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3 protocols using uas ubx

1

Genetic Toolkit for Drosophila Research

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Fly lines w1118, FRT82, LabialRNAi (BL26753), UAS-mcherry (BL38245), UAS-TkvQD (BL36536), UAS-Dpp (BL1486), UAS-Ubx (BL911), Ubx1 (BL529), UbxRNAi line 1 (BL31913), UbxRNAi line 2 (BL34993), DadRNAi (BL33759) were obtained from Bloomington Drosophila Stock Center. esg-Gal4, UAS-GFP was a gift from Shigeo Hayashi; FRT82B, Dad212 from Hannele Ruohola-Baker; Btl-Gal4ts, UAS-GFP from Dirk Bohmann; Dad::nlsGFP from Georgios Pyrowolakis; Su(H)-GBE-lacZ from Sarah Bray; esgtsF/O (esgGal4, tubG80ts, UAS-GFP; UAS-flp, act > STOP > Gal4) from Huaqi Jiang; UAS::Dad from Thomas Kornberg; NP1::Gal4 from Dominique Ferrandon; MARCM82 (hsFlp; tub-Gal4, UAS-GFP; FRT82, tubGal80) from Norbert Perrimon.
Flies were cultured on yeast/molasses-based standard fly food (Recipe: 10 L H2O, 138 g agar, 220 g molasses, 750 g malt extract, 180 dry yeast, 800 g corn flour, 100 g soy flour, 62.5 ml propionic acid, 20 g Methyl 4-Hydroxybenzoate, and 72 ml ethanol) at 25 °C with a 12 h light/dark cycle. For TARGET (tubGal80ts) experiments, flies were raised at 18 °C to allow Gal80 to inhibit Gal4, and 3–4 days after eclosion shifted to 29 °C to inhibit Gal80 and to allow Gal4 to drive UAS-linked transgene expression.
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2

Targeted Gene Expression in Drosophila

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Drosophila stocks were maintained at 25°C. The w1118 strain was used as wild type. The targeted expression experiments were performed using the UAS-GAL4 system (Brand and Perrimon, 1993 (link)) on the following GAL4 and UAS lines: eme-GAL4 (kindly provided by R. Bodmer, Burnham Institute, San Diego, CA, USA); UAS-Rpr (BL5824), UAS-Antp (BL7301), UAS-Ubx (BL911), UAS-AbdA (BL912), UAS-AbdB (BL913), UAS-mcd8-GFP (BL32184) and UAS-LifeAct-GFP (BL58718) from Bloomington Stock Center; UAS-Tup RNAi (45859) and UAS-Eve RNAi (9284) from VDRC; UAS-Tin (kindly provided by M. Frasch, Erlangen-Nürnberg University, Germany); UAS-Lbe (Jagla et al., 1997 (link)); and UAS-Kr (a gift from G. Vorbrüggen, Max Planck Institute, Goettingen, Germany). The following additional lines were used: UAS-Antp RNAi (101774) and UAS-AbdA RNAi (106155) from VDRC; Antp25 (3020) from Bloomington Stock Center; and AbdAM1 (kindly provided by L. Perrin; Aix-Marseille University, France). The Tup-GFP line was kindly provided by Stephan Thor (Linköping University, Sweden), the Hand-GFP line was a gift from E. Olson (Utah University, Salt Lake City, USA) and the UAS-H2B::YFP line was kindly provided by Michel Gho (IBPS, Paris, France). UAS-Ubx was re-balanced with TM3, twi-lacZ, and homozygous mutant embryos were selected by absence of β-galactosidase staining.
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3

Genetic Toolkit for Drosophila Research

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Fly lines w1118, FRT82, LabialRNAi (BL26753), UAS-mcherry (BL38245), UAS-TkvQD (BL36536), UAS-Dpp (BL1486), UAS-Ubx (BL911), Ubx1 (BL529), UbxRNAi line 1 (BL31913), UbxRNAi line 2 (BL34993), DadRNAi (BL33759) were obtained from Bloomington Drosophila Stock Center. esg-Gal4, UAS-GFP was a gift from Shigeo Hayashi; FRT82B, Dad212 from Hannele Ruohola-Baker; Btl-Gal4ts, UAS-GFP from Dirk Bohmann; Dad::nlsGFP from Georgios Pyrowolakis; Su(H)-GBE-lacZ from Sarah Bray; esgtsF/O (esgGal4, tubG80ts, UAS-GFP; UAS-flp, act > STOP > Gal4) from Huaqi Jiang; UAS::Dad from Thomas Kornberg; NP1::Gal4 from Dominique Ferrandon; MARCM82 (hsFlp; tub-Gal4, UAS-GFP; FRT82, tubGal80) from Norbert Perrimon.
Flies were cultured on yeast/molasses-based standard fly food (Recipe: 10 L H2O, 138 g agar, 220 g molasses, 750 g malt extract, 180 dry yeast, 800 g corn flour, 100 g soy flour, 62.5 ml propionic acid, 20 g Methyl 4-Hydroxybenzoate, and 72 ml ethanol) at 25 °C with a 12 h light/dark cycle. For TARGET (tubGal80ts) experiments, flies were raised at 18 °C to allow Gal80 to inhibit Gal4, and 3–4 days after eclosion shifted to 29 °C to inhibit Gal80 and to allow Gal4 to drive UAS-linked transgene expression.
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