Genetic Evidence for Function of the bHLH-PAS Protein Gce/Met As a Juvenile Hormone Receptor

Juvenile hormones (JHs) play a major role in controlling development and reproduction in insects and other arthropods. Synthetic JH-mimicking compounds such as methoprene are employed as potent insecticides against significant agricultural, household and disease vector pests. However, a receptor mediating effects of JH and its insecticidal mimics has long been the subject of controversy. The bHLH-PAS protein Methoprene-tolerant (Met), along with its Drosophila melanogaster paralog germ cell-expressed (Gce), has emerged as a prime JH receptor candidate, but critical evidence that this protein must bind JH to fulfill its role in normal insect development has been missing. Here, we show that Gce binds a native D. melanogaster JH, its precursor methyl farnesoate, and some synthetic JH mimics. Conditional on this ligand binding, Gce mediates JH-dependent gene expression and the hormone's vital role during development of the fly. Any one of three different single amino acid mutations in the ligand-binding pocket that prevent binding of JH to the protein block these functions. Only transgenic Gce capable of binding JH can restore sensitivity to JH mimics in D. melanogaster Met-null mutants and rescue viability in flies lacking both Gce and Met that would otherwise die at pupation. Similarly, the absence of Gce and Met can be compensated by expression of wild-type but not mutated transgenic D. melanogaster Met protein. This genetic evidence definitively establishes Gce/Met in a JH receptor role, thus resolving a long-standing question in arthropod biology.

Introduction with nanomolar affinities. Specific mutations within the PAS-B domain of T. castaneum or A. aegypti Met preclude this JH binding [29,30]. JH induces Met to bind to another bHLH-PAS protein Taiman (Tai), also known as FISC or SRC [29,[31][32][33]. The resulting complex binds JHresponse DNA motifs and activates target gene transcription [30][31][32][33][34][35]. Similarly to Met, Tai has also been shown to mediate effects of JH on metamorphosis [36] and reproduction [37,38] in some insects. The D. melanogaster Met and Gce proteins interact with a chaperone Hsp83, which facilitates nuclear import of Met and expression of JH-induced genes such as Krüppel homolog 1 (Kr-h1) [34]. Most recently, Met and Gce were shown to mediate the effect of the JH precursor MF, which has been established as a circulating hormone in D. melanogaster [39].
Taken together, the above results favor Gce/Met as a JH receptor candidate. However, to establish conclusively that Gce/Met is a JH receptor, it must also be demonstrated that binding of the hormone is a necessary condition for functioning of the candidate receptor in vivo, during normal insect development. This study employs the power of Drosophila genetics to provide this critical missing evidence. It shows that transgenic Gce or Met proteins restore the natural sensitivity to JH mimics in the Methoprene-tolerant mutants and rescue the non-conditionally lethal Met gce double-mutant flies as long as their JH-binding pocket is intact.

Results and Discussion
Gce and Tai activate transcription in response to JH III, synthetic JH mimics, and MF The D. melanogaster S2 cell line expresses endogenous mRNAs encoding both Met and Gce paralogs and their single partner protein Tai (S1 Fig). We initially tested whether Met, Gce and Tai mediated ligand-dependent transcriptional activation in the S2 cells. A luciferase reporter JHRE-luc was constructed using eight tandem copies of a JH-response element (JHRE) from the A. aegypti early trypsin gene [30,31] (Fig 1A). JHRE-luc was activated by a native JH (JH III), the JH mimic methoprene, and by MF in a dose-dependent manner (Fig 1B). Mutation of the JHRE inhibited the response to JH III ( Fig 1B). RNAi-mediated knockdown of either tai or gce but not of Met prevented JH III or MF from inducing JHRE-luc ( Fig 1C). Expression of additional Tai enhanced this hormone-dependent activation, again in a manner dependent primarily on gce and tai ( Fig 1D). Similar results were obtained utilizing pyriproxyfen, a potent JH mimic of distinct, pyridine-based chemical structure [40] (S2 Fig).
The observation that Gce and Tai were required for activation of JHRE-luc by MF ( Fig 1C  and 1D), is consistent with a previous finding that MF activated transcription through an ortholog of Gce/Met from the silkworm, Bombyx mori [29,[31][32][33] and the recent finding that this natural JH precursor is a circulating hormone in D. melanogaster [39].

