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Fig. 5. srt7E4 mitotic clones result in Wg accumulation at
the dorsoventral boundary and blocks the activation of targets in Wg receiving
cells in the wing disc. The wild-type expression pattern for Wg (red;
A) and its downstream targets Senseless (Sen, blue; B) and
Achaete (Ac, red; J) in third instar wing imaginal discs. (C)
Images A and B merged with wild-type Green Fluorescent Protein (GFP).
(D-I) The effects of srt7E4 homozygous mutant
tissues on the expression of Wg and Sen at two different magnifications.
(K-L) Anterior Ac expression.
srt7E4-homozygous-mutant cells are marked by the absence
of GFP shown in merged images (F,I,L,N). Retention of Wg within Wg-expressing
cells at the dorsoventral boundary blocks dorsal and ventral expression of Sen
(E,H). Sen is expressed when GFP-positive (heterozygous) cells are present at
the dorsoventral boundary, but does not require wild-type srt because
many srt7E4-homozygous cells are present (Senexpressing
cells excluded from outlined region in E and H). Arrows in G and H show two
srt7E4-mutant cells that express high levels of Sen, but
not Wg. Similarly, anterior Achaete expression also requires a wild-type
srt in Wg-expressing cells at the dorsoventral boundary (K,L).
(M-O) A projection of optical sections of a Wg-stained (red) third
instar wing disc shows the dramatic difference in the presence of Wg within
the cells that express it between srt7E4-mutant (left
side) and heterozygous tissue (right side). Homozygous mutant cells are
identified by the absence of GFP (O). Punctate Wg endocytic vesicles
(arrowheads) are present adjacent to Wg-expressing heterozygous cells and
absent near srt7E4-homozygous tissue. There also appears
to be an expansion in the number of cells that express Wg at the dorsoventral
boundary when srt function is absent. All wing discs are orientated
dorsal up and anterior left. Images A-I are single optical sections focusing
on the Sen-expressing nuclei. (J-O) Projection of eight optical sections
acquired at 1 µm z-intervals. Scale bars: 20 µm.