Precocious Metamorphosis in the Juvenile Hormone–Deficient Mutant of the Silkworm, Bombyx mori

Larvae of standard B. mori strains undergo molting four times and thus have five larval instars; these larvae are conventionally termed “tetramolter” in silkworm genetics. The spontaneous mutant mod was identified in a standard strain [11] and mod larvae undergo precocious metamorphosis in the third (dimolter) or fourth instar (trimolter). First, we obtained a detailed developmental profile of larvae from two batches of the mod strain. All mod larvae underwent precocious metamorphosis in the fourth instar and no individuals reached the fifth instar (Figure 1A and 1B). We plotted the timing of the onset of spinning in the mod larvae (Figure 1C and 1D). Consistent with previous reports [11], [12], we found that spinning occurred at two clearly distinguishable timings: (1) from 56 to 80 h and (2) from 112 to 144 h after the third molt: these larvae were termed early- and late-maturing trimolters, respectively. This segregation in the timing of the onset of spinning was not observed in the standard strain p50T (Figure 1C) or other moltinism strains [11], and thus is a unique characteristic of the mod strain. Importantly, development in almost all early-maturing trimolters was arrested and they remained as larval-pupal intermediates (93.4%, 85/91 larvae); only 3 of the 91 larvae (3.3%) successfully survived to adulthood (Figure 1B). In contrast, the late-maturing trimolters did not show such severe developmental impairment and 88.5% (77/87) became miniature adults (Figure 1B). In the larval-pupal intermediates, we usually observed prothetelic phenotypes such as a mixed pupal cuticle on the exoskeleton of animals having overall a larval appearance (Figure 1A), suggesting that hormonal switching of molting and metamorphosis may be aberrant in the mod strain. Notably, despite their small body size, reproduction in mod moths seemed normal, and their eggs hatched without apparent abnormalities.

In the silkworm, premature metamorphosis can be induced by the loss of or low levels of JH signaling, which can occur due to the surgical removal of the CA [17] or to overexpression of the JH-degrading enzyme [16]. We therefore hypothesized that precocious metamorphosis in the mod strain was caused by the prevention of JH biosynthesis or signaling. To examine this hypothesis, we first determined whether the mod phenotype could be rescued by treatment with methoprene, a JH analogue. We topically applied several doses of methoprene to newly-molted third or fourth instar mod larvae and found that a fourth larval molting was induced by the treatment (Figure 1E). Fifth instar larvae that had undergone fourth larval ecdysis grew normally, began to spin after ∼6 days, and eventually metamorphosed to pupae and adults that were normal and fertile. This result suggests that JH reception and subsequent JH signaling is normal in the mod strain. Therefore, we next compared the JH titers in the hemolymph of third instar larvae of mod and p50T strains at 24 h after molting to the third instar. JHs were extracted from the hemolymph and their methoxyhydrin derivatives were analyzed by liquid chromatography-mass spectrometry (LC-MS). We detected JH I and JH II in the hemolymph of p50T, whereas the JH titer in the hemolymph of the mod strain was below the detectable level (Figure 1F). These results indicate that the mod strain is a JH-deficient mutant in which complete (or almost complete) loss of JH caused precocious metamorphosis.

To identify the gene responsible for the mod locus, we performed positional cloning using backcross 1 progeny (BC₁) obtained from crossing females of the mod strain (t011 strain, see http://www.shigen.nig.ac.jp/silkwormbase/index.jsp↗) with F₁ heterozygote males of mod and p50T strains (see Figure S1). We mapped the mod locus within ∼400 kb region on the scaffold Bm_scaf16 (chromosome 11) [8] using 792 BC₁ individuals. Twenty-five genes were predicted to be present within this region. Among them, we focused on BGIBMGA011708, a gene encodes a cytochrome P450 monooxygenase. Based on sequence homology and phylogenetic analysis (Figure 2B), the gene was designated as CYP15C1. We found that CYP15C1 shares high homology with the CYP15A1 of the cockroach Diploptera punctata, which is involved in JH biosynthesis in CA of the cockroach [18]. Given that the mod phenotype is a result of the loss of the JH titer (Figure 1F), we speculated that the mod phenotype is due to the loss of function of CYP15C1. To examine this possibility, we first determined the nucleotide sequence of the full-length CYP15C1 cDNA from p50T and mod strains. We identified a 68-bp deletion in the mod allele that introduces a premature stop codon in the coding region of CYP15C1 (Figure 2C–2E). This deletion seemed to produce a functionally null mutation in CYP15C1, since a heme-binding motif, which is essential for enzymatic activities in P450s [19], was eliminated in the mod allele (Figure 2D). This result indicates that CYP15C1 is a strong candidate for the mod locus. Therefore, we further characterized CYP15C1 and its gene product.

