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NvPrdm14d-expressing neural progenitor cells contribute to non-ectodermal neurogenesis in Nematostella vectensis

Neurogenesis has been studied extensively in the ectoderm, from which most animals generate the majority of their neurons. Neurogenesis from non-ectodermal tissue is, in contrast, poorly understood. Here we use the cnidarian Nematostella vectensis as a model to provide new insights into the molecula...

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Autores principales: Lemaître, Quentin I. B., Bartsch, Natascha, Kouzel, Ian U., Busengdal, Henriette, Richards, Gemma Sian, Steinmetz, Patrick R. H., Rentzsch, Fabian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10415408/
https://www.ncbi.nlm.nih.gov/pubmed/37563174
http://dx.doi.org/10.1038/s41467-023-39789-4
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author Lemaître, Quentin I. B.
Bartsch, Natascha
Kouzel, Ian U.
Busengdal, Henriette
Richards, Gemma Sian
Steinmetz, Patrick R. H.
Rentzsch, Fabian
author_facet Lemaître, Quentin I. B.
Bartsch, Natascha
Kouzel, Ian U.
Busengdal, Henriette
Richards, Gemma Sian
Steinmetz, Patrick R. H.
Rentzsch, Fabian
author_sort Lemaître, Quentin I. B.
collection PubMed
description Neurogenesis has been studied extensively in the ectoderm, from which most animals generate the majority of their neurons. Neurogenesis from non-ectodermal tissue is, in contrast, poorly understood. Here we use the cnidarian Nematostella vectensis as a model to provide new insights into the molecular regulation of non-ectodermal neurogenesis. We show that the transcription factor NvPrdm14d is expressed in a subpopulation of NvSoxB(2)-expressing endodermal progenitor cells and their NvPOU4-expressing progeny. Using a new transgenic reporter line, we show that NvPrdm14d-expressing cells give rise to neurons in the body wall and in close vicinity of the longitudinal retractor muscles. RNA-sequencing of NvPrdm14d::GFP-expressing cells and gene knockdown experiments provide candidate genes for the development and function of these neurons. Together, the identification of a population of endoderm-specific neural progenitor cells and of previously undescribed putative motoneurons in Nematostella provide new insights into the regulation of non-ectodermal neurogenesis.
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spelling pubmed-104154082023-08-12 NvPrdm14d-expressing neural progenitor cells contribute to non-ectodermal neurogenesis in Nematostella vectensis Lemaître, Quentin I. B. Bartsch, Natascha Kouzel, Ian U. Busengdal, Henriette Richards, Gemma Sian Steinmetz, Patrick R. H. Rentzsch, Fabian Nat Commun Article Neurogenesis has been studied extensively in the ectoderm, from which most animals generate the majority of their neurons. Neurogenesis from non-ectodermal tissue is, in contrast, poorly understood. Here we use the cnidarian Nematostella vectensis as a model to provide new insights into the molecular regulation of non-ectodermal neurogenesis. We show that the transcription factor NvPrdm14d is expressed in a subpopulation of NvSoxB(2)-expressing endodermal progenitor cells and their NvPOU4-expressing progeny. Using a new transgenic reporter line, we show that NvPrdm14d-expressing cells give rise to neurons in the body wall and in close vicinity of the longitudinal retractor muscles. RNA-sequencing of NvPrdm14d::GFP-expressing cells and gene knockdown experiments provide candidate genes for the development and function of these neurons. Together, the identification of a population of endoderm-specific neural progenitor cells and of previously undescribed putative motoneurons in Nematostella provide new insights into the regulation of non-ectodermal neurogenesis. Nature Publishing Group UK 2023-08-10 /pmc/articles/PMC10415408/ /pubmed/37563174 http://dx.doi.org/10.1038/s41467-023-39789-4 Text en © The Author(s) 2023 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 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/) .
spellingShingle Article
Lemaître, Quentin I. B.
Bartsch, Natascha
Kouzel, Ian U.
Busengdal, Henriette
Richards, Gemma Sian
Steinmetz, Patrick R. H.
Rentzsch, Fabian
NvPrdm14d-expressing neural progenitor cells contribute to non-ectodermal neurogenesis in Nematostella vectensis
title NvPrdm14d-expressing neural progenitor cells contribute to non-ectodermal neurogenesis in Nematostella vectensis
title_full NvPrdm14d-expressing neural progenitor cells contribute to non-ectodermal neurogenesis in Nematostella vectensis
title_fullStr NvPrdm14d-expressing neural progenitor cells contribute to non-ectodermal neurogenesis in Nematostella vectensis
title_full_unstemmed NvPrdm14d-expressing neural progenitor cells contribute to non-ectodermal neurogenesis in Nematostella vectensis
title_short NvPrdm14d-expressing neural progenitor cells contribute to non-ectodermal neurogenesis in Nematostella vectensis
title_sort nvprdm14d-expressing neural progenitor cells contribute to non-ectodermal neurogenesis in nematostella vectensis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10415408/
https://www.ncbi.nlm.nih.gov/pubmed/37563174
http://dx.doi.org/10.1038/s41467-023-39789-4
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