Lysine post‐translational modification of glyceraldehyde‐3‐phosphate dehydrogenase regulates hepatic and systemic metabolism. Issue 6 (3rd March 2017)

• Record Type: Journal Article
• Authors: Bond, Simon T.; Howlett, Kirsten F.; Kowalski, Greg M.; Mason, Shaun; Connor, Timothy; Cooper, Adrian; Streltsov, Victor; Bruce, Clinton R.; Walder, Ken R.; McGee, Sean L.
• Is Part Of: FASEB journal. Volume 31:Issue 6(2017)
• Page Start: 2592
• Page End: 2602
• Publication Date: 2017-03-03
• Subjects: glycolysis -- gluconeogenesis -- liver metabolism -- ketones -- lysine acetylation; Biology -- Periodicals; Biology, Experimental -- Periodicals; 570
• DOI: 10.1096/fj.201601215R
• Languages: English
• ISSNs: 0892-6638

Abstract

ABSTRACT: Reciprocal regulation of hepatic glycolysis and gluconeogenesis contributes to systemic metabolic homeostasis. Recent evidence from lower order organisms has found that reversible post‐translational modification of glyceraldehyde‐3‐phosphate dehydrogenase (GAPDH), particularly acetylation, contributes to the reciprocal regulation of glycolysis/gluconeogenesis. However, whether this occurs in mammalian hepatocytes in vitro or in vivo is unknown. Several proteomics studies have identified 4 lysine residues in critical regions of mammalian GAPDH that are altered by multiple post‐translational modifications. In FAO hepatoma cells, mutation of all 4 lysine residues (4K‐R GAPDH) to mimic their unmodified state reduced GAPDH glycolytic activity and glycolytic flux and increased gluconeogenic GAPDH activity and glucose production. Hepatic expression of 4K‐R GAPDH in mice increased GAPDH gluconeogenic activity and the contribution of gluconeogenesis to endogenous glucose production in the unfed state. Consistent with the increased reliance on the energy‐consuming gluconeogenic pathway, plasma free fatty acids and ketones were elevated in mice expressing 4K‐R GAPDH, suggesting enhanced lipolysis and hepatic fatty acid oxidation. In normal mice, food withholding and refeeding, as well as hormonal regulators of reciprocal glycolysis/gluconeogenesis, such as insulin, glucagon, and norepinephrine, had no effect on global GAPDH acetylation. However, GAPDH acetylation was reduced in obese and type 2 diabetic db/db mice. These findings show that post‐translational modification of GAPDH lysine residues regulates hepatic and systemic metabolism, revealing an unappreciated role for hepatic GAPDH in substrate selection and utilization.—Bond, S. T., Howlett, K. F., Kowalski, G. M., Mason, S., Connor, T., Cooper, A., Streltsov, V., Bruce, C. R., Walder, K. R., McGee, S. L. Lysine post‐translational modification of glyceraldehyde‐3‐phosphate dehydrogenase regulates hepatic and systemic metabolism. FASEB J. 31, 2592–2602 (2017). www.fasebj.org