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Loss of functional Dicer in mouse radial glia cell-autonomously prolongs cortical neurogenesis()

Radial glia of the mouse cerebral cortex emerge from neuroepithelial stem cells around embryonic day 11 and produce excitatory cortical neurons until a few days before birth. The molecular mechanisms that regulate the end of cortical neurogenesis remain largely unknown. Here we investigated if the D...

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Autores principales: Nowakowski, Tomasz Jan, Mysiak, Karolina Sandra, O‘Leary, Timothy, Fotaki, Vassiliki, Pratt, Thomas, Price, David Jonathan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3793872/
https://www.ncbi.nlm.nih.gov/pubmed/24012747
http://dx.doi.org/10.1016/j.ydbio.2013.08.023
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author Nowakowski, Tomasz Jan
Mysiak, Karolina Sandra
O‘Leary, Timothy
Fotaki, Vassiliki
Pratt, Thomas
Price, David Jonathan
author_facet Nowakowski, Tomasz Jan
Mysiak, Karolina Sandra
O‘Leary, Timothy
Fotaki, Vassiliki
Pratt, Thomas
Price, David Jonathan
author_sort Nowakowski, Tomasz Jan
collection PubMed
description Radial glia of the mouse cerebral cortex emerge from neuroepithelial stem cells around embryonic day 11 and produce excitatory cortical neurons until a few days before birth. The molecular mechanisms that regulate the end of cortical neurogenesis remain largely unknown. Here we investigated if the Dicer-dependent microRNA (miRNA) pathway is involved. By electroporating a cre-recombinase expression vector into the cortex of E13.5 embryos carrying a conditional allele of Dicer1, we induced mosaic recombination causing Dicer1 deletion and reporter activation in a subset of radial glia. We analysed the long-term fates of their progeny. We found that mutant radial glia produced abnormally large numbers of Cux1-positive neurons, many of which populated the superficial cortical layers. Injections of the S-phase marker bromodeoxyuridine between postnatal days 3 and 14 showed that much of this population was generated postnatally. Our findings suggest a role for Dicer-dependent processes in limiting the timespan of cortical neurogenesis.
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spelling pubmed-37938722013-10-15 Loss of functional Dicer in mouse radial glia cell-autonomously prolongs cortical neurogenesis() Nowakowski, Tomasz Jan Mysiak, Karolina Sandra O‘Leary, Timothy Fotaki, Vassiliki Pratt, Thomas Price, David Jonathan Dev Biol Article Radial glia of the mouse cerebral cortex emerge from neuroepithelial stem cells around embryonic day 11 and produce excitatory cortical neurons until a few days before birth. The molecular mechanisms that regulate the end of cortical neurogenesis remain largely unknown. Here we investigated if the Dicer-dependent microRNA (miRNA) pathway is involved. By electroporating a cre-recombinase expression vector into the cortex of E13.5 embryos carrying a conditional allele of Dicer1, we induced mosaic recombination causing Dicer1 deletion and reporter activation in a subset of radial glia. We analysed the long-term fates of their progeny. We found that mutant radial glia produced abnormally large numbers of Cux1-positive neurons, many of which populated the superficial cortical layers. Injections of the S-phase marker bromodeoxyuridine between postnatal days 3 and 14 showed that much of this population was generated postnatally. Our findings suggest a role for Dicer-dependent processes in limiting the timespan of cortical neurogenesis. Elsevier 2013-10-15 /pmc/articles/PMC3793872/ /pubmed/24012747 http://dx.doi.org/10.1016/j.ydbio.2013.08.023 Text en © 2013 The Authors https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license
spellingShingle Article
Nowakowski, Tomasz Jan
Mysiak, Karolina Sandra
O‘Leary, Timothy
Fotaki, Vassiliki
Pratt, Thomas
Price, David Jonathan
Loss of functional Dicer in mouse radial glia cell-autonomously prolongs cortical neurogenesis()
title Loss of functional Dicer in mouse radial glia cell-autonomously prolongs cortical neurogenesis()
title_full Loss of functional Dicer in mouse radial glia cell-autonomously prolongs cortical neurogenesis()
title_fullStr Loss of functional Dicer in mouse radial glia cell-autonomously prolongs cortical neurogenesis()
title_full_unstemmed Loss of functional Dicer in mouse radial glia cell-autonomously prolongs cortical neurogenesis()
title_short Loss of functional Dicer in mouse radial glia cell-autonomously prolongs cortical neurogenesis()
title_sort loss of functional dicer in mouse radial glia cell-autonomously prolongs cortical neurogenesis()
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3793872/
https://www.ncbi.nlm.nih.gov/pubmed/24012747
http://dx.doi.org/10.1016/j.ydbio.2013.08.023
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