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2 protocols using yolk gal4

1

Drosophila Lipid Metabolism Regulation

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The following fly lines were used: w1118 (background control), yw (background control), FB-Gal4 (Schmid et al., 2014 (link)), tub-Gal4 (Bloomington Stock Center no. 5138), yolk-Gal4 (Bloomington Stock Center no. 58814), UAS-LipinRNAi (VDRC transformant ID 36007), UAS-rel (Bloomington Stock Center no.9459), UAS-Toll10b (Bloomington Stock Center no. 58987), plin138 (Bi et al., 2012 (link)), UAS-plin1 (Bi et al., 2012 (link)), UAS-TK RNAi (Bloomington Stock Center no. 25800), UAS-wRNAi (Bloomington Stock Center no. 28980), TKg-Gal4 (Song et al., 2014 (link)), PGRP-LE112 (Bloomington Stock Center no. 33055), PGRP-LCΔE (Bloomington Stock Center no. 55713). Genetic recombination was used to generate UAS-plin1; tub-Gal4.
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2

Drosophila Starvation Response Assay

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Flies were raised on standard agar-yeast-based food at 25°C, 50%–60% humidity with 12-hour light: 12-hour dark cycle. Starvation experiments were performed on 1% agar food for 24 hours. upd2Δ3–62 was kindly provided by J. Hombria [33 (link)]. The following stocks were from Bloomington Drosophila Stock Center (BDSC), yw (#1495), yolk-GAL4 (#58814), UAS-upd2RNAi (#33988, HMS00901) [110 (link)], UAS-domeRNAi (#32860), Ilp2-Gal4 (#37516), 24B-GAL4 (#1757), R57C10-GAL4 (#39171), R38H02-GAL4 (#47352) [111 (link)], UAS-CaLexa (#66542) [65 (link)]. Flies were crossed into a w+ (Canton-S) background (lab stock, originally obtained from BDSC) for all knockdown experiments.
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