Dietary inclusion of plant ingredients induces epigenetic changes in the intestine of zebrafish.
Anusha K S DhanasiriXianquan ChenDalia DahlePrabhugouda SiriyappagouderChristiane K FæsteJorge Manuel De Oliveira FernandesPublished in: Epigenetics (2020)
Epigenetic modifications, such as DNA methylation, can be regulated by nutrition and dietary factors. There has been a large increase in the use of sustainable plant-based protein sources in fish feed due to limitations of fishmeal resources, which are needed to sustain a rapidly growing aquaculture industry. With this major transition from marine ingredients to plant-based diets, fish are abruptly introduced to changes in dietary composition and exposed to a variety of phytochemicals, some of which known to cause epigenetic changes in mammals. However, the effect of plant ingredients on the epigenome of fish is barely understood. In the present study, the nutriepigenomic effects of the addition of pea, soy, and wheat gluten protein concentrate to aquafeeds were investigated using zebrafish as a model. A genome-wide analysis of DNA methylation patterns was performed by reduced representation bisulphite sequencing to examine global epigenetic alterations in the mid intestine after a 42-day feeding trial. We found that inclusion of 30% of wheat gluten, pea and soy protein concentrate in the diet induced epigenetic changes in the mid intestine of zebrafish. A large number of genes and intergenic regions were differentially methylated with plant-based diets. The genes concerned were related to immunity, NF-κB system, ubiquitin-proteasome pathway, MAPK pathway, and the antioxidant defence system. Epigenetic regulation of several biological processes, including neurogenesis, cell adhesion, response to stress and immunity was also observed. Ultimately, the observed epigenetic changes may enable zebrafish to rapidly regulate inflammation and maintain intestinal homoeostasis when fed plant protein-based diets.
Keyphrases
- dna methylation
- genome wide
- gene expression
- oxidative stress
- copy number
- weight loss
- cell adhesion
- signaling pathway
- protein protein
- amino acid
- cell wall
- physical activity
- clinical trial
- small molecule
- study protocol
- pi k akt
- transcription factor
- mass spectrometry
- high resolution
- subarachnoid hemorrhage
- phase iii
- irritable bowel syndrome
- heat stress
- toll like receptor
- genome wide identification