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dc.contributor.authorLemaitre, Quentin Indiana Bruno
dc.contributor.authorBartsch, Natascha
dc.contributor.authorKouzel, Ivan
dc.contributor.authorBusengdal, Henriette
dc.contributor.authorRichards, Gemma Sian
dc.contributor.authorSteinmetz, Patrick
dc.contributor.authorRentzsch, Fabian
dc.date.accessioned2024-01-17T12:51:25Z
dc.date.available2024-01-17T12:51:25Z
dc.date.created2023-10-10T12:24:21Z
dc.date.issued2023
dc.identifier.issn2041-1723
dc.identifier.urihttps://hdl.handle.net/11250/3112177
dc.description.abstractNeurogenesis 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.en_US
dc.language.isoengen_US
dc.publisherNatureen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleNvPrdm14d-expressing neural progenitor cells contribute to non-ectodermal neurogenesis in Nematostella vectensisen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2023 The Author(s)en_US
dc.source.articlenumber4854en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2
dc.identifier.doi10.1038/s41467-023-39789-4
dc.identifier.cristin2183309
dc.source.journalNature Communicationsen_US
dc.identifier.citationNature Communications. 2023, 14 (1), 4854.en_US
dc.source.volume14en_US
dc.source.issue1en_US


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