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Fig. 8. Robo family knockdown disrupts photoreceptor axon targeting. (A-C)
Photoreceptor axons visualized using anti-Chaoptin. (A)
Tubulin-Gal4;UAS-GFP control. (B)
Tubulin-Gal4;UAS-GFP;UAS-RoboRNAi;UAS-Robo2RNAi;UAS-Robo3RNAi animal,
showing many photoreceptor axons extending through the lamina (arrow) and too
many photoreceptor axons entering the medulla (arrowhead). (C)
GMR-Gal4;UAS-GFP;UAS-RoboRNAi;UAS-Robo2RNAi;UAS-Robo3RNAi animal.
(D-F) Animals express GFP (green) under control of Sca-Gal4, while
photoreceptor axons are visualized using anti-Chaoptin (magenta). (D)
Sca-Gal4;UAS-GFP animal. (E)
Sca-Gal4;UAS-GFP;UAS-RoboRNAi,UAS-Robo3RNAi;UAS-RoboRNAi,UAS-Robo3RNAi
animal in which GFP-expressing cells in the lamina correspond to regions of
photoreceptor axon mistargeting (arrow). (F)
Sca-Gal4;UAS-GFP;UAS-RoboRNAi;UAS-Robo2RNAi;UAS-Robo3RNAi animal. (G)
Schematic of observed disruptions in visual system development. In wild type,
distal cell neurons (blue) express Robos (orange outline), while Slit protein
(red) surrounds glia (yellow with black outline) at the base of the lamina.
Lamina glia serve as initial targets of incoming R1-R6 photoreceptor axons
(green). When expression of all three Robo family members is inhibited in
distal cell neurons (robo, robo2, robo3), distal cell neurons
intermingle with the lamina glia and photoreceptor axon targeting is
disrupted. Loss of Slit expression (slit) causes an indistinguishable
defect.