Endoplasmic reticulum membranes are continuously required to maintain mitotic spindle size and forces

Detalhes bibliográficos
Autor(a) principal: Araújo, Margarida
Data de Publicação: 2022
Outros Autores: Tavares, Alexandra, Vieira, Diana V., Telley, Ivo A., Oliveira, Raquel A.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.14/39489
Resumo: Membrane organelle function, localization, and proper partitioning upon cell division depend on interactions with the cytoskeleton. Whether membrane organelles also impact the function of cytoskeletal elements remains less clear. Here, we show that acute disruption of the ER around spindle poles affects mitotic spindle size and function in Drosophila syncytial embryos. Acute ER disruption was achieved through the inhibition of ER membrane fusion by the dominant-negative cytoplasmic domain of atlastin. We reveal that when centrosome-proximal ER membranes are disrupted, specifically at metaphase, mitotic spindles become smaller, despite no significant changes in microtubule dynamics. These smaller spindles are still able to mediate sister chromatid separation, yet with decreased velocity. Furthermore, by inducing mitotic exit, we found that nuclear separation and distribution are affected by ER disruption. Our results suggest that ER integrity around spindle poles is crucial for the maintenance of mitotic spindle shape and pulling forces. In addition, ER integrity also ensures nuclear spacing during syncytial divisions.
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spelling Endoplasmic reticulum membranes are continuously required to maintain mitotic spindle size and forcesMembrane organelle function, localization, and proper partitioning upon cell division depend on interactions with the cytoskeleton. Whether membrane organelles also impact the function of cytoskeletal elements remains less clear. Here, we show that acute disruption of the ER around spindle poles affects mitotic spindle size and function in Drosophila syncytial embryos. Acute ER disruption was achieved through the inhibition of ER membrane fusion by the dominant-negative cytoplasmic domain of atlastin. We reveal that when centrosome-proximal ER membranes are disrupted, specifically at metaphase, mitotic spindles become smaller, despite no significant changes in microtubule dynamics. These smaller spindles are still able to mediate sister chromatid separation, yet with decreased velocity. Furthermore, by inducing mitotic exit, we found that nuclear separation and distribution are affected by ER disruption. Our results suggest that ER integrity around spindle poles is crucial for the maintenance of mitotic spindle shape and pulling forces. In addition, ER integrity also ensures nuclear spacing during syncytial divisions.Veritati - Repositório Institucional da Universidade Católica PortuguesaAraújo, MargaridaTavares, AlexandraVieira, Diana V.Telley, Ivo A.Oliveira, Raquel A.2022-12-07T09:22:15Z2023-01-012023-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.14/39489eng2575-107710.26508/lsa.20220154085141996496PMC967106836379670000898376200001info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-12T17:45:00Zoai:repositorio.ucp.pt:10400.14/39489Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T18:32:19.463366Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Endoplasmic reticulum membranes are continuously required to maintain mitotic spindle size and forces
title Endoplasmic reticulum membranes are continuously required to maintain mitotic spindle size and forces
spellingShingle Endoplasmic reticulum membranes are continuously required to maintain mitotic spindle size and forces
Araújo, Margarida
title_short Endoplasmic reticulum membranes are continuously required to maintain mitotic spindle size and forces
title_full Endoplasmic reticulum membranes are continuously required to maintain mitotic spindle size and forces
title_fullStr Endoplasmic reticulum membranes are continuously required to maintain mitotic spindle size and forces
title_full_unstemmed Endoplasmic reticulum membranes are continuously required to maintain mitotic spindle size and forces
title_sort Endoplasmic reticulum membranes are continuously required to maintain mitotic spindle size and forces
author Araújo, Margarida
author_facet Araújo, Margarida
Tavares, Alexandra
Vieira, Diana V.
Telley, Ivo A.
Oliveira, Raquel A.
author_role author
author2 Tavares, Alexandra
Vieira, Diana V.
Telley, Ivo A.
Oliveira, Raquel A.
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Veritati - Repositório Institucional da Universidade Católica Portuguesa
dc.contributor.author.fl_str_mv Araújo, Margarida
Tavares, Alexandra
Vieira, Diana V.
Telley, Ivo A.
Oliveira, Raquel A.
description Membrane organelle function, localization, and proper partitioning upon cell division depend on interactions with the cytoskeleton. Whether membrane organelles also impact the function of cytoskeletal elements remains less clear. Here, we show that acute disruption of the ER around spindle poles affects mitotic spindle size and function in Drosophila syncytial embryos. Acute ER disruption was achieved through the inhibition of ER membrane fusion by the dominant-negative cytoplasmic domain of atlastin. We reveal that when centrosome-proximal ER membranes are disrupted, specifically at metaphase, mitotic spindles become smaller, despite no significant changes in microtubule dynamics. These smaller spindles are still able to mediate sister chromatid separation, yet with decreased velocity. Furthermore, by inducing mitotic exit, we found that nuclear separation and distribution are affected by ER disruption. Our results suggest that ER integrity around spindle poles is crucial for the maintenance of mitotic spindle shape and pulling forces. In addition, ER integrity also ensures nuclear spacing during syncytial divisions.
publishDate 2022
dc.date.none.fl_str_mv 2022-12-07T09:22:15Z
2023-01-01
2023-01-01T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.14/39489
url http://hdl.handle.net/10400.14/39489
dc.language.iso.fl_str_mv eng
language eng
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10.26508/lsa.202201540
85141996496
PMC9671068
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