The strict regulation of JH biosynthesis in CA is critical for the successful development and reproduction of insects [14], [15], [20]. We next examined the spatial expression pattern of CYP15C1 mRNA. We examined 12 tissues at four different developmental stages and found that CYP15C1 mRNA was highly specific to the corpus cardiacum (CC)-CA complex (Figure 3A). A whole mount in situ hybridization experiment in the brain (Br)-CC-CA complex (Figure 3B and Figure S2) showed that the signal for CYP15C1 was strictly limited to CA, where JH is synthesized, and could not be detected in the brain or CC. These results showed a close spatial correlation between CYP15C1 expression and JH biosynthesis.

Next, we carried out a detailed analysis of the temporal expression pattern of CYP15C1 in the CC-CA complex and compared it to that of the gene for JHA methyltransferase (JHAMT), a key enzyme that acts in the final step of the JH biosynthetic pathway in CA [21]. CYP15C1 mRNA was constitutively expressed in CA from the first instar larval to adult stages (Figure 3D), even when JH is not synthesized (Figure 3C) [20]; no apparent differences in levels of CYP15C1 mRNA were observed between males and females during pupal and adult stages (Figure 3D). In contrast, the temporal expression pattern of JHAMT correlates well with the JH synthetic activity of CA (Figure 3D and Figure S2). JHAMT transcript completely disappeared by day 4 of the fifth instar when CA ceased production of JH (see Figure 3C). It reappeared from the mid-pupal stage and increased to a very high level in the female CA. This was consistent with the temporal profile of JH biosynthesis activity in CA as this occurs only in females during the pupal and adult stages [20]. Taken together, our results strongly indicate that CYP15C1 is involved in JH biosynthesis in CA, but does not appear to act as a rate-limiting factor for JH biosynthesis.

The cockroach CYP15A1, the ortholog of B. mori CYP15C1, catalyzes the epoxidation of (2E,6E)-methyl farnesoate (MF) to JH III [18]. Although biochemical studies predicted the presence of FA epoxidase in the CA of the lepidopteran insect Manduca sexta[22], [23], the corresponding gene has not been identified to date. Therefore we examined the enzymatic activity of B. mori CYP15C1 against two plausible substrates, FA and MF. First, we employed a transient expression system using Drosophila S2 cells. When S2 cells expressing CYP15C1 were incubated with medium containing FA, a major HPLC peak was generated that had the same retention time (15.1 min) as standard JH III acid (JHA III) (Figure 4A, middle). This peak did not appear when S2 cells expressing GFP were used (Figure 4A, bottom). The ESI-MS spectrum of this peak gave an [M-H]⁻ at m/z 251, consistent with the C₁₅H₂₄O₃ formula of JHA III, confirming that CYP15C1 catalyzes the conversion of FA to JHA III. The enzymatic properties of CYP15C1 was further examined in a stable Sf9 cell line (Sf9/BmCYP15C1) that constitutively expresses CYP15C1. When the Sf9/BmCYP15C1 cells were cultured in medium containing FA, significant levels of JHA III were detected; in contrast, JHA III production was difficult to detect when original Sf9 cells were used (Table S2, Exp.1). When Sf9/BmCYP15C1 cells were cultured in medium containing MF, JH III generation was detected at low levels. However, a similar level of JH III production was also detected in the original Sf9 cells when they were cultured in the same medium (Table S2, Exp.1). These results suggest that JH III production observed in Sf9/BmCYP15C1 was might be due to the presence of endogenous P450 epoxidases in Sf9 cells, which have been reported previously to have lower substrate specificity and stereospecificity [18], [24]. The addition of the JH esterase inhibitor 3-octylthio-1,1,1- trifluropropan-2-one (OTFP) did not increase production of JHA III (Table S2, Exp. 2), indicating that the degradation of JH III by intrinsic JH esterases in the cells was negligible. Therefore, we were able to estimate the conversion ratio of FA and MF to JH III by CYP15C1. This showed that CYP15C1 exhibited at least 18-fold higher activity for FA than MF (Table S2, Exp. 1), a result that is consistent with previous biochemical studies on lepidopteran FA epoxidase in CA.

