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Fig. 7. ß-Spectrin affects the guidance of the Apterous (Ap) neurons.
(A-E) All embryos have AptGal4, UAS-TauMycGFP in the
background. (F,G) Embryos have AptGal4; UAS-TauGFP in
the background. (A) Wild-type embryos have no `thick' bundles of Ap neurons
crossing the midline. (B) slit/+ heterozygous embryos have less than
one thick bundle of Ap neurons crossing the midline (arrow). (C)
ß-spectrin mutant embryos have approximately one to two thick Ap
bundles crossing the midline (arrow). (D) Ap neuron guidance defects in a
slit/+ heterozygous background are enhanced by removing
ß-spectrin (arrows). (E) The genetic interaction seen in D
cannot be rescued by expressing UAS-ß-Spectrin in the Ap neurons
(arrows). (F) In robo mutants, Ap neurons in every segment cross and
recross the midline (starred arrowheads). (G) Unlike what is observed in the
ß-spectrin background, Ap neuron defects seen in robo1
mutants can be rescued by expressing UAS-RoboMyc specifically in the Ap
neurons themselves (arrowheads). (H) Quantification of genotypes: a,
AptTMG/+ (n=12); b, slit, AptTMG/+ (n=14);
c, em6/Y; AptTMG (n=10); d, em6/Y; slit, AptTMG/+
(n=16); e, em6/Y; slit, AptTMG/UAS-ßSpec
(n=20); f, G0198/Y; AptTMG/+ (n=14); g,
G0198/Y; slit, AptTMG/+ (n=13). Asterisk denotes a
significant difference between genotypes d and c (P=0.0144;
two-sample Student's t-test). There is no significant difference
between genotypes d and e. Double asterisk denotes a significant difference
between genotypes g and f (P=0.00139; two-sample Student's
t-test). AptTMG, ApterousGal4, UAS-TauMycGFP.