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首页> 外文期刊>Journal of Animal Science >Prenatal transportation stress alters genome-wide DNA methylation in suckling Brahman bull calves
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Prenatal transportation stress alters genome-wide DNA methylation in suckling Brahman bull calves

机译:产前运输压力改变乳脂牛犊的基因组DNA甲基化

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摘要

The objective of this experiment was to identify genome-wide differential methylation of DNA in young prenatally stressed (PNS) bull calves. Mature Brahman cows (n = 48) were transported for 2-h periods at 60 +/- 5, 80 +/- 5, 100 +/- 5, 120 +/- 5, and 140 +/- 5 d of gestation or maintained as nontransported Controls (n = 48). Methylation of DNA from white blood cells from a subset of 28-d-old intact male offspring (n = 7 PNS; n = 7 Control) was assessed via reduced representation bisulfite sequencing. Samples from PNS bulls contained 16,128 CG, 226 CHG, and 391 CHH (C = cytosine; G = guanine; H = either adenine, thymine, or cytosine) sites that were differentially methylated compared to samples from Controls. Of the CG sites, 7,407 were hypermethylated (at least 10% more methylated than Controls; P &= 0.05) and 8,721 were hypomethylated (at least 10% less methylated than Controls; P &= 0.05). Increased DNA methylation in gene promoter regions typically results in decreased transcriptional activity of the region. Therefore, differentially methylated CG sites located within promoter regions (n = 1,205) were used to predict (using Ingenuity Pathway Analysis software) alterations to canonical pathways in PNS compared with Control bull calves. In PNS bull calves, 113 pathways were altered (P = 0.05) compared to Controls. Among these were pathways related to behavior, stress response, metabolism, immune function, and cell signaling. Genome-wide differential DNA methylation and predicted alterations to pathways in PNS compared with Control bull calves suggest epigenetic programming of biological systems in utero.
机译:该实验的目的是确定在年轻产前应激(PNS)公牛犊DNA的全基因组差异甲基化。成熟婆罗门牛(N = 48)在60 +/- 5运往2小时时段,80 +/- 5,100 +/- 5,120 +/- 5,和妊娠的140 +/- 5 d或保持为nontransported对照组(n = 48)。从白血细胞的DNA的甲基从28-d-老完整雄性后代的一个子集(N = 7个PNS; N = 7控制)通过减少表示硫酸氢盐测序评估。从PNS公牛样品含有16128 CG,226 CHG,和391 CHH(C =胞嘧啶; G =鸟嘌呤; H =要么腺嘌呤,胸腺嘧啶或胞嘧啶)与来自对照样品的是被差异甲基化的位点。所述CG位点的,7407被超甲基化的(比对照组的至少10%以上的甲基化; P&安培; LT = 0.05)和8721被低甲基化(比对照组至少10%更少的甲基化; P&安培; LT; = 0.05)。在基因的启动子区域增加的DNA甲基化通常导致降低的区域的转录活性。因此,差异甲基化的启动子位于区域(N = 1205)内CG位点被用来预测(使用独创性途径分析软件)改建经典途径在PNS与控制公牛犊相比较。在PNS公牛犊,与对照相比,113点的途径被改变(P = 0.05)。在这些之中有关的行为,应激反应,代谢,免疫功能,以及细胞信号传导途径。基因组范围的差动DNA甲基化和预测的变化,以与控制小公牛相比PNS途径建议在子宫内的生物系统的表观遗传编程。

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