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Notch signaling is a critical initiator of roof plate formation as revealed by the use of RNA profiling of the dorsal neural tube
BACKGROUND: The dorsal domain of the neural tube is an excellent model to investigate the generation of complexity during embryonic development. It is a highly dynamic and multifaceted region being first transiently populated by prospective neural crest (NC) cells that sequentially emigrate to gener...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8063321/ https://www.ncbi.nlm.nih.gov/pubmed/33892704 http://dx.doi.org/10.1186/s12915-021-01014-3 |
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author | Ofek, Shai Wiszniak, Sophie Kagan, Sarah Tondl, Markus Schwarz, Quenten Kalcheim, Chaya |
author_facet | Ofek, Shai Wiszniak, Sophie Kagan, Sarah Tondl, Markus Schwarz, Quenten Kalcheim, Chaya |
author_sort | Ofek, Shai |
collection | PubMed |
description | BACKGROUND: The dorsal domain of the neural tube is an excellent model to investigate the generation of complexity during embryonic development. It is a highly dynamic and multifaceted region being first transiently populated by prospective neural crest (NC) cells that sequentially emigrate to generate most of the peripheral nervous system. Subsequently, it becomes the definitive roof plate (RP) of the central nervous system. The RP, in turn, constitutes a patterning center for dorsal interneuron development. The factors underlying establishment of the definitive RP and its segregation from NC and dorsal interneurons are currently unknown. RESULTS: We performed a transcriptome analysis at trunk levels of quail embryos comparing the dorsal neural tube at premigratory NC and RP stages. This unraveled molecular heterogeneity between NC and RP stages, and within the RP itself. By implementing these genes, we asked whether Notch signaling is involved in RP development. First, we observed that Notch is active at the RP-interneuron interface. Furthermore, gain and loss of Notch function in quail and mouse embryos, respectively, revealed no effect on early NC behavior. Constitutive Notch activation caused a local downregulation of RP markers with a concomitant development of dI1 interneurons, as well as an ectopic upregulation of RP markers in the interneuron domain. Reciprocally, in mice lacking Notch activity, both the RP and dI1 interneurons failed to form and this was associated with expansion of the dI2 population. CONCLUSIONS: Collectively, our results offer a new resource for defining specific cell types, and provide evidence that Notch is required to establish the definitive RP, and to determine the choice between RP and interneuron fates, but not the segregation of RP from NC. |
format | Online Article Text |
id | pubmed-8063321 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-80633212021-04-23 Notch signaling is a critical initiator of roof plate formation as revealed by the use of RNA profiling of the dorsal neural tube Ofek, Shai Wiszniak, Sophie Kagan, Sarah Tondl, Markus Schwarz, Quenten Kalcheim, Chaya BMC Biol Research Article BACKGROUND: The dorsal domain of the neural tube is an excellent model to investigate the generation of complexity during embryonic development. It is a highly dynamic and multifaceted region being first transiently populated by prospective neural crest (NC) cells that sequentially emigrate to generate most of the peripheral nervous system. Subsequently, it becomes the definitive roof plate (RP) of the central nervous system. The RP, in turn, constitutes a patterning center for dorsal interneuron development. The factors underlying establishment of the definitive RP and its segregation from NC and dorsal interneurons are currently unknown. RESULTS: We performed a transcriptome analysis at trunk levels of quail embryos comparing the dorsal neural tube at premigratory NC and RP stages. This unraveled molecular heterogeneity between NC and RP stages, and within the RP itself. By implementing these genes, we asked whether Notch signaling is involved in RP development. First, we observed that Notch is active at the RP-interneuron interface. Furthermore, gain and loss of Notch function in quail and mouse embryos, respectively, revealed no effect on early NC behavior. Constitutive Notch activation caused a local downregulation of RP markers with a concomitant development of dI1 interneurons, as well as an ectopic upregulation of RP markers in the interneuron domain. Reciprocally, in mice lacking Notch activity, both the RP and dI1 interneurons failed to form and this was associated with expansion of the dI2 population. CONCLUSIONS: Collectively, our results offer a new resource for defining specific cell types, and provide evidence that Notch is required to establish the definitive RP, and to determine the choice between RP and interneuron fates, but not the segregation of RP from NC. BioMed Central 2021-04-23 /pmc/articles/PMC8063321/ /pubmed/33892704 http://dx.doi.org/10.1186/s12915-021-01014-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Ofek, Shai Wiszniak, Sophie Kagan, Sarah Tondl, Markus Schwarz, Quenten Kalcheim, Chaya Notch signaling is a critical initiator of roof plate formation as revealed by the use of RNA profiling of the dorsal neural tube |
title | Notch signaling is a critical initiator of roof plate formation as revealed by the use of RNA profiling of the dorsal neural tube |
title_full | Notch signaling is a critical initiator of roof plate formation as revealed by the use of RNA profiling of the dorsal neural tube |
title_fullStr | Notch signaling is a critical initiator of roof plate formation as revealed by the use of RNA profiling of the dorsal neural tube |
title_full_unstemmed | Notch signaling is a critical initiator of roof plate formation as revealed by the use of RNA profiling of the dorsal neural tube |
title_short | Notch signaling is a critical initiator of roof plate formation as revealed by the use of RNA profiling of the dorsal neural tube |
title_sort | notch signaling is a critical initiator of roof plate formation as revealed by the use of rna profiling of the dorsal neural tube |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8063321/ https://www.ncbi.nlm.nih.gov/pubmed/33892704 http://dx.doi.org/10.1186/s12915-021-01014-3 |
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