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MicroRNA expression analysis in the liver of high fat diet-induced obese mice

机译:高脂饮食诱导的肥胖小鼠肝脏中MicroRNA表达分析

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A previous study indicated a causal link between certain miRNAs induced by obesity and the development of hepatic insulin resistance and type 2 diabetes. Here we provide accompanying data collected using Affymetrix GeneChip miRNAs microarrays to identify the changes in miRNAs expression in the liver of mice fed a high fat diet (HFD). Differentially expressed microRNA analyses in the liver of the HFD-fed mice revealed a range of upregulated (1.5-fold) or downregulated (0.5-fold) miRNAs. Among those upregulated miRNAs, in silico target analysis, such as TargetScan, PicTar, and miRWalk, identified miRNAs with the putative binding sites on the 3’UTRs of INSR and/or IRS-1 . Interpretation of the data and further extensive insights into the implication of miRNAs, particularly miR-15b, in hepatic insulin resistance can be found in "Obesity-induced miR-15b is linked causally to the development of insulin resistance through the repression of the insulin receptor in hepatocytes." (W.M. Yang, H.J. Jeong, S.W. Park, W. Lee, 2015).
机译:先前的研究表明,肥胖引起的某些miRNA与肝胰岛素抵抗和2型糖尿病的发展之间存在因果关系。在这里,我们提供使用Affymetrix GeneChip miRNA微阵列收集的伴随数据,以鉴定喂高脂饮食(HFD)的小鼠肝脏中miRNA表达的变化。在喂食HFD的小鼠肝脏中差异表达的microRNA分析显示了一系列上调(> 1.5倍)或下调(<0.5倍)的miRNA。在那些上调的miRNA中,计算机靶标分析(例如TargetScan,PicTar和miRWalk)识别出了在INSR和/或IRS-1的3’UTR上具有假定结合位点的miRNA。数据的解释和对miRNA尤其是miR-15b在肝胰岛素抵抗中的意义的进一步深入了解可以在以下文献中找到:“肥胖诱导的miR-15b通过抑制胰岛素受体与胰岛素抵抗的发展有因果关系在肝细胞中。” (杨万美,郑汉杰,朴世伟,李永杰,2015年)。

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