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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2014
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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. |
format | Online Article Text |
id | pubmed-3912533 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
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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