Research Group Functional Genomics, Leibniz Institute for Farm Animal Biology, Wilhelm-Stahl-Allee 2, D-18196 Dummerstorf, Germany.
Br J Nutr. 2012 Mar;107(6):791-9. doi: 10.1017/S0007114511003667. Epub 2011 Sep 1.
There is growing evidence that maternal nutrition during gestation has an important effect on offspring development as well as on their gene expression with long-term effects on the metabolic state. A potential mechanism forming long-lasting gene expression patterns is DNA methylation of cytosine in CpG dinucleotides within the promoter region of distinct genes. There has been special focus on mitochondrial dysfunction by prenatal malnourishment over the recent years. To this end, we investigated the gene expression of somatic cytochrome c (CYCS), an important member of the respiratory chain, in a porcine model of gestational protein over- and undersupply at 94 d post-conception and 1, 28 and 188 d of age, and analysed the association with the DNA methylation status within the CYCS promoter. Gene expression on day 1 post natum showed a significant increase in the low protein (LP) group (P = 0·0005) and a slight increase in the high protein (HP) group (P = 0·079) compared with the control (CO) group in the liver. The mean of the methylation level over forty-seven CpG sites from nucleotide (nt) - 417 to - 10 was significantly decreased in the LP (P = 0·007) and HP (P = 0·009) groups compared with that in the CO group. Excess and restricted protein supply during pregnancy led to hypomethylation of a number of CpG sites in the CYCS promoter, including those representing putative transcription factor-binding sites, associated with elevated expression levels. However, the impact of the low-protein gestation diet is more pronounced, indicating that the offspring could better adapt to excess rather than restricted protein supply.
越来越多的证据表明,妊娠期间的母体营养对后代的发育以及对其基因表达具有重要影响,从而对代谢状态产生长期影响。一种形成持久基因表达模式的潜在机制是,在特定基因启动子区域内的胞嘧啶(CpG 二核苷酸)中的 DNA 甲基化。近年来,人们特别关注产前营养不良引起的线粒体功能障碍。为此,我们在妊娠蛋白供应过多和过少的猪模型中,研究了体细胞细胞色素 c(CYCS)的基因表达,CYCS 是呼吸链的重要成员,在妊娠后 94 天、1 天、28 天和 188 天以及分析与 CYCS 启动子内的 DNA 甲基化状态的关联。与对照组(CO)相比,新生后 1 天,低蛋白(LP)组(P = 0.0005)和高蛋白(HP)组(P = 0.079)的肝脏中 CYCS 基因表达显著增加。LP(P = 0.007)和 HP(P = 0.009)组中从核苷酸(nt)-417 到-1047 个 CpG 位点的平均甲基化水平与 CO 组相比显著降低。与对照组相比,妊娠期间过量和限制蛋白质供应导致 CYCS 启动子中多个 CpG 位点发生低甲基化,包括那些代表潜在转录因子结合位点的 CpG 位点,与升高的表达水平相关。然而,低蛋白妊娠饮食的影响更为显著,这表明后代可以更好地适应过量而非限制蛋白质的供应。