The autism-linked UBE3A T485A mutant E3 ubiquitin ligase activates the Wnt/β-catenin pathway by inhibiting the proteasome
| Autor: | Matthew P. Walker, Justin M. Wolter, Michael B. Major, Michael J. Emanuele, Mark J. Zylka, Jason J. Yi, Smita R. Paranjape, Rajarshi Choudhury, Giulia Fragola |
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| Rok vydání: | 2017 |
| Předmět: |
0301 basic medicine
HECT domain Proteasome Endopeptidase Complex congenital hereditary and neonatal diseases and abnormalities Ubiquitin-Protein Ligases Biology Biochemistry 03 medical and health sciences Neurobiology Humans Autistic Disorder Wnt Signaling Pathway Molecular Biology beta Catenin Wnt signaling pathway LRP6 LRP5 Cell Biology Ubiquitin ligase HEK293 Cells 030104 developmental biology Proteasome Catenin Mutation biology.protein Cancer research Phosphorylation Proteasome Inhibitors |
| Zdroj: | Journal of Biological Chemistry. 292:12503-12515 |
| ISSN: | 0021-9258 |
| Popis: | UBE3A is a HECT domain E3 ubiquitin ligase whose dysfunction is linked to autism, Angelman syndrome, and cancer. Recently, we characterized a de novo autism-linked UBE3A mutant (UBE3AT485A) that disrupts phosphorylation control of UBE3A activity. Through quantitative proteomics and reporter assays, we found that the UBE3AT485A protein ubiquitinates multiple proteasome subunits, reduces proteasome subunit abundance and activity, stabilizes nuclear β-catenin, and stimulates canonical Wnt signaling more effectively than wild-type UBE3A. We also found that UBE3AT485A activates Wnt signaling to a greater extent in cells with low levels of ongoing Wnt signaling, suggesting that cells with low basal Wnt activity are particularly vulnerable to UBE3AT485A mutation. Ligase-dead UBE3A did not stimulate Wnt pathway activation. Overexpression of several proteasome subunits reversed the effect of UBE3AT485A on Wnt signaling. We also observed that subunits that interact with UBE3A and affect Wnt signaling are located along one side of the 19S regulatory particle, indicating a previously unrecognized spatial organization to the proteasome. Altogether, our findings indicate that UBE3A regulates Wnt signaling in a cell context-dependent manner and that an autism-linked mutation exacerbates these signaling effects. Our study has broad implications for human disorders associated with UBE3A gain or loss of function and suggests that dysfunctional UBE3A might affect additional proteins and pathways that are sensitive to proteasome activity. |
| Databáze: | OpenAIRE |
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