AI Article Synopsis

  • p62/SQSTM1 is a protein that promotes liquid-liquid phase separation and is crucial for selective autophagy cargo isolation and the Keap1-Nrf2 oxidative stress response.
  • NBR1, a similar protein to p62/SQSTM1, influences the formation of p62 liquid droplets and assists in activating the Nrf2 pathway by preventing the autophagic degradation of p62.
  • NBR1 is elevated during oxidative stress, facilitating the activation of Nrf2 via p62, while the absence of NBR1 diminishes both liquid droplet formation and Nrf2 activation under these conditions.

Article Abstract

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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7054683PMC
http://dx.doi.org/10.15252/embr.201948902DOI Listing

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