Abstract
Ubiquitin C-terminal hydrolase L1 (UCHL1) is a component of the ubiquitin-proteasome system (UPS) linked to neurodegeneration. Despite its exceptionally high abundance in neurons, UCHL1's precise role remains unclear. This review critically examines the proposed functions of UCHL1 and the challenges to understanding its role in neuronal cells. While UCHL1 hydrolyzes small adducts from the C-terminus of ubiquitin, its occluded active site limits the range of possible substrates and restricts its activity as an efficient deubiquitinase (DUB). These constraints, alongside the paucity of identified substrates, challenge the centrality of this proposed role. We also explore the potential of UCHL1 acting as a ubiquitin ligase and its nonenzymatic role in stabilizing mono-ubiquitin by preventing its lysosomal degradation. By highlighting the unresolved complexities surrounding UCHL1, this perspective proposes several approaches to elucidate UCHL1's significance in the brain.
Original language | Danish |
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Journal | BioEssays |
DOIs | |
State | Accepted/In press - 2025 |
Keywords
- Alzheimer's disease
- deubiquitinases
- neurodegeneration
- proteostasis
- ubiquitin
- ubiquitin ligases
All Science Journal Classification (ASJC) codes
- General Biochemistry,Genetics and Molecular Biology