Gce binds JH and its agonists including MF
As the effect of JH in the S2 cell-based assay was essentially mediated by Tai and Gce, we examined the ability of the Gce protein in vitro to bind the activating ligands. [ 3 H]JH III bound to Gce with a K d of 19.3 ± 4.5 nM (Fig 2A), an affinity within the physiological hormone range [13]. Following on from the reporter gene activation data (Fig 1B), methoprene, pyriproxyfen, and MF all effectively competed with [ 3 H]JH III for binding to Gce (Fig 2B), consistent with both JH mimics and MF acting as JH receptor agonists. Similarly to binding affinities previously determined for the PAS-B domain of T. castaneum Met [29], pyriproxyfen was the strongest competitor for binding to Gce, followed by methoprene and MF (Fig 2B). The higher potency of methoprene to activate JHRE-luc, relative to JH III (Fig 1B) may be explained by the fact that the synthetic insecticide is chemically and biologically more stable than JH III.
Due to marginal levels of total [ 3 H]JH III bound to the in-vitro translated D. melanogaster Met protein [29], we were unable to determine the ligand-binding affinities for Met.
The activation and binding of Gce by MF is significant, as this circulating JH precursor prevails over JH III in D. melanogaster larvae [13,39] and exerts its own hormonal function [39]. Interestingly, MF has been reported to bind D. melanogaster USP with a high affinity (K d = 40 nM) [12], comparable to the K i of 87.9 nM we observed for MF binding to Gce (Fig 2B). USP has therefore been proposed as an intracellular MF receptor [6,13,14]. However, in agreement with genetic evidence [39], our RNAi data (Fig 1C and 1D) clearly show that Gce and Tai are essential for MF to induce expression of the JHRE-dependent reporter and thus act as a MF receptor.
MF is a "juvenile hormone" of crustaceans, where it promotes reproductive maturation and specific developmental events [41,42]. Interestingly, similar to JH in insects [29,[31][32][33], MF has been shown to stimulate interaction between Met and Tai/SRC orthologs from the cladoceran  [30,31]. The core (capital letters) of the JHRE was mutated to produce mutJHRE. (B) S2 cells responded to the indicated compounds by activating the JHRE-luc reporter, but not mutJHRE-luc (1 μM JH III). Farnesol is a biologically inactive control. (C-D) Activation of JHRE-luc by 1 μM JH III or 10 μM MF relative to basal activity (ethanol) required both Gce and Tai as revealed by dsRNA-mediated knockdown of either protein; egfp dsRNA served as a control. Cotransfection with a Tai-expressing plasmid enhanced the Gce-dependent activation by JH III and MF (D). Data were normalized to Renilla luciferase activity and plotted as mean ± SD (n = 3). crustaceans, Daphnia pulex and D. magna [43]. Moreover, when a threonine residue in the PAS-B domain of Daphnia Met was replaced with valine that occurs in the corresponding position critical for JH III binding in insects, namely V315 in D. melanogaster Gce (Fig 3A and 3B) or V297 in T. castaneum Met [29], the Daphnia Met protein became more responsive to JH III, without losing its responsiveness to MF [43]. Together with our current findings, this recent evidence suggests that Gce/Met has evolved as a receptor for sesquiterpenoid hormones in a common ancestor of crustaceans and insects.  (C) Similar results were obtained for Met, which also lost its ability to activate JHRE-luc in response to JH III when its PAS-B domain was mutated at the corresponding conserved residues. In both experiments (B and C), the endogenous gce and Met were suppressed by RNAi. Data were normalized to Renilla luciferase activity and plotted as mean ± SD (n = 3). The WT and mutated Gce and Met variants were all stable as detected on immunoblots (insets) using their FLAG tags; antibody against the Mbf1 or Cheerio proteins served as controls.

