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Oxidation of SQSTM1/p62 mediates the link between redox state and protein homeostasis.

Bernadette Carroll | Elsje G Otten | Diego Manni | Rhoda Stefanatos | Fiona M Menzies | Graham R Smith | Diana Jurk | Niall Kenneth | Simon Wilkinson | Joao F Passos | Johannes Attems | Elizabeth A Veal | Elisa Teyssou | Danielle Seilhean | Stéphanie Millecamps | Eeva-Liisa Eskelinen | Agnieszka K Bronowska | David C Rubinsztein | Alberto Sanz | Viktor I Korolchuk
Nature communications | 2018

Cellular homoeostatic pathways such as macroautophagy (hereinafter autophagy) are regulated by basic mechanisms that are conserved throughout the eukaryotic kingdom. However, it remains poorly understood how these mechanisms further evolved in higher organisms. Here we describe a modification in the autophagy pathway in vertebrates, which promotes its activity in response to oxidative stress. We have identified two oxidation-sensitive cysteine residues in a prototypic autophagy receptor SQSTM1/p62, which allow activation of pro-survival autophagy in stress conditions. The Drosophila p62 homologue, Ref(2)P, lacks these oxidation-sensitive cysteine residues and their introduction into the protein increases protein turnover and stress resistance of flies, whereas perturbation of p62 oxidation in humans may result in age-related pathology. We propose that the redox-sensitivity of p62 may have evolved in vertebrates as a mechanism that allows activation of autophagy in response to oxidative stress to maintain cellular homoeostasis and increase cell survival.

Pubmed ID: 29343728

Associated grants

  • Agency: Biotechnology and Biological Sciences Research Council, United Kingdom
    Id: BB/H022384/1
  • Agency: Medical Research Council, United Kingdom
    Id: MR/L016354/1
  • Agency: Medical Research Council, United Kingdom
    Id: G1100540
  • Agency: Medical Research Council, United Kingdom
    Id: G0900652
  • Agency: Cancer Research UK, United Kingdom
    Id: 12825
  • Agency: Medical Research Council, United Kingdom
    Id: G0400074
  • Agency: Medical Research Council, United Kingdom
    Id: G0502157

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