Mitochondria-Targeted DNA Repair Glycosylase hOGG1 Protects Against HFD-Induced Liver Oxidative Mitochondrial DNA Damage and Insulin Resistance in OGG1-Deficient Mice

Int J Mol Sci. 2024 Nov 13;25(22):12168. doi: 10.3390/ijms252212168.

Abstract

8-oxoguanine DNA glycosylase-1 (OGG1) is a DNA glycosylase mediating the first step in base excision repair which removes 7,8-dihydro-8-oxoguanine (8-oxoG) and repairs oxidized nuclear and mitochondrial DNA. Previous studies showed that OGG1 deficiency results in an increased susceptibility to high-fat diet (HFD)-induced obesity and metabolic dysfunction in mice, suggesting a crucial role of OGG1 in metabolism. However, the tissue-specific mechanisms of how OGG1 deficiency leads to insulin resistance is unknown. Thus, in the current study, we used a hyperinsulinemic-euglycemic clamp to evaluate in-depth glucose metabolism in male wild-type (WT) mice and Ogg1-/- (Ogg1-KO) mice fed an HFD. Ogg1-KO mice fed HFD were more obese, with significantly lower hepatic insulin action compared to WT/HFD mice. Targeting human OGG1 to mitochondria protected against HFD-induced obesity, insulin resistance, oxidative mitochondrial DNA damage in the liver and showed decreased expression of liver gluconeogenic genes in Ogg1-KO mice, suggesting a putative protective mechanism. Additionally, several subunits of oxidative phosphorylation protein levels were noticeably increased in Ogg1-KO/Tg compared to Ogg1-KO mice fed an HFD which was associated with improved insulin signaling. Our findings demonstrate the crucial role of mitochondrial hOGG1 in HFD-induced insulin resistance and propose several protective mechanisms which can further direct the development of therapeutic treatment.

Keywords: DNA methylation; Ogg1; gluconeogenesis; high-fat diet; insulin resistance; liver; mitochondrial DNA damage; obesity.

MeSH terms

  • Animals
  • DNA Damage*
  • DNA Glycosylases* / deficiency
  • DNA Glycosylases* / genetics
  • DNA Glycosylases* / metabolism
  • DNA Repair
  • DNA, Mitochondrial* / genetics
  • DNA, Mitochondrial* / metabolism
  • Diet, High-Fat* / adverse effects
  • Humans
  • Insulin Resistance* / genetics
  • Liver* / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout*
  • Mitochondria / metabolism
  • Obesity / etiology
  • Obesity / genetics
  • Obesity / metabolism
  • Oxidative Stress

Substances

  • DNA Glycosylases
  • Ogg1 protein, mouse
  • DNA, Mitochondrial
  • oxoguanine glycosylase 1, human