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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2017
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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. |
format | Online Article Text |
id | pubmed-5731517 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
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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