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Resolution: standard / high Figure 3.
miR-449 targets cell cycle controller genes. A - Ingenuity Pathway Analysis (IPA) of deregulated genes upon miR-449 re-introduction
into SNU638 cells showing enrichment for the gene categories cancer, cell death and
cell cycle pathways among others. B - qPCR validation of Affymetrix arrays showing down-regulation of MET, CDK6, GMNN, MYC and HDAC1 upon miR-449 re-introduction compared to scrambled RNA controls. C - Western blot validation of down-regulated genes upon miR-449 re-introduction into
SNU638 cells compared to scrambled RNA controls. Vinculin (VCL) and tubulin beta (TUBB)
were used as loading controls D - verification of direct and functional target binding using luciferase constructs
holding wild type 3'UTRs and mutated 3'UTRs (two mutations in miR-449 binding site),
* indicates statistical significance in luciferase expression between wild type 3'UTRs
transfected with miR449a/b compared to RNA scrambled control, # indicates statistical
difference in luciferase expression between wild type 3'UTRs compared to mutant 3'UTRs
transfected with miR-449a and miR-449b. "ns" not significant p value > 0.05, "*" or
"#" significant 0.01 < p value < 0.05, "**" or "##" very significant 0.01 < p value
< 0.001, "***" or "###" extremely significant p value < 0.001
Bou Kheir et al. Molecular Cancer 2011 10:29 doi:10.1186/1476-4598-10-29 |