Key Laboratory of Agricultural Animal Genetics, Breeding & Reproduction of Ministry of Education, Huazhong Agricultural University, Wuhan, People's Republic of China.
Mol Cell Biochem. 2013 Sep;381(1-2):105-13. doi: 10.1007/s11010-013-1692-9. Epub 2013 May 29.
MicroRNAs (miRNAs), a novel class of post-transcriptional gene regulators, have been demonstrated to be involved in several cellular processes regulating the expression of protein-coding genes. To investigate the mechanisms of miRNA-mediated regulation during the process of muscle atrophy, we performed miRNA microarray hybridization between normal differentiated C2C12 cells and dexamethasone (DEX)-treated C2C12 cells. We observed that 11 miRNAs were significantly up-regulated and six miRNAs were down-regulated in the differentiated C2C12 cells after being treated with DEX. Stem-loop real-time RT-PCR confirmed the differential expression of six selected miRNAs (miR-1, miR-147, miR-322, miR-351, and miR-503*, miR-708). miRNA potential target prediction was accomplished using TargetScan, and many target genes related to muscle growth and atrophy have been reported in previous studies. The results of the current study suggested the potential roles of these differentially expressed miRNAs in skeletal muscle atrophy.
微小 RNA(miRNA)是一类新的转录后基因调控因子,已被证明参与调节蛋白质编码基因表达的几种细胞过程。为了研究 miRNA 介导的调节在肌肉萎缩过程中的机制,我们在正常分化的 C2C12 细胞和地塞米松(DEX)处理的 C2C12 细胞之间进行了 miRNA 微阵列杂交。我们观察到,在 DEX 处理后,分化的 C2C12 细胞中有 11 个 miRNA 明显上调,6 个 miRNA 下调。茎环实时 RT-PCR 证实了 6 个选定 miRNA(miR-1、miR-147、miR-322、miR-351、miR-503*和 miR-708)的差异表达。使用 TargetScan 进行了 miRNA 潜在靶基因预测,先前的研究报道了许多与肌肉生长和萎缩相关的靶基因。本研究结果表明这些差异表达的 miRNA 在骨骼肌萎缩中可能发挥作用。