Abstract

Diet has been shown to influence epigenetic key players, such as DNA methylation, which can regulate the gene expression potential in both parents and offspring. Diets enriched in omega-6 and deficient in omega-3 PUFAs (low dietary omega-3/omega-6 PUFA ratio), have been associated with the promotion of pathogenesis of diseases in humans and other mammals. In this study, we investigated the impact of increased dietary intake of arachidonic acid (ARA), a physiologically important omega-6 PUFA, on 2 generations of zebrafish. Parental fish were fed either a low or a high ARA diet, while the progeny of both groups were fed the low ARA diet. We screened for DNA methylation on single base-pair resolution using reduced representation bisulfite sequencing (RRBS). The DNA methylation profiling revealed significant differences between the dietary groups in both parents and offspring. The majority of differentially methylated loci associated with high dietary ARA were found in introns and intergenic regions for both generations. Common loci between the identified differentially methylated loci in F0 and F1 livers were reported. We described overlapping gene annotations of identified methylation changes with differential expression, but based on a small number of overlaps. The present study describes the diet-associated methylation profiles across genomic regions, and it demonstrates that parental high dietary ARA modulates DNA methylation patterns in zebrafish liver.

Highlights

  • Methylation of the cytosine nucleotide, generally referred to as DNA methylation, is the most widely studied epigenetic mechanism

  • The F0 generation was clearly separated between the dietary groups there were only three samples left in the control group as the other three samples did not meet DNA quality cut-offs for sequencing

  • We found that the number of differentially methylated loci (DML) between high arachidonic acid (ARA) and control group was marginally higher in F0 livers (2338) than in F1 livers (2142)

Read more

Summary

Introduction

Methylation of the cytosine nucleotide, generally referred to as DNA methylation, is the most widely studied epigenetic mechanism. DNA methylation is crucial for regulating cell differentiation and development [1,2,3], and can be affected in response to environmental stimuli, such as nutrition [4,5,6,7]. Cytosine methylation plays a key role in transcriptional regulation, and can thereby influence physiological processes [8, 9]. Methylation primarily occurs in CpG sites where a cytosine is followed by a guanine. CpG islands are genomic regions highly enriched in CpG sequences, and often associated with promoter regions of a gene.

Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call