Gce/Met requires ligand binding to induce transcription in response to JH
To determine whether Gce required direct binding of JH for its function, we individually mutated three amino acids (T272Y, V315F, and C366M) in the ligand-binding pocket of Gce PAS-B (Fig 3A). The same substitutions of the corresponding residues have been shown to abolish binding to JH III in the Met proteins from T. castaneum [29] and A. aegypti [30]. As expected, all three mutated Gce proteins lost the ability to bind indicating that these conserved T, V and C residues are critical for hormone binding by D. melanogaster Gce.
To test whether binding of JH was necessary for Gce to activate transcription, FLAG epitope-tagged wild-type (FLAG-Gce WT ) or mutated (FLAG-Gce T272Y ,-Gce V315F , and-Gce C366M ) proteins were expressed in S2 cells, in which the endogenous Gce and Met were suppressed by RNAi. Clearly, only FLAG-Gce WT responded to JH III to activate the JHRE-luc reporter, whereas the three Gce variants incapacitated for hormone binding did not ( Fig 3B). The wildtype and mutated Gce proteins all appeared to be stable in the S2 cells (Fig 3B, inset).
Although the endogenous Met protein did not appear to play a major role in the JH-dependent activation of JHRE-luc in the S2 cell line (Fig 1C and 1D), D. melanogaster Met could in fact substitute for Gce in this reporter assay when transfected to the cells ( Fig 3C). The S2 cells were again subjected to RNAi-mediated depletion of the endogenous Met and Gce proteins but not of the added Met protein that was expressed from a synthetic DNA construct. Like Gce, Met but not its mutated versions, mediated induction of JHRE-luc by JH III (Fig 3C). Importantly, the functional JHRE-luc reporter was not activated by Met that had been mutated in its PAS-B domain with individual substitutions T406Y, V449F, and C500M that correspond to the T272Y, V315F, and C366M mutations in Gce ( Fig 3C). These mutations did not lead to degradation of Met (Fig 3C, inset). Although we have been unable to directly confirm the effect of these mutations on the ligand-binding activity of D. melanogaster Met, it is most likely that they prevent JH III binding just as equivalent substitutions of these highly conserved residues do in Gce (S3 Fig) and in the Met proteins from T. castaneum [29] and A. aegypti [30]. These results strongly suggest that the JH-binding capacity is required for the normal function of D. melanogaster Met.
Expression of an endogenous JH-response gene relies on the JHbinding activity of Gce In D. melanogaster the Met and gce genes reside on the X chromosome and their simultaneous loss in females that are homozygous or males that are hemizygous for the Met 27 and gce 2.5k null alleles is lethal at the onset of pupation [22]. The Met 27 gce 2.5k double mutants are known to express reduced mRNA levels of the Kr-h1 gene, which is a direct target of Gce/Met [22,34,39]. In order to demonstrate that the JH-binding capacity of Gce is important in vivo for transcription of this relevant JH-response gene, we expressed the wild-type and mutated forms of Gce using the ubiquitous armadillo-Gal4 driver (arm-Gal4) in the Met 27 gce 2.5k background. To avoid the lethal phase in this strain, we examined Kr-h1 expression in Met 27 gce 2.5k /Y male larvae that were selected and genotyped during mid-third instar. The equal performance of the Gce variants was ensured by inserting all transgenic UAS-gce constructs into the same genetic locus [44].
