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Dual topology of co-chaperones at the membrane of the endoplasmic reticulum
Dual topologies of proteins at the ER membrane are known for a variety of proteins allowing the same protein to exert different functions according to the topology adopted. A dual topology of the co-chaperone ERdj4, which resides in the endoplasmic reticulum (ER), was proposed recently, a thesis tha...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8342575/ https://www.ncbi.nlm.nih.gov/pubmed/34354047 http://dx.doi.org/10.1038/s41420-021-00594-x |
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author | Daverkausen-Fischer, Lea Pröls, Felicitas |
author_facet | Daverkausen-Fischer, Lea Pröls, Felicitas |
author_sort | Daverkausen-Fischer, Lea |
collection | PubMed |
description | Dual topologies of proteins at the ER membrane are known for a variety of proteins allowing the same protein to exert different functions according to the topology adopted. A dual topology of the co-chaperone ERdj4, which resides in the endoplasmic reticulum (ER), was proposed recently, a thesis that we found to align all published data and existing controversies into one whole picture. The aim of this review is to reassess all primary data available in the literature on ER-resident Hsp40 co-chaperones with respect to their topology. After careful and critical analyses of all experimental data published so far, we identified, next to ERdj4, two other co-chaperones, ERdj3 and ERdj6, that also display features of a dual topology at the ER membrane. We assume that during cellular stress subpools of some ER-resident J protein can alter their topology so that these proteins can exert different functions in order to adapt to cellular stress. |
format | Online Article Text |
id | pubmed-8342575 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-83425752021-08-20 Dual topology of co-chaperones at the membrane of the endoplasmic reticulum Daverkausen-Fischer, Lea Pröls, Felicitas Cell Death Discov Review Article Dual topologies of proteins at the ER membrane are known for a variety of proteins allowing the same protein to exert different functions according to the topology adopted. A dual topology of the co-chaperone ERdj4, which resides in the endoplasmic reticulum (ER), was proposed recently, a thesis that we found to align all published data and existing controversies into one whole picture. The aim of this review is to reassess all primary data available in the literature on ER-resident Hsp40 co-chaperones with respect to their topology. After careful and critical analyses of all experimental data published so far, we identified, next to ERdj4, two other co-chaperones, ERdj3 and ERdj6, that also display features of a dual topology at the ER membrane. We assume that during cellular stress subpools of some ER-resident J protein can alter their topology so that these proteins can exert different functions in order to adapt to cellular stress. Nature Publishing Group UK 2021-08-05 /pmc/articles/PMC8342575/ /pubmed/34354047 http://dx.doi.org/10.1038/s41420-021-00594-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Article Daverkausen-Fischer, Lea Pröls, Felicitas Dual topology of co-chaperones at the membrane of the endoplasmic reticulum |
title | Dual topology of co-chaperones at the membrane of the endoplasmic reticulum |
title_full | Dual topology of co-chaperones at the membrane of the endoplasmic reticulum |
title_fullStr | Dual topology of co-chaperones at the membrane of the endoplasmic reticulum |
title_full_unstemmed | Dual topology of co-chaperones at the membrane of the endoplasmic reticulum |
title_short | Dual topology of co-chaperones at the membrane of the endoplasmic reticulum |
title_sort | dual topology of co-chaperones at the membrane of the endoplasmic reticulum |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8342575/ https://www.ncbi.nlm.nih.gov/pubmed/34354047 http://dx.doi.org/10.1038/s41420-021-00594-x |
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