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Recent progress in understanding the role of ecdysteroids in adult insects: Germline development and circadian clock in the fruit fly Drosophila melanogaster
Zoological Letters volume 1, Article number: 32 (2015)
Steroid hormones are one of the major bioactive molecules responsible for the coordinated regulation of biological processes in multicellular organisms. In insects, the principal steroid hormones are ecdysteroids, including 20-hydroxyecdysone. A great deal of research has investigated the roles played by ecdysteroids during insect development, especially the regulatory role in inducing molting and metamorphosis. However, little attention has been paid to the roles of these hormones in post-developmental processes, despite their undisputed presence in the adult insect body. Recently, molecular genetics of the fruit fly Drosophila melanogaster has revealed that ecdysteroid biosynthesis and signaling are indeed active in adult insects, and involved in diverse processes, including oogenesis, stress resistance, longevity, and neuronal activity. In this review, we focus on very recent progress in the understanding of two adult biological events that require ecdysteroid biosynthesis and/or signaling in Drosophila at the molecular level: germline development and the circadian clock.
Steroid hormones play indispensable roles in modulating a broad range of biological processes in nearly all multicellular organisms [1–3]. Steroid hormones are biosynthesized from sterols, such as cholesterol, by members of specific steroidogenic enzymes in specialized steroidogenic tissues . Once produced, steroid hormones are circulated in hemolymph and are easily transported to target cells to act as ligands for the nuclear receptor family of transcription factors . The steroid hormone-nuclear receptor complexes affect gene expression in target cells, triggering a hormone-dependent response.
In insects, the major steroid hormones are ecdysteroids, also known as molting hormones. Ecdysteroids, especially the most biologically active form 20-hydroxyecdysone (20E), play essential roles in coordinating developmental transitions, such as larval molting and metamorphosis [2, 6]. 20E activates a heterodimeric nuclear hormone receptor complex of proteins encoded by the Ecdysone receptor (EcR) and ultraspiracle (usp) genes [7–10]. This heterodimer regulates the expression of ecdysone-responsive genes by binding to specific promoter sequences called ecdysone response elements. In contrast to the long history of studies of EcR/USP and its downstream gene cascades, identification and characterization of ecdysteroidogenic enzymes have only been achieved within the last 15 years. So far, there are at least 10 essential ecdysteroidogenic enzymes that are expressed in ecdysteroidogenic tissues/organs, such as the larval prothoracic gland (PG), during embryonic and larval development .
The timing of molting and metamorphosis are mainly determined by dynamic temporal fluctuations of hemolymph ecdysteroid pulses and the subsequent activation of the ecdysteroid-dependent gene cascade . Previous studies have also demonstrated that many genetic mutants of EcR, usp, ecdysteroid-inducible genes and ecdysteroidogenic enzyme genes exhibit clear defects of molting and/or metamorphosis [2, 12]. Therefore, a large body of literature has described the roles of ecdysteroids to trigger such drastic developmental changes. By contrast, whereas a low but significant amount of ecdysteroids are undoubtedly present in adult stages, temporal changes of the hemolymph titer are ill-defined . Furthermore, after the completion of development, the adult insects no longer display visible changes of either morphology or physiology. Perhaps for these reasons little attention had been paid to the functions of ecdysteroids in adult insects.
In the past decade, however, molecular genetic studies using Drosophila have revealed some important aspects of ecdysteroids in adult physiology . In this review, we specifically focus on very recent progress in understanding two adult biological events that require ecdysteroid biosynthesis and/or signaling in Drosophila at the molecular level: germline development and the circadian clock.
Oocyte maturation and ecdysteroids: Stage-8 checkpoint and lipid accumulation
The first evidence showing the role of ecdysteroids in adult insects was reported by studies using the ovaries of adult mosquitoes in the 1970s [15, 16]. These studies demonstrated that vitellogenin synthesis in the fat body of mosquitoes is regulated by ovarian ecdysteroids . After this discovery, genetic studies of ecdysteroids and oogenesis have mainly been conducted using the convenient genetic model, the fruit fly D. melanogaster.
In Drosophila, ecdysteroids are also detected in the adult ovary [13, 17–19]. Genetic studies using mutants of genes required for ecdysteroid biosynthesis have proved that ovarian ecdysteroids are biosynthesized in the ovary itself. For example, adult females with a temperature-sensitive allele of ecdysoneless have a low ecdysteroid titer in the ovary [19, 20]. More recently, identification and characterization of a number of ecdysteroidogenic enzyme genes have enabled researchers to show that these genes are expressed in nurse cells and/or follicle cells of the adult ovary [19, 21–30]. Genetic studies have also confirmed that at least two of the ecdysteroidogenic genes, spook and phantom, are required for proper development of the ovary [27, 31]. In addition, some ecdysone response genes also play essential roles in oogenesis .
