UAS-cg17282 RNAi and UAS-dbt RNAi stocks were obtained from the Vienna Drosophila RNAi Center and the GAL4 driver lines from the Bloomington Stock Center. These lines, the genetic crosses employing them, and the activity assays are described in greater detail in Supplemental Experimental Procedures in Supplemental Information. UAS-dbt-myc lines have been previously described ( Muskus et al., 2007). A cDNA clone for cg17282 (RE50353) was obtained from the Drosophila Genomics Resource Center (DGRC). In order to clone it into vectors allowing expression in Drosophila S2 cells or flies, the DGRC Gateway collection was employed. BDBT was cloned into pGateway

vector pAWF (cat 1112) or pTWF (cat 1116), thereby generating a C-terminal 3× FLAG-tag and

allowing constitutive expression from the Act5C promoter in S2 cells or flies (with a GAL4 driver), respectively. Transformants were produced by Genetic BMN 673 purchase Services. More complete descriptions are given in Supplemental Experimental Procedures. S2 cells were transiently transfected with pAC-bdbt-flag, pMT-dbt-myc, and/or pAC-per-ha by cellfectin II (Life Technologies) treatment as previously described ( Muskus et al., 2007) or were treated with double-stranded RNAi (dsRNAi) for BDBT. To make http://www.selleckchem.com/products/azd9291.html the dsRNAi, a PCR product was amplified from BDBT clone RE50353 with Bull’s eye Taq polymerase (Midwest Scientific) and primers that introduced T7 promoters on each end of the product (forward primer: 5′-GTAATACGACTCACTATAGGG-3′; reverse primer: 5′-TTAATACGACTCACTATAGGGAGAACTAAACATACGTTGCACCA). Then, T7 RNA polymerase (Megascript RNAi kit, cat AM1626; Life Technologies) was used to produce dsRNAi, and this was

applied to S2 cells according to the procedure of the Perrimon lab (http://www.flyrnai.org/DRSC-PRR.html). These included GST pull-down assays and immunoprecipitations from Drosophila S2 cells, fly heads, and human embryonic kidney cells, as described in Supplemental Experimental Procedures. Antibodies to BDBT were generated to the first 120 or to the first 238 amino acids of BDBT expressed in E. coli and purified as described in Supplemental Experimental Procedures. The antibodies were generated in guinea pig by Covance Research others Products. For immunoblot assays, crude extracts or immunoprecipitates were subjected to SDS-PAGE, transferred to nitrocellulose, and antigens detected with the appropriate antibodies as described in Supplemental Experimental Procedures. Extracts were analyzed on either 5.7% (for PER) or 10% (for DBT, tubulin, actin, and BDBT) SDS-PAGE gels with the ECL procedure (GE Healthcare) (Muskus et al., 2007). Typically, immunoblots of independent experiments were performed three times for each figure (see figure legends). For analysis of DBT modification in bdbt RNAi flies, head extracts were prepared at ZT7 by sonication in 1× phosphatase buffer (7 μl per head in 1.