Genetic tools to study juvenile hormone action in Drosophila

Baumann, A. A.; Texada, M. J.; Chen, H. M.; Etheredge, J. N.; Miller, D. L.; Picard, S.; Warner, R.; Truman, J. W.; Riddiford, L. M.

doi:10.1038/s41598-017-02264-4

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Published: 18 May 2017

Genetic tools to study juvenile hormone action in Drosophila

A. A. Baumann^1,2,
M. J. Texada ORCID: orcid.org/0000-0003-2479-1241¹,
H. M. Chen¹,
J. N. Etheredge¹,
D. L. Miller^1,3,
S. Picard¹,
R. Warner¹,
J. W. Truman^1,4 &
…
L. M. Riddiford^1,4

Scientific Reports volume 7, Article number: 2132 (2017) Cite this article

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Abstract

The insect juvenile hormone receptor is a basic helix-loop-helix (bHLH), Per-Arnt-Sim (PAS) domain protein, a novel type of hormone receptor. In higher flies like Drosophila, the ancestral receptor germ cell-expressed (gce) gene has duplicated to yield the paralog Methoprene-tolerant (Met). These paralogous receptors share redundant function during development but play unique roles in adults. Some aspects of JH function apparently require one receptor or the other. To provide a foundation for studying JH receptor function, we have recapitulated endogenous JH receptor expression with single cell resolution. Using Bacteria Artificial Chromosome (BAC) recombineering and a transgenic knock-in, we have generated a spatiotemporal expressional atlas of Met and gce throughout development. We demonstrate JH receptor expression in known JH target tissues, in which temporal expression corresponds with periods of hormone sensitivity. Larval expression largely supports the notion of functional redundancy. Furthermore, we provide the neuroanatomical distribution of JH receptors in both the larval and adult central nervous system, which will serve as a platform for future studies regarding JH action on insect behavior.

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Introduction

Juvenile hormone (JH) drives various aspects of insect physiology. A well-documented role for this hormone is to prevent early metamorphosis. In most insects, JH prevents early induction of key metamorphosis-initiating genes. As larvae gain competence to undergo metamorphosis¹, the JH titer drops, reducing expression of the antimetamorphic, JH response gene Kr-h1, which lifts suppression on pupal or adult developmental programs^{2, 3}. This aspect of JH activity has promoted the synthesis of batteries of compounds employed to combat pest insects. These JH analog (JHA) insecticides have been used in various formulations to combat medical and agricultural pests^{4, 5} since their exogenous application can disrupt normal development. Methoprene, a JHA that shares structural similarity with endogenous JH, has proven valuable as both a research tool and as a key component of flea and tick preventative products for companion animals.

Unlike beetles and moths, in which JHAs can induce supernumerary larval instars, JH exposure does not override metamorphosis in flies⁶, which instead die as pharate adults that fail to eclose from the puparium. Furthermore, the best candidate for a Drosophila JH receptor, the bHLH PAS protein Met, was demonstrated to be encoded by a nonvital gene⁷. Thus, despite its utility as a powerful genetic model, progress toward understanding JH signaling in Drosophila has been frustratingly slow. However, Konopova and Jindra⁸ demonstrated that suppressing the presumed Met ortholog in Tribolium using RNAi induced developmental phenotypes that were typical of a loss of JH signaling; specifically, TcMet-deficient animals experienced precocious metamorphosis. Sequence analysis demonstrated that TcMet is ancestral to another Drosophila bHLH PAS gene called gce ⁹, and that DmMet arose during dipteran evolution^{10, 11}. Met ²⁷ gce ^2.5k double null larvae suffer developmental arrest during pupariation¹², which phenocopies the effects of the loss of JH achieved through genetic ablation of the JH-producing gland, the corpus allatum (CA) (allatectomy, CAX;¹³). Unlike CAX larvae¹⁴, Met ²⁷ gce ^2.5k larvae cannot be rescued by supplying exogenous JHA¹². However, they can be rescued with a single ectopic copy of either gene, demonstrating redundancy. Recent work has demonstrated that Met and Gce proteins each bind JH with high affinity and that this binding is eliminated when the ligand-binding pocket is mutated¹⁵. As bona fide paralogous JH receptors (JHR), these proteins represent a novel class of metazoan hormone receptor¹⁶.

Paralog-specific function for each JH receptor has primarily been described in adults^{17, 18}. In addition to its developmental and reproductive roles, JH signaling also influences insect behaviors, including courtship^{17, 19}, aggression²⁰, and the onset of foraging behavior in honey bees²¹. While studies have demonstrated how JH acts during nervous system development^{14, 22}, we understand virtually nothing about how JH influences the neuronal circuits underlying various insect behaviors.