While versatile roles of ecdysteroid signaling in the development of the ovary of Drosophila have been proposed , one important role is to act as a developmental checkpoint during mid-oogenesis to ensure proper egg production. The ovary of Drosophila is composed of 15–20 ovarioles that have continuously developing egg chambers  (Figure 1a). Each egg chamber can be divided into 14 stages based on morphological criteria. Stage 14 is the mature egg, and stage 1 is budding of the egg chamber in the anterior of ovarioles, called the germarium (Fig. 1a). During Drosophila oogenesis, there is a critical developmental checkpoint around stage 8 . In this stage, a developmental decision is made in each egg chamber to determine whether it will develop or die. While a low concentration of ecdysteroids is essential for normal oogenesis, a high concentration of ecdysteroids caused by nutritional shortage induces apoptosis in the nurse cells of stage 8 and 9 egg chambers [34, 35]. In this checkpoint, ecdysone-induced protein 75 (E75) isoforms are involved in inducing or suppressing apoptosis. While overexpression of E75A in the egg chamber induces apoptosis of the nurse cells at stages 8 and 9 in fed flies, overexpression of E75B suppresses it at stages 8 and 9 in starved flies, suggesting that E75A and E75B have the opposite effect on apoptosis: E75A induces apoptosis and E75B inhibits apoptosis . In addition, expression of E75 isoforms is regulated by the BR-C isoform. BR-C Z2 and Z3 are not expressed in the egg chambers at stages 8 and 9 under feeding conditions, but are expressed in the follicle cells under apoptotic conditions. Overexpression of BR-C Z2 or Z3 induces E75A expression and suppresses E75B expression in the egg chambers at stages 8 and 9 . This suggests that BR-C isoforms respond to the nutritional signals and regulate the expression of E75A and E75B expression to control apoptosis in the stage 8 egg chamber (Fig. 2).
Notably, the ecdysteroid-dependent mid-oogenesis checkpoint is also influenced by organismal metabolism and external nutrient conditions, as illustrated by a recent study . During oogenesis, lipids are maternally supplied to oocytes and the lipid storage is crucial for the early stages of embryogenesis in many animals [38, 39]. In Drosophila, lipids accumulate in the stage 10 oocyte via a low-density lipoprotein (LDL) receptor. A recent study has demonstrated that ecdysteroid signaling is required for lipid accumulation, and feeding behavior is required for proper nutrition uptake (Fig. 2) . EcR mutant females have a defect in lipid accumulation and exhibit reduced levels of the LDL receptor LpR2. The expression of LpR2 is regulated by Sterol regulatory element-binding proteins (SREBP), the important lipogenic transcription factor in response to ecdysteroid signaling and dietary nutrients. In addition, adult-specific dominant-negative EcR expression in the central nervous system (CNS) causes decreased levels in feeding behavior and nutrient uptake in females. As oral administration of 20E induces nutrient storage , it is possible that ecdysteroid signaling in the CNS may promote nutrient accumulation required for the proper level of egg laying in females. However, it is unclear how follicle cells perceive nutrient information regarding starvation or feeding of individuals to control ecdysteroid levels.
Germline stem cells and ecdysteroids
In addition to the previously reported ecdysteroid-dependent regulation of oogenesis, such as in mid-oogenesis as described above, as well as oocyte maturation and oviposition [32, 40], recent studies have revealed that ecdysteroids also control very early steps of oogenesis, namely niche formation, germline stem cell (GSC) behavior, and cyst cell differentiation.
In the germarium in adult Drosophila females, 1–3 GSCs give rise to mature eggs (Fig. 1b). GSCs reside in a specialized microenvironment called the niche that maintains stem cell function by sending local niche signals into GSCs and controls symmetric or asymmetric GSC division [41, 42]. GSCs can divide symmetrically to produce daughter stem cells, or asymmetrically to produce daughter cells called cystoblasts that differentiate into nurse cells and oocytes. The cystoblast undergoes four mitotic divisions with incomplete cytokinesis to form 15 nurse cells and one oocyte in each egg chamber that is surrounded by somatic follicle cells.
The ovary of Drosophila has long been recognized as one of the most powerful tools for investigating GSCs and niches . GSCs receive a somatic signal from niches consisting of the terminal filament and cap cells, which maintain GSC function (Fig. 1b). In the larval ovary, both primordial germ cells (PGC, the precursors of GSCs) and gonadal somatic cells (the precursors of niche cells) proliferate and develop to form 16–20 GSC units of the adult ovary . Ecdysteroid signaling controls formation of niche and stem cell precursors in the larval ovarian development. Although knocking down of EcR or Usp function in the somatic ovary at the early third instar does not change developmental timing, precocious differentiation of both niches and PGCs occurs in gonads of EcR or usp RNAi animals at the early third instar . However, overexpression of the dominant negative form of EcR at the mid-third instar causes reduced size in the ovary and niche . These results suggest that the ecdysone receptor represses precocious differentiation of both niches and PGCs at the early third instar, and is required for niche formation and gonadal development at the mid-third instar (Fig. 2). In addition, this mechanism involves the early ecdysone response gene, Broad-Z1. Ecdysteroid signaling non-cell-autonomously activates Broad expression in the somatic ovary through EcR/Usp to form niche and differentiating PGCs at the mid-third instar and later, but not the early third instar . In addition, loss of ecdysone-induced transcription factor, E78 results in decreased cap cell numbers and fewer germline stem cells , suggesting that ecdysteroid signaling controls niche assembly to maintain the proper number of GSCs via E78 and Broad (Fig. 2).
