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Fig. 2. EGFR is required for Delta expression in pupal cone cells.
(A-C) Delta expression in EGFRts1-mutant clones
subjected to a nonpermissive temperature during pupal development. (A) GFP
expression marks wild-type cells (green); non-GFP cells are mutant for
EGFRts1. (B) The same disc as in A was co-stained for
Delta expression (red). (C) The merged panel shows that the Delta
protein is restricted to wild-type cells. (D-F) Expression of the
cone-cell marker, Cut, in EGFRts1 clones transferred to
non-permissive conditions during the mid-pupal stages. (D) GFP marks wild-type
tissue; non-GFP cells are mutant for EGFR. (E) The same disc as in D
was co-stained for Cut (red). (F) The merged panel shows that the loss of
EGFR function in pupal stages does not compromise cone-cell fate.
(G-J) Expression of a dominant-negative version of EGFR
(EGFRDN) in cone cells blocks Delta expression. (G,H)
Wild-type (control) pupal eye discs stained for Delta showed its expression in
cone cells (red, G); the spa-Gal4 driver was also expressed in cone
cells (red, H). spa-Gal4, UAS-EGFRDN pupal eye discs
stained for Delta showed loss of Delta expression in the cone cells (I),
whereas spa-Gal4, UAS-EGFRDN pupal eye discs stained for
Cut showed that a loss of EGFR function during pupal stages does not disrupt
cone-cell fate specification (J). (K-N) Ectopic activation of EGFR in
cone cells promotes Delta expression. MAPK activation in wild-type third
instar eye disc (K) is seen in cells at the furrow followed by low levels of
activation in the differentiated R cells behind the furrow (K). (L) In
spa-Gal4, UASEGFRact third instar eye disc, MAPK is
activated at high levels at later stages in the developing cone cells, which
express spa-Gal4. (M) Wild-type expression of Delta (green)
in the third instar eye disc is limited to R cells and is not expressed in
cone cells (red). (N) In spa-Gal4, UAS-EGFRact third
instar eye disc, ectopic activation of Delta (green) is seen in cone cells
(red, arrow).