Food Nutrition & Health Team, Food & Bio-based Products Group, AgResearch Grasslands, Palmerston North 4442, New Zealand.
BMC Med Genomics. 2013 Mar 5;6:7. doi: 10.1186/1755-8794-6-7.
Consumption of high-fat diets has negative impacts on health and well-being, some of which may be epigenetically regulated. Selenium and folate are two compounds which influence epigenetic mechanisms. We investigated the hypothesis that post-weaning supplementation with adequate levels of selenium and folate in offspring of female mice fed a high-fat, low selenium and folate diet during gestation and lactation will lead to epigenetic changes of potential importance for long-term health.
Female offspring of mothers fed the experimental diet were either maintained on this diet (HF-low-low), or weaned onto a high-fat diet with sufficient levels of selenium and folate (HF-low-suf), for 8 weeks. Gene and protein expression, DNA methylation, and histone modifications were measured in colon and liver of female offspring.
Adequate levels of selenium and folate post-weaning affected gene expression in colon and liver of offspring, including decreasing Slc2a4 gene expression. Protein expression was only altered in the liver. There was no effect of adequate levels of selenium and folate on global histone modifications in the liver. Global liver DNA methylation was decreased in mice switched to adequate levels of selenium and folate, but there was no effect on methylation of specific CpG sites within the Slc2a4 gene in liver.
Post-weaning supplementation with adequate levels of selenium and folate in female offspring of mice fed high-fat diets inadequate in selenium and folate during gestation and lactation can alter global DNA methylation in liver. This may be one factor through which the negative effects of a poor diet during early life can be ameliorated. Further research is required to establish what role epigenetic changes play in mediating observed changes in gene and protein expression, and the relevance of these changes to health.
高脂肪饮食对健康和幸福感有负面影响,其中一些可能受到表观遗传调控。硒和叶酸是两种影响表观遗传机制的化合物。我们假设,在妊娠和哺乳期喂食高脂肪、低硒和叶酸饮食的雌性小鼠的后代,在断奶后补充足够水平的硒和叶酸,将导致对长期健康有重要意义的表观遗传变化。
喂食实验饮食的雌性后代继续喂食该饮食(HF-low-low),或断奶后喂食高脂肪饮食,其中含有足够水平的硒和叶酸(HF-low-suf),持续 8 周。测量雌性后代结肠和肝脏中的基因和蛋白质表达、DNA 甲基化和组蛋白修饰。
断奶后补充足够水平的硒和叶酸影响了后代结肠和肝脏中的基因表达,包括降低 Slc2a4 基因表达。蛋白质表达仅在肝脏中发生改变。在肝脏中,足够水平的硒和叶酸对整体组蛋白修饰没有影响。切换到足够水平的硒和叶酸会降低肝脏中的整体肝 DNA 甲基化,但对 Slc2a4 基因内特定 CpG 位点的甲基化没有影响。
在妊娠和哺乳期喂食高脂肪、低硒和叶酸饮食的雌性小鼠的后代,在断奶后补充足够水平的硒和叶酸,可以改变肝脏中的整体 DNA 甲基化。这可能是减轻早期不良饮食负面影响的一个因素。需要进一步研究以确定表观遗传变化在调节观察到的基因和蛋白质表达变化中的作用,以及这些变化与健康的相关性。