Detalle de: USP-48 enables insulin-mediated longevity and modulates the mitochondrial stress response
| Title | USP-48 enables insulin-mediated longevity and modulates the mitochondrial stress response |
| Abstract |
The mitochondrial prohibitin (PHB) complex is essential for mitochondrial homeostasis, yet its depletion produces opposite effects on lifespan: shortening it in wild-type C. elegans but extending it in insulin/IGF-1 receptor daf-2 mutants, which show an attenuated mitochondrial unfolded protein response (UPR mt ). To identify regulators of this differential stress response and its role in aging, we conducted the first genome-wide double-RNAi screen in C. elegans. We identify the ubiquitin-specific peptidase USP-48 as a modulator of the UPR mt , specially required for lifespan extension under reduced insulin signaling. USP-48 influences mitochondrial structure and function and cooperates with the transcription factor DVE-1 to regulate the UPR mt largely independent of activating transcription factor associated with stress-1 (ATFS-1). Tissue-specific analysis shows that USP-48 is required for lifespan primarily in the hypodermis, with a smaller germline contribution, but is dispensable in muscle and intestine. Mechanistically, USP-48 promotes histone H2B deubiquitination to shape stress-responsive transcription, revealing ubiquitination as a key determinant of metabolism-dependent longevity. |
| Apa Reference | Gordillo-García, S., Fernandez-Abascal, J., Hernando-Rodríguez, B., Rodríguez-Palero, M.J., Cantalejo-Carrasco, L., Jarit-Cabanillas, A., Martínez-Bueno, M.D., Pérez-Jiménez, M.M., Clavijo-Bernal, E.J., Cambón, A., Cases, I., Eder, M. & Artal-Sanz, M. (2026). USP-48 enables insulin-mediated longevity and modulates the mitochondrial stress response. Cell Reports, 45(10), 118067. 10.1016/j.celrep.2026.118067 |
| Doi | 10.1016/j.celrep.2026.118067 |
| Publication Date | Oct 2026 |
| Publication Type | Article |
| Ontology | Model organisms, Genomics, Regulatory biology, Mutation Analysis and design, Structure-function relationship, Histone structure and regulation |
| Researchers | Ildefonso Cases |
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