GSCs are maintained by local niche signals and are also affected by systemic ecdysteroid signaling. EcR mutant females show a reduced number of GSCs independent of insulin signaling, suggesting that ecdysteroid signaling directly regulates adult GSC proliferation and self-renewal . This regulation is mediated by E74, a transcription factor known as an early responsive gene of ecdysteroids, while other transcription factors, E75 and BR-C, are not required for proper GSC proliferation (Fig. 2) . Moreover, ecdysteroid signaling controls GSC proliferation by interacting with chromatin remodeling factors such as ISWI (an intrinsic epigenetic factor required for GSC fate and activity) and Nurf301 (the largest subunit of the ISWI-containing NURF chromatin remodeling complex), suggesting that there is an essential link between ecdysteroid signaling and the intrinsic chromatin remodeling machinery as a potential mechanism for promoting the general transcriptional program .
GSCs undergo four rounds of synchronous division to produce 2, 4, 8, and eventually 16 interconnected developing cysts (called cystocytes), the precursors of ovarian follicles. Somatic follicle cells envelop each cystocyte to form a follicle through 14 developmental stages and support proper differentiation. Ecdysteroid signaling is also required for cyst differentiation. Overexpression of the dominant-negative form of EcR in somatic escort cells that envelop the GSC progeny disrupts early germ cell differentiation . In addition, mutants for ecdysteroid signaling pathway components in escort cells show increased levels of the cell adhesion molecules β-Catenin/Armadillo, DE-Cadherin and a cytoskeleton component Adducin . These data suggest that ecdysteroid signaling in somatic escort cells plays an important role in controlling germ cell differentiation via regulation of cell adhesion complexes required for the establishment of physiological germline–soma interaction [48, 49]. Moreover, knocking down the components of EcR or E75 in escort cells causes a reduced number of 16-cell cysts, but not 2-, 4- and 8-cell cysts and disrupted follicle cell formation, suggesting that ecdysteroid signaling has a specific role in controlling entry into meiosis of 16-cell cysts (Fig. 2) . In addition, mutants for E78 show a significant decrease in ovarian follicle cell numbers, suggesting that ecdysteroid signaling is also required for follicle cell survival (Fig. 2) .
In addition to the ovary, ecdysteroids are also detected in the testis [13, 17, 18]. The role of ecdysteroids in stem cell maintenance in the testis has been reported recently. The Drosophila testis stem cell niche consists of a cluster of non-mitotic somatic cells called the hub, which produces signals that maintain surrounding GSCs as well as cyst stem cells (CySCs). CySCs produce cyst cells that are required for differentiation to sperm from GSC daughters. In this system, ecdysteroid signaling pathway components are essential for the maintenance and survival of both GSCs and CySCs . Moreover, as well as the ovarian GSC system, EcR genetically interacts with Nurf301 to maintain these stem cells in the testis niche. These results imply that ecdysteroid signaling is required for stem cell maintenance beyond sexes at least in Drosophila .
Ecdysteroid signaling factors in the molecular machinery of the circadian clock
Besides the germline, which is the most classical site of action of ecdysteroids in adult insects, ecdysteroids also influence many other adult organs and tissues. Recent studies have shown that ecdysteroids are involved in adult neuronal function, including the control of learning, memory, and behavior [52–55]. Particularly, very recent studies have unraveled the ecdysteroid-dependent regulation of circadian clocks in insects, especially Drosophila.
Circadian clocks coordinate rhythmic behaviors and help living organisms adapt to the daily cycling of environmental conditions . Circadian clocks provide the obvious advantage of anticipatory preparation for predictably recurrent conditions, which cannot be achieved by direct responses to conditions that have already commenced. The molecular machinery of the circadian clock has been extensively studied in Drosophila, where the circadian master clock comprises about 150 neurons located in the central brain . The oscillation of the clock is thought to be generated by a molecular mechanism that is composed of transcriptional-translational autoregulatory feedback loops of the clock genes, such as period (per), timeless (tim) Clock (Clk), and cycle (cyc) [58, 59]. The CLK-CYC heterodimer directly activates transcription of per, tim, vrille (vri), Par Domain Protein 1 (Pdp1ϵ) and clockwork orange (cwo) by binding to their promoters [60, 61]. Conversely, the induced TIM and PER inhibit the activity of CLK-CYC in the nucleus, which allows the clock to be oscillated. The clock oscillation is also modulated by Clk transcription, which is first repressed by VRI and then activated by PDP1ϵ. CWO also directly activates transcription of per, tim, vri, Pdp1ϵ by binding to their promoters.
The timing of developmental transitions, such as molting and eclosion, are regulated by a circadian clock in some insects, in which the circadian clock appears to control ecdysteroid biosynthesis in the PGs. For example, in the blood-sucking bug Rhodnius prolixus and the leafworm Spodoptera littoralis, ecdysteroid titers fluctuate with a daily rhythm and such temporal changes control the timing of molting during development [62, 63]. In Drosophila, the timing of transition from pupae to adults is gated by the timing of ecdysteroid biosynthesis, which is under control of the circadian clock components in not only PG cells, but also in neuronal cells of the brain [64, 65]. By contrast, the relationship between ecdysteroids and circadian clocks has been largely unknown until recently, but some pioneer studies focusing on this issue have been reported in recent years.