To provide a framework for addressing the tissue- and cell-specific action of JH, we determined the spatiotemporal expression of JH receptors through Drosophila development using a series of genetic tools. Specifically, we recapitulated endogenous Met and gce expression in both larval and adult Drosophila melanogaster using both recombineered BAC drivers and a viral T2A peptide-mediated transgenic knock-in to drive the expression of a variety of fluorescent reporter constructs. Our results suggest that Met and gce share considerable expressional overlap in larval Drosophila, supporting the notion of functional redundancy during preadult development¹². There were a few key exceptions to this finding, in which one receptor was expressed at substantially higher levels than, or in exclusion to, its paralog. Furthermore, we demonstrate JH receptor expression in known JH target tissues, the temporal dynamics of which are consistent with periods of hormone sensitivity. In both larvae and adults, paralog-specific expression was evident predominantly in the central nervous system (CNS), suggesting that they have distinct contributions to JH-regulated behavior and CNS development. Here, we provide a neuroanatomical atlas of JHR expression, which will ultimately facilitate future studies regarding JH action in CNS development and function.

Results

BAC Validation

In this study we recapitulated endogenous JHR expression using transgenic D. melanogaster carrying either (1) one of several BACs comprised of a gce or Met coding sequence, interrupted by a GAL4::p65 or LexA::p65 driver fragment replacing the first exon, and flanked bilaterally by 40 kb of genomic DNA (Fig. 1a,b), or (2) a T2A-GAL4 fusion construct inserted in frame into the native gce genomic locus (Fig. 1a). These constructs were used to drive the expression of a number of fluorescent reporter constructs. We used several experimental approaches to validate the reported expression patterns.

First, we generated genomic rescue stocks containing the native BAC clones for Met or gce, which lacked a driver cassette. We crossed these lines to Met ²⁷ gce ^2.5k/FM7c females and scored the survival of progeny. Met ²⁷ gce ^2.5k animals die early in pupal development, but can be rescued to adulthood with an ectopic Met or gce transgene¹². Crosses of Met ²⁷ gce ^2.5k/FM7c females to w ¹¹¹⁸ control males resulted in only FM7c/Y males, and their vials showed 25.9% pupal mortality (n = 194), accounting for wvMet ²⁷, gce ^2.5k/Y males that did not complete metamorphosis. Males carrying the native gce BAC eclosed at levels comparable with balancer sibs, indicating complete rescue (n = 174). By contrast, transformants carrying the native Met BACs rescued only 12% of Met ²⁷ gce ^2.5k double mutants (n = 164) and the rescued males showed mosaic w ⁺ expression in their compound eyes. Therefore, while we were satisfied that the native gce BAC contained sufficient regulatory sequence to direct expression of functional gce, the native Met construct either could not restore JH signaling or contained genes which, when duplicated in the genome via ectopic expression, were incompatible with the JH receptor mutant background.

To determine whether Met-GAL4::p65 could rescue Met phenotypes, we crossed the Met-GAL4::p65 reagent into the Met ²⁷ mutant line, but this stock was fragile and could not be maintained. We elected to sequence the genome of the Met-GAL4::p65 reagent to evaluate the integrity of the construct. We discovered that the BAC contained small deletions in a 5′ gene, CG1703 (see Fig. 1b for position of CG1703). However, adjacent sequence corresponding to that contained in either the St-H fragment²³ or the p[EN71] genomic rescue construct²⁴ was intact. We therefore proceeded under the assumption that the Met expression reported using this BAC might represent the endogenous pattern.

Since we successfully generated multiple gce drivers, we compared the expression patterns reported among these various iterations. We compared gce-LexA::p65 and gce-GAL4::p65 directly in the same line: gce-LexA::p65 (attP40) > 13xLexAop2-IVS-myr-tdTomato-p10 (attP40); gce-Gal4::p65 (VK00033) > 10xUAS-IVS-myr-GFP-p10 (attP2). Confocal analysis revealed considerable overlap between LexA::p65 and GAL4::p65 reagents, both in adults and larvae (Fig. 1c–g”). Observed differences in spatial partitioning or expression strength of GFP reporters driven by the GAL4 and LexA BAC constructs were likely due to a combination of position (chromatin) effects, driver strength, and reporter architecture, as previously reported^{25, 26}. In contrast, there were substantial differences in BAC- and T2A-reported GFP CNS expression for the gce gene, discussed below.

