Disruption of Acetyl-Lysine Turnover in Muscle Mitochondria Promotes Insulin Resistance and Redox Stress without Overt Respiratory Dysfunction

Cell Metab. 2020 Jan 7;31(1):131-147.e11. doi: 10.1016/j.cmet.2019.11.003. Epub 2019 Dec 5.

Abstract

This study sought to examine the functional significance of mitochondrial protein acetylation using a double knockout (DKO) mouse model harboring muscle-specific deficits in acetyl-CoA buffering and lysine deacetylation, due to genetic ablation of carnitine acetyltransferase and Sirtuin 3, respectively. DKO mice are highly susceptible to extreme hyperacetylation of the mitochondrial proteome and develop a more severe form of diet-induced insulin resistance than either single KO mouse line. However, the functional phenotype of hyperacetylated DKO mitochondria is largely normal. Of the >120 measures of respiratory function assayed, the most consistently observed traits of a markedly heightened acetyl-lysine landscape are enhanced oxygen flux in the context of fatty acid fuel and elevated rates of electron leak. In sum, the findings challenge the notion that lysine acetylation causes broad-ranging damage to mitochondrial quality and performance and raise the possibility that acetyl-lysine turnover, rather than acetyl-lysine stoichiometry, modulates redox balance and carbon flux.

Keywords: NAD biology; bioenergetics; diabetes; fat oxidation; fatty acid oxidation; insulin action; lysine acetylation; mitochondria; muscle; nutrition; obesity; proteomics; reactive oxygen species; redox; respiration; sirtuins.

Publication types

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

MeSH terms

  • Acetyl Coenzyme A / metabolism
  • Acetylation
  • Animals
  • Carnitine O-Acetyltransferase / genetics*
  • Carnitine O-Acetyltransferase / metabolism
  • Creatine Kinase / metabolism
  • Diet, High-Fat
  • Energy Metabolism / genetics
  • Homeostasis
  • Hydrogen Peroxide / metabolism
  • Insulin / blood
  • Insulin Resistance / genetics*
  • Lysine / analogs & derivatives
  • Lysine / metabolism*
  • Male
  • Membrane Potential, Mitochondrial / genetics
  • Membrane Potential, Mitochondrial / physiology
  • Mice
  • Mice, Knockout
  • Mitochondria, Muscle / genetics
  • Mitochondria, Muscle / metabolism*
  • Mitochondrial Proteins / genetics
  • Mitochondrial Proteins / metabolism*
  • Oxidation-Reduction
  • Oxidative Stress / genetics*
  • Proteome / genetics
  • Proteome / metabolism
  • Sirtuin 3 / genetics*
  • Sirtuin 3 / metabolism
  • Thermodynamics

Substances

  • Insulin
  • Mitochondrial Proteins
  • Proteome
  • Sirt3 protein, mouse
  • Acetyl Coenzyme A
  • Hydrogen Peroxide
  • Carnitine O-Acetyltransferase
  • Creatine Kinase
  • Sirtuin 3
  • Lysine