SCF/β-TrCP Promotes Glycogen Synthase Kinase 3-Dependent Degradation of the Nrf2 Transcription Factor in a Keap1-Independent Manner
Biomedical Research Networking Center on Neurodegenerative Diseases · Instituto de Investigaciones Biomédicas Sols-Morreale · +3 more institutions
Abstract
Regulation of transcription factor Nrf2 (NF-E2-related factor 2) involves redox-sensitive proteasomal degradation via the E3 ubiquitin ligase Keap1/Cul3. However, Nrf2 is controlled by other mechanisms that have not yet been elucidated. We now show that glycogen synthase kinase 3 (GSK-3) phosphorylates a group of Ser residues in the Neh6 domain of mouse Nrf2 that overlap with an SCF/β-TrCP destruction motif (DSGIS, residues 334 to 338) and promotes its degradation in a Keap1-independent manner. Nrf2 was stabilized by GSK-3 inhibitors in Keap1-null mouse embryo fibroblasts. Similarly, an Nrf2(ΔETGE) mutant, which cannot be degraded via Keap1, accumulated when GSK-3 activity was blocked. Phosphorylation of a Ser…
Citation impact
- FWCI
- 11.71
- Percentile
- 100%
- References
- 55
Authors
6- PRPatricia Rada
Biomedical Research Networking Center on Neurodegenerative Diseases, Instituto de Investigaciones Biomédicas Sols-Morreale, Universidad Autónoma de Madrid
- AIAna I. Rojo
Biomedical Research Networking Center on Neurodegenerative Diseases, Instituto de Investigaciones Biomédicas Sols-Morreale, Universidad Autónoma de Madrid
- SCSudhir Chowdhry
University of Dundee, Ninewells Hospital
- MMMichael McMahon
University of Dundee, Ninewells Hospital
- JDJohn D. Hayes
University of Dundee, Ninewells Hospital
Topics & keywords
- Ubiquitin ligase
- GSK-3
- Ubiquitin
- KEAP1
- Phosphorylation
- Biology
- Transcription factor
- GSK3B