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. Author manuscript; available in PMC: 2017 Nov 21.
Published in final edited form as: Dev Cell. 2016 Oct 13;39(4):438–451. doi: 10.1016/j.devcel.2016.09.014

Figure 4. Sumoylation of Smo at K851 is required for its optimal activity in vivo.

Figure 4

(A-A′) Wing imaginal discs of late third instar larvae containing smo3 clones induced by the MARCM system were immunostained to show the expression of GFP, Ci, En (blue in A) or Ptc (blue in A′). smo3 clones are marked by the GFP expression (arrowheads). (B–F′) Wing discs containing smo3 clones that express Myc-Smo (B-B′), Myc-SmoK851R (C-C′), Myc-SmoK851R-SUMO (D-D′), Myc-SmoSD123 (E-E′), or Myc-SmoSD123 K851R (F-F′) driven by the C765 Gal4 driver were immunostained with Myc, Ci, En or Ptc antibodies. smo3 clones expressing Smo transgenes are marked by the Myc expression. Arrows and arrowheads indicate clones distant from or close to the A/P compartment boundary, respectively. See also Figure S4.