All stocks were maintained at 18°C on standard media, and crosses were cultured at 29°C unless otherwise indicated. Stocks used were: drm-Gal4, UAS-GFP (drm > GFP) (Green et al. 2002 (link)), smg132AP; btl-Gal4, UAS-Moesin::GFP (btl > MoeGFP, smg132AP is an allele of smg1 [courtesy of M.Metzstein]; male progeny of crosses using virgins from this stock show enhanced expression of UAS constructs due to interference with nonsense mediated decay (Metzstein and Krasnow 2006 (link)). btl > MoeGFP crosses were incubated at 25°C and high GFP progeny were assessed), UAS-trc RNAi (41591, Bloomington), UAS-luciferase RNAi (31603, Bloomington), UAS-Ccm3 RNAi (109453, VDRC), UAS-coracle RNAi (51845, TRiP), UAS-furry RNAi (60103, Bloomington), UAS-Mob2 RNAi (107327, VDRC), UAS-Mo25 RNAi (55681, Bloomington), UAS-PyK RNAi 1 and 2 (49533 & 35165, VDRC), UAS-HexA RNAi 1 and 2 (104680, VDRC and 35155, Bloomington), UAS-Pfk RNAi 1 and 2 (105666, VDRC and 36782, Bloomington), UAS-blw RNAi (28059, Bloomington), UAS-ATPsyn-beta RNAi (28056, Bloomington), and UAS-ND75 RNAi 1 and 2 (33911 and 27739, Bloomington). Refer to Supplementary Table 2 and 3 for transgenic flies used in this study.
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