The protein acetylase GCN5L1 modulates hepatic fatty acid oxidation activity via acetylation of the mitochondrial β-oxidation enzyme HADHA

J Biol Chem. 2018 Nov 16;293(46):17676-17684. doi: 10.1074/jbc.AC118.005462. Epub 2018 Oct 15.

Abstract

Sirtuin 3 (SIRT3) deacetylates and activates several mitochondrial fatty acid oxidation enzymes in the liver. Here, we investigated whether the protein acetylase GCN5 general control of amino acid synthesis 5-like 1 (GCN5L1), previously shown to oppose SIRT3 activity, is involved in the regulation of hepatic fatty acid oxidation. We show that GCN5L1 abundance is significantly up-regulated in response to an acute high-fat diet (HFD). Transgenic GCN5L1 overexpression in the mouse liver increased protein acetylation levels, and proteomic detection of specific lysine residues identified numerous sites that are co-regulated by GCN5L1 and SIRT3. We analyzed several fatty acid oxidation proteins identified by the proteomic screen and found that hyperacetylation of hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit α (HADHA) correlates with increased GCN5L1 levels. Stable GCN5L1 knockdown in HepG2 cells reduced HADHA acetylation and increased activities of fatty acid oxidation enzymes. Mice with a liver-specific deletion of GCN5L1 were protected from hepatic lipid accumulation following a chronic HFD and did not exhibit hyperacetylation of HADHA compared with WT controls. Finally, we found that GCN5L1-knockout mice lack HADHA that is hyperacetylated at three specific lysine residues (Lys-350, Lys-383, and Lys-406) and that acetylation at these sites is significantly associated with increased HADHA activity. We conclude that GCN5L1-mediated regulation of mitochondrial protein acetylation plays a role in hepatic metabolic homeostasis.

Keywords: GCN5L1; HADHA; acetylation; fatty acid oxidation; lipid metabolism; liver metabolism; mitochondria; mitochondrial metabolism; post-translational modification (PTM).

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylation
  • Animals
  • Diet, High-Fat / adverse effects
  • Fatty Acids / metabolism*
  • Fatty Liver / prevention & control
  • Hep G2 Cells
  • Humans
  • Lysine / chemistry
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mitochondrial Proteins
  • Mitochondrial Trifunctional Protein, alpha Subunit / metabolism
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism*
  • Oxidation-Reduction
  • Protein Isoforms / metabolism
  • Protein Processing, Post-Translational
  • Proteomics
  • Sirtuin 3 / genetics

Substances

  • BLOC1S1 protein, human
  • BLOC1S1 protein, mouse
  • Fatty Acids
  • Mitochondrial Proteins
  • Nerve Tissue Proteins
  • Protein Isoforms
  • Sirt3 protein, mouse
  • Mitochondrial Trifunctional Protein, alpha Subunit
  • Sirtuin 3
  • Hadha protein, mouse
  • Lysine