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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.