NBR 1‐mediated p62‐liquid droplets enhance the Keap1‐Nrf2 system
| Autor: | Masaaki Komatsu, Masato Koike, Pablo Sánchez-Martín, Satoshi Waguri, Yu-shin Sou, Shun Kageyama |
|---|---|
| Rok vydání: | 2020 |
| Předmět: |
NF-E2-Related Factor 2
medicine.disease_cause environment and public health Biochemistry Nrf2 activation Selective autophagy Mice 03 medical and health sciences 0302 clinical medicine Sequestosome-1 Protein Autophagy Genetics medicine Animals Receptor Molecular Biology 030304 developmental biology 0303 health sciences Kelch-Like ECH-Associated Protein 1 Chemistry Articles respiratory system Keap1 nrf2 Cell biology Selective degradation Phosphorylation 030217 neurology & neurosurgery Oxidative stress Signal Transduction |
| Zdroj: | EMBO Rep |
| ISSN: | 1469-3178 1469-221X |
| DOI: | 10.15252/embr.201948902 |
| Popis: | p62/SQSTM1 is a multivalent protein that has the ability to cause liquid–liquid phase separation and serves as a receptor protein that participates in cargo isolation during selective autophagy. This protein is also involved in the non‐canonical activation of the Keap1‐Nrf2 system, a major oxidative stress response pathway. Here, we show a role of neighbor of BRCA1 gene 1 (NBR1), an autophagy receptor structurally similar to p62/SQSTM1, in p62‐liquid droplet formation and Keap1‐Nrf2 pathway activation. Overexpression of NBR1 blocks selective degradation of p62/SQSTM1 through autophagy and promotes the accumulation and phosphorylation of p62/SQSTM1 in liquid‐like bodies, which is required for the activation of Nrf2. NBR1 is induced in response to oxidative stress, which triggers p62‐mediated Nrf2 activation. Conversely, loss of Nbr1 suppresses not only the formation of p62/SQSTM1‐liquid droplets, but also of p62‐dependent Nrf2 activation during oxidative stress. Taken together, our results show that NBR1 mediates p62/SQSTM1‐liquid droplet formation to activate the Keap1‐Nrf2 pathway. |
| Databáze: | OpenAIRE |
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