For example, E75 and unfulfilled (unf; DHR51), which encode nuclear receptors, have been identified as components of the molecular clocks in the Drosophila pacemaker neurons, as knockdown of E75 and unf in the clock neurons lengthen the free-running period . E75 and UNF bind to per regulatory sequences and act together to enhance the CLK/CYC-mediated transcription of the per gene (Fig. 3) . Notably, E75 has also been recognized as a component of molecular clocks in other animals. For example, in the firebrat Thermobia domestica, a primitive insect, normal rhythmic expression of E75 and nuclear hormone receptor 3 (HR3) is required for the persistence of locomotor rhythms . Interestingly, HR3 and E75 are orthologs of mammalian clock genes, Rorα and Rev-erbα. Despite these mechanistic divergences, the notion that Rorα and Rev-erbα homologs are integral to the molecular oscillators in both insects and mammals highlights the significance of transcriptional regulations via nuclear receptors in metazoan circadian clocks [66, 67].
In addition to nuclear receptor-mediated regulation, another type of the feedback loop of ecdysteroid signaling has been implicated in the Drosophila circadian clock by studies on a gene called Early gene at 23 (E23) encoding the ABC transporter (Fig. 3) [68, 69]. The E23 knockdown flies lengthen circadian period with an increased expression of the clock gene vri. E23 and vri are positively regulated by 20E in pacemaker neurons, whereas E23 negatively regulates 20E-dependent signaling . Considering that E23 protein depresses the 20E response in cultured cells , this ABC transporter might cause the reduction in intracellular level of 20E. Taken together, E23 forms its own feedback loop in the ecdysteroid response through the E23 function itself and ecdysteroid-mediated vri expression (Fig. 3) .
Consistent with the fact that 20E is involved in the regulation of the circadian clock, EcR is expressed in circadian neurons , and the double knockdown flies of EcR and usp exhibit the abnormal circadian phenotype . It is therefore important to identify transcriptional targets of EcR/USP. E75 and E23 are the EcR-USP targets in the clock neurons . A recent study has also reported that the microRNA let-7 is a target of EcR/USP . let-7 is the evolutionarily-well conserved microRNA and involved in temporal regulation of development and physiology in many animals . Importantly, let-7 targets the crucial clock component CWO. The ecdysteroid-induced let-7 regulates the circadian rhythm via repression of CWO, as up-regulation of cwo rescues the circadian clock phenotype in flies overexpressing the let-7-complex . Taken together, ecdysteroid signaling has multiple functions in controlling the circadian clock in Drosophila adults at several levels of regulation, such as the transporter-mediated, transcriptional and post-transcriptional levels.
There is a growing body of evidence of the importance of ecdysteroids in adult insects. Steroid hormones are small and fat-soluble bioactive molecules that can be easily circulated throughout the body and pass through the cell membrane into cells . Steroid hormones, therefore, have the potential to rapidly and systemically orchestrate many types of cells in the whole body. It is feasible that ecdysteroid signaling is used to orchestrate individual biological events not only in developing animals but also in adults, although an actual benefit of signaling for adult insects has not been fully elucidated. Curiously, steroid hormones are involved in controlling germline development  and circadian rhythms in mammals , implying that the functions of steroid hormones in adults are, at least in part, evolutionarily conserved.
One important unanswered question is the ecdysteroidogenic cell(s) or organ(s) (other than the ovary) responsible for biosynthesizing ecdysteroids after eclosion. While the PG is the organ responsible for biosynthesizing ecdysteroids during larval and early pupal stages, the PG degenerates during pupal development and is eventually lost in the adult stage [76–79]. It is possible that the ovary is the source of circulating ecdysteroids in adult female hemolymph, as has been shown in the cockroach Blattella germanica . Although the ovariectomized Blattella female exhibits a reduced ecdysteroid titer, a substantial amount of the hemolymph ecdysteroids remain . In the case of male adults, while several recent studies have identified the accessory gland as a site of ecdysteroid production [80, 81], it is unclear whether accessory gland-producing ecdysteroids systemically act in the whole body. Neuronal subpopulations are a strong candidate for the unidentified adult ecdysteroidogenic cells. 20E is detected in the brain of Drosophila, and its expression is regulated by the clock gene . Second, some ecdysteroidogenic enzymes are expressed in the brain in the honeybee Apis mellifera  and in Drosophila (Yuko Shimada-Niwa, Sora Enya and R.N., unpublished observation). Third, a clock neuron-specific knockdown of the ecdysteroidogenic gene phantom exhibits an abnormal free-running period in Drosophila . It should be noted that vertebrate nervous systems can biosynthesize de novo steroids, known as neurosteroids, which modulate neuronal activities [83, 84]. By extension, the possibility that de novo biosynthesized ecdysteroids also act as neuromodulators and are required for adult neuronal functions represents an attractive hypothesis. To understand the regulatory mechanisms controlling production of ecdysteroids in adult flies, it is important to examine where ecdysteroidogenic enzyme genes are expressed, and how their expression and activity are regulated at cellular resolution.
Another interesting issue to be addressed is whether ecdysteroids regulate GSCs and the circadian clock cooperatively with juvenile hormone (JH), which is also a key insect hormone that regulates molting and metamorphosis [85, 86]. It is well known that JH plays a crucial role in controlling adult ovarian maturation in many insects. In female Drosophila there is a functional interaction between 20E and JH to regulate ovarian maturation and oviposition . A role of JH in regulating the circadian clock has also been implied by a study on the gene takeout, which encodes the JH binding protein. takeout is essential for a circadian output pathway that conveys temporal information to feeding-relevant metabolism and activities . However, whether and how GSCs and circadian clocks are regulated by a crosstalk between 20E and JH is still an intriguing open question.
