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. 2020 Nov 17;117(48):30520–30530. doi: 10.1073/pnas.2013449117

Fig. 4.

Fig. 4.

The yki 3′ UTR is necessary and sufficient for Rox8-mediated mRNA decay in vivo. (AF) Fluorescence micrographs of wing discs are shown. Rox8 overexpression dramatically suppressed the overgrowth induced by Myc-Yki-UTR (A and B) or Myc-Yki-UTRM2 (E and F), but not that by Myc-Yki-UTRM1 (C and D). Consistently, Myc-Yki expression from Myc-Yki-UTR or Myc-Yki-UTRM2, but not from Myc-Yki-UTRM1, was impeded by Rox8 (AF). (GN) Light micrographs of Drosophila adult eyes are shown. Compared with the GMR > GFP control (G), GMR > Rox8 displayed no obvious phenotype (H). However, overexpression of Rox8 significantly impeded tumor-like overgrowth triggered by ectopic expression of Myc-Yki-UTR (I and J) or Myc-Yki-UTRM2 (M and N), but not of Myc-Yki-UTRM1 (K and L). (OQ) Fluorescent images of third instar larval wing discs. Expressing Rox8 strikingly attenuated the expression of GFP from GFP-UTR (O) or GFP-UTRM2 (Q), but not that from GFP-UTRM1 (P). (R) RT-qPCR and immunoblot assays were performed in cultured S2 cells. Rox8 overexpression decreased the expression of GFP-UTR and GFP-UTRM2 at both the mRNA and protein level, but had no significant effect on that of GFP-UTRM1. ***P < 0.001. ns, no significant difference. Magnification for IN: 6.3×.