Larval expression

Met-GAL4::p65 and gce-GAL4::p65 or gce-T2A-GAL4 each exhibited widespread tissue expression during larval growth including in epidermis, fat body, muscles, salivary glands (Fig. 2) and the central nervous system (CNS; Fig. 3). As in most other larval tissues, JHR expression was widespread in the larval CNS (Fig. 3a–d). One significant distinguishing characteristic was that Met > myr-GFP-p10 showed strong expression in the mushroom bodies (mb) (Fig. 3a,e’), while gce > myr-GFP-p10 showed moderate mb expression (Fig. 3b,f’), and gce-LexA > myr-tdTomato-p10 showed none (Fig. 3f). In contrast to the BAC construction, the gce knock-in, gce-T2A-GAL4, showed obvious expression in the mushroom body (Fig. 3e). Met > myr-GFP-p10 showed broad expression in the developing optic lobe, including the nascent lobula and medulla neuropils in WL3 stage larvae (Fig. 3a,e’), whereas gce neuronal expression using all three gce constructs and different reporters was essentially absent from the developing optic lobes (Fig. 3b–e,f and f’), but was evident in surface glia (Fig. 3d,e,f and f’). Both receptors were present in key peptidergic neurons whose axons project into the ring gland, including the prothoracicotropic hormone (PTTH) neurons that stimulate ecdysteroid production by the prothoracic glands (PG) (Fig. 3g,h,k and l) and the CA-LP1 and −2 neurons whose axons terminate in the corpus allatum (see Fig. 3g–j and m).

In wild type flies, JH I or JH III application during the sensitive period severely disrupts adult abdominal differentiation by suppressing the proliferation and spreading of the abdominal histoblasts that normally give rise to the adult abdominal epidermis^{27, 28}. Met mutants are refractory to this effect of JH treatment²⁹. We detected both JHRs in wandering stage larva (WL3) histoblasts, with expression persisting through pupariation, and then tapering off by 9 h APF (Fig. 4).

Imaginal discs

Met-GAL4::p65 was expressed in wing, eye, leg, and genital discs (Fig. 5a–c and data not shown). In contrast, there was no gce-GAL4::p65 or gce-T2-GAL4 expression in the wing, leg, eye, or genital imaginal discs of larvae (Fig. 5d–f) with any driver/reporter combination. To validate these results, we performed qPCR analyses with Met- and gce-specific primers, using cDNA libraries prepared from either pooled leg discs and wing discs, or from larval CNS’s which included associated leg discs. We employed two tissue-specific control genes to verify the integrity of the disc-specific sample: Notum was chosen for its enrichment in wing discs (ModEncode;³⁰) while bruchpilot (brp), which marks presynaptic active zones in the CNS³¹, was used as a CNS-specific control gene. Consistent with our confocal data, we detected no gce transcript in wing/leg disc samples, while Met showed low expression in these tissues (Fig. 5g).

In contrast to the effects of exogenous JH on the differentiation of the adult abdomen derived from the histoblasts, structures derived from imaginal discs are not affected by JH treatment^{27, 28}. We hypothesized that an absence (gce) or modest level (Met) of JHR expression in the discs might explain their JH insensitivity. To test this, we attempted to induce JH sensitivity, and presumably a reinduction of pupal cuticle, in wing discs, by supplying ectopic gce, Met, or both transgenes, using the c765-GAL4 driver, which expresses strongly in wing discs³², and rearing these larvae on food containing 1 ppm pyriproxyfen [a potent JHA for Drosophila ⁶]. However, none of these manipulations shifted the response of the wing discs to JHA (Fig. 5h and data not shown), suggesting that simply supplying additional JHR to imaginal discs is not sufficient to confer JH sensitivity to these tissues.

Ring gland

The ring gland of higher dipteran larvae contains the endocrine cells of the JH-producing corpus allatum (CA) and the paired, lateral prothoracic glands (PG), which synthesize and secrete ecdysone (Fig. 6a). As shown in Fig. 6b, we observed strong Met and gce expression in both the CA and PG during larval life; gce-T2A-GAL4 > nls-GFP additionally showed strong expression in the corpus cardiacum (Fig. 6b, bottom row).

We sought to address the significance of JHR expression specifically in the PG, since this organ is considered a size-assessing tissue that regulates the time of metamorphosis³³. We used RNAi to suppress Met expression specifically in the PG of gce ^2.5k mutants, effectively eliminating both receptors from the PG. Met RNAi was functionally validated since its expression driven by Act5C-GAL4 in gce mutants produces the double mutant phenotype¹². gce ^2.5k; Act5c > Met RNAi larvae (either 1x Met RNAi in gce ^2.5k ; Act5C > 45854 or 2x Met RNAi in gce ^2.5k ; Act5C > 45854, 45852) showed nearly 100% pupal lethality (Fig. 6c; n = 195, 1x Met RNAi; n = 183, 2x Met RNAi), while balancer sibs showed approximately 100% survival to adulthood (n = 214, 1x Met RNAi cross; n = 142, 2x Met RNAi). Met suppression in the PG using gce ^2.5k ; phm > 45852 was inconsequential for survival (n = 152/152).

