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Proper symmetric and asymmetric endoplasmic reticulum partitioning requires astral microtubules

Mechanisms that regulate partitioning of the endoplasmic reticulum (ER) during cell division are largely unknown. Previous studies have mostly addressed ER partitioning in cultured cells, which may not recapitulate physiological processes that are critical in developing, intact tissues. We have addr...

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Autores principales: Smyth, Jeremy T., Schoborg, Todd A., Bergman, Zane J., Riggs, Blake, Rusan, Nasser M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4554919/
https://www.ncbi.nlm.nih.gov/pubmed/26289801
http://dx.doi.org/10.1098/rsob.150067
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author Smyth, Jeremy T.
Schoborg, Todd A.
Bergman, Zane J.
Riggs, Blake
Rusan, Nasser M.
author_facet Smyth, Jeremy T.
Schoborg, Todd A.
Bergman, Zane J.
Riggs, Blake
Rusan, Nasser M.
author_sort Smyth, Jeremy T.
collection PubMed
description Mechanisms that regulate partitioning of the endoplasmic reticulum (ER) during cell division are largely unknown. Previous studies have mostly addressed ER partitioning in cultured cells, which may not recapitulate physiological processes that are critical in developing, intact tissues. We have addressed this by analysing ER partitioning in asymmetrically dividing stem cells, in which precise segregation of cellular components is essential for proper development and tissue architecture. We show that in Drosophila neural stem cells, called neuroblasts, the ER asymmetrically partitioned to centrosomes early in mitosis. This correlated closely with the asymmetric nucleation of astral microtubules (MTs) by centrosomes, suggesting that astral MT association may be required for ER partitioning by centrosomes. Consistent with this, the ER also associated with astral MTs in meiotic Drosophila spermatocytes and during syncytial embryonic divisions. Disruption of centrosomes in each of these cell types led to improper ER partitioning, demonstrating the critical role for centrosomes and associated astral MTs in this process. Importantly, we show that the ER also associated with astral MTs in cultured human cells, suggesting that this centrosome/astral MT-based partitioning mechanism is conserved across animal species.
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spelling pubmed-45549192015-09-09 Proper symmetric and asymmetric endoplasmic reticulum partitioning requires astral microtubules Smyth, Jeremy T. Schoborg, Todd A. Bergman, Zane J. Riggs, Blake Rusan, Nasser M. Open Biol Research Mechanisms that regulate partitioning of the endoplasmic reticulum (ER) during cell division are largely unknown. Previous studies have mostly addressed ER partitioning in cultured cells, which may not recapitulate physiological processes that are critical in developing, intact tissues. We have addressed this by analysing ER partitioning in asymmetrically dividing stem cells, in which precise segregation of cellular components is essential for proper development and tissue architecture. We show that in Drosophila neural stem cells, called neuroblasts, the ER asymmetrically partitioned to centrosomes early in mitosis. This correlated closely with the asymmetric nucleation of astral microtubules (MTs) by centrosomes, suggesting that astral MT association may be required for ER partitioning by centrosomes. Consistent with this, the ER also associated with astral MTs in meiotic Drosophila spermatocytes and during syncytial embryonic divisions. Disruption of centrosomes in each of these cell types led to improper ER partitioning, demonstrating the critical role for centrosomes and associated astral MTs in this process. Importantly, we show that the ER also associated with astral MTs in cultured human cells, suggesting that this centrosome/astral MT-based partitioning mechanism is conserved across animal species. The Royal Society 2015-08-19 /pmc/articles/PMC4554919/ /pubmed/26289801 http://dx.doi.org/10.1098/rsob.150067 Text en © 2015 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Research
Smyth, Jeremy T.
Schoborg, Todd A.
Bergman, Zane J.
Riggs, Blake
Rusan, Nasser M.
Proper symmetric and asymmetric endoplasmic reticulum partitioning requires astral microtubules
title Proper symmetric and asymmetric endoplasmic reticulum partitioning requires astral microtubules
title_full Proper symmetric and asymmetric endoplasmic reticulum partitioning requires astral microtubules
title_fullStr Proper symmetric and asymmetric endoplasmic reticulum partitioning requires astral microtubules
title_full_unstemmed Proper symmetric and asymmetric endoplasmic reticulum partitioning requires astral microtubules
title_short Proper symmetric and asymmetric endoplasmic reticulum partitioning requires astral microtubules
title_sort proper symmetric and asymmetric endoplasmic reticulum partitioning requires astral microtubules
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4554919/
https://www.ncbi.nlm.nih.gov/pubmed/26289801
http://dx.doi.org/10.1098/rsob.150067
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