TP53/p53-FBXO22-TFEB controls basal autophagy to govern hormesis

Autophagy. 2021 Nov;17(11):3776-3793. doi: 10.1080/15548627.2021.1897961. Epub 2021 Mar 11.

Abstract

Preconditioning with a mild stressor such as fasting is a promising way to reduce severe side effects from subsequent chemo- or radiotherapy. However, the underlying mechanisms have been largely unexplored. Here, we demonstrate that the TP53/p53-FBXO22-TFEB (transcription factor EB) axis plays an essential role in this process through upregulating basal macroautophagy/autophagy. Mild stress-activated TP53 transcriptionally induced FBXO22, which in turn ubiquitinated KDM4B (lysine-specific demethylase 4B) complexed with MYC-NCOR1 suppressors for degradation, leading to transcriptional induction of TFEB. Upregulation of autophagy-related genes by increased TFEB dramatically enhanced autophagic activity and cell survival upon following a severe stressor. Mitogen-induced AKT1 activation counteracted this process through the phosphorylation of KDM4B, which inhibited FBXO22-mediated ubiquitination. Additionally, fbxo22-/- mice died within 10 h of birth, and their mouse embryonic fibroblasts (MEFs) showed a lowered basal autophagy, whereas FBXO22-overexpressing mice were resistant to chemotherapy. Taken together, these results suggest that TP53 upregulates basal autophagy through the FBXO22-TFEB axis, which governs the hormetic effect in chemotherapy.Abbreviations: BBC3/PUMA: BCL2 binding component 3; CDKN1A/p21: cyclin dependent kinase inhibitor 1A; ChIP-seq: chromatin immunoprecipitation followed by sequencing; DDB2: damage specific DNA binding protein 2; DRAM: DNA damage regulated autophagy modulator; ESR/ER: estrogen receptor 1; FMD: fasting mimicking diet; HCQ: hydroxychloroquine; KDM4B: lysine-specific demethylase 4B; MAP1LC3/LC3: microtubule associated protein 1 light chain 3 alpha; MEFs: mouse embryonic fibroblasts; MTOR: mechanistic target of rapamycin kinase; NCOR1: nuclear receptor corepressor 1; SCF: SKP1-CUL-F-box protein; SQSTM1: sequestosome 1; TFEB: transcription factor EB.

Keywords: AKT1; FBXO22; KDM4B; MYC; TP53; autophagy; hormesis; ubiquitination.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autophagy*
  • Basic Helix-Loop-Helix Leucine Zipper Transcription Factors / metabolism*
  • Basic Helix-Loop-Helix Leucine Zipper Transcription Factors / physiology
  • Cells, Cultured
  • F-Box Proteins / metabolism*
  • F-Box Proteins / physiology
  • Female
  • Fibroblasts / metabolism
  • Hormesis*
  • Humans
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Receptors, Cytoplasmic and Nuclear / metabolism*
  • Receptors, Cytoplasmic and Nuclear / physiology
  • Tumor Suppressor Protein p53 / metabolism*
  • Tumor Suppressor Protein p53 / physiology
  • Ubiquitination

Substances

  • Basic Helix-Loop-Helix Leucine Zipper Transcription Factors
  • F-Box Proteins
  • FBXO22 protein, human
  • Receptors, Cytoplasmic and Nuclear
  • TFEB protein, human
  • TP53 protein, human
  • Tumor Suppressor Protein p53

Grants and funding

This work was supported by the Japan Agency for Medical Research and Development [16ck0106085h0003]; Japan Agency for Medical Research and Development [JP17gm5010001]; Japan Agency for Medical Research and Development [JP17fk0310111]; Japan Agency for Medical Research and Development [JP17cm0106122]; Japan Society for the Promotion of Science [JP16K15239]; Japan Society for the Promotion of Science [17K08676]; Japan Society for the Promotion of Science [JP26250027]; Japan Society for the Promotion of Science [JP22118003]; Japan Society for the Promotion of Science [JP24112005]; Japan Society for the Promotion of Science [17H03585]; Japan Society for the Promotion of Science [JP18H05026m]; Japan Society for the Promotion of Science [JP16H06148]; Japan Society for the Promotion of Science [JP16K15238]; Ono Medical Research Foundation; RELAY FOR LIFE JAPAN CANCER SOCIETY; Princess Takamatsu Cancer Research Fund.