Since an earlier study showed that Met suppression in the PG did not alter timing from the L2/L3 transition to pupariation³⁴, we tested the hypothesis that gce expression may provide functional redundancy. We staged larvae in 6-hour egg collections and scored time to pupariation as the proportion of puparia to wandering larvae (Fig. 6d). wgce ^2.5k;;phm-GAL4 homozygotes were developmentally delayed beyond wgce ^2.5k;;phm > Met-RNAi or wgce ^2.5k;;phm > TM6b lines. The two phm-GAL4 heterozygous lines showed nearly identical developmental timing profiles, but were slightly delayed relative to the wgce ^2.5k;;Met-RNAi/TM6b parental stock. These data indicate that while phm-GAL4 expression alone can induce a dose-dependent developmental phenotype, Met and gce suppression together in the PG does not alter developmental timing beyond the shift incurred by simply expressing phm-GAL4.

Adult expression

Recent studies have revealed that reproductive behaviors are influenced by JH signaling, some of which require either Met or Gce¹⁷. The driver lines indicated that both JHRs were widely expressed in adults, with wide expressional overlap in many tissues. Here, we focus on expression in reproductive tissues and the adult CNS.

Met mutants suffer substantial reproductive deficiency, while gce mutants show only minor reductions in reproductive capacity¹². Figure 7 provides an overview of Met and gce expression in male and female reproductive tissues as reported by the nuclear reporter UAS-nls-GFP. In males, both receptors show widespread expression; the ejaculatory duct and ejaculatory bulb, accessory glands and vas deferens all showed moderate to high level of Met and gce expression (Fig. 7a,b,g,k and k’). In females, both receptors showed strong expression in the spermathecae (Fig. 7f,h and m), regardless of mating status, as well as in the seminal receptacle (Fig. 7c,m), and uterus (Fig. 7e,h and m), but not in early stage oocytes (pvO in Fig. 7d,i, and data not shown). However, both receptors showed expression in the follicle cells of stage 8–10 oocytes, but gce UAS-nls-GFP expression in these cells was moderate compared to that of Met (Fig. 7j,l). We boosted expression with either cytoplasmic GFP or myr-GFP-p10 to unequivocally identify gce in stage 8–10 oocytes (vO; Fig. 7d,i;). Reproductive tissues showed similar reporter expression for the gce-GAL4::p65 and gce-T2A-GAL4 drivers (Fig. 7a–j).

To evaluate Met/gce expression in the brain, we employed a series of reporters specifically tailored for neuroanatomy^{26, 35}. Overall, both receptors expressed broadly across the adult CNS, with each showing a unique and reproducible pattern. Indeed, the most striking examples of divergent JHR expression were observed across the various cell types of the adult CNS. For example, we observed distinct partitioning across compartments in the central complex and optic lobes (OL). An overview of both JHRs as reported with myr-GFP-p10 is shown in Fig. 8(a,a’,f,f’,k and k’).

In the central complex, Met and gce expressed with variable intensity across the ring neurons of the ellipsoid body (EB), and either shared or occupied discrete layers of the fan-shaped body (FB). Across the layers of the FB, gce > myr-GFP-p10 showed the most intense expression in layers 4 and 6, with comparatively weak expression in layer 5 (Fig. 8h), and also expressed in the asymmetrical body (AB), a unilateral structure associated with long term memory formation and retrieval³⁶. gce-T2A-GAL4 > myr-GFP exhibited a similar expression pattern, with weaker GFP signal evident in layers 2, 3, and 5 relative to other layers (Fig. 8m). Met > myr-GFP-p10 showed global expression across the FB, with strongest expression shown in layers 1 and 5 (Fig. 8c). Met > myr-GFP-p10 expression in the EB (Fig. 8b) was comparatively weaker than gce > myr-GFP-p10 and gce-T2A-GAL4 > myr-GFP (Fig. 8g,l), the latter of which was exceptionally strong relative to expression across the entire brain. The paired noduli (NO) displayed prominent dorso-ventral segregation of JHRs. Met > myr-GFP-p10 showed highly enriched expression in the ventral NO3, with moderate expression in NO1 and NO2 (Fig. 8d’). In contrast, gce-GAL4::p65 > myr-GFP-p10 signal across the NO was moderate to strong in NO2 and NO1 (Fig. 8i), while gce-T2A-GAL4 > myr-GFP showed minimal expression in NO2, with moderate expression in both NO1 and NO3 (Fig. 8n).

Given the staggering diversity of cell types in the OL, we focused on a handful of distinctive features that characterized the expression pattern of each receptor. Met > myr-GFP-p10 and gce > myr-GFP-p10 either coexpressed or expressed individually in the various cell types that constitute the layers of two of the major OL neuropils, the lobula and the medulla³⁷, thus establishing a paralog-specific banding pattern in each neuropil (Fig. 8e,j). Some features of optic lobe expression were consistent between the BAC and knock-in gce reagents. None of the gce constructs drove reporter expression in the T4 or T5 layers of the medulla or lobula, respectively (Fig. 8j,o). There were also notable differences in the gce drivers. For instance, while BAC reagents showed moderate lobula plate expression (Fig. 8j), the T2A-GAL4 reagent did not drive myr-GFP expression in the lobula plate (Fig. 8o).

