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Intersectin-1 interacts with the golgin GCC88 to couple the actin network and Golgi architecture
The maintenance of the Golgi ribbon relies on a dynamic balance between the actin and microtubule networks; however, the pathways controlling actin networks remain poorly defined. Previously, we showed that the trans-Golgi network (TGN) membrane tether/golgin, GCC88, modulates the Golgi ribbon archi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6589577/ https://www.ncbi.nlm.nih.gov/pubmed/30540523 http://dx.doi.org/10.1091/mbc.E18-05-0313 |
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author | Makhoul, Christian Gosavi, Prajakta Duffield, Regina Delbridge, Bronwen Williamson, Nicholas A. Gleeson, Paul A. |
author_facet | Makhoul, Christian Gosavi, Prajakta Duffield, Regina Delbridge, Bronwen Williamson, Nicholas A. Gleeson, Paul A. |
author_sort | Makhoul, Christian |
collection | PubMed |
description | The maintenance of the Golgi ribbon relies on a dynamic balance between the actin and microtubule networks; however, the pathways controlling actin networks remain poorly defined. Previously, we showed that the trans-Golgi network (TGN) membrane tether/golgin, GCC88, modulates the Golgi ribbon architecture. Here, we show that dispersal of the Golgi ribbon by GCC88 is dependent on actin and the involvement of nonmuscle myosin IIA. We have identified the long isoform of intersectin-1 (ITSN-1), a guanine nucleotide exchange factor for Cdc42, as a novel Golgi component and an interaction partner of GCC88 responsible for mediating the actin-dependent dispersal of the Golgi ribbon. We show that perturbation of Golgi morphology by changes in membrane flux, mediated by silencing the retromer subunit Vps26, or in a model of neurodegeneration, induced by Tau overexpression, are also dependent on the ITSN-1-GCC88 interaction. Overall, our study reveals a role for a TGN golgin and ITSN-1 in linking to the actin cytoskeleton and regulating the balance between a compact Golgi ribbon and a dispersed Golgi, a pathway with relevance to pathophysiological conditions. |
format | Online Article Text |
id | pubmed-6589577 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-65895772019-06-28 Intersectin-1 interacts with the golgin GCC88 to couple the actin network and Golgi architecture Makhoul, Christian Gosavi, Prajakta Duffield, Regina Delbridge, Bronwen Williamson, Nicholas A. Gleeson, Paul A. Mol Biol Cell Articles The maintenance of the Golgi ribbon relies on a dynamic balance between the actin and microtubule networks; however, the pathways controlling actin networks remain poorly defined. Previously, we showed that the trans-Golgi network (TGN) membrane tether/golgin, GCC88, modulates the Golgi ribbon architecture. Here, we show that dispersal of the Golgi ribbon by GCC88 is dependent on actin and the involvement of nonmuscle myosin IIA. We have identified the long isoform of intersectin-1 (ITSN-1), a guanine nucleotide exchange factor for Cdc42, as a novel Golgi component and an interaction partner of GCC88 responsible for mediating the actin-dependent dispersal of the Golgi ribbon. We show that perturbation of Golgi morphology by changes in membrane flux, mediated by silencing the retromer subunit Vps26, or in a model of neurodegeneration, induced by Tau overexpression, are also dependent on the ITSN-1-GCC88 interaction. Overall, our study reveals a role for a TGN golgin and ITSN-1 in linking to the actin cytoskeleton and regulating the balance between a compact Golgi ribbon and a dispersed Golgi, a pathway with relevance to pathophysiological conditions. The American Society for Cell Biology 2019-02-01 /pmc/articles/PMC6589577/ /pubmed/30540523 http://dx.doi.org/10.1091/mbc.E18-05-0313 Text en © 2019 Makhoul, Gosavi, et al. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. http://creativecommons.org/licenses/by-nc-sa/3.0 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. |
spellingShingle | Articles Makhoul, Christian Gosavi, Prajakta Duffield, Regina Delbridge, Bronwen Williamson, Nicholas A. Gleeson, Paul A. Intersectin-1 interacts with the golgin GCC88 to couple the actin network and Golgi architecture |
title | Intersectin-1 interacts with the golgin GCC88 to couple the actin network and Golgi architecture |
title_full | Intersectin-1 interacts with the golgin GCC88 to couple the actin network and Golgi architecture |
title_fullStr | Intersectin-1 interacts with the golgin GCC88 to couple the actin network and Golgi architecture |
title_full_unstemmed | Intersectin-1 interacts with the golgin GCC88 to couple the actin network and Golgi architecture |
title_short | Intersectin-1 interacts with the golgin GCC88 to couple the actin network and Golgi architecture |
title_sort | intersectin-1 interacts with the golgin gcc88 to couple the actin network and golgi architecture |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6589577/ https://www.ncbi.nlm.nih.gov/pubmed/30540523 http://dx.doi.org/10.1091/mbc.E18-05-0313 |
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