To further examine the stereospecificity of CYP15C1, the JHA III generated by Sf9/CYP15C1 was chemically methylated and analyzed by a Chiral-HPLC. The methylated product had a major (R)-JH III and a minor (S)-JH III peak (R∶S = 97∶3) (Figure 4B). These results show that B. mori CYP15C1 encodes a functional P450 epoxidase that preferentially converts FA to JHA III rather than MF to JH III, and does so in a highly (R)-enantioselective manner (Figure 4C).

To obtain direct evidence that CYP15C1 is responsible for the mod mutation, we performed transgenic rescue experiments using the GAL4/UAS system [25]. We generated transgenic silkworm lines carrying the UAS-CYP15C1 transgene with the eye-specific 3xP3-EGFP marker [26]. The UAS-CYP15C1 transgene was driven using a silkworm enhancer trap line ET14 in which GAL4 was strongly expressed in CA (Figure 5A), although weak expression was also detected in peripheral tissues including fat bodies and the midgut [9], [27]. As these lines were generated using the standard Shiro-C (w-1; +^mod) strain, we changed the genetic background to w-1/w-1; mod/mod by crossing to the mod strain. The resultant w-1; mod; ET14/+ females were then crossed with w-1; mod; UAS-CYP15C1/+ males to determine whether the mod phenotype could be rescued by CYP15C1 overexpression. We used two independent UAS-CYP15C1 lines with ET-14 (Figure 5B). In both UAS-CYP15C1 lines, CYP15C1 overexpression efficiently prevented precocious metamorphosis and 97.1% of the larvae (34/35 in total) underwent the fourth larval molt to become fifth instar larvae (Figure 5B and 5C). Only one larva (1/35) became a late-maturing trimolter, but neither dimolters nor early-maturing trimolters appeared. This result was in contrast to what was observed in control larvae or larvae carrying either the GAL4 or UAS construct alone: approximately half of the larvae became dimolters and the remainder became trimolters, while no larvae became tetramolters. We also measured the JH titer in the hemolymph (Figure 5D). As expected, the JH titers in control, ET14, and UAS larvae were below the detectable limit. In contrast, we were able to detect JH I and JH II in the hemolymph of mod larvae carrying both ET14 and UAS-CYP15C1 constructs. Taken together, these results provide direct evidence that CYP15C1 is responsible for the mod mutation and is essential for JH biosynthesis.

JH III is the most common JH in many insect orders, although its ethyl-branched homologs (JH I and II) are the major JHs in the order Lepidoptera [22], [28]. Biochemical studies have shown that in the late steps of JH biosynthesis in many insect species, including cockroaches and locusts, FA is first methylated to MF and then epoxidized to JH III in CA [22]. However, the final two steps of JH biosynthesis are reversed in Lepidoptera: ethyl-branched homologs of FA (homo-FAs) are first epoxidized and the resultant JHAs (i.e., JHA I and II) are then methylated to the authentic JHs (i.e., JH I and II) [22]. This study showed that B. mori CYP15C1 epoxidizes FA to JHA III in a highly stereospecific manner. CYP15C1 might also epoxidize MF to JH III, but in a far less efficient manner (Table S2). Given that B. mori JHAMT can methylate both FA and JHAs with similar efficiencies [21], our data clearly demonstrate the major JH biosynthetic pathway in B. mori: homo-FAs are first epoxidized to JHAs by CYP15C1, and then methylated to JHs by JHAMT (Figure 4C and Figure 6A). Interestingly, D. punctata CYP15A1 does not convert FA to JHA III [18]. Thus, the difference in specificity of CYP15 to the substrates FA and MF may determine the order of the final steps of JH biosynthesis in insects.

