Loss of RNA-binding protein GRSF1 activates mTOR to elicit a proinflammatory transcriptional program

Nucleic Acids Res. 2019 Mar 18;47(5):2472-2486. doi: 10.1093/nar/gkz082.

Abstract

The RNA-binding protein GRSF1 (G-rich RNA sequence-binding factor 1) critically maintains mitochondrial homeostasis. Accordingly, loss of GRSF1 impaired mitochondrial respiration and increased the levels of reactive oxygen species (ROS), triggering DNA damage, growth suppression, and a senescent phenotype characterized by elevated production and secretion of interleukin (IL)6. Here, we characterize the pathways that govern IL6 production in response to mitochondrial dysfunction in GRSF1-depleted cells. We report that loss of GRSF1 broadly altered protein expression programs, impairing the function of respiratory complexes I and IV. The rise in oxidative stress led to increased DNA damage and activation of mTOR, which in turn activated NF-κB to induce IL6 gene transcription and orchestrate a pro-inflammatory program. Collectively, our results indicate that GRSF1 helps preserve mitochondrial homeostasis, in turn preventing oxidative DNA damage and the activation of mTOR and NF-κB, and suppressing a transcriptional pro-inflammatory program leading to increased IL6 production.

Publication types

  • Research Support, N.I.H., Intramural

MeSH terms

  • DNA Damage / genetics
  • Electron Transport Complex I / genetics
  • Gene Expression Regulation / genetics
  • Humans
  • Inflammation / genetics*
  • Inflammation / pathology
  • Interleukin-6 / genetics*
  • Mitochondria / genetics
  • Mitochondria / metabolism
  • NF-kappa B / genetics
  • Oxidative Stress / genetics
  • Poly(A)-Binding Proteins / genetics*
  • RNA-Binding Proteins / genetics
  • Reactive Oxygen Species / metabolism
  • Signal Transduction / genetics
  • TOR Serine-Threonine Kinases / genetics*
  • Transcription, Genetic

Substances

  • GRSF1 protein, human
  • Interleukin-6
  • NF-kappa B
  • Poly(A)-Binding Proteins
  • RNA-Binding Proteins
  • Reactive Oxygen Species
  • MTOR protein, human
  • TOR Serine-Threonine Kinases
  • Electron Transport Complex I