neurulation
title_short Single-cell atlas of early chick development reveals gradual segregation of neural crest lineage from the neural plate border during neurulation
title_sort single-cell atlas of early chick development reveals gradual segregation of neural crest lineage from the neural plate border during neurulation
topic Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798042/
https://www.ncbi.nlm.nih.gov/pubmed/35088714
http://dx.doi.org/10.7554/eLife.74464
work_keys_str_mv AT williamsruthm singlecellatlasofearlychickdevelopmentrevealsgradualsegregationofneuralcrestlineagefromtheneuralplateborderduringneurulation
AT lukoseviciutemartyna singlecellatlasofearlychickdevelopmentrevealsgradualsegregationofneuralcrestlineagefromtheneuralplateborderduringneurulation
AT saukaspenglertatjana singlecellatlasofearlychickdevelopmentrevealsgradualsegregationofneuralcrestlineagefromtheneuralplateborderduringneurulation
AT bronnermariannee singlecellatlasofearlychickdevelopmentrevealsgradualsegregationofneuralcrestlineagefromtheneuralplateborderduringneurulation