Skip to main content
Fig. 6 | BMC Biology

Fig. 6

From: Deciphering the roles of subcellular distribution and interactions involving the MEF2 binding region, the ankyrin repeat binding motif and the catalytic site of HDAC4 in Drosophila neuronal morphogenesis

Fig. 6

Expression of nuclear and cytoplasmic-restricted HDAC4 exacerbates disruption to eye development, which is reduced in the Y1142H mutant. A Stereomicrographs of Drosophila eyes. Genotypes were generated by crossing GMR-GAL4/CyO;UAS-HDAC4 females to males carrying each UAS-HDAC4 transgene and to the w(CS10) control and collecting non Cy progeny. Representative images of n = 5 males and n = 5 females per genotype are shown. × 110 magnification. B Quantification of the severity of eye phenotypes. In comparison to HDAC4WT, the severity of HDAC43SA, HDAC4ΔANK, and HDAC4ΔNLS phenotypes was significantly increased. In contrast, the HDAC4ΔMEF2 and HDAC4Y1142H phenotypes were both significantly reduced in males and females (females: ANOVA, F(8,36) = 218.5, p = 1.11 × 10−16. Tukey’s post hoc test, **p < 0.01; males: ANOVA, F(8,36) = 157.58, p = 1.11 × 10−16. Tukey’s post hoc test, **p < 0.01). Error bars = mean ± SEM. C Anti-Myc immunohistochemistry on eye imaginal discs from wandering third instar larvae expressing HDAC4WT and mutants with GMR-GAL4. Representative images from n = 15 discs per genotype are shown. Scale bar = 10 μm

Back to article page