In addition to the role of ecdysteroids in the adult stage summarized in this paper, other ecdysteroid-dependent biological events in the adult stage have also been reported, such as stress resistance , lifespan [14, 89, 90], and innate immunity . A number of studies on vertebrates have revealed that the actions of steroid hormones play crucial roles in adult homeostasis. In this sense, further investigation of the roles of ecdysteroids in adult insects is needed to establish a secure foundation for the use of insects as model organisms in steroid hormone research. Considering the recent remarkable advances in knowledge and resources of ecdysteroid biosynthesis and signaling, it is likely that additional essential adult events that are regulated by ecdysteroids will be found in the future.
- Br :
- Clk :
- cwo :
- cyc :
Central nervous system
Cyst stem cell
- E23 :
Early gene at 23
- E75 :
Ecdysone-induced protein 75
- E78 :
Ecdysone-induced protein 78
- EcR :
Germline stem cell
- HR3 :
Nuclear hormone receptor 3
An intrinsic epigenetic factor
- Pdp1ϵ :
Par Domain Protein 1
- per :
Primordial germ cell
- Rorα :
RAR-related orphan receptor alpha
- SREBP :
Sterol regulatory element-binding proteins
- tim :
- unf :
- vri :
Baker ME. Origin and diversification of steroids: Co-evolution of enzymes and nuclear receptors. Mol Cell Endocrinol. 2011;334:14–20.
Niwa R, Niwa YS. Enzymes for ecdysteroid biosynthesis: their biological functions in insects and beyond. Biosci Biotechnol Biochem. 2014;78:1283–92.
Markov GV, Tavares R, Dauphin-Villemant C, Demeneix BA, Baker ME, Laudet V. Independent elaboration of steroid hormone signaling pathways in metazoans. Proc Natl Acad Sci USA. 2009;106:11913–8.
Miller WL, Auchus RJ. The molecular biology, biochemistry, and physiology of human steroidogenesis and its disorders. Endocr Rev. 2011;32:81–151.
Rousseau GG. Fifty years ago: The quest for steroid hormone receptors. Mol Cell Endocrinol. 2013;375:10–3.
Niwa YS, Niwa R. Neural control of steroid hormone biosynthesis during development in the fruit fly Drosophila melanogaster. Genes Genet Syst. 2014;89:27–34.
Koelle MR, Talbot WS, Segraves WA, Bender MT, Cherbas P, Hogness DS. The Drosophila EcR gene encodes an ecdysone receptor, a new member of the steroid receptor superfamily. Cell. 1991;67:59–77.
Yao T-P, Forman BM, Jiang Z, Cherbas L, Chen JD, Cherbas P, et al. Functional ecdysone receptor is the product of EcR and Ultraspiracle genes. Nature. 1993;366:476–9.
Yao T, Segraves WA, Oro AE, Mckeown M, Evans RM. Drosophila ultraspiracle modulates ecdysone receptor function via heterodimer formation. Cell. 1992;71:63–72.
Thomas HE, Stunnenberg HG. Stewart a F. Heterodimerization of the Drosophila ecdysone receptor with retinoid X receptor and ultraspiracle. Nature. 1993;362:471–5.
Riddiford LM. Hormones and Drosophila development. In: Bate M, Martinez Arias A, editors. The Development of Drosophila melanogaster. Cold Spring Harbor: Cold Spring Harbor Laboratory Press; 1993. p. 899–939.
Thummel CS. Molecular Mechanisms of Developmental Timing in C. elegans and Drosophila. Dev Cell. 2001 Oct;1:453–65.
Handler AM. Ecdysteroid titers during pupal and adult development in Drosophila melanogaster. Dev Biol. 1982;93:73–82.
Schwedes CC, Carney GE. Ecdysone signaling in adult Drosophila melanogaster. J Insect Physiol. 2012 Mar;58:293–302.
Hagedorn HH, O’Connor JD, Fuchs MS, Sage B, Schlaeger DA, Bohm MK. The ovary as a source of alpha-ecdysone in an adult mosquito. Proc Natl Acad Sci USA. 1975;72:3255–9.
Belles X, Piulachs MD. Ecdysone signalling and ovarian development in insects: from stem cells to ovarian follicle formation. Biochim Biophys Acta - Gene Regul Mech. 1849;2014:181–6.
Hodgetts RB, Sage B, O’Connor JD. Ecdysone titers during postembryonic development of Drosophila melanogaster. Dev Biol. 1977;60:310–7.
Bownes M, Dubendorfer A, Smith T. Steroids in adult males and females of Drosophila melanogaster. J Insect Physiol. 1984;30:823–30.
Garen A, Kauvar L, Lepesant JA. Roles of ecdysone in Drosophila development. Proc Natl Acad Sci USA. 1977;74:5099–103.
Gaziova I, Bonnette PC, Henrich VC, Jindra M. Cell-autonomous roles of the ecdysoneless gene in Drosophila development and oogenesis. Development. 2004;131:2715–25.
