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. Author manuscript; available in PMC: 2011 Jun 1.
Published in final edited form as: Dev Biol. 2010 Mar 17;342(1):1–10. doi: 10.1016/j.ydbio.2010.03.005

Figure 7. Distinct rescue of the D-cbl over-recruitment phenotype by expression of the D-cbl isoforms.

Figure 7

Shown are pupal (42h APF) eye discs labeled with anti-Pros/Elav antibodies (red/blue) for R7/photoreceptor (R) cells and anti-Cut antibody (red) for cone cells. D-cbl mutant clones are positively labeled by GFP due to the MARCM technique (outlined by white lines) and express either no transgene (A,A,B,B′), D-cblL (C,C,D,D′) or D-cblS (E,EF,F′). GFP-negative cells are non-mutant (wild-type or heterozygous) and do not express any transgene. Arrows point to representative examples of the phenotypes in the mutant clones as explained in the text. The null allele D-cblK26, and the transgenes UAS-D-cblL (line A18) and UAS-D-cblS (line A1) transgenes were used.

Genotypes:

(A,B) hs-Flp actin-Gal4 UAS-GFP; D-cblK26 FRT80/tub-Gal80 FRT80;

(C,D) hs-Flp actin-Gal4 UAS-GFP; UAS-D-cblL/+; D-cblK26 FRT80/tub-Gal80 FRT80;

(E,F) hs-Flp actin-Gal4 UAS-GFP; UAS-D-cblS/+; D-cblK26 FRT80/tub-Gal80 FRT80.