The expression of most early JH biosynthetic enzyme genes and JHAMT in B. mori is limited to the CA and shows dynamic developmental fluctuations [20], [21], [29]. In particular, the temporal expression profile of JHAMT correlates well with JH biosynthetic activity in B. mori[20], [21], [30], [31] and in the Eri silkworm Samia cynthia ricini[32], indicating that JHAMT is a key regulatory gene whose transcriptional control is critical for the regulation of JH biosynthesis in Lepidoptera. Here, we found that expression of CYP15C1 was also limited in CA but in a different pattern to other JH biosynthesis genes in that it was constitutively expressed from larval to adult stages. This result suggests that the transcriptional regulation of CYP15C1 is less important than JHAMT for the temporal regulation of JH production in B. mori. CA of the silkworm ceases JH biosynthesis by day 3 of the last (fifth) instar [20]; however, it is speculated that CA synthesizes and secretes JHAs during the following prepupal period. Our data indicate that this endocrine switch can be explained by constitutive CYP15C1 expression and the shut-off of JHAMT expression in CA (Figure 6A). During the larval-pupal transition, homo-FAs are constantly converted to JHA I and II by CYP15C1, and the resultant JHAs are secreted from the gland without further conversion because of the absence of JHAMT.

CYP15 P450 family members are found in both hemimetabolous and holometabolous insects [33]. In a similar manner as CYP15C1 expression in B. mori, CA-specific CYP15 expression has also been observed in two cockroach species, D. punctata and Blattella germanica[18], [34], in the locust Schistocerca gregaria[35], and in the mosquito Aedes aegypti[36], suggesting a conserved function in JH biosynthesis. However, the enzymatic properties of CYP15 products, with the exception of those of D. punctata[18] and B. mori (this study), have not been studied and the physiological role of CYP15s in the development of other insects remains unknown. By characterizing the CYP15C1-null mutant silkworm, we have demonstrated here that CYP15C1 plays an essential role in JH biosynthesis and for the maintenance of the proper timing of metamorphosis.

Accumulating data have suggested that CYP15 genes are evolutionarily diversified in terms of their gene regulation and nature. For example, unlike B. mori CYP15C1, A. aegypti CYP15 shows developmentally and dynamically regulated changes of expression, which appear to correlate well with the JH synthetic activity in the CA [36]. In addition, CYP15 is not present in the genome of D. melanogaster, but a P450 gene (Cyp6g2) is expressed in CA in a highly tissue-specific manner [37]. More extensive research on the transcriptional controls and enzymatic properties of JH epoxidases across a broader range of insect taxa will shed light on the roles of these enzymes.

Our results consistently indicate that the mod strain is a JH-deficient mutant that is unable to synthesize JHs in CA. One unique characteristic of the precocious pupation in the mod strain is the variation in the timing of the onset of spinning (Figure 1). The feeding period in early-maturing trimolters was unusually short (50 h after molting) compared with that observed in surgical allatectomy of newly molted fourth instar larvae. In the latter larvae, the feeding period was comparable in length to that of the late-maturing trimolters [e.g. ∼130 h [17]] and no timing segregation was observed [17]. In addition, most of the early-maturing trimolters displayed a larval-pupal intermediate phenotype and eventually died, unlike allatectomized larvae, most of which successfully developed into small but normal pupae [17]. One explanation for this phenomenon is that the early-maturing trimolters were destined to undergo larval molting to the fifth instar on day 2, while the late-maturing trimolters were destined for pupation after a prolonged fourth instar, similar to allatectomized larvae [17] (Figure 1D). Molting in early-maturing trimolters on day 2 usually resulted in the formation of larval-pupal intermediates. One possible explanation for this mixed phenotype is that metamorphosis in the mod strain is induced in the presence of homo-MFs (unepoxidized JH I and II), presumed products instead of epoxidized JH I and II in CA of the mod strain (see Figure 6B). MF is known as a crustacean JH and has recently been reported to have JH activity in D. melanogaster[38], [39]. Therefore, MF and its homologs might have JH-like activity but not able to fully substitute for authentic (epoxidized) JHs in the physiology of the silkworm. Alternatively, other P450 epoxidases in B. mori that have low substrate specificity and stereospecificity, like CYP9E1 [18] and CYP6A1 [24] in other insects, might substitute for the absence of CYP15C1 in peripheral tissues of mod larvae, and such locally-synthesized JHs may prevent precocious metamorphosis in the first and second instar larvae carrying the mod mutation. Further studies are needed to elucidate the mechanism for this unique characteristic of the mod strain.