Chávez VM, Marqués G, Delbecque JP, Kobayashi K, Hollingsworth M, Burr J, et al. The Drosophila disembodied gene controls late embryonic morphogenesis and codes for a cytochrome P450 enzyme that regulates embryonic ecdysone levels. Development. 2000;127:4115–26.
Warren JT, Petryk A, Marque G, Jarcho M, Parvy J-P, Dauphin-villemant C, et al. Molecular and biochemical characterization of two P450 enzymes in the ecdysteroidogenic pathway of Drosophila melanogaster. Proc Natl Acad Sci USA. 2002;99:11043–8.
Petryk A, Warren JT, Marqués G, Jarcho MP, Gilbert LI, Kahler J, et al. Shade is the Drosophila P450 enzyme that mediates the hydroxylation of ecdysone to the steroid insect molting hormone 20-hydroxyecdysone. Proc Natl Acad Sci USA. 2003;100:13773–8.
Niwa R, Matsuda T, Yoshiyama T, Namiki T, Mita K, Fujimoto Y, et al. CYP306A1, a cytochrome P450 enzyme, is essential for ecdysteroid biosynthesis in the prothoracic glands of Bombyx and Drosophila. J Biol Chem. 2004;279:35942–9.
Warren JT, Petryk A, Marqués G, Parvy J-P, Shinoda T, Itoyama K, et al. Phantom encodes the 25-hydroxylase of Drosophila melanogaster and Bombyx mori: a P450 enzyme critical in ecdysone biosynthesis. Insect Biochem Mol Biol. 2004;34:991–1010.
Namiki T, Niwa R, Sakudoh T, Shirai KI, Takeuchi H, Kataoka H. Cytochrome P450 CYP307A1/Spook: A regulator for ecdysone synthesis in insects. Biochem Biophys Res Commun. 2005;337:367–74.
Ono H, Rewitz KF, Shinoda T, Itoyama K, Petryk A, Rybczynski R, et al. Spook and Spookier code for stage-specific components of the ecdysone biosynthetic pathway in Diptera. Dev Biol. 2006;298:555–70.
Niwa R, Namiki T, Ito K, Shimada-Niwa Y, Kiuchi M, Kawaoka S, et al. Non-molting glossy/shroud encodes a short-chain dehydrogenase/reductase that functions in the “Black Box” of the ecdysteroid biosynthesis pathway. Development. 2010;137:1991–9.
Enya S, Ameku T, Igarashi F, Iga M, Kataoka H, Shinoda T, et al. A Halloween gene noppera-bo encodes a glutathione S-transferase essential for ecdysteroid biosynthesis via regulating the behaviour of cholesterol in Drosophila. Sci Rep. 2014;4:6586.
Freeman MR, Dobritsa A, Gaines P, Segraves WA, Carlson JR. The dare gene: steroid hormone production, olfactory behavior, and neural degeneration in Drosophila. Development. 1999;126:4591–602.
Domanitskaya E, Anllo L, Schüpbach T. Phantom, a cytochrome P450 enzyme essential for ecdysone biosynthesis, plays a critical role in the control of border cell migration in Drosophila. Dev Biol. 2014;386:408–18.
Buszczak M, Freeman MR, Carlson JR, Bender M, Cooley L, Segraves WA. Ecdysone response genes govern egg chamber development during mid-oogenesis in Drosophila. Development. 1999;126:4581–9.
Bastock R, St JD. Drosophila oogenesis. Curr Biol. 2008;18:R1082–7.
Terashima J, Bownes M. Translating available food into the number of eggs laid by Drosophila melanogaster. Genetics. 2004;167:1711–9.
Terashima J, Takaki K, Sakurai S, Bownes M. Nutritional status affects 20-hydroxyecdysone concentration and progression of oogenesis in Drosophila melanogaster. J Endocrinol. 2005;187:69–79.
Terashima J, Bownes M. E75A and E75B have opposite effects on the apoptosis/development choice of the Drosophila egg chamber. Cell Death Differ. 2006;13:454–64.
Sieber MH, Spradling AC. Steroid signaling establishes a female metabolic state and regulates SREBP to control oocyte lipid accumulation. Curr Biol. 2015;25:993–1004.
Tennessen JM, Bertagnolli NM, Evans J, Sieber MH, Cox J, Thummel CS. Coordinated metabolic transitions during Drosophila embryogenesis and the onset of aerobic glycolysis. G3. 2014;4:839–50.
Dunning KR, Cashman K, Russell DL, Thompson JG, Norman RJ, Robker RL. β-oxidation is essential for mouse oocyte developmental competence and early embryo development. Biol Reprod. 2010;83:909–18.
Carney GE, Bender M. The Drosophila ecdysone receptor (EcR) gene is required maternally for normal oogenesis. Genetics. 2000;154:1203–11.
Spradling A, Fuller MT, Braun RE, Yoshida S. Germline stem cells. Cold Spring Harb Perspect Biol. 2011;3:a002642.
Spradling A, Drummond-Barbosa D, Kai T. Stem cells find their niche. Nature. 2001;414:98–104.
Kirilly D, Xie T. The Drosophila ovary: an active stem cell community. Cell Res. 2007;17:15–25.
Gilboa L, Lehmann R. Soma-germline interactions coordinate homeostasis and growth in the Drosophila gonad. Nature. 2006;443:97–100.