Consistent with previous reports [22,34,39], we observed reduced Kr-h1 levels in Met 27 gce 2.5k mutants (Fig 4) albeit the difference was less dramatic, likely due to the earlier stage of our animals at which Kr-h1 expression is lower and less dependent on JH [45]. Addition of the transgenic Gce WT protein to the Met 27 gce 2.5k background significantly augmented Kr-h1 expression near levels occurring in Met + gce + sibling male larvae (Fig 4). In contrast, the Kr-h1 transcript remained low when any of the three mutated forms of Gce were expressed (Fig 4). Therefore, only when capable of binding its hormonal ligand (S3 Fig), Gce could compensate for the missing endogenous receptor proteins in restoring the normal expression of their target gene. As the function of Kr-h1 is essential for D. melanogaster to complete the prepupal stage [45], compromised Kr-h1 expression may be contributing to the lethality resulting from the absence of Gce and Met.
The ligand-binding capacity of Gce/Met is necessary for the normal response of Drosophila to JH mimics To further investigate the receptor function of Gce in vivo, we tested the relationship of JH binding to the phenomenon of "methoprene tolerance"-the insecticide resistance phenotype for which the D. melanogaster Met mutants were originally isolated and named [20]. Strains singly mutant either for Met or, to a lesser extent gce, resist doses of JH mimics that kill flies possessing both wild-type genes [20,22,46,47]. It has been shown that ubiquitous expression of a gce + transgene using the Gal4/UAS system is sufficient to reinstate sensitivity to methoprene in the Met 27 null mutants [46].
We took this approach with our Gce WT , Gce T272Y , Gce V315F , and Gce C366M transgenic constructs. When expressed under the arm-Gal4 driver, only Gce WT restored sensitivity to dietary methoprene in Met 27 homozygotes (Fig 5A). In fact, these Met 27 animals expressing Gce WT became more sensitive to methoprene than Met + controls, reflecting a dominant effect of the additional Gce WT protein. In contrast, Met 27 males and females expressing any of the three mutated Gce variants remained resistant and emerged as adults after feeding on methoprene The male progeny were selected as mid-third instar larvae and genotyped by PCR detecting the gce 2.5k deletion [22] to distinguish Met 27 gce 2.5k /Y from Met + gce + /Y siblings carrying the FM7c balancer chromosome. Groups of four larvae were subjected to qRT-PCR with primers detecting the endogenous Kr-h1α and gce transcripts (S2 Table). Values relative to mRNA levels in Met + gce + /Y controls (set to 1) are mean ± SD from three biological replicates for each genotype, five replicates for Gce WT . The significance levels of differences determined by t-test were P < 0.02 (*), P = 0.0002 (**), and P < 0.0002 (***).  ; arm-Gal4 (or tub-Gal4) females were crossed with males bearing the UAS-gce or UAS-Met transgenes, and emerged Met 27 gce 2.5k /Y adult males were scored relative to their FM7c/Y (Met + gce + ) siblings (1:1 ratio was considered 100% rescue). Non-conditionally lethal Met 27 gce 2.5k /Y males were rescued to adulthood by transgenic Gce WT , FLAG-Gce WT , and Met WT proteins but not by their mutated versions except for a few flies rescued by one randomly inserted FLAG-Gce V315F construct expressed under arm-Gal4 (C). Data are mean ± SD; numbers of ( Fig 5A). Similar results were obtained with pyriproxyfen ( S4 Fig). Thus, the lethal action of the insecticidal JH mimics relies on the ligand-binding capacity of the transgenic Gce protein.
To obtain similar information for Met, we repeated this experiment with fly strains expressing the D. melanogaster wild-type Met protein or its mutated versions Met V449F and Met C500M (our initial attempt to transform flies with UAS-Met T406Y failed). Although the flies expressing Met WT under the arm-Gal4 driver did not become more sensitive than control Met + flies, their response to dietary methoprene significantly increased relative to the original Met 27 mutants or the same mutants carrying the Met V449F and Met C500M transgenes (Fig 5B). Our data thus demonstrate that Gce and Met are mutual substitutes in rendering flies sensitive to exogenous JH mimics as long their ligand-binding pockets are unaffected by specific mutations.

