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Microtubules are necessary for proper Reticulon localization during mitosis

During mitosis, the structure of the Endoplasmic Reticulum (ER) displays a dramatic reorganization and remodeling, however, the mechanism driving these changes is poorly understood. Hairpin-containing ER transmembrane proteins that stabilize ER tubules have been identified as possible factors to pro...

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Autores principales: Diaz, Ulises, Bergman, Zane J., Johnson, Brittany M., Edington, Alia R., de Cruz, Matthew A., Marshall, Wallace F., Riggs, Blake
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6932760/
https://www.ncbi.nlm.nih.gov/pubmed/31877164
http://dx.doi.org/10.1371/journal.pone.0226327
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author Diaz, Ulises
Bergman, Zane J.
Johnson, Brittany M.
Edington, Alia R.
de Cruz, Matthew A.
Marshall, Wallace F.
Riggs, Blake
author_facet Diaz, Ulises
Bergman, Zane J.
Johnson, Brittany M.
Edington, Alia R.
de Cruz, Matthew A.
Marshall, Wallace F.
Riggs, Blake
author_sort Diaz, Ulises
collection PubMed
description During mitosis, the structure of the Endoplasmic Reticulum (ER) displays a dramatic reorganization and remodeling, however, the mechanism driving these changes is poorly understood. Hairpin-containing ER transmembrane proteins that stabilize ER tubules have been identified as possible factors to promote these drastic changes in ER morphology. Recently, the Reticulon and REEP family of ER shaping proteins have been shown to heavily influence ER morphology by driving the formation of ER tubules, which are known for their close proximity with microtubules. Here, we examine the role of microtubules and other cytoskeletal factors in the dynamics of a Drosophila Reticulon, Reticulon-like 1 (Rtnl1), localization to spindle poles during mitosis in the early embryo. At prometaphase, Rtnl1 is enriched to spindle poles just prior to the ER retention motif KDEL, suggesting a possible recruitment role for Rtnl1 in the bulk localization of ER to spindle poles. Using image analysis-based methods and precise temporal injections of cytoskeletal inhibitors in the early syncytial Drosophila embryo, we show that microtubules are necessary for proper Rtnl1 localization to spindles during mitosis. Lastly, we show that astral microtubules, not microfilaments, are necessary for proper Rtnl1 localization to spindle poles, and is largely independent of the minus-end directed motor protein dynein. This work highlights the role of the microtubule cytoskeleton in Rtnl1 localization to spindles during mitosis and sheds light on a pathway towards inheritance of this major organelle.
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spelling pubmed-69327602020-01-07 Microtubules are necessary for proper Reticulon localization during mitosis Diaz, Ulises Bergman, Zane J. Johnson, Brittany M. Edington, Alia R. de Cruz, Matthew A. Marshall, Wallace F. Riggs, Blake PLoS One Research Article During mitosis, the structure of the Endoplasmic Reticulum (ER) displays a dramatic reorganization and remodeling, however, the mechanism driving these changes is poorly understood. Hairpin-containing ER transmembrane proteins that stabilize ER tubules have been identified as possible factors to promote these drastic changes in ER morphology. Recently, the Reticulon and REEP family of ER shaping proteins have been shown to heavily influence ER morphology by driving the formation of ER tubules, which are known for their close proximity with microtubules. Here, we examine the role of microtubules and other cytoskeletal factors in the dynamics of a Drosophila Reticulon, Reticulon-like 1 (Rtnl1), localization to spindle poles during mitosis in the early embryo. At prometaphase, Rtnl1 is enriched to spindle poles just prior to the ER retention motif KDEL, suggesting a possible recruitment role for Rtnl1 in the bulk localization of ER to spindle poles. Using image analysis-based methods and precise temporal injections of cytoskeletal inhibitors in the early syncytial Drosophila embryo, we show that microtubules are necessary for proper Rtnl1 localization to spindles during mitosis. Lastly, we show that astral microtubules, not microfilaments, are necessary for proper Rtnl1 localization to spindle poles, and is largely independent of the minus-end directed motor protein dynein. This work highlights the role of the microtubule cytoskeleton in Rtnl1 localization to spindles during mitosis and sheds light on a pathway towards inheritance of this major organelle. Public Library of Science 2019-12-26 /pmc/articles/PMC6932760/ /pubmed/31877164 http://dx.doi.org/10.1371/journal.pone.0226327 Text en © 2019 Diaz et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Diaz, Ulises
Bergman, Zane J.
Johnson, Brittany M.
Edington, Alia R.
de Cruz, Matthew A.
Marshall, Wallace F.
Riggs, Blake
Microtubules are necessary for proper Reticulon localization during mitosis
title Microtubules are necessary for proper Reticulon localization during mitosis
title_full Microtubules are necessary for proper Reticulon localization during mitosis
title_fullStr Microtubules are necessary for proper Reticulon localization during mitosis
title_full_unstemmed Microtubules are necessary for proper Reticulon localization during mitosis
title_short Microtubules are necessary for proper Reticulon localization during mitosis
title_sort microtubules are necessary for proper reticulon localization during mitosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6932760/
https://www.ncbi.nlm.nih.gov/pubmed/31877164
http://dx.doi.org/10.1371/journal.pone.0226327
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