Lysine Methyltransferase SETD7 (SET7/9) Regulates ROS Signaling through mitochondria and NFE2L2/ARE pathway

Sci Rep. 2015 Oct 5:5:14368. doi: 10.1038/srep14368.

Abstract

Reactive oxygen species (ROS) homeostasis requires stringent regulation. ROS imbalance, especially ROS accumulation, has profound implications in various disease pathogenesis. Lysine methylation of histone and non-histone proteins has been implicated in various cellular responses. The main objective of this study is to investigate the role of SET domain containing lysine methyltransferase SETD7 (SET7/9) in the regulation of ROS-mediated signaling. Here we report that inhibition of SETD7 with siRNA or a SETD7 small molecule inhibitor in both macrophages and a human bronchial epithelial cell line (Beas-2B) were able to counter NF-ĸB-induced oxidative stress and pro-inflammatory cytokine production. Meanwhile, inhibition of SETD7 elevates mitochondria antioxidant functions via negative regulation of PPARGC1A and NFE2L2. Using a co-expression system and purified proteins, we detected direct interaction between SETD7 and NFE2L2. These results indicate that lysine methylation by SETD7 is important for the fine-tuning of ROS signaling through its regulation on pro-inflammatory responses, mitochondrial function and the NFE2L2/ARE pathway. Up-regulation of multiple antioxidant genes and improved ROS clearance by inhibition of SETD7 suggests the potential benefit of targeting SETD7 in treating ROS-associated diseases.

MeSH terms

  • Antioxidant Response Elements
  • Catalase / genetics
  • Catalase / metabolism
  • Cell Line
  • Cytokines / genetics
  • Cytokines / metabolism
  • Gene Expression
  • Gene Expression Regulation
  • Gene Knockdown Techniques
  • Histone-Lysine N-Methyltransferase / physiology*
  • Humans
  • Mitochondria / enzymology*
  • Mitochondrial Dynamics
  • NF-E2-Related Factor 2 / metabolism*
  • NF-kappa B / metabolism
  • Oxidative Stress
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
  • Reactive Oxygen Species / metabolism
  • Signal Transduction
  • Superoxide Dismutase / genetics
  • Superoxide Dismutase / metabolism
  • Transcription Factors / metabolism
  • Up-Regulation

Substances

  • Cytokines
  • NF-E2-Related Factor 2
  • NF-kappa B
  • NFE2L2 protein, human
  • PPARGC1A protein, human
  • Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
  • Reactive Oxygen Species
  • Transcription Factors
  • Catalase
  • Superoxide Dismutase
  • superoxide dismutase 2
  • Histone-Lysine N-Methyltransferase
  • SETD7 protein, human