We found that the precocious phenotype was more severe in the w-1; mod strain compared to that in t011, a genetic stock of the mod strain. We rarely observed dimolter larvae in the t011 stock (Figure 1B). However, in the original manuscript in 1956, it was reported that 28–92% of mod larvae became dimolters [11]. This difference might have developed as a consequence of unintended artificial selection during stock maintenance that favored broods producing trimolters in higher proportions, as it is difficult to obtain sufficient number of eggs using dimolter moths [11], [12]. Thus, we speculate that the present t011 stock may be genetically fixed to produce mostly trimolters, and that this attribute can be varied by outcrossing to other strains.

In the silkworm, premature metamorphosis can be induced by surgical removal of JH-producing CA (allatectomy) [17], by application of an imidazole-based insect growth regulator KK-42 [40] or an anti-juvenile hormone agent KF-13S [41], [42], or by continuous overexpression of the JH-degrading enzyme, JH esterase [16]. In any case, however, premature pupation is not induced in larvae younger than the third instar. In agreement with these studies, we did not observe precocious pupation in first or second instar mod larvae, nor did we observe apparent developmental abnormalities during these early instars. Therefore, our data support the hypothesis that there are two physiological phases in the life of silkworm larvae [16]: the JH-independent phase (first and second instar) in which JH does not have a morphogenetic function; and, the JH-dependent phase (third instar and thereafter) in which the morphostatic action of JH is required to prolong the larval stage until the attainment of the appropriate body size for metamorphosis. Given that most generally the minimum number of the larval instar in insects is three [1], [2], our data further imply that insect larvae need to experience at least one [e.g., L2 pupae in D. melanogaster[43]] or two (e.g., B. mori) larval-larval molts and/or require a certain length of time of postembryonic development in order to acquire competence for metamorphosis.

The silkworm is a classic model organism that has been used for pioneering studies in genetics, physiology, and biochemistry [5]. The availability of whole genome data [8], post-genomic tools [10], and unique mutant resources [6], together with the classic “status quo” responses to JHs in this insect [14], [15], [17], makes the silkworm well-suited for study of hormonal control of growth and development. Indeed, these advantages have greatly contributed to the identification of essential components in the biosynthesis of ecdysteroids, the insect molting hormones [44]. Moreover, recent success in targeted gene disruption using a zinc-finger nuclease [45] increases the utility of this model organism. We are hopeful that our present study will encourage further studies on other “moltinism” strains in the silkworm, and consequently pave the way for a greater understanding of physiological control, developmental plasticity, and evolutionary history of the number of larval molting in insects, which may reflect adaptive strategies of insects to diverse environmental conditions. It is also noteworthy that the late step of the JH biosynthetic pathway is insect-specific and is therefore a potential target for biorational insecticides [46].

Silkworms were reared on an artificial diet or mulberry leaves at 25–27°C under standard conditions as described previously [47]. The silkworm strain t011 (mod/mod) was obtained from Kyushu University [6]. The Spodoptera frugiperda Sf9 and Drosophila melanogaster S2 cells were maintained as described previously [48]. To determine the developmental profile of mod, larvae from two batches of t011 were individually reared in plastic dishes, and their developmental stages were recorded at ∼8-h intervals.

The JH analog, methoprene (a kind gift from S. Sakurai) was applied to newly molted third or fourth instar larvae (∼8–12 h after molting). Methoprene was diluted with acetone and the selected doses (0.01–10 µg/larva) were topically applied to the dorsum using a 10-µl Hamilton microsyringe. The same volume of acetone was applied as a control.