Expression of the JHRs in the medulla was complex with some layers showing expression of both receptors, other showing expression of neither, and still others with enhanced expression of Met or gce. Both Met > myr-GFP-p10 and gce > -myr-GFP-p10 as well as gce-T2A-GAL4 expressed in axon bundles of cells crossing the inner chiasm (Fig. 8e,j and o). In the lobula, Met > myrGFP showed highest expression in layer 1 (Fig. 8e). By contrast, gce > myr-GFP-p10 and gce-T2A-GAL4 are lacking in layer 1 but are at high levels in the other layers of the lobula (Fig. 8j,o). Also, Met > myr-GFP-p10 showed moderate expression in the medial-most layer 10 of the medulla occupied by arborizations of T4 cells, where gce was absent (Fig. 8j,o).

Discussion

In this study we used a set of genetic tools to probe developmental expression of the duplicate Drosophila JH receptors Met and gce, by recapitulating their expression with fluorescent reporters. We have systematically surveyed larval and adult tissues, with emphasis on neuronal expression. Coexpression experiments in which the GAL4 and LexA gce reagents drove simultaneous GFP and tdTomato constructs demonstrated extensive expressional overlap between these reagents, but also illustrated some differences (Fig. 1e–g”). The T2A-GAL4 knock-in and BAC reagents showed substantially divergent expression patterns in key CNS structures in both larvae and adults, likely a consequence of position effects and construct architecture, though there were shared features. Peripheral tissue expression was essentially the same between the T2A and BAC iterations of the gce constructs, indicating that at least in non-CNS tissues, BAC expression is a reliable proxy for endogenous gce expression. We obtained only a single Met-GAL4::p65 BAC reagent; several efforts to produce a Met knock-in reagent were fruitless. Given the differences between BAC and knock-in data for gce, we propose that the Met BAC reagent faithfully recapitulates peripheral tissue expression but likely only approximates Met expression in the CNS, since we were unable to generate the “gold standard” genomic knock-in reagent for Met.

Overall, our confocal data are consistent with characterized aspects of tissue-specific JH action and therefore represent a working foundation for future studies regarding JH action at the cellular level in Drosophila. An overview of key expression features in the larva is given in Fig. 9a–a”. JHR redundancy during larval life¹² is supported by their near global coexpression. A key exception to this finding was that gce but not Met was conspicuously absent from the imaginal discs (Fig. 5a,b and c). Following JHA challenge, disc-derived structures develop normally in Drosophila ^{6,27, 28}. In contrast, exogenous JHA reprograms the abdominal histoblasts by maintaining the expression of the pupal specifier Broad, promoting a second pupal, rather than adult, epidermis³⁸. We demonstrate here that Met and gce coexpress in histoblasts during the window of JH sensitivity²⁸, following which their expression declines, with gce levels declining followed by Met, beginning at 9 h APF (Fig. 4). Under the rationale that JH sensitivity requires both receptors, we created lines in which Met, gce, or both were ectopically expressed specifically in the wing disc. However, following dietary JH treatment, wing development in both experimental and balancer flies was normal (Fig. 5h), indicating that ectopic JHR expression was not sufficient to confer JH sensitivity to this tissue. To address the possibility that another component of the JH receptor machinery was absent in wing discs, we labeled the discs with antibodies against the JH-dependent Met binding partner Taiman (Tai)^{39, 40}. Tai was observed in discs in late wandering larvae, before the onset of pupariation (Fig. S1). Therefore, the canonical JH signaling pathway is present. Perhaps unidentified inhibitory factors block JH action in wing discs or downstream components are missing.

Removing JH signaling in Drosophila larvae, through genetic ablation of the CA [allatectomy (CAX); 13, 14] or by suppressing Met/gce function¹², cannot prevent the onset of metamorphosis, but does alter developmental timing in the third instar. During this instar, the PG establishes the timing of pupariation by assessing larval size to determine whether the critical weight checkpoint, which corresponds to the time after which starvation cannot prevent metamorphosis, has been attained³³. By suppressing Met expression specifically in the PG, Mirth et al.³⁴ demonstrated that this treatment is insufficient to alter time to pupariation relative to phm/+ control larvae. In this study we found Met and Gce were coexpressed in the PG during larval development (Fig. 6b), suggesting the possibility that Mirth et al.³⁴ failed to override functional redundancy between JHRs in the PG. To address this, we performed the same manipulation in gce mutants, eliminating PG expression of both JHRs. There was no difference in pupariation time between the Met RNAi larvae and the Tm6b balancer sibs although both were delayed slightly in comparison to the parental stock, indicating that the phm-GAL4 construct itself can influence the time to pupariation. Our finding that the gce mutant with two copies of the phm-GAL4 construct showed a large delay in pupariation time indicates that this delay is dose-dependent. Thus, the phm-GAL4 construct alone is sufficient to shift time to pupariation, a phenotype that is consistent with perturbed ecdysone synthesis or PG function⁴¹. When we attempted to create a wvMet ²⁷;;phm/TM6b line, the stock was fragile and showed extensive preadult mortality, indicating that Met flies are sensitive to PG manipulation, and that expression of GAL4 alone in the PG has developmental consequences.

