Joaquim, Mariana
ORCID: 0000-0003-4669-4493, Altin, Selver, Bulimaga, Maria-Bianca
ORCID: 0000-0002-2050-6098, Simões, Tânia, Nolte, Hendrik
ORCID: 0000-0003-1560-5099, Bader, Verian
ORCID: 0000-0001-5260-4728, Franchino, Camilla Aurora
ORCID: 0009-0002-4502-6514, Plouzennec, Solenn, Szczepanowska, Karolina
ORCID: 0000-0003-4689-2350, Marchesan, Elena, Hofmann, Kay
ORCID: 0000-0002-2289-9083, Krüger, Marcus
ORCID: 0000-0002-5846-6941, Ziviani, Elena, Trifunovic, Aleksandra
ORCID: 0000-0002-5472-3517, Chevrollier, Arnaud, Winklhofer, Konstanze F.
ORCID: 0000-0002-7256-8231, Motori, Elisa
ORCID: 0000-0001-5997-6866, Odenthal, Margarete
ORCID: 0000-0002-2424-0960 and Escobar-Henriques, Mafalda
ORCID: 0000-0002-0879-3119
(2025).
Mitofusin 2 displays fusion-independent roles in proteostasis surveillance.
Nature Communications, 16 (1).
p. 1501.
Springer Nature.
ISSN 2041-1723
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PDF
s41467-025-56673-5.pdf Bereitstellung unter der CC-Lizenz: Creative Commons Attribution. Download (10MB) |
Abstract
Mitochondria are essential organelles and their functional state dictates cellular proteostasis. However, little is known about the molecular gatekeepers involved, especially in absence of external stress. Here we identify a role of MFN2 in quality control independent of its function in organellar shape remodeling. MFN2 ablation alters the cellular proteome, marked for example by decreased levels of the import machinery and accumulation of the kinase PINK1. Moreover, MFN2 interacts with the proteasome and cytosolic chaperones, thereby preventing aggregation of newly translated proteins. Similarly to MFN2-KO cells, patient fibroblasts with MFN2-disease variants recapitulate excessive protein aggregation defects. Restoring MFN2 levels re-establishes proteostasis in MFN2-KO cells and rescues fusion defects of MFN1-KO cells. In contrast, MFN1 loss or mitochondrial shape alterations do not alter protein aggregation, consistent with a fusion-independent role of MFN2 in cellular homeostasis. In sum, our findings open new possibilities for therapeutic strategies by modulation of MFN2 levels.
| Item Type: | Article |
| Creators: | Creators Email ORCID ORCID Put Code Altin, Selver UNSPECIFIED UNSPECIFIED UNSPECIFIED Simões, Tânia UNSPECIFIED UNSPECIFIED UNSPECIFIED Plouzennec, Solenn UNSPECIFIED UNSPECIFIED UNSPECIFIED Marchesan, Elena UNSPECIFIED UNSPECIFIED UNSPECIFIED Ziviani, Elena UNSPECIFIED UNSPECIFIED UNSPECIFIED Chevrollier, Arnaud UNSPECIFIED UNSPECIFIED UNSPECIFIED |
| URN: | urn:nbn:de:hbz:38-792310 |
| Identification Number: | 10.1038/s41467-025-56673-5 |
| Journal or Publication Title: | Nature Communications |
| Volume: | 16 |
| Number: | 1 |
| Page Range: | p. 1501 |
| Date: | 10 February 2025 |
| Publisher: | Springer Nature |
| ISSN: | 2041-1723 |
| Language: | English |
| Faculty: | Central Institutions / Interdisciplinary Research Centers External institution Faculty of Mathematics and Natural Sciences Faculty of Medicine |
| Divisions: | Außeruniversitäre Forschungseinrichtungen > MPI for Biology of Ageing CECAD - Cluster of Excellence Cellular Stress Responses in Aging-Associated Diseases Faculty of Mathematics and Natural Sciences > Department of Biology > Institute for Genetics Faculty of Medicine > Pathologie und Neuropathologie > Institut für Pathologie Zentrum für Molekulare Medizin |
| Subjects: | Life sciences Medical sciences Medicine |
| ['eprint_fieldname_oa_funders' not defined]: | Publikationsfonds UzK |
| Refereed: | Yes |
| URI: | http://kups.ub.uni-koeln.de/id/eprint/79231 |
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https://orcid.org/0000-0003-4669-4493