Supplementation with N-3 long-chain polyunsaturated fatty acids or olive oil in men and women with renal disease induces differential changes in the DNA methylation of FADS2 and ELOVL5 in peripheral blood mononuclear cells

PLoS One. 2014 Oct 17;9(10):e109896. doi: 10.1371/journal.pone.0109896. eCollection 2014.

Abstract

Background: Studies in animal models and in cultured cells have shown that fatty acids can induce alterations in the DNA methylation of specific genes. There have been no studies of the effects of fatty acid supplementation on the epigenetic regulation of genes in adult humans.

Methods and results: We investigated the effect of supplementing renal patients with 4 g daily of either n-3 long-chain polyunsaturated fatty acids (n-3 LCPUFA) or olive oil (OO) for 8 weeks on the methylation status of individual CpG loci in the 5' regulatory region of genes involved in PUFA biosynthesis in peripheral blood mononuclear cells from men and women (aged 53 to 63 years). OO and n-3 LCPUFA each altered (>10% difference in methylation) 2/22 fatty acid desaturase (FADS)-2 CpGs, while n-3 LCPUFA, but not OO, altered (>10%) 1/12 ELOVL5 CpGs in men. OO altered (>6%) 8/22 FADS2 CpGs and (>3%) 3/12 elongase (ELOVL)-5 CpGs, while n-3 LCPUFA altered (>5%) 3/22 FADS2 CpGs and 2/12 (>3%) ELOVL5 CpGs in women. FADS1 or ELOVL2 methylation was unchanged. The n-3 PUFA supplementation findings were replicated in blood DNA from healthy adults (aged 23 to 30 years). The methylation status of the altered CpGs in FADS2 and ELOVL5 was associated negatively with the level of their transcripts.

Conclusions: These findings show that modest fatty acid supplementation can induce altered methylation of specific CpG loci in adult humans, contingent on the nature of the supplement and on sex. This has implications for understanding the effect of fatty acids on PUFA metabolism and cell function.

Publication types

  • Controlled Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetyltransferases / genetics*
  • Acetyltransferases / metabolism
  • Adult
  • Base Sequence
  • DNA Methylation*
  • Delta-5 Fatty Acid Desaturase
  • Dietary Supplements*
  • Fatty Acid Desaturases / genetics*
  • Fatty Acid Desaturases / metabolism
  • Fatty Acid Elongases
  • Fatty Acids, Omega-3 / administration & dosage
  • Fatty Acids, Omega-3 / pharmacology*
  • Female
  • Humans
  • Leukocytes, Mononuclear / drug effects
  • Leukocytes, Mononuclear / metabolism*
  • Male
  • Middle Aged
  • Molecular Sequence Data
  • Olive Oil
  • Plant Oils / administration & dosage
  • Plant Oils / pharmacology*
  • Renal Insufficiency, Chronic / genetics
  • Renal Insufficiency, Chronic / metabolism*

Substances

  • Delta-5 Fatty Acid Desaturase
  • ELOVL2 protein, human
  • ELOVL5 protein, human
  • Fatty Acids, Omega-3
  • Olive Oil
  • Plant Oils
  • Fatty Acid Desaturases
  • FADS1 protein, human
  • FADS2 protein, human
  • Acetyltransferases
  • Fatty Acid Elongases

Grants and funding

The generation of the samples used in Study 1 was supported by a grant from the National Health and Medical Research Council of Australia (APP303151) and the Hollywood Private Hospital Research Foundation to TAM. The generation of the samples used in Study 2 was funded by the European Union’s Seventh Framework Programme FP7 2007–2013 under grant agreement number 244995 (BIOCLAIMS: Biomarkers of robustness of metabolic homeostasis for nutrigenomics-derived health claims made on food) awarded to PCC. All other analyses reported here were supported by departmental funds at the University of Southampton (GCB). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.