Abstract

Within the past decade, epigenetic mechanisms and their modulation by natural products have gained increasing interest. Dietary bioactive compounds from various sources, including green tea, soya, fruit and berries, cruciferous vegetables, whole grain foods, fish and others, have been shown to target enzymes involved in epigenetic gene regulation, including DNA methyltransferases, histone acetyltransferases, deacetylases and demethylases in vitro and in cell culture. Also, many dietary agents were shown to alter miRNA expression. In vivo studies in animal models and humans are still limited. Recent research has indicated that the gut microbiota and gut microbial metabolites might be important mediators of diet–epigenome interactions. Inter-individual differences in the gut microbiome might affect release, metabolism and bioavailability of dietary agents and explain variability in response to intervention in human studies. Only a few microbial metabolites, including folate, phenolic acids, S-(−)equol, urolithins, isothiocyanates, and short- and long-chain fatty acids have been tested with respect to their potential to influence epigenetic mechanisms. Considering that a complex mixture of intermediary and microbial metabolites is present in human circulation, a more systematic interdisciplinary investigation of nutri-epigenetic activities and their impact on human health is called for.This article is part of a discussion meeting issue ‘Frontiers in epigenetic chemical biology’.

Highlights

  • Studies have identified large inter-individual differences in gut microbial composition, with consequences for human health [1,2]

  • In an in vitro inflammation model of monocytes stimulated with tumour necrosis factor a (TNFa), 5 mM ellagic acid prevented TNFa-mediated reduction of histone deacetylases (HDACs) activity, whereas ellagic acid and urolithins B and C inhibited the concomitant induction of histone acetyltransferases (HATs) activity by greater than 50%

  • Whereas activation of the acetyl-coenzyme A (CoA)/ HAT pathway induces genes involved in cell proliferation, HDAC inhibition upregulates genes involved in cell-cycle arrest and induction of apoptosis and cell differentiation [48]

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Summary

Introduction

Studies have identified large inter-individual differences in gut microbial composition, with consequences for human health [1,2]. Of Dutch and Belgian populations, low microbial diversity has been linked to consumption of high-fat whole milk, sugarsweetened drinks, higher total energy and carbohydrate intake, and snacking, whereas high microbial diversity has been associated with consumption of coffee, tea, red wine and dark chocolate as sources of polyphenols [9,10]. Overall, these studies indicate that the metagenomic composition can be modified by (long-term) dietary patterns [1,2]. Identification and functional evaluation of long noncoding (lnc) RNAs 2 (greater than 200 nt) has become an additional area of scientific interest [24,25]

Impact of microbial metabolites on the epigenome
Summary and conclusion
Findings
21. Allis CD et al 2007 New nomenclature for
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