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Fig. 5. Tub
1>vg clones act at short range to induce
vg and QE reporter expression in neighboring
UAS-Nrt-wg clones. (A-D) ap0 discs
containing Tub
1>vg clones (black by absence of
DsRed, left column), C765-Gal4/UAS-Nrt-wg clones (yellow by
coincident expression of Flu-tagged Nrt-Wg, green, and DsRed), and `double'
Tub
1>vg C765-Gal4/UAS-Nrt-wg clones (green by
expression of Nrt-Wg in the absence of DsRed) are shown stained for Vg (A,C)
or 1XQE-lacZ (B,D) expression (blue). (A,B) Double clones (green)
within the prospective Drosophila wing pouch (A,B, 2) show peak
expression of Vg (bright blue) and 1XQE-lacZ and induce peak
expression in adjacent cells outside of the clone (note that the green
territories are nested inside the larger bright blue territories, right
column). Tub
1>vg clones (A, black, 1) show only
moderate Vg expression (derived only from Tub
1>vg,
dull blue). (C,D) Tub
1>vg clones (1, black) that
abut C765-Gal4/UAS-Nrt-wg clones (3, yellow) induce cells in the
latter to express peak levels of Vg and 1XQE-lacZ. The induction is
not limited to those C765-Gal4/UAS-Nrt-wg cells that abut the
Tub
1>vg clone, but propagates over many cell
diameters into the C765-Gal4/UAS-Nrt-wg clone. Vg and
1XQE-lacZ expression are also upregulated in the
Tub
1>vg cells that abut the
C765-Gal4/UAS-Nrt-wg clone.