Fig. 3. Wing veins deviate toward nearby mew- clones.
mewM6 clones were generated in a sog
misexpression background (sogEP7) using FLP/FRT-mediated
recombination and were scored by the marker forked (f). (A)
A dorsal mewM6 clone adjacent to the L2 vein displaces the
vein towards the clone. The broken black line indicates the normal trajectory
of the L2 vein. (B) A small mewM6 clone adjacent to a
distal region of L2 has a similar vein deviating effect. (C) A
mewM6 clone between veins L3 and L4 alters the course of
the L3 vein. The distance between the tips of L2 and L3 is increased as a
function of L3 being displaced posteriorly (arrow) towards the
mewM6 clone. The broken black line indicates the
approximate location where the L3 vein would normally form. (D) A
mewM6 clone that straddles the L2 vein by several cells on
each side of the vein does not significantly disrupt the course of the vein.
(E) A mewM6 clone adjacent to the posterior crossvein
induces formation of ectopic vein material between the normal vein and the
clone. (F) Ventral mewM6 clones adjacent to veins have no
effect. Broken red lines indicate the limits of dorsal clones, broken purple
lines indicate ventral clones.