Gancz D, Lengil T, Gilboa L. Coordinated regulation of niche and stem cell precursors by hormonal signaling. PLoS Biol. 2011;9, e1001202.
Ables ET, Bois KE, Garcia CA, Drummond-Barbosa D. Ecdysone response gene E78 controls ovarian germline stem cell niche formation and follicle survival in Drosophila. Dev Biol. 2015;400:33–42.
Ables ET, Drummond-Barbosa D. The steroid hormone ecdysone functions with intrinsic chromatin remodeling factors to control female germline stem cells in Drosophila. Cell Stem Cell. 2010;7:581–92.
König A, Yatsenko AS, Weiss M, Shcherbata HR. Ecdysteroids affect Drosophila ovarian stem cell niche formation and early germline differentiation. EMBO J. 2011;30:1549–62.
König A, Shcherbata HR. Soma influences GSC progeny differentiation via the cell adhesion-mediated steroid-let-7-Wingless signaling cascade that regulates chromatin dynamics. Biol Open. 2015;4:285–300.
Morris LX, Spradling AC. Steroid signaling within Drosophila ovarian epithelial cells sex-specifically modulates early germ cell development and meiotic entry. PLoS One. 2012;7, e46109.
Li Y, Ma Q, Cherry CM, Matunis EL. Steroid signaling promotes stem cell maintenance in the Drosophila testis. Dev Biol. 2014;394:129–41.
Ishimoto H, Sakai T, Kitamoto T. Ecdysone signaling regulates the formation of long-term courtship memory in adult Drosophila melanogaster. Proc Natl Acad Sci U S A. 2009;106:6381–6.
Ishimoto H, Kitamoto T. The steroid molting hormone Ecdysone regulates sleep in adult Drosophila melanogaster. Genetics. 2010;185:269–81.
Ishimoto H, Kitamoto T. Beyond molting--roles of the steroid molting hormone ecdysone in regulation of memory and sleep in adult Drosophila. Fly. 2011;5:215–20.
Ishimoto H, Wang Z, Rao Y, Wu CF, Kitamoto T. A novel role for ecdysone in Drosophila conditioned behavior: Linking GPCR-mediated non-canonical steroid action to cAMP signaling in the adult brain. PLoS Genet. 2013;9, e1003843.
Dunlap JC, Loros JJ, DeCoursey PJ, editors. Chronobiology - Biological timekeeping. Sunderland, MA, USA: Sinauer; 2004.
Helfrich-Förster C. The circadian clock in the brain: a structural and functional comparison between mammals and insects. J Comp Physiol A Neuroethol Sens Neural Behav Physiol. 2004;190:601–13.
Dunlap J. Molecular bases for circadian clocks. Cell. 1999;96:271–90.
Hardin PE. The circadian timekeeping system of Drosophila. Curr Biol. 2005;15:R714–22.
Cyran SA, Buchsbaum AM, Reddy KL, Lin MC, Glossop NRJ, Hardin PE, et al. vrille, Pdp1, and dClock form a second feedback loop in the Drosophila circadian clock. Cell. 2003;112:329–41.
Matsumoto A, Ukai-Tadenuma M, Yamada RG, Houl J, Uno KD, Kasukawa T, et al. A functional genomics strategy reveals clockwork orange as a transcriptional regulator in the Drosophila circadian clock. Genes Dev. 2007;21:1687–700.
Ampleford EJ, Steel CG. Circadian control of a daily rhythm in hemolymph ecdysteroid titer in the insect Rhodnius prolixus (Hemiptera). Gen Comp Endocrinol. 1985;59:453–9.
Polanska MA, Maksimiuk-Ramirez E, Ciuk MA, Kotwica J, Bebas P. Clock-controlled rhythm of ecdysteroid levels in the haemolymph and testes, and its relation to sperm release in the Egyptian cotton leafworm, Spodoptera littoralis. J Insect Physiol. 2009;55:426–34.
Lee E, Jeong EH, Jeong H-J, Yildirim E, Vanselow JT, Ng F, et al. Phosphorylation of a central clock transcription factor is required for thermal but not photic entrainment. PLoS Genet. 2014;10, e1004545.
Plautz JD. Independent Photoreceptive circadian clocks throughout Drosophila. Science. 1997;278:1632–5.
Jaumouillé E, Machado Almeida P, Stähli P, Koch R, Nagoshi E. Transcriptional regulation via nuclear receptor crosstalk required for the Drosophila circadian clock. Curr Biol. 2015;25:1502–8.
Kamae Y, Uryu O, Miki T, Tomioka K. The Nuclear Receptor Genes HR3 and E75 are required for the circadian rhythm in a primitive insect. PLoS One. 2014;9, e114899.
Hock T, Cottrill T, Keegan J, Garza D. The E23 early gene of Drosophila encodes an ecdysone-inducible ATP-binding cassette transporter capable of repressing ecdysone-mediated gene activation. Proc Natl Acad Sci U S A. 2000;97:9519–24.
Itoh TQ, Tanimura T, Matsumoto A. Membrane-bound transporter controls the circadian transcription of clock genes in Drosophila. Genes Cells. 2011;16:1159–67.
Kumar S, Chen D, Jang C, Nall A, Zheng X, Sehgal A. An ecdysone-responsive nuclear receptor regulates circadian rhythms in Drosophila. Nat Commun. 2014;5:5697.
