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Prolonged high-fat diet induces gradual and fat depot-specific DNA methylation changes in adult mice

High-fat diets (HFD) are thought to contribute to the development of metabolism-related diseases. The long-term impact of HFD may be mediated by epigenetic mechanisms, and indeed, HFD has been reported to induce DNA methylation changes in white adipose tissue (WAT) near metabolism related genes. How...

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Autores principales: Zwamborn, Ramona A. J., Slieker, Roderick C., Mulder, Petra C. A., Zoetemelk, Inge, Verschuren, Lars, Suchiman, H. Eka D., Toet, Karin H., Droog, Simone, Slagboom, P. Eline, Kooistra, Teake, Kleemann, Robert, Heijmans, Bastiaan T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5335669/
https://www.ncbi.nlm.nih.gov/pubmed/28256596
http://dx.doi.org/10.1038/srep43261
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author Zwamborn, Ramona A. J.
Slieker, Roderick C.
Mulder, Petra C. A.
Zoetemelk, Inge
Verschuren, Lars
Suchiman, H. Eka D.
Toet, Karin H.
Droog, Simone
Slagboom, P. Eline
Kooistra, Teake
Kleemann, Robert
Heijmans, Bastiaan T.
author_facet Zwamborn, Ramona A. J.
Slieker, Roderick C.
Mulder, Petra C. A.
Zoetemelk, Inge
Verschuren, Lars
Suchiman, H. Eka D.
Toet, Karin H.
Droog, Simone
Slagboom, P. Eline
Kooistra, Teake
Kleemann, Robert
Heijmans, Bastiaan T.
author_sort Zwamborn, Ramona A. J.
collection PubMed
description High-fat diets (HFD) are thought to contribute to the development of metabolism-related diseases. The long-term impact of HFD may be mediated by epigenetic mechanisms, and indeed, HFD has been reported to induce DNA methylation changes in white adipose tissue (WAT) near metabolism related genes. However, previous studies were limited to a single WAT depot, a single time-point and primarily examined the pre-pubertal period. To define dynamic DNA methylation patterns specific for WAT depots, we investigated DNA methylation of Pparg2 and Leptin in gonadal adipose tissue (GAT) and subcutaneous adipose tissue (SAT), at baseline and after 6, 12 and 24 weeks of HFD exposure in adult mice. HFD induced hypermethylation of both the Leptin promoter (max. 19.6% at week 24, P = 2.6·10(−3)) and the Pparg2 promoter in GAT (max. 10.5% at week 12, P = 0.001). The differential methylation was independent of immune cell infiltration upon HFD exposure. In contrast, no differential methylation in the Pparg2 and Leptin promoter was observed in SAT. Leptin and Pparg2 DNA methylation were correlated with gene expression in GAT. Our study shows that prolonged exposure to HFD in adulthood is associated with a gradually increasing DNA methylation level at the Leptin and Pparg2 promoters in a depot-specific manner.
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spelling pubmed-53356692017-03-07 Prolonged high-fat diet induces gradual and fat depot-specific DNA methylation changes in adult mice Zwamborn, Ramona A. J. Slieker, Roderick C. Mulder, Petra C. A. Zoetemelk, Inge Verschuren, Lars Suchiman, H. Eka D. Toet, Karin H. Droog, Simone Slagboom, P. Eline Kooistra, Teake Kleemann, Robert Heijmans, Bastiaan T. Sci Rep Article High-fat diets (HFD) are thought to contribute to the development of metabolism-related diseases. The long-term impact of HFD may be mediated by epigenetic mechanisms, and indeed, HFD has been reported to induce DNA methylation changes in white adipose tissue (WAT) near metabolism related genes. However, previous studies were limited to a single WAT depot, a single time-point and primarily examined the pre-pubertal period. To define dynamic DNA methylation patterns specific for WAT depots, we investigated DNA methylation of Pparg2 and Leptin in gonadal adipose tissue (GAT) and subcutaneous adipose tissue (SAT), at baseline and after 6, 12 and 24 weeks of HFD exposure in adult mice. HFD induced hypermethylation of both the Leptin promoter (max. 19.6% at week 24, P = 2.6·10(−3)) and the Pparg2 promoter in GAT (max. 10.5% at week 12, P = 0.001). The differential methylation was independent of immune cell infiltration upon HFD exposure. In contrast, no differential methylation in the Pparg2 and Leptin promoter was observed in SAT. Leptin and Pparg2 DNA methylation were correlated with gene expression in GAT. Our study shows that prolonged exposure to HFD in adulthood is associated with a gradually increasing DNA methylation level at the Leptin and Pparg2 promoters in a depot-specific manner. Nature Publishing Group 2017-03-03 /pmc/articles/PMC5335669/ /pubmed/28256596 http://dx.doi.org/10.1038/srep43261 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Zwamborn, Ramona A. J.
Slieker, Roderick C.
Mulder, Petra C. A.
Zoetemelk, Inge
Verschuren, Lars
Suchiman, H. Eka D.
Toet, Karin H.
Droog, Simone
Slagboom, P. Eline
Kooistra, Teake
Kleemann, Robert
Heijmans, Bastiaan T.
Prolonged high-fat diet induces gradual and fat depot-specific DNA methylation changes in adult mice
title Prolonged high-fat diet induces gradual and fat depot-specific DNA methylation changes in adult mice
title_full Prolonged high-fat diet induces gradual and fat depot-specific DNA methylation changes in adult mice
title_fullStr Prolonged high-fat diet induces gradual and fat depot-specific DNA methylation changes in adult mice
title_full_unstemmed Prolonged high-fat diet induces gradual and fat depot-specific DNA methylation changes in adult mice
title_short Prolonged high-fat diet induces gradual and fat depot-specific DNA methylation changes in adult mice
title_sort prolonged high-fat diet induces gradual and fat depot-specific dna methylation changes in adult mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5335669/
https://www.ncbi.nlm.nih.gov/pubmed/28256596
http://dx.doi.org/10.1038/srep43261
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