Localization of Dsh::GFP in 30 h APF pupal wing stained for Fmi, and GFP and F‐actin (shown in Fig
EV2). The Dsh::GFP localization was analyzed in intervein region between L3 and L4 veins. We obtained
ens
KO36
/ens
KO39 pupae by selecting third instar larvae, which were identified by the loss of mCherry fluorescence from the balancer chromosome.
w; dsh::EGFP was used as wild type.