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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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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 |
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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 |
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