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Early endosome motility spatially organizes polysome distribution

Early endosomes (EEs) mediate protein sorting, and their cytoskeleton-dependent motility supports long-distance signaling in neurons. Here, we report an unexpected role of EE motility in distributing the translation machinery in a fungal model system. We visualize ribosomal subunit proteins and show...

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Detalles Bibliográficos
Autores principales: Higuchi, Yujiro, Ashwin, Peter, Roger, Yvonne, Steinberg, Gero
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3912533/
https://www.ncbi.nlm.nih.gov/pubmed/24493587
http://dx.doi.org/10.1083/jcb.201307164
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author Higuchi, Yujiro
Ashwin, Peter
Roger, Yvonne
Steinberg, Gero
author_facet Higuchi, Yujiro
Ashwin, Peter
Roger, Yvonne
Steinberg, Gero
author_sort Higuchi, Yujiro
collection PubMed
description Early endosomes (EEs) mediate protein sorting, and their cytoskeleton-dependent motility supports long-distance signaling in neurons. Here, we report an unexpected role of EE motility in distributing the translation machinery in a fungal model system. We visualize ribosomal subunit proteins and show that the large subunits diffused slowly throughout the cytoplasm (D(c,60S) = 0.311 µm(2)/s), whereas entire polysomes underwent long-range motility along microtubules. This movement was mediated by “hitchhiking” on kinesin-3 and dynein-driven EEs, where the polysomes appeared to translate EE-associated mRNA into proteins. Modeling indicates that this motor-driven transport is required for even cellular distribution of newly formed ribosomes. Indeed, impaired EE motility in motor mutants, or their inability to bind EEs in mutants lacking the RNA-binding protein Rrm4, reduced ribosome transport and induced ribosome aggregation near the nucleus. As a consequence, cell growth was severely restricted. Collectively, our results indicate that polysomes associate with moving EEs and that “off- and reloading” distributes the protein translation machinery.
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spelling pubmed-39125332014-08-03 Early endosome motility spatially organizes polysome distribution Higuchi, Yujiro Ashwin, Peter Roger, Yvonne Steinberg, Gero J Cell Biol Research Articles Early endosomes (EEs) mediate protein sorting, and their cytoskeleton-dependent motility supports long-distance signaling in neurons. Here, we report an unexpected role of EE motility in distributing the translation machinery in a fungal model system. We visualize ribosomal subunit proteins and show that the large subunits diffused slowly throughout the cytoplasm (D(c,60S) = 0.311 µm(2)/s), whereas entire polysomes underwent long-range motility along microtubules. This movement was mediated by “hitchhiking” on kinesin-3 and dynein-driven EEs, where the polysomes appeared to translate EE-associated mRNA into proteins. Modeling indicates that this motor-driven transport is required for even cellular distribution of newly formed ribosomes. Indeed, impaired EE motility in motor mutants, or their inability to bind EEs in mutants lacking the RNA-binding protein Rrm4, reduced ribosome transport and induced ribosome aggregation near the nucleus. As a consequence, cell growth was severely restricted. Collectively, our results indicate that polysomes associate with moving EEs and that “off- and reloading” distributes the protein translation machinery. The Rockefeller University Press 2014-02-03 /pmc/articles/PMC3912533/ /pubmed/24493587 http://dx.doi.org/10.1083/jcb.201307164 Text en © 2014 Higuchi et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Research Articles
Higuchi, Yujiro
Ashwin, Peter
Roger, Yvonne
Steinberg, Gero
Early endosome motility spatially organizes polysome distribution
title Early endosome motility spatially organizes polysome distribution
title_full Early endosome motility spatially organizes polysome distribution
title_fullStr Early endosome motility spatially organizes polysome distribution
title_full_unstemmed Early endosome motility spatially organizes polysome distribution
title_short Early endosome motility spatially organizes polysome distribution
title_sort early endosome motility spatially organizes polysome distribution
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3912533/
https://www.ncbi.nlm.nih.gov/pubmed/24493587
http://dx.doi.org/10.1083/jcb.201307164
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