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. 2017 May 2;45(10):5653–5665. doi: 10.1093/nar/gkx331

Figure 7.

Figure 7.

In vitro experimental validation of rs11540855-miR-4707-3p-ABHD8-AXIN1. (A) Graphic representation of genetic effect on miR-4707-3p-ABHD8-AXIN1, circle: ceD and ceT; triangle: miRNA; suppression line with label: the miRNA-ceD regulation, G for gain-of-function mutation; other suppression lines: the miRNA-ceT regulation; arrow: ceD activate ceTs in gain-of-function situation (Inline graphic and Inline graphic). (B) Fold change of luciferase activity ratio for ABHD8 A-allele or ABHD8 G-allele (Firefly luciferase) and the internal control (Renilla luciferase) in response to miR-4707-3p agomir, n = 6 experiments; (C) Fold change of relative ABHD8 A-allele or ABHD8 G-allele mRNA expression level (with GAPDH) in response to miR-4707-3p agomir, n = 6 experiments; (D) A representative immunoblot and fold change of MCF116 native AXIN1 expression in response to miR-4707-3p agomir, n = 5 experiments; (E) A representative immunoblot and fold change of AXIN1 expression in MCF116 cells stably expressing the two ABHD8 alleles in response to miR-4707-3p agomir, n = 5 experiments; (F) Relative expression level of miR-4707-3p, ABHD8 and AXIN1, as a function of miR-4707-3p agomir dosage (range: 0, 5, 10, 15, 20 pmol/well), n = 6 experiments.