Positional cloning of the mod locus was performed as described previously [49]. Codominant PCR markers and p50T-specific PCR markers were generated for each position of the scaffold Bm_scaf16 (chromosome 11) [9], and used for genetic analysis (Figure 2A and Figure S1). Homozygotes of the mod locus were collected from the BC₁ population [t011×(p50×t011)] based on the phenotype of precocious pupation.

Total RNAs were collected from CA of day 0 fifth instar larvae of p50T and Kinshu×Showa strains and used for 5′- and 3′-rapid amplification of cDNA ends (RACE) using the GeneRacer Kit (Invitrogen). PCR was performed using the primers listed in Table S1. The PCR products were subcloned and sequenced as described previously [47]. The obtained cDNA sequence was deposited in the GeneBank (accession number: AB124839↗).

qRT-PCR was performed essentially as described previously [21]. The primers used for the quantification of the CYP15C1 transcript are listed in Table S1.

In situ hybridization was performed essentially as described previously [50]. A CYP15C1 cDNA fragment (∼1.1 kb) was amplified by PCR listed in Table S1 and subcloned into a pDrive plasmid vector (QIAGEN).

(2E,6E)-farnesoic acid (FA) and (2E,6E)-methyl farnesoate (MF) were purchased from Echelon Research Laboratories (Salt Lake City) and racemic JH III from Sigma. JH III acid was prepared from the racemic JH III as described previously [21]. (R)-JH III was a kind gift from W.G. Goodman.

CYP15C1 overexpression in S2 cells was achieved using a GAL4/UAS system [51]. To generate a vector for expressing CYP15C1 under the control of the UAS promoter (UAS-CYP15C1-HA), a cDNA fragment coding the entire CYP15C1 ORF was ligated into the pUAST vector. UAS-GFP.RN3[52] was used as a negative control. UAS-CYP15C1-HA or UAS-GFP.RN3 was transfected with the Actin5C-GAL4 construct (a gift from Yasushi Hiromi, National Institute of Genetics, Japan). Forty-eight hours after transfection of S2 cells in a 60-mm dish, the old medium was replaced with 2 ml of fresh medium. S2 cells were detached from the bottom of the dish by pipetting, and 1 ml of the cell suspension was transferred to a siliconized glass test tube. FA or MF (100 µM at final concentration) was then added to the tube. After incubation at 25°C for 16 h, 500 µl of medium was collected and mixed with 500 µl of acetonitrile. Samples were centrifuged for 10 min at 15,000 rpm, followed by incubation at 25°C for 10 min. After filtration using a 0.2 µm filter, 10–20 µl of each sample was subjected to HPLC analysis as described below.

A cDNA with the full ORF of CYP15C1 cDNA was subcloned into the pIZT/V5-His vector (Invitrogen). The plasmid was transfected into Sf9 cells with Cellfectin reagent (Invitrogen), then cells transiently expressing CYP15C1 were selected successively with Zeocin according to the manufacture's instruction and a cell line (Sf9/CYP15C1) stably expressing CYP15C1 was established. Sf9/CYP15C1 cells were placed in a glass tube (12×75 mm) coated with PEG20,000 and cultured in SF900-II SFM medium containing FA or MF (10 µg/ml) for either 2 or 6 h at 26°C. In some experiments, the specific JH esterase-specific inhibitor OTFP (6 µM) was added to the medium to prevent possible degradation of the generated JH III by intrinsic JH esterase present in the cells. After incubation, an equal volume of CH₃CN was added to the medium, vortexed vigorously and centrifuged for 4,800 rpm for 10 min to remove cell debris. The supernatant was directly subjected to an HPLC analysis as described below for JH III acid or JH III, which were expected to be generated from FA and MF, respectively.

JH III was analyzed by reversed-phase HPLC as described previously [21]. JH III acid was analyzed by reversed-phase HPLC (column, Shiseido ODS UG80, 150 mm×3.0 mm ID; solvent, CH₃CN-20 mM CH₃COONH₄, pH 5.5, 35∶65, flow rate, 0.5 ml/min; detection, UV 219 nm). ESI-MS spectrum of JH III acid was obtained by TSQ system (Thermo Quest Finnigan, USA).

