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HMMR acts in the PLK1-dependent spindle positioning pathway and supports neural development
Oriented cell division is one mechanism progenitor cells use during development and to maintain tissue homeostasis. Common to most cell types is the asymmetric establishment and regulation of cortical NuMA-dynein complexes that position the mitotic spindle. Here, we discover that HMMR acts at centro...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5681225/ https://www.ncbi.nlm.nih.gov/pubmed/28994651 http://dx.doi.org/10.7554/eLife.28672 |
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author | Connell, Marisa Chen, Helen Jiang, Jihong Kuan, Chia-Wei Fotovati, Abbas Chu, Tony LH He, Zhengcheng Lengyell, Tess C Li, Huaibiao Kroll, Torsten Li, Amanda M Goldowitz, Daniel Frappart, Lucien Ploubidou, Aspasia Patel, Millan S Pilarski, Linda M Simpson, Elizabeth M Lange, Philipp F Allan, Douglas W Maxwell, Christopher A |
author_facet | Connell, Marisa Chen, Helen Jiang, Jihong Kuan, Chia-Wei Fotovati, Abbas Chu, Tony LH He, Zhengcheng Lengyell, Tess C Li, Huaibiao Kroll, Torsten Li, Amanda M Goldowitz, Daniel Frappart, Lucien Ploubidou, Aspasia Patel, Millan S Pilarski, Linda M Simpson, Elizabeth M Lange, Philipp F Allan, Douglas W Maxwell, Christopher A |
author_sort | Connell, Marisa |
collection | PubMed |
description | Oriented cell division is one mechanism progenitor cells use during development and to maintain tissue homeostasis. Common to most cell types is the asymmetric establishment and regulation of cortical NuMA-dynein complexes that position the mitotic spindle. Here, we discover that HMMR acts at centrosomes in a PLK1-dependent pathway that locates active Ran and modulates the cortical localization of NuMA-dynein complexes to correct mispositioned spindles. This pathway was discovered through the creation and analysis of Hmmr-knockout mice, which suffer neonatal lethality with defective neural development and pleiotropic phenotypes in multiple tissues. HMMR over-expression in immortalized cancer cells induces phenotypes consistent with an increase in active Ran including defects in spindle orientation. These data identify an essential role for HMMR in the PLK1-dependent regulatory pathway that orients progenitor cell division and supports neural development. |
format | Online Article Text |
id | pubmed-5681225 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-56812252017-11-13 HMMR acts in the PLK1-dependent spindle positioning pathway and supports neural development Connell, Marisa Chen, Helen Jiang, Jihong Kuan, Chia-Wei Fotovati, Abbas Chu, Tony LH He, Zhengcheng Lengyell, Tess C Li, Huaibiao Kroll, Torsten Li, Amanda M Goldowitz, Daniel Frappart, Lucien Ploubidou, Aspasia Patel, Millan S Pilarski, Linda M Simpson, Elizabeth M Lange, Philipp F Allan, Douglas W Maxwell, Christopher A eLife Cell Biology Oriented cell division is one mechanism progenitor cells use during development and to maintain tissue homeostasis. Common to most cell types is the asymmetric establishment and regulation of cortical NuMA-dynein complexes that position the mitotic spindle. Here, we discover that HMMR acts at centrosomes in a PLK1-dependent pathway that locates active Ran and modulates the cortical localization of NuMA-dynein complexes to correct mispositioned spindles. This pathway was discovered through the creation and analysis of Hmmr-knockout mice, which suffer neonatal lethality with defective neural development and pleiotropic phenotypes in multiple tissues. HMMR over-expression in immortalized cancer cells induces phenotypes consistent with an increase in active Ran including defects in spindle orientation. These data identify an essential role for HMMR in the PLK1-dependent regulatory pathway that orients progenitor cell division and supports neural development. eLife Sciences Publications, Ltd 2017-10-10 /pmc/articles/PMC5681225/ /pubmed/28994651 http://dx.doi.org/10.7554/eLife.28672 Text en © 2017, Connell et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Cell Biology Connell, Marisa Chen, Helen Jiang, Jihong Kuan, Chia-Wei Fotovati, Abbas Chu, Tony LH He, Zhengcheng Lengyell, Tess C Li, Huaibiao Kroll, Torsten Li, Amanda M Goldowitz, Daniel Frappart, Lucien Ploubidou, Aspasia Patel, Millan S Pilarski, Linda M Simpson, Elizabeth M Lange, Philipp F Allan, Douglas W Maxwell, Christopher A HMMR acts in the PLK1-dependent spindle positioning pathway and supports neural development |
title | HMMR acts in the PLK1-dependent spindle positioning pathway and supports neural development |
title_full | HMMR acts in the PLK1-dependent spindle positioning pathway and supports neural development |
title_fullStr | HMMR acts in the PLK1-dependent spindle positioning pathway and supports neural development |
title_full_unstemmed | HMMR acts in the PLK1-dependent spindle positioning pathway and supports neural development |
title_short | HMMR acts in the PLK1-dependent spindle positioning pathway and supports neural development |
title_sort | hmmr acts in the plk1-dependent spindle positioning pathway and supports neural development |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5681225/ https://www.ncbi.nlm.nih.gov/pubmed/28994651 http://dx.doi.org/10.7554/eLife.28672 |
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