The capacity of Gce/Met to prevent lethality in Met gce double-mutant flies depends on hormone binding
The non-conditional lethality of the Met 27 gce 2.5k double-mutants can be rescued with transgenic constructs providing either Met + or gce + function, thus reflecting partial redundancy between Met and Gce [22]. This genetic rescue offers an ideal system to answer the ultimate question as to whether Gce/Met requires its JH-binding capacity to sustain normal development of the animal. Using two ubiquitous drivers, arm-Gal4 and α-tubulin (tub-Gal4), and transgenic UAS-gce and UAS-Met constructs uniformly inserted to the attP2 chromosomal site [44], we expressed the functional or mutated proteins in the Met 27 gce 2.5k background. Indeed, expression of Gce WT or Met WT under both drivers rescued a major proportion of Met 27 gce 2.5k / Y hemizygous males to adulthood (Fig 5C and 5D). In striking contrast, the mutated Gce T272Y , Gce V315F , Gce C366M , Met V449F or Met C500M proteins did not allow any Met 27 gce 2.5k /Y adults to emerge (Fig 5C and 5D). Therefore, only Gce/Met with intact JH-binding function can substitute for the absence of both genes during normal development.
To examine whether Gce incapacitated for JH binding was stable in vivo, we expressed FLAG-tagged versions of Gce WT , Gce T272Y , and Gce V315F in transgenic D. melanogaster. Again, only the functional but not the JH binding-deficient tagged protein provided a clear rescue of the Met 27 gce 2.5k mutants (Fig 5C). Interestingly, marginal rescue of 7.5% of emerging adults was observed, albeit only with the arm-Gal4 driver, with FLAG-Gce V315F (Fig 5C), suggesting that this mutated protein might retain some residual functionality. The discrepancy between this weak effect and the total absence of rescue by untagged Gce V315F (Fig 5C) might result from variable expression level of the FLAG-tagged construct that, unlike the untagged constructs, had been integrated to random loci rather than to the specific attP2 site. Indeed, from three independent FLAG-Gce V315F transgenic lines, only one showed the partial genetic rescue.
Importantly, all three FLAG-tagged Gce variants were detected on immunoblots from whole transgenic flies (Fig 5E), and all were observed primarily in the nuclei of larval fat body cells (Fig 5F), regardless of whether or not Gce was mutated to prevent binding of JH. Thus, the failure of mutated Gce to compensate for the loss of the endogenous Met and Gce proteins was more likely caused by inability to bind JH rather than by degradation or mislocalization of the mutated protein.
In conclusion, our study shows that the capacity of Gce, and most likely also of Met, to promote gene expression and sustain normal development requires direct hormone binding to the protein in vivo. The case that Gce/Met acts as a JH receptor in insects is now unequivocal. Establishment of the nature of this receptor resolves a central problem in arthropod endocrinology. The ability of Gce to respond to methyl farnesoate, the crustacean JH, suggests that the role of Gce/Met in sesquiterpenoid signaling predates the evolutionary separation of the hexapod and crustacean lineages. Furthermore, it is of interest that Gce/Met provides the first clear example of a bHLH-PAS protein acting as a receptor for a genuine animal hormone.

