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ER-driven membrane contact sites: Evolutionary conserved machineries for stress response and autophagy regulation?

Endoplasmic Reticulum (ER), spreading in the whole cell cytoplasm, is a central player in eukaryotic cell homeostasis, from plants to mammals. Beside crucial functions, such as membrane lipids and proteins synthesis and outward transport, the ER is able to connect to virtually every endomembrane com...

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Autores principales: Molino, Diana, Nascimbeni, Anna Chiara, Giordano, Francesca, Codogno, Patrice, Morel, Etienne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5731517/
https://www.ncbi.nlm.nih.gov/pubmed/29259731
http://dx.doi.org/10.1080/19420889.2017.1401699
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author Molino, Diana
Nascimbeni, Anna Chiara
Giordano, Francesca
Codogno, Patrice
Morel, Etienne
author_facet Molino, Diana
Nascimbeni, Anna Chiara
Giordano, Francesca
Codogno, Patrice
Morel, Etienne
author_sort Molino, Diana
collection PubMed
description Endoplasmic Reticulum (ER), spreading in the whole cell cytoplasm, is a central player in eukaryotic cell homeostasis, from plants to mammals. Beside crucial functions, such as membrane lipids and proteins synthesis and outward transport, the ER is able to connect to virtually every endomembrane compartment by specific tethering molecular machineries, which enables the establishment of membrane-membrane contact sites. ER-mitochondria contact sites have been shown to be involved in autophagosome biogenesis, the main organelle of the autophagy degradation pathway. More recently we demonstrated that also ER-plasma membrane contact sites are sites for autophagosomes assembly, suggesting that more generally ER-organelles contacts are involved in autophagy and organelle biogenesis. Here we aim to discuss the functioning of ER-driven contact sites in mammals and plants and more in particular emphasize on their recently highlighted function in autophagy to finally conclude on some key questions that may be useful for further research in the field.
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spelling pubmed-57315172017-12-19 ER-driven membrane contact sites: Evolutionary conserved machineries for stress response and autophagy regulation? Molino, Diana Nascimbeni, Anna Chiara Giordano, Francesca Codogno, Patrice Morel, Etienne Commun Integr Biol Original Articles Endoplasmic Reticulum (ER), spreading in the whole cell cytoplasm, is a central player in eukaryotic cell homeostasis, from plants to mammals. Beside crucial functions, such as membrane lipids and proteins synthesis and outward transport, the ER is able to connect to virtually every endomembrane compartment by specific tethering molecular machineries, which enables the establishment of membrane-membrane contact sites. ER-mitochondria contact sites have been shown to be involved in autophagosome biogenesis, the main organelle of the autophagy degradation pathway. More recently we demonstrated that also ER-plasma membrane contact sites are sites for autophagosomes assembly, suggesting that more generally ER-organelles contacts are involved in autophagy and organelle biogenesis. Here we aim to discuss the functioning of ER-driven contact sites in mammals and plants and more in particular emphasize on their recently highlighted function in autophagy to finally conclude on some key questions that may be useful for further research in the field. Taylor & Francis 2017-12-13 /pmc/articles/PMC5731517/ /pubmed/29259731 http://dx.doi.org/10.1080/19420889.2017.1401699 Text en © 2017 The Author(s). Published with license by Taylor & Francis http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Molino, Diana
Nascimbeni, Anna Chiara
Giordano, Francesca
Codogno, Patrice
Morel, Etienne
ER-driven membrane contact sites: Evolutionary conserved machineries for stress response and autophagy regulation?
title ER-driven membrane contact sites: Evolutionary conserved machineries for stress response and autophagy regulation?
title_full ER-driven membrane contact sites: Evolutionary conserved machineries for stress response and autophagy regulation?
title_fullStr ER-driven membrane contact sites: Evolutionary conserved machineries for stress response and autophagy regulation?
title_full_unstemmed ER-driven membrane contact sites: Evolutionary conserved machineries for stress response and autophagy regulation?
title_short ER-driven membrane contact sites: Evolutionary conserved machineries for stress response and autophagy regulation?
title_sort er-driven membrane contact sites: evolutionary conserved machineries for stress response and autophagy regulation?
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5731517/
https://www.ncbi.nlm.nih.gov/pubmed/29259731
http://dx.doi.org/10.1080/19420889.2017.1401699
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