Skip to main content
. Author manuscript; available in PMC: 2018 Feb 21.
Published in final edited form as: Nat Cell Biol. 2017 Aug 21;19(9):1049–1060. doi: 10.1038/ncb3592

Figure 2. MRCK/gek regulates apical Myosin activation and morphogenesis in differentiating Drosophila photoreceptors.

Figure 2

(a) Scheme illustrating the similarities and corresponding plasma membrane domains of vertebrate epithelial cells and Drosophila photoreceptors. Indicated are apical microvilli and the apical zone enriched in active Myosin-II. (b-d) Confocal sections of Drosophila pupal mosaic retinas showing wild type cells (blue nuclei) and cells mutant for gek were stained for F-actin (c) or p-MLC (b). Mutant cells are labelled with asterisks. Quantification of apical actin enrichment shows analysis of wild type and mutant cells (paired within sections; n represents 11 animals, a t-test was used to calculate the p value). (e,f) Analysis of rhabdomere integrity in wild type and gek mutant cells using 2 different gek alleles (gekNP5192 or gek1080) demonstrates severe defects including splitting. (g,h) Confocal sections of Drosophila eyes showing wild type cells and cells mutant for gekNP5192 but expressing sqh-SqhEE (blue nuclei; labelled with asterisks; the quantification represents pairs within sections and is based on n = 8 animals, a t-test was used to calculate the p value).