Reciprocal biosynthetic regulation between JH and ecdysone pathways has been demonstrated in several species, though the mechanisms segregate along taxonomic lines. In the hemimetabolous Diploptera punctata, expression of the ecdysone receptor proteins EcR and RXR (USP) coincides with an elevation in JH titer in 5-day old adult females; suppressing these genes lowers ecdysteroid titer and elevates JH biosynthesis in 6-day old females⁴². In holometabolous insects, 20E has an evolutionarily-conserved allatotropic role. JH biosynthesis is irreversibly stimulated in cultured Aedes aegypti CA following 20-hydroxyecdysone (20E) addition at a concentration of 10⁻⁶ M⁴³. Fourth instar Bombyx mori CC-CA complexes likewise increased JH biosynthesis when cultured with 20E in a narrow concentration range, and this JH synthesis profile was concomitant with the elevation and subsequent decline in the transcript abundance of two JH biosynthetic enzymes⁴⁴. In both A. aegypti ⁴³ and B. mori ⁴⁴, 20E overrides an inhibitory factor from the brain that prevents JH synthesis at a developmentally inappropriate time.

In Drosophila such a factor(s) may be a product of the CA-LP1/2 neurons that innervate the CA⁴⁵, and which according to the present study, show JHR expression in WL3 larvae. Further, JH receptor expression in CA/PG cells, as well as in CA-LP and PTTH neurons suggests a potential role in coordinating hormone biosynthesis. For instance, by responding to changes in hormone titer, JHRs may participate in a feedback mechanism through which one or both receptors monitor the rate of biosynthesis or release of JH, ecdysone, or both. Experiments in other insects have shown that JH can inhibit PTTH release to indirectly suppress ecdysone production^{46, 47}, or act directly on the PG to suppress ecdysteroid synthesis⁴⁸. Met and Gce both express in the PTTH cells (Fig. 3k,l) and PG (Fig. 6b) during the third instar. The coexpression of JH and ecdysone receptor machinery in the endocrine cells and associated neurons supports these tissues as critical sites for the convergence of signaling pathways, and the sensitivity of wvMet ²⁷;;phm/TM6b flies to PG manipulation suggests that Met may be the key player in integrating these signals.

In adult flies, JH-Met regulates reproductive physiology in both sexes^{7, 49}. Met mutants produce and oviposit fewer vitellogenic oocytes than wild type flies⁷, while flies lacking gce exhibit considerably milder reproductive consequences¹². We observed widespread Met and gce coexpression in both male and female reproductive tracts (Figs 7 and 9b).

In Drosophila oogenesis, JH is necessary for entry into the vitellogenic phase⁵⁰. The vitellogenic checkpoint occurs in stage 9⁵¹ oocytes where JH is required for both yolk protein synthesis by the follicle cells and yolk protein uptake from the hemolymph⁵⁰. It also suppresses 20E-induced apoptosis of the oocyte at stages 8–9 when the females are starved^{52, 53}. This apoptosis is mediated by the ecdysone-induced E75A⁵³. Both Met and gce are expressed in the follicle cells surrounding the primary oocyte in stage 8–10 egg chambers, which corresponds with the vitellogenic checkpoint (Fig. 7h,m and n). Met and gce in stage 8 and 9 follicle cells may mediate the action of JH, 20E, or both to oppose apoptosis of egg chambers. The comparatively severe oogenesis phenotype exhibited by Met mutants argues for a scenario under which Met-JH suppresses ecdysone-driven apoptosis, possibly by downregulating the apoptosis inducer E75A, which is a JH and 20E responsive gene, and a demonstrated transcriptional target of JH-Gce in cell culture⁵⁴. If gce regulates E75A expression in check-point stage egg chambers, gce overexpression, rather than loss of function, might be expected to promote apoptosis in egg chambers.

Virtually nothing is known about Met and gce function in the brain, but a handful of studies have addressed the more general issue of JH action on nervous system development. Widespread and dramatic neurological damage results from a lethal dose of the JH analog methoprene in OR-C wildtype flies, including fusion of the subesophageal ganglion with the thoracicoabdominal ganglion, an incomplete fusion of the optic lobe neuropils with the central brain, and disorganization and degeneration of the optic lobe, particularly in the chiasma²². Riddiford et al.¹⁴ describe a gross malformation of the lobula in Met ²⁷ null mutants, evident as finger-like projections that encroach laterally into the inner chiasm, attributed partially to premature EcR B1 expression. gce mutants do not display this phenotype⁵⁵. Accordingly, gce expression in the developing optic lobe of WL3 larvae is sparse (Fig. 3b,e), and the T5 cells that arborize along the margin of the lobula likewise show Met but not gce expression (Fig. 8e vs. 8j,o), suggesting a potential maintenance function for Met-JH in the morphological integrity of the developing lobula.

