Cargando…

MicroRNA‐34/449 controls mitotic spindle orientation during mammalian cortex development

Correct orientation of the mitotic spindle determines the plane of cellular cleavage and is crucial for organ development. In the developing cerebral cortex, spindle orientation defects result in severe neurodevelopmental disorders, but the precise mechanisms that control this important event are no...

Descripción completa

Detalles Bibliográficos
Autores principales: Fededa, Juan Pablo, Esk, Christopher, Mierzwa, Beata, Stanyte, Rugile, Yuan, Shuiqiao, Zheng, Huili, Ebnet, Klaus, Yan, Wei, Knoblich, Juergen A, Gerlich, Daniel W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5109238/
https://www.ncbi.nlm.nih.gov/pubmed/27707753
http://dx.doi.org/10.15252/embj.201694056
_version_ 1782467496342716416
author Fededa, Juan Pablo
Esk, Christopher
Mierzwa, Beata
Stanyte, Rugile
Yuan, Shuiqiao
Zheng, Huili
Ebnet, Klaus
Yan, Wei
Knoblich, Juergen A
Gerlich, Daniel W
author_facet Fededa, Juan Pablo
Esk, Christopher
Mierzwa, Beata
Stanyte, Rugile
Yuan, Shuiqiao
Zheng, Huili
Ebnet, Klaus
Yan, Wei
Knoblich, Juergen A
Gerlich, Daniel W
author_sort Fededa, Juan Pablo
collection PubMed
description Correct orientation of the mitotic spindle determines the plane of cellular cleavage and is crucial for organ development. In the developing cerebral cortex, spindle orientation defects result in severe neurodevelopmental disorders, but the precise mechanisms that control this important event are not fully understood. Here, we use a combination of high‐content screening and mouse genetics to identify the miR‐34/449 family as key regulators of mitotic spindle orientation in the developing cerebral cortex. By screening through all cortically expressed miRNAs in HeLa cells, we show that several members of the miR‐34/449 family control mitotic duration and spindle rotation. Analysis of miR‐34/449 knockout (KO) mouse embryos demonstrates significant spindle misorientation phenotypes in cortical progenitors, resulting in an excess of radial glia cells at the expense of intermediate progenitors and a significant delay in neurogenesis. We identify the junction adhesion molecule‐A (JAM‐A) as a key target for miR‐34/449 in the developing cortex that might be responsible for those defects. Our data indicate that miRNA‐dependent regulation of mitotic spindle orientation is crucial for cell fate specification during mammalian neurogenesis.
format Online
Article
Text
id pubmed-5109238
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-51092382016-11-25 MicroRNA‐34/449 controls mitotic spindle orientation during mammalian cortex development Fededa, Juan Pablo Esk, Christopher Mierzwa, Beata Stanyte, Rugile Yuan, Shuiqiao Zheng, Huili Ebnet, Klaus Yan, Wei Knoblich, Juergen A Gerlich, Daniel W EMBO J Articles Correct orientation of the mitotic spindle determines the plane of cellular cleavage and is crucial for organ development. In the developing cerebral cortex, spindle orientation defects result in severe neurodevelopmental disorders, but the precise mechanisms that control this important event are not fully understood. Here, we use a combination of high‐content screening and mouse genetics to identify the miR‐34/449 family as key regulators of mitotic spindle orientation in the developing cerebral cortex. By screening through all cortically expressed miRNAs in HeLa cells, we show that several members of the miR‐34/449 family control mitotic duration and spindle rotation. Analysis of miR‐34/449 knockout (KO) mouse embryos demonstrates significant spindle misorientation phenotypes in cortical progenitors, resulting in an excess of radial glia cells at the expense of intermediate progenitors and a significant delay in neurogenesis. We identify the junction adhesion molecule‐A (JAM‐A) as a key target for miR‐34/449 in the developing cortex that might be responsible for those defects. Our data indicate that miRNA‐dependent regulation of mitotic spindle orientation is crucial for cell fate specification during mammalian neurogenesis. John Wiley and Sons Inc. 2016-10-05 2016-11-15 /pmc/articles/PMC5109238/ /pubmed/27707753 http://dx.doi.org/10.15252/embj.201694056 Text en © 2016 The Authors. Published under the terms of the CC BY 4.0 license This is an open access article under the terms of the Creative Commons Attribution 4.0 (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Fededa, Juan Pablo
Esk, Christopher
Mierzwa, Beata
Stanyte, Rugile
Yuan, Shuiqiao
Zheng, Huili
Ebnet, Klaus
Yan, Wei
Knoblich, Juergen A
Gerlich, Daniel W
MicroRNA‐34/449 controls mitotic spindle orientation during mammalian cortex development
title MicroRNA‐34/449 controls mitotic spindle orientation during mammalian cortex development
title_full MicroRNA‐34/449 controls mitotic spindle orientation during mammalian cortex development
title_fullStr MicroRNA‐34/449 controls mitotic spindle orientation during mammalian cortex development
title_full_unstemmed MicroRNA‐34/449 controls mitotic spindle orientation during mammalian cortex development
title_short MicroRNA‐34/449 controls mitotic spindle orientation during mammalian cortex development
title_sort microrna‐34/449 controls mitotic spindle orientation during mammalian cortex development
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5109238/
https://www.ncbi.nlm.nih.gov/pubmed/27707753
http://dx.doi.org/10.15252/embj.201694056
work_keys_str_mv AT fededajuanpablo microrna34449controlsmitoticspindleorientationduringmammaliancortexdevelopment
AT eskchristopher microrna34449controlsmitoticspindleorientationduringmammaliancortexdevelopment
AT mierzwabeata microrna34449controlsmitoticspindleorientationduringmammaliancortexdevelopment
AT stanyterugile microrna34449controlsmitoticspindleorientationduringmammaliancortexdevelopment
AT yuanshuiqiao microrna34449controlsmitoticspindleorientationduringmammaliancortexdevelopment
AT zhenghuili microrna34449controlsmitoticspindleorientationduringmammaliancortexdevelopment
AT ebnetklaus microrna34449controlsmitoticspindleorientationduringmammaliancortexdevelopment
AT yanwei microrna34449controlsmitoticspindleorientationduringmammaliancortexdevelopment
AT knoblichjuergena microrna34449controlsmitoticspindleorientationduringmammaliancortexdevelopment
AT gerlichdanielw microrna34449controlsmitoticspindleorientationduringmammaliancortexdevelopment