Literature DB >> 27261364

Acetylation and succinylation contribute to maturational alterations in energy metabolism in the newborn heart.

Arata Fukushima1, Osama Abo Alrob2, Liyan Zhang1, Cory S Wagg1, Tariq Altamimi1, Sonia Rawat1, Ivan M Rebeyka1, Paul F Kantor1, Gary D Lopaschuk3.   

Abstract

Dramatic maturational changes in cardiac energy metabolism occur in the newborn period, with a shift from glycolysis to fatty acid oxidation. Acetylation and succinylation of lysyl residues are novel posttranslational modifications involved in the control of cardiac energy metabolism. We investigated the impact of changes in protein acetylation/succinylation on the maturational changes in energy metabolism of 1-, 7-, and 21-day-old rabbit hearts. Cardiac fatty acid β-oxidation rates increased in 21-day vs. 1- and 7-day-old hearts, whereas glycolysis and glucose oxidation rates decreased in 21-day-old hearts. The fatty acid oxidation enzymes, long-chain acyl-CoA dehydrogenase (LCAD) and β-hydroxyacyl-CoA dehydrogenase (β-HAD), were hyperacetylated with maturation, positively correlated with their activities and fatty acid β-oxidation rates. This alteration was associated with increased expression of the mitochondrial acetyltransferase, general control of amino acid synthesis 5 like 1 (GCN5L1), since silencing GCN5L1 mRNA in H9c2 cells significantly reduced acetylation and activity of LCAD and β-HAD. An increase in mitochondrial ATP production rates with maturation was associated with the decreased acetylation of peroxisome proliferator-activated receptor-γ coactivator-1α, a transcriptional regulator for mitochondrial biogenesis. In addition, hypoxia-inducible factor-1α, hexokinase, and phosphoglycerate mutase expression declined postbirth, whereas acetylation of these glycolytic enzymes increased. Phosphorylation rather than acetylation of pyruvate dehydrogenase (PDH) increased in 21-day-old hearts, accounting for the low glucose oxidation postbirth. A maturational increase was also observed in succinylation of PDH and LCAD. Collectively, our data are the first suggesting that acetylation and succinylation of the key metabolic enzymes in newborn hearts play a crucial role in cardiac energy metabolism with maturation.
Copyright © 2016 the American Physiological Society.

Entities:  

Keywords:  lysine acetylation; lysine succinylation; myocardial fatty acid oxidation; newborn heart

Mesh:

Substances:

Year:  2016        PMID: 27261364     DOI: 10.1152/ajpheart.00900.2015

Source DB:  PubMed          Journal:  Am J Physiol Heart Circ Physiol        ISSN: 0363-6135            Impact factor:   4.733


  33 in total

1.  Cardiac-specific deletion of GCN5L1 restricts recovery from ischemia-reperfusion injury.

Authors:  Janet R Manning; Dharendra Thapa; Manling Zhang; Michael W Stoner; Javier Traba; Charles F McTiernan; Catherine Corey; Sruti Shiva; Michael N Sack; Iain Scott
Journal:  J Mol Cell Cardiol       Date:  2019-02-15       Impact factor: 5.000

2.  Acetylation of mitochondrial proteins by GCN5L1 promotes enhanced fatty acid oxidation in the heart.

Authors:  Dharendra Thapa; Manling Zhang; Janet R Manning; Danielle A Guimarães; Michael W Stoner; Robert M O'Doherty; Sruti Shiva; Iain Scott
Journal:  Am J Physiol Heart Circ Physiol       Date:  2017-05-19       Impact factor: 4.733

3.  Dual peroxisome-proliferator-activated-receptor-α/γ activation inhibits SIRT1-PGC1α axis and causes cardiac dysfunction.

Authors:  Charikleia Kalliora; Ioannis D Kyriazis; Shin-Ichi Oka; Melissa J Lieu; Yujia Yue; Estela Area-Gomez; Christine J Pol; Ying Tian; Wataru Mizushima; Adave Chin; Diego Scerbo; P Christian Schulze; Mete Civelek; Junichi Sadoshima; Muniswamy Madesh; Ira J Goldberg; Konstantinos Drosatos
Journal:  JCI Insight       Date:  2019-08-08

4.  Adropin treatment restores cardiac glucose oxidation in pre-diabetic obese mice.

Authors:  Dharendra Thapa; Bingxian Xie; Manling Zhang; Michael W Stoner; Janet R Manning; Brydie R Huckestein; Lia R Edmunds; Steven J Mullett; Charles F McTiernan; Stacy G Wendell; Michael J Jurczak; Iain Scott
Journal:  J Mol Cell Cardiol       Date:  2019-02-26       Impact factor: 5.000

Review 5.  Succinylation Links Metabolism to Protein Functions.

Authors:  Yun Yang; Gary E Gibson
Journal:  Neurochem Res       Date:  2019-03-22       Impact factor: 3.996

6.  Acetylation contributes to hypertrophy-caused maturational delay of cardiac energy metabolism.

Authors:  Arata Fukushima; Liyan Zhang; Alda Huqi; Victoria H Lam; Sonia Rawat; Tariq Altamimi; Cory S Wagg; Khushmol K Dhaliwal; Lisa K Hornberger; Paul F Kantor; Ivan M Rebeyka; Gary D Lopaschuk
Journal:  JCI Insight       Date:  2018-05-17

Review 7.  Mechanisms of transcription factor acetylation and consequences in hearts.

Authors:  Devi Thiagarajan; Srinivasan Vedantham; Radha Ananthakrishnan; Ann Marie Schmidt; Ravichandran Ramasamy
Journal:  Biochim Biophys Acta       Date:  2016-08-17

8.  GCN5L1 interacts with αTAT1 and RanBP2 to regulate hepatic α-tubulin acetylation and lysosome trafficking.

Authors:  Kaiyuan Wu; Lingdi Wang; Yong Chen; Mehdi Pirooznia; Komudi Singh; Sarah Wälde; Ralph H Kehlenbach; Iain Scott; Marjan Gucek; Michael N Sack
Journal:  J Cell Sci       Date:  2018-11-20       Impact factor: 5.285

Review 9.  GCN5L1/BLOS1 Links Acetylation, Organelle Remodeling, and Metabolism.

Authors:  Iain Scott; Lingdi Wang; Kaiyuan Wu; Dharendra Thapa; Michael N Sack
Journal:  Trends Cell Biol       Date:  2018-02-21       Impact factor: 20.808

10.  miR-21-5p regulates mitochondrial respiration and lipid content in H9C2 cells.

Authors:  Victoria L Nasci; Sandra Chuppa; Lindsey Griswold; Kathryn A Goodreau; Ranjan K Dash; Alison J Kriegel
Journal:  Am J Physiol Heart Circ Physiol       Date:  2019-01-18       Impact factor: 4.733

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