The neuroanatomical atlas of JHR expression presented here will allow targeted studies regarding JH effects on behavior. Key expression in the adult CNS is summarized in Fig. 9c. In Drosophila, JH application or the pharmacological suppression of JH synthesis via precocene application in the adult induces changes in basic locomotor behaviors and courtship⁵⁶. The central complex is a major locomotor control center in the brain⁵⁷ and shows strong Met and gce expression in distinct cell types (Fig. 8). A recent study by Wolff et al.⁵⁸ provides an exquisite reconstruction of the central complex at single-cell resolution and identifies a collection of GAL4 lines that grant genetic access to these neurons. Such collections will facilitate future research regarding JHR action in coordinating CNS development and function. A general strategy will require defining JHR-carrying, hormone-responsive neurons via co-expression of Met/Gce-GAL4 lines with LexA driver lines that express in characterized sets of neurons. We envision that the genetic tools presented herein will facilitate such research and help elucidate how developmental hormones interact to direct behavior.

Materials and Methods

Bacterial Artificial Chromosome (BAC) generation for making driver lines

BAC recombineering was performed in SW102 cells⁵⁹ using a kanamycin/streptomycin positive/negative-selection cassette modified from pSK + -RpsL-kana ⁶⁰. Landing-site cassettes were created by ligating ~500-base-pair GAL4 or LexA 5′ and 3′ homology arms amplified from pBPGUw ²⁵ and pBPnlsLexA::p65Uw ²⁶, creating pGKU and pLKU. Landing-site cassettes were amplified from pGKU and pLKU using primers that added 50 bases of 5′ and 3′ Met and gce homology to the GAL4/LexA-flanked selectable markers. These cassettes were recombined into the Met or gce BACs (CH321-28O05 and CH321-09E09:⁶¹) (obtained from Children’s Hospital Oakland Research Institute, Oakland, CA), and recombinants were selected on kanamycin medium. Putative clones were analyzed by colony PCR to ensure that proper recombination had occurred. Full-length GAL4, GAL4::p65, or NLS::LexA::p65 transgene cassettes were recombined into these modified BACs making use of the 500-bp homology arms added earlier. Potential recombinants were identified by faster growth on streptomycin medium. Clones were analyzed by colony PCR, and putative recombinant BACs were sequenced at the recombined regions. Correct BACs were isolated and electroporated into EPI300 cells (Epicentre) and EPI300 clones were shipped to Genetic Services, Inc. (Cambridge, MA), as agar stabs for preparation and injection into y w nos phi C3-nls #12; attP40; VK00033 flies (hereafter referred to as the injection line). Integrant flies were analyzed by PCR to ensure proper integration of the transgene.

Fly lines

Reporter lines used in this study include the membrane-bound GFP reporters 10xUAS-IVS-mCD8-GFP (pJFRC2; attP2), 10xUAS-IVS-myr-GFP (pJFRC12; attP2), 10xUAS-IVS-GFP-p10 (pJFRC28; attP2), 10xUAS-IVS-myr-GFP-p10 (pJFRC29; attP2;²⁶), 13xLexAop2-IVS-myr-GFP (pJFRC19; attP2;²⁶), LexAop2-IVS-myr-tdTomato-p10 (attP40), and the nuclear GFP reporter UAS-nls-eGFP (pStinger;⁶²). Other Drosophila lines used in this study include: wgce ^2.5k ¹², phm-GAL4 ³³, Met RNAi lines (BDSC #v45852 (w ¹¹¹⁸; P{GD4384}v45852) and #v45854 (w ¹¹¹⁸; P{GD4384}v45854)), Act5C-GAL4 (BDSC# 4414, P{w ^+mC = Act5C-GAL4}25FO1/CyO, y ⁺), w; UAS-Met (attP40), and w; UAS-gce (attP2). The PTTH-HA line was a gift from Dr. Michael O’Connor.

Quantitative PCR

Quantitative real-time PCR was performed on a LightCycler 480 (Roche Molecular Diagnostics, Basel, Switzerland) using SYBR Green detection. Data were analyzed using the ΔΔCT method.

