A transient increase of HIF-1α during the G1 phase (G1-HIF) ensures cell survival under nutritional stress

Cell Death Dis. 2023 Jul 27;14(7):477. doi: 10.1038/s41419-023-06012-7.

Abstract

The family of hypoxia-inducible transcription factors (HIF) is activated to adapt cells to low oxygen conditions, but is also known to regulate some biological processes under normoxic conditions. Here we show that HIF-1α protein levels transiently increase during the G1 phase of the cell cycle (designated as G1-HIF) in an AMP-activated protein kinase (AMPK)-dependent manner. The transient elimination of G1-HIF by a degron system revealed its contribution to cell survival under unfavorable metabolic conditions. Indeed, G1-HIF plays a key role in the cell cycle-dependent expression of genes encoding metabolic regulators and the maintenance of mTOR activity under conditions of nutrient deprivation. Accordingly, transient elimination of G1-HIF led to a significant reduction in the concentration of key proteinogenic amino acids and carbohydrates. These data indicate that G1-HIF acts as a cell cycle-dependent surveillance factor that prevents the onset of starvation-induced apoptosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis* / genetics
  • Cell Cycle / genetics
  • Cell Hypoxia / physiology
  • Cell Survival / genetics
  • G1 Phase
  • Hypoxia-Inducible Factor 1, alpha Subunit* / genetics

Substances

  • Hypoxia-Inducible Factor 1, alpha Subunit