King-Jones K, Thummel CS. Nuclear receptors--a perspective from Drosophila. Nat Rev Genet. 2005;6:311–23.
Chen W, Liu Z, Li T, Zhang R, Xue Y, Zhong Y, et al. Regulation of Drosophila circadian rhythms by miRNA let-7 is mediated by a regulatory cycle. Nat Commun. 2014;5:5549.
Niwa R, Slack FJ. The evolution of animal microRNA function. Curr Opin Genet Dev. 2007;17:145–50.
Edson MA, Nagaraja AK, Matzuk MM. The mammalian ovary from genesis to revelation. Endocr Rev. 2009;30:624–712.
Mong JA, Baker FC, Mahoney MM, Paul KN, Schwartz MD, Semba K, et al. Sleep, rhythms, and the endocrine brain: Influence of sex and gonadal hormones. J Neurosci. 2011;31:16107–16.
Dai JD, Gilbert LI. Metamorphosis of the corpus allatum and degeneration of the prothoracic glands during the larval-pupal-adult transformation of Drosophila melanogaster: a cytophysiological analysis of the ring gland. Dev Biol. 1991;144:309–26.
Romañá I, Bellés X. The ovary is a source of circulating ecdysteroids in Blattella germanica (Dictyoptera: Blattellidae). Eur J Entomol. 1995;92:93–103.
Martau T, Romer F. Degeneration of moulting glands in male crickets. J Insect Physiol. 1998;44:981–9.
Dai JD, Gilbert LI. Juvenile hormone prevents the onset of programmed cell death in the prothoracic glands of Manduca sexta. Gen Comp Endocrinol. 1998;109:155–65.
Pondeville E, Maria A, Jacques J-C, Bourgouin C, Dauphin-Villemant C. Anopheles gambiae males produce and transfer the vitellogenic steroid hormone 20-hydroxyecdysone to females during mating. Proc Natl Acad Sci USA. 2008;105:19631–6.
Hentze JL, Moeller ME, Jørgensen AF, Bengtsson MS, Bordoy AM, Warren JT, et al. Accessory gland as a site for prothoracicotropic hormone controlled ecdysone synthesis in adult male insects. PLoS One. 2013;8, e55131.
Yamazaki Y, Kiuchi M, Takeuchi H, Kubo T. Ecdysteroid biosynthesis in workers of the European honeybee Apis mellifera L. Insect Biochem Mol Biol. 2011;41:283–93.
Tsutsui K, Haraguchi S. Breakthrough in neuroendocrinology by discovering novel neuropeptides and neurosteroids: 2. Discovery of neurosteroids and pineal neurosteroids. Gen Comp Endocrinol. 2014;205:11–22.
do Regoa JL, Vaudry H. Comparative aspects of neurosteroidogenesis: From fish to mammals. Comp Endocrinol. 2015;doi:10.1016/j.ygcen.2015.05.014
Di Cara F, King-Jones K. How clocks and hormones act in concert to control the timing of insect development. Curr Top Dev Biol. 2013;105:1–36.
Belles X, Santos CG. The MEKRE93 (Methoprene tolerant-Krüppel homolog 1-E93) pathway in the regulation of insect metamorphosis, and the homology of the pupal stage. Insect Biochem Mol Biol. 2014;52:60–8.
Gruntenko NE, Rauschenbach IY. Interplay of JH, 20E and biogenic amines under normal and stress conditions and its effect on reproduction. J Insect Physiol. 2008;54:902–8.
Sarov-Blat L, So WV, Liu L, Rosbash M. The Drosophila takeout gene is a novel molecular link between circadian rhythms and feeding behavior. Cell. 2000;101:647–56.
Simon AF, Shih C, Mack A, Benzer S. Steroid control of longevity in Drosophila melanogaster. Science. 2003;299:1407–10.
Gáliková M, Klepsatel P, Senti G, Flatt T. Steroid hormone regulation of C. elegans and Drosophila aging and life history. Exp Gerontol. 2011;46:141–7.
Rus F, Flatt T, Tong M, Aggarwal K, Okuda K, Kleino A, et al. Ecdysone triggered PGRP-LC expression controls Drosophila innate immunity. EMBO J. 2013;32:1626–38.
Itoh TQ, Matsumoto A. 40 years of molecular genetics of circadian clock in Drosophila - II. Drosophila yet again -. Jikan Seibutsugaku. 2013;19:70–8.
This work was supported by grants to RN from JST/PRESTO, MEXT KAKENHI Grant Number 23116701 on Innovative Areas ‘Regulatory Mechanism of Gamete Stem Cells’, and JSPS KAKENHI Grant Number 25712010.
The authors declare that they have no competing interests.
All authors wrote, read, and approved the manuscript.
OU and TA are recipients of the research fellowships for young scientists from the Japan Society for the Promotion of Science.
Outa Uryu and Tomotsune Ameku contributed equally to this work.
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Uryu, O., Ameku, T. & Niwa, R. Recent progress in understanding the role of ecdysteroids in adult insects: Germline development and circadian clock in the fruit fly Drosophila melanogaster . Zoological Lett 1, 32 (2015) doi:10.1186/s40851-015-0031-2
- Steroid hormone
- Germline stem cell
- Circadian clock