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Alterations in hepatic miRNA expression during negative energy balance in postpartum dairy cattle

机译:产后奶牛负能平衡期间肝miRNA表达的改变

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Background Negative energy balance (NEB), an altered metabolic state, occurs in early postpartum dairy cattle when energy demands to support lactation exceed energy intake. During NEB the liver undergoes oxidative stress and increased breakdown of fatty acids accompanied by changes in gene expression. It is now known that micro RNAs (miRNA) can have a role in mediating such alterations in gene expression through repression or degradation of target mRNAs. miRNA expression is known to be altered by metabolism and environmental factors and miRNAs are implicated in expression modulation of metabolism related genes. Results miRNA expression was profiled in the liver of moderate yielding dairy cattle under severe NEB (SNEB) and mild NEB (MNEB) using the Affymetrix Gene Chip miRNA_2.0 array with 679 probe sets for Bos-taurus miRNAs. Ten miRNAs were found to be differentially expressed using the ‘samr’ statistical package (delta = 0.6) at a q-value FDR of GPR37 (G protein-coupled receptor 37), HEYL (hairy/enhancer-of-split related with YRPW motif-like), DNJA1, CD14 (Cluster of differentiation 14) and GNS (glucosamine (N-acetyl)-6-sulfatase) are known to be associated with hepatic metabolic disorders. In addition miR-140 and miR-2885 have binding sites on the most down-regulated of these genes, FADS2 (Fatty acid desaturase 2) which encodes an enzyme critical in lipid biosynthesis. Furthermore, HNF3-gamma (Hepatocyte nuclear factor 3-gamma), a hepatic transcription factor (TF) that is involved in IGF-1 expression regulation and maintenance of glucose homeostasis is a putative target of miR-31. Conclusions This study shows that SNEB affects liver miRNA expression and these miRNAs have putative targets in hepatic genes down-regulated under this condition. This study highlights the potential role of miRNAs in transcription regulation of hepatic gene expression during SNEB in dairy cattle.
机译:背景技术负能量平衡(NEB),改变的代谢状态,发生在后乳制的乳制品早期,当能量要求支持哺乳期超过能量摄入量时。在NEB期间,肝脏经历氧化应激并增加脂肪酸的崩解伴随基因表达的变化。现在已知通过抑制或降解靶mRNA的抑制或降解,微rNA(miRNA)可以具有在介导基因表达中的这种改变中的作用。已知miRNA表达通过代谢和环境因素和米兰语涉及代谢相关基因的表达调节。结果在严重的NEB(SNEB)和MILDNEB(MNEB)下,使用Affymetrix基因芯片MiRNA_2.0阵列,在中等屈服奶牛的肝脏中肝脏中的MiRNA表达在具有679探针MiRNA的探针组中进行了肝脏。发现10个miRNA在GPR37(G蛋白偶联受体37)的Q值FDR处使用“SAMR”统计包(Delta = 0.6)差异表达(Delta = 0.6),Heyl(与YRPW主题相关的毛茸茸/增强型分裂已知已知DNJA1,CD14(分化14)和GNS(氨基甲胺(N-乙酰基)-6-硫酸酶)与肝代谢紊乱相关。此外,MiR-140和miR-2885在这些基因中最下调的结合位点,编码在脂质生物合成中关键的酶的FADS2(脂肪酸去饱和酶2)。此外,HNF3-Gamma(肝细胞核因子3-Gamma),参与IGF-1表达调节和葡萄糖稳态的维持的肝脏转录因子(TF)是miR-31的推定靶标。结论本研究表明,SNEB影响肝miRNA表达,这些miRNA在这种情况下下调下调的肝基因靶向靶标。本研究突出了miRNA在乳制品中SNEB期间肝基因表达转录调节中的潜在作用。

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