Gce-T2A-GAL4 construction

To knock-in the T2A-Gal4 coding sequence immediately preceding the gce stop codon^{63, 64}, 5′ and 3′ homology arms approximately 3 kb in length were amplified with the following primers: gce_55_AgeI: TACGACCGGTCCACATTATTCTGACATTTTAGTCTGAG; gce_53StuI: AAGGCCTGTCCTGGTCGTCCTCCTG; gce_35PmeI: TACGGTTTAAACTAGAGTGATGGAGAGCGCC; gce_33MluI: TACGACGCGTACACCTTGCCAAACAATGACAC BAC from clone BACR48D17, and cloned into pTL1⁶⁵. T2A-Gal4 was generated by cloning Gal4 from pBPGAL4.2Uw-2²⁶ into pTL1 (StuI/SacI) using a forward primer containing the T2A coding sequence. Donor DNA was integrated at attP40 to create the corresponding transgenic fly, which was then mated with+/Y, hs-hid; 5X-ri6TS-Rac1 ^V12 ; hs-FLP, hs-I-SceI/TM3, Sb ⁶⁶. The progeny were heat shocked (37 °C for 1 hour) twice, once during the second instar (L2) and once during the mid-third instar (L3) to promote donor release. Females, Donor/5X-ri6TS-Rac1 ^V12 ; hs-FLP, hs-I-SceI/+, were crossed to nSyb-LexA::p65 for lethality selection. Surviving candidates were subjected to chromosomal mapping and genomic PCR confirmation. An identical approach was taken to construct a Met-T2A-GAL4 reagent, but we were unsuccessful in generating transformant lines.

JH treatment

Five µg pyriproxifen (Sumitomo Chemical Company, Osaka, Japan) (a JHA) in 50 µl 95% ethanol was mixed into 5 ml molten standard molasses/cornmeal/yeast diet after cooling to 60 °C to make a 1 ppm pyriproxifen diet. Control food contained 50 µl of 95% ethanol only. Flies were monitored for pharate adult mortality, the typical wild type response to high doses of JHAs⁶.

Genomic rescue

Native BACs (CH321-28O05 and CH321-09E09⁶¹; called “Native Gce” or “Native Met”) lacking a driver cassette were used to transform the same injection line used for driver line construction. Transformants were homozygosed in a w ¹¹¹⁸ background. Restoration of functional JH signaling was assayed by scoring male survival from crosses with Met ²⁷, gce ^2.5k/FM7c females.

Immunocytochemistry

Animals were dissected in phosphate-buffered saline (PBS; pH 7.4, from 10x biology grade PBS, Corning 46-013-CM) and fixed in 4% formaldehyde in PBS for at least 2 hours. Following three washes with PBS +1% TritonX (1% PBST), tissues were blocked in normal donkey serum at a final concentration of 1:50 for at least 2 hours. Primary antibodies were supplied in the following concentrations: chicken anti-GFP monoclonal at 1:1000; mouse anti-Histone H1 at 1:1000; rat anti-N-cadherin (DNEX-8) at 1:20; mouse anti-Fas2 (1D4) at 1:50; rabbit anti-dsRed at 1:500. Following incubation at 4 °C for at least one night, tissues were washed three times in 1% PBST and secondary antibodies in 1% PBST were added at the following concentrations: goat anti-chicken AlexaFluor 488 at 1:1000, donkey anti-mouse Cy5 at 1:1000, donkey-anti rabbit AlexaFluor 594 at 1:1000, and donkey anti-rat AlexaFluor 649 at 1:1000. Following overnight incubation at 4 °C for at least one night, tissues were washed three times in 1% PBST, placed on poly-L-lysine coated cover slips, dehydrated and cleared through an ethanol/xylene series, mounted in DPX mounting medium, and visualized by confocal microscopy on a Zeiss 510 LSM⁶⁷.

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Acknowledgements

We thank Dr. Michael O’Connor for the Ptth-HA lines. This work was supported by the Howard Hughes Medical Institute.

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Authors and Affiliations

Howard Hughes Medical Institute, Janelia Research Campus, Ashburn, VA, 21047, USA
A. A. Baumann, M. J. Texada, H. M. Chen, J. N. Etheredge, D. L. Miller, S. Picard, R. Warner, J. W. Truman & L. M. Riddiford
University of Tennessee, College of Veterinary Medicine, Knoxville, TN, 37996, USA
A. A. Baumann
National Institute of Neurological Disease and Stroke, NIH, Bethesda, MD, 20892, USA
D. L. Miller
Friday Harbor Laboratories, University of Washington, Friday Harbor, WA, 98250, USA
J. W. Truman & L. M. Riddiford

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A. A. Baumann
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M. J. Texada
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H. M. Chen
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Contributions

A.B. and L.M.R. wrote the paper. A.B., L.M.R. and J.T. analyzed the data. A.B., M.T., H.M.C., R.W., S.P., J.E., D.M. and R.W. performed the experiments.

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Baumann, A.A., Texada, M.J., Chen, H.M. et al. Genetic tools to study juvenile hormone action in Drosophila . Sci Rep 7, 2132 (2017). https://doi.org/10.1038/s41598-017-02264-4

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Received: 23 November 2016
Accepted: 10 April 2017
Published: 18 May 2017
DOI: https://doi.org/10.1038/s41598-017-02264-4

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