The stereospecificity of the epoxide group of JH III acid formed by CYP15C1 was analyzed as follows under semi-dark conditions. Sf9/CYP15 cells were cultured in medium containing 10 µg/ml FA for 48 hrs. An equal volume of CH₃CN was added to the medium (2 ml), vortexed vigorously and centrifuged at 4,800 rpm for 10 min. One ml of 1 M CH₃COONH, (pH 5.5) was added to the supernatant and extracted with 5 ml of CH₂CH₂; this step was performed 5 times. The extract was dehydrated with anhydrous Na₂SO₄ and evaporated to dryness in vacuo at 40°C, then the residue was dissolved in 200 µl of CH₂Cl₂, 50 µl of MeOH and 100 µl of TMS-diazomethane were then added and the solution was incubated at room temperature for 30 min. The reaction was dried with an N₂ gas stream, the residue dissolved in 100 µl of hexane, and subjected to a normal-phase HPLC (column, Shiseido SG80, 250×4.6 mm ID; solvent, hexane-EtOH, 99∶1; flow rate, 0.5 ml/min; detection, UV 211 nm). The peak corresponding to JH III (r.t. = 9.8 min) was collected. The stereospecificity of the epoxide group of the JH III was analyzed by a chiral-HPLC (column, Chiralapack IA, 250×4.6 mm ID, DAICEL; solvent, hexane-EtOH, 99∶1; flow rate, 0.5 ml/min; detection UV 219 nm) as described previously [31].

Ten microliters of deuterium-substituted JH III (d₃-JH III) [53] in toluene (67.1 pg/ml) was transferred to a clean glass tube to which 0.5 ml of methanol was added. The hemolymph sample (100 µl) was then added and mixed vigorously, and 1.5 ml of 2% NaCl was added to the JH sample. JH was extracted by partition with 0.5 ml hexane; this step was performed three times. The combined solvent containing JH (1.5 ml) was evaporated under a stream of nitrogen. One hundred microliters of methanol and 2 µl trifluoroacetic acid were added to the crude JH extract and mixture heated at 60°C for 30 min. After removal of the methanol, methoxyhydrin derivatives of JH (JH-MHs) were purified using a Pasture pipette packed with 1.0 g of aluminum oxide (activity grade III, ICN Ecochrom) prewashed with hexane. After loading the extract and washing with 2 ml of 30% ether in hexane, JH-MHs were eluted with 2 ml of 50% ethyl acetate in hexane and then dried under a stream of nitrogen. The residue was dissolved in 25 ml of 80% acetonitrile containing 5 µM sodium acetate.

The HP1100MSD system (Agilent) was equipped with a 150×3 mm C18 reversed phase column (UG80, Shiseido) protected by a guard column with 70% acetonitrile containing 5 µM sodium acetate at a flow rate of 0.4 ml/min. For MS analysis, electrospray ionization in the positive mode was used under the conditions of drying gas temperature at 320°C with 10 l/min flow rate, ionization voltage of 70 V. Under these conditions, selected ion masses for each JH-MH were monitored as [M+Na]+, i.e., m/z 321, 324, 335, and 349 for JH III, d₃-JH III, JH II, and JH I, respectively.

Overexpression of CYP15C1 was performed in transgenic silkworms using the GAL4/UAS system as described previously [25], [27], [54]. A coding sequence of CYP15C1 was introduced into a silkworm UAS vector carrying the marker gene 3xP3-EGFP. B. mori transformants were established using standard protocols [10]. To overexpress CYP15C1 on the mod/mod background, established UAS lines and an enhancer trap line ET14[27] were crossed with the t011 strain, and the resultant F₁ animals were sib mated to obtain the F₂ generation. In the F₂ generation, we collected animals showing premature pupation with white eyes (i.e., mod/mod; w-1/w-1) and confirmed the presence of the fluorescent marker gene using a fluorescent microscope (SZX12, Olympus). The established w-1; mod lines carrying UAS-CYP15C1 or ET14 were crossed, and their offspring were examined to determine whether precocious metamorphosis was blocked by CYP15C1 overexpression.