All wing imaginal discs shown in this study were oriented with anterior on the left and ventral on the top.
(A-A’) UAS-GFP (green) marks the apG4-mediated gene expression pattern. apG4 drives UAS transgenes to be specifically expressed in the dorsal region of wing discs.
(B-B’) Knockdown of usp7 by apG4 attenuated the expression of dpp-lacZ (arrow).
(C-J’) Knockdown of usp7 with apG4 attenuated the expression of ptc-lacZ (compared D-D’ with C-C’), kn-lacZ (compared F-F’ with E-E’), En (compared H-H’ with G-G’) and Ci (compared J-J’ with I-I’). Arrows indicate the decrease of ptc-lacZ, kn-lacZ, En and Ci.
(K-L”) Low (K) and high (L-L”) magnifications of wing disc carrying usp7KG06814 clones was immunostained to show the expression of GFP (green) and Ci (red). usp7KG06814 clones are recognized by the lack of GFP.
(L-L”) are enlarged views of the region marked by dashed lines in (K).
(M-N”) Wing discs carrying usp7KG06814 clones were immunostained to show the expression of GFP (green) and En (white). The clones in A compartment near A/P boundary showed decrease of En (M-M”, arrows), while the clones in P compartment did not show En decrease (N-N”).
(O-P”) usp7KG06814 clones showed a decrease of ptc-lacZ expression (arrow). (P-P”) are enlarged views of the region marked by dashed lines in (O).
See also Figure S1.