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. 2018 Jul 30;115(33):8358–8363. doi: 10.1073/pnas.1807343115

Fig. 4.

Fig. 4.

Cno is necessary for RhoA-induced apical delamination and invasion in RasV12; M6−/− clones. (A) RasV12 and RasV12; M6−/− eye-disk clones were stained for Cno (n = 10 discs of each genotype). (Scale bar: 50 um.) (Right) Boxed area enlarged. (Scale bar: Right, 50 um.) (B) RhoA mean stain intensity was quantified for clones of the indicated genotypes (n = 59 RasV12 clones, 116 RasV12; M6−/− clones, and 113 Cno RNAi; RasV12, M6−/− clones). Significance was calculated using a Mann–Whitney U test. **P < 0.01. Data presented as mean with 95% CI. (C) Quantification of the localization of clones of indicated genotypes (n = 102 RasV12; M6−/− clones and 90 Cno RNAi; RasV12; M6−/− clones). Statistical significance was analyzed using χ2 analysis. **P < 0.01. (D) The VNCs from flies of the indicated genotypes were dissected and scored for the presence of GFP+ invasive cells (n = 31 RasV12; M6−/− clones and 35 Cno RNAi; RasV12; M6−/− clones). Significance was calculated using Fisher’s exact text. **P < 0.01.