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Actin and Microtubules Differently Contribute to Vacuolar Targeting Specificity during the Export from the ER

Plants rely on both actin and microtubule cytoskeletons to fine-tune sorting and spatial targeting of membranes during cell growth and stress adaptation. Considerable advances have been made in recent years in the comprehension of the relationship between the trans-Golgi network/early endosome (TGN/...

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Autores principales: De Caroli, Monica, Barozzi, Fabrizio, Renna, Luciana, Piro, Gabriella, Di Sansebastiano, Gian-Pietro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8074374/
https://www.ncbi.nlm.nih.gov/pubmed/33924184
http://dx.doi.org/10.3390/membranes11040299
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author De Caroli, Monica
Barozzi, Fabrizio
Renna, Luciana
Piro, Gabriella
Di Sansebastiano, Gian-Pietro
author_facet De Caroli, Monica
Barozzi, Fabrizio
Renna, Luciana
Piro, Gabriella
Di Sansebastiano, Gian-Pietro
author_sort De Caroli, Monica
collection PubMed
description Plants rely on both actin and microtubule cytoskeletons to fine-tune sorting and spatial targeting of membranes during cell growth and stress adaptation. Considerable advances have been made in recent years in the comprehension of the relationship between the trans-Golgi network/early endosome (TGN/EE) and cytoskeletons, but studies have mainly focused on the transport to and from the plasma membrane. We address here the relationship of the cytoskeleton with different endoplasmic reticulum (ER) export mechanisms toward vacuoles. These emergent features of the plant endomembrane traffic are explored with an in vivo approach, providing clues on the traffic regulation at different levels beyond known proteins’ functions and interactions. We show how traffic of vacuolar markers, characterized by different vacuolar sorting determinants, diverges at the export from the ER, clearly involving different components of the cytoskeleton.
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spelling pubmed-80743742021-04-27 Actin and Microtubules Differently Contribute to Vacuolar Targeting Specificity during the Export from the ER De Caroli, Monica Barozzi, Fabrizio Renna, Luciana Piro, Gabriella Di Sansebastiano, Gian-Pietro Membranes (Basel) Article Plants rely on both actin and microtubule cytoskeletons to fine-tune sorting and spatial targeting of membranes during cell growth and stress adaptation. Considerable advances have been made in recent years in the comprehension of the relationship between the trans-Golgi network/early endosome (TGN/EE) and cytoskeletons, but studies have mainly focused on the transport to and from the plasma membrane. We address here the relationship of the cytoskeleton with different endoplasmic reticulum (ER) export mechanisms toward vacuoles. These emergent features of the plant endomembrane traffic are explored with an in vivo approach, providing clues on the traffic regulation at different levels beyond known proteins’ functions and interactions. We show how traffic of vacuolar markers, characterized by different vacuolar sorting determinants, diverges at the export from the ER, clearly involving different components of the cytoskeleton. MDPI 2021-04-20 /pmc/articles/PMC8074374/ /pubmed/33924184 http://dx.doi.org/10.3390/membranes11040299 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
De Caroli, Monica
Barozzi, Fabrizio
Renna, Luciana
Piro, Gabriella
Di Sansebastiano, Gian-Pietro
Actin and Microtubules Differently Contribute to Vacuolar Targeting Specificity during the Export from the ER
title Actin and Microtubules Differently Contribute to Vacuolar Targeting Specificity during the Export from the ER
title_full Actin and Microtubules Differently Contribute to Vacuolar Targeting Specificity during the Export from the ER
title_fullStr Actin and Microtubules Differently Contribute to Vacuolar Targeting Specificity during the Export from the ER
title_full_unstemmed Actin and Microtubules Differently Contribute to Vacuolar Targeting Specificity during the Export from the ER
title_short Actin and Microtubules Differently Contribute to Vacuolar Targeting Specificity during the Export from the ER
title_sort actin and microtubules differently contribute to vacuolar targeting specificity during the export from the er
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8074374/
https://www.ncbi.nlm.nih.gov/pubmed/33924184
http://dx.doi.org/10.3390/membranes11040299
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