<p>(<b>A</b>) Wt and mut miR-21 targets within the 3′UTR of murine YOD1 mRNA. The target sites were predicted by using TargetScan program. Mutated sites were designed for luciferase assay controls. (<b>B</b>) miR-21 suppressed YOD1 expression. HL-1 cells were transfected and infected as indicated. YOD1 expression levels were measured by WB. (<b>C</b>) Luciferase assay to validate miR-21 targeting effect on YOD1 translation. HL-1 cells were co-transfected with miRNA mimics and luciferase reporters harboring wt or mut YOD1 3′UTR fragments. Dual luciferase assays were conducted to compare the relative luciferase activities (Firefly/Renilla) among different groups.</p
<p>Schematic diagram of the luciferase reporter plasmids including <i>F11</i> WT 3′UTR or <i>F11</i>...
<p>A, Predicted miR-21 binding sites within the 3′-UTR of PTEN mRNA. The arrows display the mutation...
<p><b>A:</b> C2C12 cells transfected with luciferase constructs. MO25 3′ UTR target sequences (as in...
<p>(<i>A</i>) Sequence alignment of miR-21 and its binding sites in the 3′ UTRs of MyD88 and IRAK1, ...
<p>Luciferase assays were performed 24 hours post-transfection on S2R+ cells transfected with miR-21...
<p>The analysis of the relative luciferase activity in PK-15 cells following transfection with candi...
<p>A) Diagram of luciferase reporter constructs. The predicted MRE, wild-type or MRE-deleted AP-2α 3...
<p>A) Direct targeting of the 15 candidate transcripts by miR-210, miR-147a and miR-47b was analyzed...
<p>(A) Putative miR-206-binding sequences in the 3’UTR of SOD1 mRNA, identified by RNAhybrid 2.2. (B...
<p>(A) Predicted target sites, A and B, of miR-1 in the 3′UTR of mouse Pax7. (B) A luciferase report...
<p>A luciferase reporter vector containing indicated stretches of the target 3′UTR or single binding...
<p>Luciferase reporter assay of NCI-H929 cells co-transfected with pLightSwitch_3′UTR Reporter Vecto...
<p>(A) Overview of miR-19a target candidate mRNAs. The miR-19a–binding sites identified using PicTar...
<p>Luciferase reporter constructs were generated through placing fragments of 185 bp (Construct I, s...
<p>(A) The expression of Myc and the predicted miRNAs was validated by real-time PCR in the presence...
<p>Schematic diagram of the luciferase reporter plasmids including <i>F11</i> WT 3′UTR or <i>F11</i>...
<p>A, Predicted miR-21 binding sites within the 3′-UTR of PTEN mRNA. The arrows display the mutation...
<p><b>A:</b> C2C12 cells transfected with luciferase constructs. MO25 3′ UTR target sequences (as in...
<p>(<i>A</i>) Sequence alignment of miR-21 and its binding sites in the 3′ UTRs of MyD88 and IRAK1, ...
<p>Luciferase assays were performed 24 hours post-transfection on S2R+ cells transfected with miR-21...
<p>The analysis of the relative luciferase activity in PK-15 cells following transfection with candi...
<p>A) Diagram of luciferase reporter constructs. The predicted MRE, wild-type or MRE-deleted AP-2α 3...
<p>A) Direct targeting of the 15 candidate transcripts by miR-210, miR-147a and miR-47b was analyzed...
<p>(A) Putative miR-206-binding sequences in the 3’UTR of SOD1 mRNA, identified by RNAhybrid 2.2. (B...
<p>(A) Predicted target sites, A and B, of miR-1 in the 3′UTR of mouse Pax7. (B) A luciferase report...
<p>A luciferase reporter vector containing indicated stretches of the target 3′UTR or single binding...
<p>Luciferase reporter assay of NCI-H929 cells co-transfected with pLightSwitch_3′UTR Reporter Vecto...
<p>(A) Overview of miR-19a target candidate mRNAs. The miR-19a–binding sites identified using PicTar...
<p>Luciferase reporter constructs were generated through placing fragments of 185 bp (Construct I, s...
<p>(A) The expression of Myc and the predicted miRNAs was validated by real-time PCR in the presence...
<p>Schematic diagram of the luciferase reporter plasmids including <i>F11</i> WT 3′UTR or <i>F11</i>...
<p>A, Predicted miR-21 binding sites within the 3′-UTR of PTEN mRNA. The arrows display the mutation...
<p><b>A:</b> C2C12 cells transfected with luciferase constructs. MO25 3′ UTR target sequences (as in...