Skip to main content
. 2016 Sep 20;6:33666. doi: 10.1038/srep33666

Figure 7.

Figure 7

(a) Control GF (GF4) was infected with lentiviruses carrying artificial miRNAs together with EmGFP. Over 99% of lentivirus-infected cells were positive for EmGFP that indicate highly efficient transduction of artificial miRNAs. Control cells were transduced with negative control miRNA (NC miR). For knockdown of DLX5 and RUNX2 long form, 4 different miRNA sequences for each transcript were designed (DLX5 miR #1 to #4, and RUNX2 long miR #1 to #4). The pictures of fluorescence microscopy for GF4 infected with lentiviruses carrying NC miR, DLX5 miR #2, and RUNX2 long miR #1 are shown. Scale bar indicates 200 μm. (b) RT-qPCR for DLX5, RUNX2 long form transcribed from p1 RUNX2 promoter, and RUNX2 short form transcribed from p2 RUNX2 promoter. RNA was collected 5 d after lentiviral infection. The expression of each gene was normalized to that of GAPDH. Bars represent mean ± SD. (c) RT-qPCR for RUNX2 long form transcribed from p1 RUNX2 promoter and RUNX2 short form transcribed from p2 RUNX2 promoter. RNA was collected 5 d after lentiviral infection. The expression of each gene was normalized to that of GAPDH. Bars represent mean ± SD. (d) Venn diagram of down-regulated genes (fold change <0.5) by knockdown of DLX5 miR #2, #4 and RUXN2 long miR #1.