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Temporal dynamics of liver mitochondrial protein acetylation and succinylation and metabolites due to high fat diet and/or excess glucose or fructose
Dietary macronutrient composition alters metabolism through several mechanisms, including post-translational modification (PTM) of proteins. To connect diet and molecular changes, here we performed short- and long-term feeding of mice with standard chow diet (SCD) and high-fat diet (HFD), with or wi...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6306174/ https://www.ncbi.nlm.nih.gov/pubmed/30586434 http://dx.doi.org/10.1371/journal.pone.0208973 |
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author | Meyer, Jesse G. Softic, Samir Basisty, Nathan Rardin, Matthew J. Verdin, Eric Gibson, Bradford W. Ilkayeva, Olga Newgard, Christopher B. Kahn, C. Ronald Schilling, Birgit |
author_facet | Meyer, Jesse G. Softic, Samir Basisty, Nathan Rardin, Matthew J. Verdin, Eric Gibson, Bradford W. Ilkayeva, Olga Newgard, Christopher B. Kahn, C. Ronald Schilling, Birgit |
author_sort | Meyer, Jesse G. |
collection | PubMed |
description | Dietary macronutrient composition alters metabolism through several mechanisms, including post-translational modification (PTM) of proteins. To connect diet and molecular changes, here we performed short- and long-term feeding of mice with standard chow diet (SCD) and high-fat diet (HFD), with or without glucose or fructose supplementation, and quantified liver metabolites, 861 proteins, and 1,815 protein level-corrected mitochondrial acetylation and succinylation sites. Nearly half the acylation sites were altered by at least one diet; nutrient-specific changes in protein acylation sometimes encompass entire pathways. Although acetyl-CoA is an intermediate in both sugar and fat metabolism, acetyl-CoA had a dichotomous fate depending on its source; chronic feeding of dietary sugars induced protein hyperacetylation, whereas the same duration of HFD did not. Instead, HFD resulted in citrate accumulation, anaplerotic metabolism of amino acids, and protein hypo-succinylation. Together, our results demonstrate novel connections between dietary macronutrients, protein post-translational modifications, and regulation of fuel selection in liver. |
format | Online Article Text |
id | pubmed-6306174 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-63061742019-01-08 Temporal dynamics of liver mitochondrial protein acetylation and succinylation and metabolites due to high fat diet and/or excess glucose or fructose Meyer, Jesse G. Softic, Samir Basisty, Nathan Rardin, Matthew J. Verdin, Eric Gibson, Bradford W. Ilkayeva, Olga Newgard, Christopher B. Kahn, C. Ronald Schilling, Birgit PLoS One Research Article Dietary macronutrient composition alters metabolism through several mechanisms, including post-translational modification (PTM) of proteins. To connect diet and molecular changes, here we performed short- and long-term feeding of mice with standard chow diet (SCD) and high-fat diet (HFD), with or without glucose or fructose supplementation, and quantified liver metabolites, 861 proteins, and 1,815 protein level-corrected mitochondrial acetylation and succinylation sites. Nearly half the acylation sites were altered by at least one diet; nutrient-specific changes in protein acylation sometimes encompass entire pathways. Although acetyl-CoA is an intermediate in both sugar and fat metabolism, acetyl-CoA had a dichotomous fate depending on its source; chronic feeding of dietary sugars induced protein hyperacetylation, whereas the same duration of HFD did not. Instead, HFD resulted in citrate accumulation, anaplerotic metabolism of amino acids, and protein hypo-succinylation. Together, our results demonstrate novel connections between dietary macronutrients, protein post-translational modifications, and regulation of fuel selection in liver. Public Library of Science 2018-12-26 /pmc/articles/PMC6306174/ /pubmed/30586434 http://dx.doi.org/10.1371/journal.pone.0208973 Text en © 2018 Meyer et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Meyer, Jesse G. Softic, Samir Basisty, Nathan Rardin, Matthew J. Verdin, Eric Gibson, Bradford W. Ilkayeva, Olga Newgard, Christopher B. Kahn, C. Ronald Schilling, Birgit Temporal dynamics of liver mitochondrial protein acetylation and succinylation and metabolites due to high fat diet and/or excess glucose or fructose |
title | Temporal dynamics of liver mitochondrial protein acetylation and succinylation and metabolites due to high fat diet and/or excess glucose or fructose |
title_full | Temporal dynamics of liver mitochondrial protein acetylation and succinylation and metabolites due to high fat diet and/or excess glucose or fructose |
title_fullStr | Temporal dynamics of liver mitochondrial protein acetylation and succinylation and metabolites due to high fat diet and/or excess glucose or fructose |
title_full_unstemmed | Temporal dynamics of liver mitochondrial protein acetylation and succinylation and metabolites due to high fat diet and/or excess glucose or fructose |
title_short | Temporal dynamics of liver mitochondrial protein acetylation and succinylation and metabolites due to high fat diet and/or excess glucose or fructose |
title_sort | temporal dynamics of liver mitochondrial protein acetylation and succinylation and metabolites due to high fat diet and/or excess glucose or fructose |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6306174/ https://www.ncbi.nlm.nih.gov/pubmed/30586434 http://dx.doi.org/10.1371/journal.pone.0208973 |
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