Vectors for Gce and Met protein expression
DNA sequences corresponding to the D. melanogaster Gce (amino acids 1-689; NCBI Reference Sequence NP_511160.1) and Met (amino acids 1-716; NCBI Reference Sequence NP_511126.2) were synthesized for optimal D. melanogaster codon usage to encode the Gce and Met wild-type (WT) and mutated (T272Y, V315F, C366M, T406Y, V449F, C500M) variants. For transcription/translation in vitro, these DNA fragments were cloned using the Eco RI and Kpn I restriction sites behind the T7 promoter in the pK-Myc-C2 plasmid [48]. The same gce and Met DNA sequences were inserted under the UAST promoter in two different vectors for D. melanogaster transformation: pTFW (Drosophila Genomics Resource Center), in which Gce was N-terminally tagged with a FLAG epitope, and pUASTattB [49] that permitted integration of the gce/Met transgenes into the specific attP2 chromosomal landing site [44].

Ligand-binding assays
Racemic (RS) tritiated JH III (10-20 Ci mMol -1 ) was purchased from Perkin Elmer. Racemic JH III, pyriproxyfen, trans,trans-farnesol and methoprene were from Sigma-Aldrich, and (E, E)-methyl farnesoate (MF) from Echelon Biosciences. The WT, T272Y, V315F, and C366M variants of Gce were produced with the rabbit reticulocyte lysate TnT Quick Coupled transcription/translation system (Promega) using 400 ng of template plasmid per 50-μl reaction. Each reaction was divided into 15-μl aliquots that were assessed for binding of [ 3 H]JH III using the dextran-coated charcoal (DCC) method as described previously [29]. The dissociation constant (K d ) was determined for Gce WT binding to [ 3 H]JH III, and the K i values for methoprene, pyriproxyfen, MF and farnesol were calculated from competition assays with the unlabeled compounds using GraphPad Prism 5.00 (GraphPad Software) as described [29].

Luciferase reporter assays
A JH-responsive luciferase reporter (JHRE-luc) was generated using a JH response element (JHRE) (5'-CCATCCCACACGCGAAGACGATAAAACCA-3') identified upstream of the Aedes aegypti early trypsin (AaET) gene [31]. A mutated version of this element (5'-CCATCC CAGTGCGCAAGACGATAAAACCA -3') was used to generate a negative-control mutJHREluc. DNA sequences were synthesized to include eight copies of either JHRE or mutJHRE, followed by a 140-bp minimal promoter of the AaET gene (nucleotides -77 to +63). These sequences were cloned to the pGL4.17 vector containing the firefly (Photinus pyralis) luc2 gene (Promega). D. melanogaster Schneider 2 (S2) cells were cultured in Shields and Sang M3 Insect Medium (Sigma-Aldrich) containing 8% of heat-inactivated fetal bovine serum (Life Technologies) at 25°C. For luciferase reporter assays, S2 cells were seeded in a 12-well plate containing 900 μl of medium per well, and cultured for 24 h. The JHRE-luc (or mutJHRE-luc) reporter plasmid (0.25 μg per well) was co-transfected with a pCopia plasmid (0.1 μg per well) encoding Renilla luciferase using the X-tremeGENE HP DNA Transfection Reagent (Roche). Where appropriate, the D. melanogaster Tai protein was expressed from a pCMA plasmid (0.25 μg per well) containing tai cDNA [31,50]. Expression of either the wild-type or mutated FLAG-tagged Gce and Met variants was achieved by co-transfecting 0.25 μg of a pTFW vector carrying the respective gce or Met DNA sequence under the UAST promoter with 0.1 μg of a plasmid expressing the Gal4 transcription factor under a D. melanogaster actin promoter. The total DNA load per well was kept constant at 1 μg by inclusion of non-specific plasmid DNA. Following transfection, cells were incubated for 48 h and treated for another 12 h with JH III, methoprene, pyriproxyfen, MF or farnesol (all dissolved in ethanol). The cells were then processed with the Dual-Luciferase reporter assay system (Promega). Relative luciferase activity was measured using the Orion II microplate luminometer (Berthold Detection Systems) and data were normalized against Renilla luciferase activity.

RNAi in S2 cells
Met, gce and tai cDNAs were obtained by reverse transcription of total D. melanogaster embryonic RNA, followed by PCR amplification with specific primer sets (S1 Table). The cDNA fragments were flanked with T7 promoter sequences to enable synthesis of double-stranded RNA (dsRNA) using T7 RNA polymerase (MEGAscript, Ambion). A 720-bp dsRNA derived from the egfp gene served as a control. To knock down Met, gce, and tai genes in S2 cells, 3 μg of dsRNA per well of a 12-well plate were added together with plasmid DNA in the transfection mixture. The dsRNA sequences targeting endogenous gce and Met did not interfere with expression of the Gce and Met (WT or mutated) proteins transfected with the pTFW vector, as those were encoded by synthetic DNA divergent from the endogenous DNA sequences. Moreover, gce dsRNA targeted an upstream region of the native gce transcript that did not overlap with the synthetic sequence included in the pTFW-gce constructs.

mRNA quantification
Total RNA isolated from whole mid-third instar D. melanogaster larvae or S2 cells using the Trizol reagent (Life Technologies) was treated with TURBO DNase (Ambion), and 1.5 μg of RNA was reverse transcribed to cDNA (Superscript II, Life Technologies). Relative transcript levels were measured in a C1000 Thermal Cycler (Bio-Rad) using the iQ SYBR Green Supermix kit (Bio-Rad) using specific primer sets (S2 Table) and normalized against levels of the ribosomal protein 49 (rp49) mRNA.

