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Temporal patterning in intermediate progenitors increases neural diversity

Human outer subventricular zone (OSVZ) neural progenitors and Drosophila type II neuroblasts both generate intermediate neural progenitors (INPs) that populate the adult cerebral cortex or central complex, respectively. It is unknown whether INPs simply expand or also diversify neural cell types. He...

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Detalles Bibliográficos
Autores principales: Bayraktar, Omer Ali, Doe, Chris Q.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3941985/
https://www.ncbi.nlm.nih.gov/pubmed/23783519
http://dx.doi.org/10.1038/nature12266
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author Bayraktar, Omer Ali
Doe, Chris Q.
author_facet Bayraktar, Omer Ali
Doe, Chris Q.
author_sort Bayraktar, Omer Ali
collection PubMed
description Human outer subventricular zone (OSVZ) neural progenitors and Drosophila type II neuroblasts both generate intermediate neural progenitors (INPs) that populate the adult cerebral cortex or central complex, respectively. It is unknown whether INPs simply expand or also diversify neural cell types. Here we show that Drosophila INPs sequentially generate distinct neural subtypes; that INPs sequentially express Dichaete>Grainyhead>Eyeless transcription factors; and that these transcription factors are required for the production of distinct neural subtypes. Moreover, parental type II neuroblasts also sequentially express transcription factors and generate different neuronal/glial progeny over time, providing a second temporal identity axis. We conclude that neuroblast and INP temporal patterning axes act combinatorially to generate increased neural diversity within adult central complex; OSVZ progenitors may use similar mechanisms to increase neural diversity in the human brain.
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spelling pubmed-39419852014-03-04 Temporal patterning in intermediate progenitors increases neural diversity Bayraktar, Omer Ali Doe, Chris Q. Nature Article Human outer subventricular zone (OSVZ) neural progenitors and Drosophila type II neuroblasts both generate intermediate neural progenitors (INPs) that populate the adult cerebral cortex or central complex, respectively. It is unknown whether INPs simply expand or also diversify neural cell types. Here we show that Drosophila INPs sequentially generate distinct neural subtypes; that INPs sequentially express Dichaete>Grainyhead>Eyeless transcription factors; and that these transcription factors are required for the production of distinct neural subtypes. Moreover, parental type II neuroblasts also sequentially express transcription factors and generate different neuronal/glial progeny over time, providing a second temporal identity axis. We conclude that neuroblast and INP temporal patterning axes act combinatorially to generate increased neural diversity within adult central complex; OSVZ progenitors may use similar mechanisms to increase neural diversity in the human brain. 2013-06-19 2013-06-27 /pmc/articles/PMC3941985/ /pubmed/23783519 http://dx.doi.org/10.1038/nature12266 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Bayraktar, Omer Ali
Doe, Chris Q.
Temporal patterning in intermediate progenitors increases neural diversity
title Temporal patterning in intermediate progenitors increases neural diversity
title_full Temporal patterning in intermediate progenitors increases neural diversity
title_fullStr Temporal patterning in intermediate progenitors increases neural diversity
title_full_unstemmed Temporal patterning in intermediate progenitors increases neural diversity
title_short Temporal patterning in intermediate progenitors increases neural diversity
title_sort temporal patterning in intermediate progenitors increases neural diversity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3941985/
https://www.ncbi.nlm.nih.gov/pubmed/23783519
http://dx.doi.org/10.1038/nature12266
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