The following fly stocks were used in this study: UAS-DDB1, UAS-DDB1
RNAi-Res,
ddb1HK-2-3,
ddb1W197 (generated in this study),
ddb15-1,
cul4G1-3,
cul4JJ11, UAS-Flag-Cul4, UAS-Flag-Cul4
KR (CT Chien);
mahj1 [36 (
link)]; UAS-Myc-Mahj, UAS-Myc-Mahj
R1120/1123E (this study). The following fly strains were obtained from BDSC:
β-
galRNAi (#50680), UAS-CD8-GFP (#32186),
wtsRNAi (#34064),
mahjRNAi1 (#34912) and UAS-Yki
S168A (#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-Gal80
ts. 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.