Drosophila transgenesis
Targeted insertion of gce transgenes into the attP2 landing site on the third chromosome (cytological position 68A4) was achieved using the bacteriophage ϕC31 integrase method [44]. The pUASTattB constructs containing the WT and mutated gce or Met sequences were injected into embryos of the y w P{nos-ϕC31\int.NLS}X; P{CaryP}attP2 host strain (Genetic Services, Inc. or BestGene, Inc.). Several independent transgenic lines for expression of the FLAG-tagged Gce WT , Gce T272Y , and Gce V315F proteins were generated through conventional P-element mediated transformation by injecting embryos of the w 1118 host strain with the pTFW-based vectors (Genetic Services, Inc.). In all cases, expression of the transgenic proteins was induced using the Gal4/UAS system [51] with the ubiquitous armadillo (arm-Gal4) or α-tubulin (tub-Gal4) drivers (Bloomington Drosophila Stock Center, Indiana).
Genetic rescue experiments D. melanogaster with unaffected Met + function are sensitive to exogenous JH or its mimics as early prepupae [52], whereas flies deficient for Met tolerate exposure to these compounds [20,47]. To test for restoration of methoprene sensitivity to Met 27 mutants, homozygous Met 27 ; arm-Gal4 females were mated with Met 27 /Y; UAS-gce or Met 27 /Y; UAS-Met males carrying the wild-type or mutated transgenes, all inserted into the same attP2 landing site [44]. The uniform Met 27 ; arm-Gal4/+; UAS-gce (or UAS-Met)/+ F1 progeny was exposed to methoprene, pyriproxyfen or ethanol alone from the outset of larval feeding, and numbers of emerged adults were scored relative to all animals forming pupae.
To test for rescue of viability in the non-conditionally lethal Met 27 gce 2.5k double mutants, balanced Met 27 gce 2.5k /FM7c; arm-Gal4 or Met 27 gce 2.5k /FM7c; tub-Gal4 females were crossed with w 1118 /Y; UAS-gce or w 1118 /Y; UAS-Met males harboring the wild-type or mutated gce or Met transgenes in the attP2 landing site. To detect the transgenic Gce proteins, we used males with UAS-FLAG-gce transgenes carried on the pTFW vector and inserted into random genomic loci.

Immunoblotting and antibody tissue staining
Immunoblots were prepared from total D. melanogaster S2 cell lysates or from entire adult transgenic flies and processed with an anti-FLAG antibody (Sigma-Aldrich; 1:4000) and with anti-Mbf1 or anti-Cheerio antibodies as previously described [53]. Clones overexpressing WT or mutant Gce proteins were induced using the heat-shock-FLPout technique [54], whereby y w hs-flp; act>y+>Gal4, UAS-GFP females were mated to UAS-FLAG-gce transgenic males. Fat bodies dissected from larval progeny one day after heat shock (37°C, 30 min) were stained with anti-FLAG (Sigma-Aldrich; 1:1000) and Cy3-conjugated (Cell Signaling) antibodies, and images were captured with the Olympus FV1000 confocal microscope. was lethal for the same Met 27 strain expressing Gce WT but none of its mutated variants incapable of binding JH. Values are per cent average numbers of emerged adults relative to total number of pupated animals. The total numbers of animals counted in three independent trials are above columns. (TIF) S1 Table. Primer sets for cloning of cDNA fragments for dsRNA synthesis. (DOC) S2 Table. Primer sets for quantitative reverse transcription-PCR (qRT-PCR).

Supporting Information
(DOC)