de la Rocha Carmen, Pérez-Mojica J Eduardo, León Silvia Zenteno-De, Cervantes-Paz Braulio, Tristán-Flores Fabiola E, Rodríguez-Ríos Dalia, Molina-Torres Jorge, Ramírez-Chávez Enrique, Alvarado-Caudillo Yolanda, Carmona F Javier, Esteller Manel, Hernández-Rivas Rosaura, Wrobel Katarzyna, Wrobel Kazimierz, Zaina Silvio, Lund Gertrud
Department of Genetic Engineering, Center for Research and Advanced Studies of the National Polytechnic Institute (CINVESTAV) Irapuato Unit, 36821 Irapuato, Gto., Mexico.
Department of Molecular Biomedicine, CINVESTAV Campus Zacatenco, Mexico D.F., Mexico.
Sci Rep. 2016 May 16;6:25867. doi: 10.1038/srep25867.
Fatty acids (FA) modify DNA methylation in vitro, but limited information is available on whether corresponding associations exist in vivo and reflect any short-term effect of the diet. Associations between global DNA methylation and FAs were sought in blood from lactating infants (LI; n = 49) and adult males (AMM; n = 12) equally distributed across the three conventional BMI classes. AMM provided multiple samples at 2-hour intervals during 8 hours after either a single Western diet-representative meal (post-prandial samples) or no meal (fasting samples). Lipid/glucose profile, HDAC4 promoter and PDK4 5'UTR methylation were determined in AMM. Multiple regression analysis revealed that global (in LI) and both global and PDK4-specific DNA methylation (in AMM) were positively associated with eicosapentaenoic and arachidonic acid. HDAC4 methylation was inversely associated with arachidonic acid post-prandially in AMM. Global DNA methylation did not show any defined within-day pattern that would suggest a short-term response to the diet. Nonetheless, global DNA methylation was higher in normal weight subjects both post-prandially and in fasting and coincided with higher polyunsaturated relative to monounsaturated and saturated FAs. We show for the first time strong associations of DNA methylation with specific FAs in two human cohorts of distinct age, diet and postnatal development stage.
脂肪酸(FA)在体外可修饰DNA甲基化,但关于体内是否存在相应关联以及是否反映饮食的任何短期影响的信息有限。我们在来自哺乳期婴儿(LI;n = 49)和成年男性(AMM;n = 12)的血液中寻找全基因组DNA甲基化与脂肪酸之间的关联,这些个体在三种传统BMI类别中均匀分布。AMM在食用一顿具有西方饮食代表性的单一餐后8小时内(餐后样本)或未进食(空腹样本),每隔2小时提供多个样本。我们测定了AMM的脂质/葡萄糖谱、HDAC4启动子和PDK4 5'UTR甲基化。多元回归分析显示,全基因组(在LI中)以及全基因组和PDK4特异性DNA甲基化(在AMM中)与二十碳五烯酸和花生四烯酸呈正相关。在AMM中,HDAC4甲基化在餐后与花生四烯酸呈负相关。全基因组DNA甲基化未显示出任何明确的日内模式,表明对饮食有短期反应。尽管如此,正常体重受试者在餐后和空腹时的全基因组DNA甲基化均较高,并且与相对于单不饱和脂肪酸和饱和脂肪酸更高的多不饱和脂肪酸含量一致。我们首次在两个年龄、饮食和产后发育阶段不同的人类队列中表明DNA甲基化与特定脂肪酸之间存在强关联。