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microRNA regulation of neural precursor self-renewal and differentiation

During early stages of development of the vertebrate central nervous system, neural precursors divide symmetrically to produce new precursors, thereby expanding the precursor population. During middle stages of neural development, precursors switch to an asymmetric division pattern whereby each mito...

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Detalles Bibliográficos
Autores principales: Hudish, Laura I, Appel, Bruce
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4973589/
https://www.ncbi.nlm.nih.gov/pubmed/27502270
http://dx.doi.org/10.4161/23262133.2014.976018
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author Hudish, Laura I
Appel, Bruce
author_facet Hudish, Laura I
Appel, Bruce
author_sort Hudish, Laura I
collection PubMed
description During early stages of development of the vertebrate central nervous system, neural precursors divide symmetrically to produce new precursors, thereby expanding the precursor population. During middle stages of neural development, precursors switch to an asymmetric division pattern whereby each mitosis produces one new precursor and one cell that differentiates as a neuron or glial cell. At late stages of development, most precursors stop dividing and terminally differentiate. Par complex proteins are associated with the apical membrane of neural precursors and promote precursor self-renewal. How Par proteins are down regulated to bring precursor self-renewal to an end has not been known. Our investigations of zebrafish neural development revealed that the microRNA miR-219 negatively regulates apical Par proteins, thereby promoting cessation of neural precursor division and driving terminal differentiation.
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spelling pubmed-49735892016-08-08 microRNA regulation of neural precursor self-renewal and differentiation Hudish, Laura I Appel, Bruce Neurogenesis (Austin) Commentary During early stages of development of the vertebrate central nervous system, neural precursors divide symmetrically to produce new precursors, thereby expanding the precursor population. During middle stages of neural development, precursors switch to an asymmetric division pattern whereby each mitosis produces one new precursor and one cell that differentiates as a neuron or glial cell. At late stages of development, most precursors stop dividing and terminally differentiate. Par complex proteins are associated with the apical membrane of neural precursors and promote precursor self-renewal. How Par proteins are down regulated to bring precursor self-renewal to an end has not been known. Our investigations of zebrafish neural development revealed that the microRNA miR-219 negatively regulates apical Par proteins, thereby promoting cessation of neural precursor division and driving terminal differentiation. Taylor & Francis 2014-11-17 /pmc/articles/PMC4973589/ /pubmed/27502270 http://dx.doi.org/10.4161/23262133.2014.976018 Text en © 2014 The Author(s). Published with license by Taylor & Francis Group, LLC http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted.
spellingShingle Commentary
Hudish, Laura I
Appel, Bruce
microRNA regulation of neural precursor self-renewal and differentiation
title microRNA regulation of neural precursor self-renewal and differentiation
title_full microRNA regulation of neural precursor self-renewal and differentiation
title_fullStr microRNA regulation of neural precursor self-renewal and differentiation
title_full_unstemmed microRNA regulation of neural precursor self-renewal and differentiation
title_short microRNA regulation of neural precursor self-renewal and differentiation
title_sort microrna regulation of neural precursor self-renewal and differentiation
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4973589/
https://www.ncbi.nlm.nih.gov/pubmed/27502270
http://dx.doi.org/10.4161/23262133.2014.976018
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