Fig. 4

miR‐27b expression phenocopies  gpr126 morphant heart phenotype in zebrafish. (A) Expression of  gpr126 at 80 hpf in zebrafish embryos, which were injected with miR‐27b at single cell stage in comparison with scr miRNA controls. White circles represent scr miRNA–injected and black circles represent miR‐27b–injected embryos of four different clutches. Expression was quantified by qPCR and is shown as normalized to a log2 scale.  n = 4;  P ≤ 0.05. (B) Relative luciferase activity in HEK293T cells expressing the control construct (control), construct containing the 3′ UTR of zebrafish  gpr126 (dre 3′ UTR), or the mutated 3′ UTR (mutated) in the presence of scr miRNA control or miR‐27b. Data are mean ± SD;  n = 8; ** P ≤ 0.01; n.s., not statistically significant. (C) Representative images of zebrafish embryonic heart ventricles of 30 or 60 pg scr miRNA– and miR‐27b–injected  Tg(myl7:EGFP‐Hsa.HRAS) embryos at 80 hpf. White arrowheads indicate trabeculae. White asterisks indicate the absence of trabeculae at 80 hpf. (D) Scatter plot graph showing the number of trabecular cardiomyocytes in scr miRNA– and miR‐27b‐3p–injected zebrafish embryos at 80 hpf. Trabecular cardiomyocytes were counted in 35 embryos for scr miRNA, 15 embryos for 30 pg miR‐27b, and in 20 embryos for 60 pg miR‐27b of four clutches for each condition. Data are mean ± SD;  n = 4; * P ≤ 0.05; ** P ≤ 0.01; *** P ≤ 0.001.