Bhajun Ricky, Guyon Laurent, Pitaval Amandine, Sulpice Eric, Combe Stéphanie, Obeid Patricia, Haguet Vincent, Ghorbel Itebeddine, Lajaunie Christian, Gidrol Xavier
1] Univ. Grenoble Alpes, iRTSV-BGE, F-38000 Grenoble, France [2] CEA, iRTSV-BGE, F-38000 Grenoble, France [3] INSERM, BGE, F-38000 Grenoble, France.
1] Center for Computational Biology - CBIO, Mines ParisTech, F-77300 Fontainebleau, France [2] Institut Curie, F-75248 Paris, France [3] INSERM, U900, F-75248 Paris, France.
Sci Rep. 2015 Feb 12;5:8336. doi: 10.1038/srep08336.
MiRNAs are key regulators of gene expression. By binding to many genes, they create a complex network of gene co-regulation. Here, using a network-based approach, we identified miRNA hub groups by their close connections and common targets. In one cluster containing three miRNAs, miR-612, miR-661 and miR-940, the annotated functions of the co-regulated genes suggested a role in small GTPase signalling. Although the three members of this cluster targeted the same subset of predicted genes, we showed that their overexpression impacted cell fates differently. miR-661 demonstrated enhanced phosphorylation of myosin II and an increase in cell invasion, indicating a possible oncogenic miRNA. On the contrary, miR-612 and miR-940 inhibit phosphorylation of myosin II and cell invasion. Finally, expression profiling in human breast tissues showed that miR-940 was consistently downregulated in breast cancer tissues.
微小RNA(miRNA)是基因表达的关键调节因子。通过与许多基因结合,它们形成了一个复杂的基因共调节网络。在此,我们采用基于网络的方法,通过紧密连接和共同靶点鉴定出miRNA枢纽组。在一个包含三个miRNA(miR-612、miR-661和miR-940)的簇中,共调节基因的注释功能表明其在小GTPase信号传导中发挥作用。尽管该簇的三个成员靶向相同的预测基因子集,但我们发现它们的过表达对细胞命运的影响不同。miR-661显示肌球蛋白II的磷酸化增强且细胞侵袭增加,表明其可能是一种致癌miRNA。相反,miR-612和miR-940抑制肌球蛋白II的磷酸化和细胞侵袭。最后,人乳腺组织中的表达谱分析表明,miR-940在乳腺癌组织中始终下调。