The following fly stocks were used in this study: UAS-DDB1, UAS-DDB1RNAi-Res, ddb1HK-2-3, ddb1W197 (generated in this study), ddb15-1, cul4G1-3, cul4JJ11, UAS-Flag-Cul4, UAS-Flag-Cul4KR (CT Chien); mahj1 [36 (link)]; UAS-Myc-Mahj, UAS-Myc-MahjR1120/1123E (this study). The following fly strains were obtained from BDSC: β-galRNAi (#50680), UAS-CD8-GFP (#32186), wtsRNAi (#34064), mahjRNAi1 (#34912) and UAS-YkiS168A (#28818); RNAi lines including ddb1RNAi (#44974) and cul4RNAi1 (#105668), cul4RNAi2 (#44829) and mahjRNAi2 (#110669) were obtained from the VDRC. Df(2R) XE2900 (#108418) is from the Kyoto Drosophila Genomics and Genetic Resource.
NSC drivers included insc-Gal4 (BDSC#8751; 1407-Gal4) or insc-Gal4, tub-Gal80ts. Glial driver was repo-Gal4 (BDSC# 7145). Ubiquitous driver was tub-Gal4 (BDSC#5138). UAS-Dcr2 (BDSC#24650) was used together with various RNAi stocks. ddb1 and mahj RNAi knockdown efficiency was verified by immunostaining of anti-DDB1 and anti-Mahj antibodies in larval brains.
All experiments with mutants were carried out at 25 °C, and experiments for RNAi knockdown or overexpression were performed at 29 °C.
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