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. Author manuscript; available in PMC: 2017 Mar 15.
Published in final edited form as: Dev Biol. 2016 Feb 2;411(2):207–216. doi: 10.1016/j.ydbio.2016.01.040

Fig. 4.

Fig. 4

Atg1-mediated suppression of Rafgof tumor formation does not rely on caspase-dependent apoptosis. (A) Progenitors in esgts>p35 midgut at 29 °C for 3 days (white arrowheads). (B) No obvious effects are observed in intestines co-expressing Atg1 and p35 at 29 °C for 3 days (white arrowheads). (C) Intestinal tumors are formed in esgts>Rafgof intestines at 29 °C for 3 days (white arrowheads). (D) ISCs in esgts>p35; Rafgof midgut at 29 °C for 3 days (white arrowheads). (E) Atg1-mediated suppression of Rafgof tumor formation cannot be rescued by co-expression of p35 (white arrowheads). (F) Quantification of the number of esg+ cells in the intestines of different genotypes. Note that because esgts>Rafgof intestines are highly deformed due to the formation of tumors, it is very difficult to accurately count the number of esg+ cells in these intestines. n=10–15 intestines. Mean ± SD is shown. **p<0.001. (G) Quantification of pH3 staining per gut in the intestines of different genotypes. n=10–15 intestines. Mean ± SD is shown. **p<0.001. Blue indicates DAPI staining for DNA. Scale bars: 20 μm.