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The Impact of One Carbon Metabolism on Histone Methylation

The effect of one carbon metabolism on DNA methylation has been well described, bridging nutrition, metabolism, and epigenetics. This modification is mediated by the metabolite S-adenosyl methionine (SAM), which is also the methyl-donating substrate of histone methyltransferases. Therefore, SAM leve...

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Autores principales: Serefidou, Magdalini, Venkatasubramani, Anuroop Venkateswaran, Imhof, Axel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6722216/
https://www.ncbi.nlm.nih.gov/pubmed/31555321
http://dx.doi.org/10.3389/fgene.2019.00764
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author Serefidou, Magdalini
Venkatasubramani, Anuroop Venkateswaran
Imhof, Axel
author_facet Serefidou, Magdalini
Venkatasubramani, Anuroop Venkateswaran
Imhof, Axel
author_sort Serefidou, Magdalini
collection PubMed
description The effect of one carbon metabolism on DNA methylation has been well described, bridging nutrition, metabolism, and epigenetics. This modification is mediated by the metabolite S-adenosyl methionine (SAM), which is also the methyl-donating substrate of histone methyltransferases. Therefore, SAM levels that are influenced by several nutrients, enzymes, and metabolic cofactors also have a potential impact on histone methylation. Although this modification plays a major role in chromatin accessibility and subsequently in gene expression in healthy or diseased states, its role in translating nutritional changes in chromatin structure has not been extensively studied. Here, we aim to review the literature of known mechanistic links between histone methylation and the central one carbon metabolism.
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spelling pubmed-67222162019-09-25 The Impact of One Carbon Metabolism on Histone Methylation Serefidou, Magdalini Venkatasubramani, Anuroop Venkateswaran Imhof, Axel Front Genet Genetics The effect of one carbon metabolism on DNA methylation has been well described, bridging nutrition, metabolism, and epigenetics. This modification is mediated by the metabolite S-adenosyl methionine (SAM), which is also the methyl-donating substrate of histone methyltransferases. Therefore, SAM levels that are influenced by several nutrients, enzymes, and metabolic cofactors also have a potential impact on histone methylation. Although this modification plays a major role in chromatin accessibility and subsequently in gene expression in healthy or diseased states, its role in translating nutritional changes in chromatin structure has not been extensively studied. Here, we aim to review the literature of known mechanistic links between histone methylation and the central one carbon metabolism. Frontiers Media S.A. 2019-08-28 /pmc/articles/PMC6722216/ /pubmed/31555321 http://dx.doi.org/10.3389/fgene.2019.00764 Text en Copyright © 2019 Serefidou, Venkatasubramani and Imhof http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Serefidou, Magdalini
Venkatasubramani, Anuroop Venkateswaran
Imhof, Axel
The Impact of One Carbon Metabolism on Histone Methylation
title The Impact of One Carbon Metabolism on Histone Methylation
title_full The Impact of One Carbon Metabolism on Histone Methylation
title_fullStr The Impact of One Carbon Metabolism on Histone Methylation
title_full_unstemmed The Impact of One Carbon Metabolism on Histone Methylation
title_short The Impact of One Carbon Metabolism on Histone Methylation
title_sort impact of one carbon metabolism on histone methylation
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6722216/
https://www.ncbi.nlm.nih.gov/pubmed/31555321
http://dx.doi.org/10.3389/fgene.2019.00764
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