Skip to main content
bioRxiv
  • Home
  • About
  • Submit
  • ALERTS / RSS
Advanced Search
New Results

GPER-dependent estrogen signaling increases cardiac GCN5L1 expression and MCAD activity

Janet R. Manning, Dharendra Thapa, Manling Zhang, Michael W. Stoner, John C. Sembrat, Mauricio Rojas, Iain Scott
doi: https://doi.org/10.1101/2021.09.20.461099
Janet R. Manning
1Division of Cardiology, Department of Medicine, University of Pittsburgh, Pittsburgh, PA
2Vascular Medicine Institute, Department of Medicine, University of Pittsburgh, Pittsburgh, PA
3Center for Metabolism and Mitochondrial Medicine, Department of Medicine, University of Pittsburgh, Pittsburgh, PA
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • For correspondence: iain.scott@pitt.edu manningj@pitt.edu
Dharendra Thapa
1Division of Cardiology, Department of Medicine, University of Pittsburgh, Pittsburgh, PA
2Vascular Medicine Institute, Department of Medicine, University of Pittsburgh, Pittsburgh, PA
3Center for Metabolism and Mitochondrial Medicine, Department of Medicine, University of Pittsburgh, Pittsburgh, PA
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Manling Zhang
1Division of Cardiology, Department of Medicine, University of Pittsburgh, Pittsburgh, PA
2Vascular Medicine Institute, Department of Medicine, University of Pittsburgh, Pittsburgh, PA
3Center for Metabolism and Mitochondrial Medicine, Department of Medicine, University of Pittsburgh, Pittsburgh, PA
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Michael W. Stoner
1Division of Cardiology, Department of Medicine, University of Pittsburgh, Pittsburgh, PA
2Vascular Medicine Institute, Department of Medicine, University of Pittsburgh, Pittsburgh, PA
3Center for Metabolism and Mitochondrial Medicine, Department of Medicine, University of Pittsburgh, Pittsburgh, PA
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
John C. Sembrat
4Division of Pulmonary, Allergy, and Critical Care Medicine, Department of Medicine, University of Pittsburgh, Pittsburgh, PA
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Mauricio Rojas
5Division of Pulmonary, Critical Care and Sleep Medicine, Department of Medicine, The Ohio State University, Columbus, OH
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Iain Scott
1Division of Cardiology, Department of Medicine, University of Pittsburgh, Pittsburgh, PA
2Vascular Medicine Institute, Department of Medicine, University of Pittsburgh, Pittsburgh, PA
3Center for Metabolism and Mitochondrial Medicine, Department of Medicine, University of Pittsburgh, Pittsburgh, PA
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • For correspondence: iain.scott@pitt.edu manningj@pitt.edu
  • Abstract
  • Full Text
  • Info/History
  • Metrics
  • Preview PDF
Loading

ABSTRACT

Reversible lysine acetylation regulates the activity of cardiac metabolic enzymes, including those controlling fuel substrate metabolism. Mitochondrial-targeted GCN5L1 and SIRT3 have been shown to regulate the acetylation status of mitochondrial enzymes, which results in alterations to the relative oxidation rates of fatty acids, glucose, and other fuels for contractile activity. However, the role that lysine acetylation plays in driving metabolic differences between male and female hearts is not currently known. In this study, we report that estrogens induce the expression of GCN5L1 via GPER agonism in cardiac cells, which increases the enzymatic activity and acetylation status of the fatty acid oxidation enzyme medium chain acyl-CoA dehydrogenase (MCAD).

Competing Interest Statement

The authors have declared no competing interest.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. All rights reserved. No reuse allowed without permission.
Back to top
PreviousNext
Posted September 21, 2021.
Download PDF
Email

Thank you for your interest in spreading the word about bioRxiv.

NOTE: Your email address is requested solely to identify you as the sender of this article.

Enter multiple addresses on separate lines or separate them with commas.
GPER-dependent estrogen signaling increases cardiac GCN5L1 expression and MCAD activity
(Your Name) has forwarded a page to you from bioRxiv
(Your Name) thought you would like to see this page from the bioRxiv website.
CAPTCHA
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.
Share
GPER-dependent estrogen signaling increases cardiac GCN5L1 expression and MCAD activity
Janet R. Manning, Dharendra Thapa, Manling Zhang, Michael W. Stoner, John C. Sembrat, Mauricio Rojas, Iain Scott
bioRxiv 2021.09.20.461099; doi: https://doi.org/10.1101/2021.09.20.461099
Reddit logo Twitter logo Facebook logo LinkedIn logo Mendeley logo
Citation Tools
GPER-dependent estrogen signaling increases cardiac GCN5L1 expression and MCAD activity
Janet R. Manning, Dharendra Thapa, Manling Zhang, Michael W. Stoner, John C. Sembrat, Mauricio Rojas, Iain Scott
bioRxiv 2021.09.20.461099; doi: https://doi.org/10.1101/2021.09.20.461099

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
  • Tweet Widget
  • Facebook Like
  • Google Plus One

Subject Area

  • Physiology
Subject Areas
All Articles
  • Animal Behavior and Cognition (4394)
  • Biochemistry (9612)
  • Bioengineering (7109)
  • Bioinformatics (24911)
  • Biophysics (12641)
  • Cancer Biology (9977)
  • Cell Biology (14375)
  • Clinical Trials (138)
  • Developmental Biology (7966)
  • Ecology (12131)
  • Epidemiology (2067)
  • Evolutionary Biology (16006)
  • Genetics (10937)
  • Genomics (14761)
  • Immunology (9886)
  • Microbiology (23700)
  • Molecular Biology (9490)
  • Neuroscience (50958)
  • Paleontology (370)
  • Pathology (1544)
  • Pharmacology and Toxicology (2688)
  • Physiology (4030)
  • Plant Biology (8676)
  • Scientific Communication and Education (1512)
  • Synthetic Biology (2402)
  • Systems Biology (6446)
  • Zoology (1346)