Sahu AK, Minetti A, Di Fraia D, Marino A, Winterhalter PR, Giustarini D, Rossi R, Simm A, Neri F, Galvagni F, Gerhardt C, Pfirrmann T, Ori A (2026)
Publication Type: Journal article
Publication year: 2026
Book Volume: 17
Article Number: 3653
Journal Issue: 1
DOI: 10.1038/s41467-026-71921-y
The ubiquitin–proteasome system is essential for neuronal proteostasis, yet its function declines with age. How aging affects deubiquitylating enzymes (DUBs) in the vertebrate brain remains unclear. Here we used activity-based proteomics to profile cysteine protease DUBs in aging mouse and killifish brains. We identified a subset of DUBs that progressively lose catalytic activity with age despite stable protein abundance. Mechanistically, oxidative stress impaired DUB function through thiol oxidation, whereas antioxidant treatment with N-acetylcysteine ethyl ester (NACET) restored activity in aging brains. In human iPSC-derived neurons, global DUB inhibition and targeted inhibition of USP7, one of the most strongly age-affected DUBs, partially recapitulated ubiquitylation changes observed in aged brains. Temporal analysis in mice further revealed that DUB inhibition precedes proteasome decline during brain aging. Together, these findings identify redox-sensitive DUBs that lose activity with age and suggest impaired deubiquitylation as an early, potentially reversible driver of proteostasis decline in the aging brain.
APA:
Sahu, A.K., Minetti, A., Di Fraia, D., Marino, A., Winterhalter, P.R., Giustarini, D.,... Ori, A. (2026). Oxidative stress causes a reversible decrease of deubiquitylases activity in old vertebrate brains. Nature Communications, 17(1). https://doi.org/10.1038/s41467-026-71921-y
MLA:
Sahu, Amit Kumar, et al. "Oxidative stress causes a reversible decrease of deubiquitylases activity in old vertebrate brains." Nature Communications 17.1 (2026).
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