Cargando…
Sigma-1 receptor chaperones rescue nucleocytoplasmic transport deficit seen in cellular and Drosophila ALS/FTD models
In a subgroup of patients with amyotrophic lateral sclerosis (ALS)/Frontotemporal dementia (FTD), the (G4C2)-RNA repeat expansion from C9orf72 chromosome binds to the Ran-activating protein (RanGAP) at the nuclear pore, resulting in nucleocytoplasmic transport deficit and accumulation of Ran in the...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7642387/ https://www.ncbi.nlm.nih.gov/pubmed/33149115 http://dx.doi.org/10.1038/s41467-020-19396-3 |
_version_ | 1783606072975556608 |
---|---|
author | Lee, Pin-Tse Liévens, Jean-Charles Wang, Shao-Ming Chuang, Jian-Ying Khalil, Bilal Wu, Hsiang-en Chang, Wen-Chang Maurice, Tangui Su, Tsung-Ping |
author_facet | Lee, Pin-Tse Liévens, Jean-Charles Wang, Shao-Ming Chuang, Jian-Ying Khalil, Bilal Wu, Hsiang-en Chang, Wen-Chang Maurice, Tangui Su, Tsung-Ping |
author_sort | Lee, Pin-Tse |
collection | PubMed |
description | In a subgroup of patients with amyotrophic lateral sclerosis (ALS)/Frontotemporal dementia (FTD), the (G4C2)-RNA repeat expansion from C9orf72 chromosome binds to the Ran-activating protein (RanGAP) at the nuclear pore, resulting in nucleocytoplasmic transport deficit and accumulation of Ran in the cytosol. Here, we found that the sigma-1 receptor (Sig-1R), a molecular chaperone, reverses the pathological effects of (G4C2)-RNA repeats in cell lines and in Drosophila. The Sig-1R colocalizes with RanGAP and nuclear pore proteins (Nups) and stabilizes the latter. Interestingly, Sig-1Rs directly bind (G4C2)-RNA repeats. Overexpression of Sig-1Rs rescues, whereas the Sig-1R knockout exacerbates, the (G4C2)-RNA repeats-induced aberrant cytoplasmic accumulation of Ran. In Drosophila, Sig-1R (but not the Sig-1R-E102Q mutant) overexpression reverses eye necrosis, climbing deficit, and firing discharge caused by (G4C2)-RNA repeats. These results on a molecular chaperone at the nuclear pore suggest that Sig-1Rs may benefit patients with C9orf72 ALS/FTD by chaperoning the nuclear pore assembly and sponging away deleterious (G4C2)-RNA repeats. |
format | Online Article Text |
id | pubmed-7642387 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-76423872020-11-10 Sigma-1 receptor chaperones rescue nucleocytoplasmic transport deficit seen in cellular and Drosophila ALS/FTD models Lee, Pin-Tse Liévens, Jean-Charles Wang, Shao-Ming Chuang, Jian-Ying Khalil, Bilal Wu, Hsiang-en Chang, Wen-Chang Maurice, Tangui Su, Tsung-Ping Nat Commun Article In a subgroup of patients with amyotrophic lateral sclerosis (ALS)/Frontotemporal dementia (FTD), the (G4C2)-RNA repeat expansion from C9orf72 chromosome binds to the Ran-activating protein (RanGAP) at the nuclear pore, resulting in nucleocytoplasmic transport deficit and accumulation of Ran in the cytosol. Here, we found that the sigma-1 receptor (Sig-1R), a molecular chaperone, reverses the pathological effects of (G4C2)-RNA repeats in cell lines and in Drosophila. The Sig-1R colocalizes with RanGAP and nuclear pore proteins (Nups) and stabilizes the latter. Interestingly, Sig-1Rs directly bind (G4C2)-RNA repeats. Overexpression of Sig-1Rs rescues, whereas the Sig-1R knockout exacerbates, the (G4C2)-RNA repeats-induced aberrant cytoplasmic accumulation of Ran. In Drosophila, Sig-1R (but not the Sig-1R-E102Q mutant) overexpression reverses eye necrosis, climbing deficit, and firing discharge caused by (G4C2)-RNA repeats. These results on a molecular chaperone at the nuclear pore suggest that Sig-1Rs may benefit patients with C9orf72 ALS/FTD by chaperoning the nuclear pore assembly and sponging away deleterious (G4C2)-RNA repeats. Nature Publishing Group UK 2020-11-04 /pmc/articles/PMC7642387/ /pubmed/33149115 http://dx.doi.org/10.1038/s41467-020-19396-3 Text en © The Author(s) 2020 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/. |
spellingShingle | Article Lee, Pin-Tse Liévens, Jean-Charles Wang, Shao-Ming Chuang, Jian-Ying Khalil, Bilal Wu, Hsiang-en Chang, Wen-Chang Maurice, Tangui Su, Tsung-Ping Sigma-1 receptor chaperones rescue nucleocytoplasmic transport deficit seen in cellular and Drosophila ALS/FTD models |
title | Sigma-1 receptor chaperones rescue nucleocytoplasmic transport deficit seen in cellular and Drosophila ALS/FTD models |
title_full | Sigma-1 receptor chaperones rescue nucleocytoplasmic transport deficit seen in cellular and Drosophila ALS/FTD models |
title_fullStr | Sigma-1 receptor chaperones rescue nucleocytoplasmic transport deficit seen in cellular and Drosophila ALS/FTD models |
title_full_unstemmed | Sigma-1 receptor chaperones rescue nucleocytoplasmic transport deficit seen in cellular and Drosophila ALS/FTD models |
title_short | Sigma-1 receptor chaperones rescue nucleocytoplasmic transport deficit seen in cellular and Drosophila ALS/FTD models |
title_sort | sigma-1 receptor chaperones rescue nucleocytoplasmic transport deficit seen in cellular and drosophila als/ftd models |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7642387/ https://www.ncbi.nlm.nih.gov/pubmed/33149115 http://dx.doi.org/10.1038/s41467-020-19396-3 |
work_keys_str_mv | AT leepintse sigma1receptorchaperonesrescuenucleocytoplasmictransportdeficitseenincellularanddrosophilaalsftdmodels AT lievensjeancharles sigma1receptorchaperonesrescuenucleocytoplasmictransportdeficitseenincellularanddrosophilaalsftdmodels AT wangshaoming sigma1receptorchaperonesrescuenucleocytoplasmictransportdeficitseenincellularanddrosophilaalsftdmodels AT chuangjianying sigma1receptorchaperonesrescuenucleocytoplasmictransportdeficitseenincellularanddrosophilaalsftdmodels AT khalilbilal sigma1receptorchaperonesrescuenucleocytoplasmictransportdeficitseenincellularanddrosophilaalsftdmodels AT wuhsiangen sigma1receptorchaperonesrescuenucleocytoplasmictransportdeficitseenincellularanddrosophilaalsftdmodels AT changwenchang sigma1receptorchaperonesrescuenucleocytoplasmictransportdeficitseenincellularanddrosophilaalsftdmodels AT mauricetangui sigma1receptorchaperonesrescuenucleocytoplasmictransportdeficitseenincellularanddrosophilaalsftdmodels AT sutsungping sigma1receptorchaperonesrescuenucleocytoplasmictransportdeficitseenincellularanddrosophilaalsftdmodels |