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Rab11 facilitates cross-talk between autophagy and endosomal pathway through regulation of Hook localization
During autophagy, double-membrane autophagosomes deliver sequestered cytoplasmic content to late endosomes and lysosomes for degradation. The molecular mechanism of autophagosome maturation is still poorly characterized. The small GTPase Rab11 regulates endosomal traffic and is thought to function a...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3923643/ https://www.ncbi.nlm.nih.gov/pubmed/24356450 http://dx.doi.org/10.1091/mbc.E13-10-0574 |
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author | Szatmári, Zsuzsanna Kis, Viktor Lippai, Mónika Hegedűs, Krisztina Faragó, Tamás Lőrincz, Péter Tanaka, Tsubasa Juhász, Gábor Sass, Miklós |
author_facet | Szatmári, Zsuzsanna Kis, Viktor Lippai, Mónika Hegedűs, Krisztina Faragó, Tamás Lőrincz, Péter Tanaka, Tsubasa Juhász, Gábor Sass, Miklós |
author_sort | Szatmári, Zsuzsanna |
collection | PubMed |
description | During autophagy, double-membrane autophagosomes deliver sequestered cytoplasmic content to late endosomes and lysosomes for degradation. The molecular mechanism of autophagosome maturation is still poorly characterized. The small GTPase Rab11 regulates endosomal traffic and is thought to function at the level of recycling endosomes. We show that loss of Rab11 leads to accumulation of autophagosomes and late endosomes in Drosophila melanogaster. Rab11 translocates from recycling endosomes to autophagosomes in response to autophagy induction and physically interacts with Hook, a negative regulator of endosome maturation. Hook anchors endosomes to microtubules, and we show that Rab11 facilitates the fusion of endosomes and autophagosomes by removing Hook from mature late endosomes and inhibiting its homodimerization. Thus induction of autophagy appears to promote autophagic flux by increased convergence with the endosomal pathway. |
format | Online Article Text |
id | pubmed-3923643 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-39236432014-04-30 Rab11 facilitates cross-talk between autophagy and endosomal pathway through regulation of Hook localization Szatmári, Zsuzsanna Kis, Viktor Lippai, Mónika Hegedűs, Krisztina Faragó, Tamás Lőrincz, Péter Tanaka, Tsubasa Juhász, Gábor Sass, Miklós Mol Biol Cell Articles During autophagy, double-membrane autophagosomes deliver sequestered cytoplasmic content to late endosomes and lysosomes for degradation. The molecular mechanism of autophagosome maturation is still poorly characterized. The small GTPase Rab11 regulates endosomal traffic and is thought to function at the level of recycling endosomes. We show that loss of Rab11 leads to accumulation of autophagosomes and late endosomes in Drosophila melanogaster. Rab11 translocates from recycling endosomes to autophagosomes in response to autophagy induction and physically interacts with Hook, a negative regulator of endosome maturation. Hook anchors endosomes to microtubules, and we show that Rab11 facilitates the fusion of endosomes and autophagosomes by removing Hook from mature late endosomes and inhibiting its homodimerization. Thus induction of autophagy appears to promote autophagic flux by increased convergence with the endosomal pathway. The American Society for Cell Biology 2014-02-15 /pmc/articles/PMC3923643/ /pubmed/24356450 http://dx.doi.org/10.1091/mbc.E13-10-0574 Text en © 2014 Szatmári et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0). “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society of Cell Biology. |
spellingShingle | Articles Szatmári, Zsuzsanna Kis, Viktor Lippai, Mónika Hegedűs, Krisztina Faragó, Tamás Lőrincz, Péter Tanaka, Tsubasa Juhász, Gábor Sass, Miklós Rab11 facilitates cross-talk between autophagy and endosomal pathway through regulation of Hook localization |
title | Rab11 facilitates cross-talk between autophagy and endosomal pathway through regulation of Hook localization |
title_full | Rab11 facilitates cross-talk between autophagy and endosomal pathway through regulation of Hook localization |
title_fullStr | Rab11 facilitates cross-talk between autophagy and endosomal pathway through regulation of Hook localization |
title_full_unstemmed | Rab11 facilitates cross-talk between autophagy and endosomal pathway through regulation of Hook localization |
title_short | Rab11 facilitates cross-talk between autophagy and endosomal pathway through regulation of Hook localization |
title_sort | rab11 facilitates cross-talk between autophagy and endosomal pathway through regulation of hook localization |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3923643/ https://www.ncbi.nlm.nih.gov/pubmed/24356450 http://dx.doi.org/10.1091/mbc.E13-10-0574 |
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