Figure 7. Kibra (Kib) degradation is patterned by mechanical tension in the wing pouch to control proportional growth.
(A–B’) Grayscale images of the wing pouch, which produces the adult wing blade, expressing UASp-Kib-GFP (A) or UASp-KibS677A-GFP (B) at identical genomic locations under the nub>Gal4 driver. Corresponding heatmap intensity images are shown in (A’) and (B’). Note that KibS677A-GFP displays a more uniform distribution across the pouch than wild-type Kib-GFP. (C) Quantification of aspect ratios of adult wings expressing nub>Gal4 alone or with UASp-Kib-GFP and UASp-KibS677A-GFP. The color-coded segments in the wing image represent the wing length (orange), distal width (green), and proximal width (red). (D) Quantification of the length of proximal (S1) or distal (S2) wing region with respect to total wing length in wings expressing nub>Gal4 alone or with UASp-Kib-GFP and UASp-KibS677A-GFP; p-cv=posterior crossvein. All quantification is represented as the mean ± SEM; n=number of wings (one wing per fly). Statistical comparison was performed using the one-way ANOVA test followed by Tukey’s HSD test. (E–F’) Kib-GFP levels are elevated in rapidly proliferating UAS-bantam clones. (G–G’’’) Increased Kib abundance is more pronounced at the center of the wing pouch (yellow arrowhead) than at its periphery (white arrow). (H–I’) KibΔWW1-GFP levels do not change in bantam-expressing clones. All scale bars=20 μm.