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. 2014 Jun;37(2):444–459. doi: 10.1590/s1415-47572014005000006

Genome-wide comparison of genes involved in the biosynthesis, metabolism, and signaling of juvenile hormone between silkworm and other insects

Daojun Cheng 1, Meng Meng 1, Jian Peng 1, Wenliang Qian 1, Lixia Kang 1, Qingyou Xia 1,✉
PMCID: PMC4094618  PMID: 25071411

Abstract

Juvenile hormone (JH) contributes to the regulation of larval molting and metamorphosis in insects. Herein, we comprehensively identified 55 genes involved in JH biosynthesis, metabolism and signaling in the silkworm (Bombyx mori) as well as 35 in Drosophila melanogaster, 35 in Anopheles gambiae, 36 in Apis mellifera, 47 in Tribolium castaneum, and 44 in Danaus plexippus. Comparative analysis showed that each gene involved in the early steps of the mevalonate (MVA) pathway, in the neuropeptide regulation of JH biosynthesis, or in JH signaling is a single copy in B. mori and other surveyed insects, indicating that these JH-related pathways or steps are likely conserved in all surveyed insects. However, each gene participating in the isoprenoid branch of JH biosynthesis and JH metabolism, together with the FPPS genes for catalyzing the final step of the MVA pathway of JH biosynthesis, exhibited an obvious duplication in Lepidoptera, including B. mori and D. plexippus. Microarray and real-time RT-PCR analysis revealed that different copies of several JH-related genes presented expression changes that correlated with the dynamics of JH titer during larval growth and metamorphosis. Taken together, the findings suggest that duplication-derived copy variation of JH-related genes might be evolutionarily associated with the variation of JH types between Lepidoptera and other insect orders. In conclusion, our results provide useful clues for further functional analysis of JH-related genes in B. mori and other insects.

Keywords: juvenile hormone, biosynthesis, metabolism, signaling, gene duplication

Introduction

In insects, the sesquiterpenoid juvenile hormone (JH) is synthesized and released from the corpora allata (CA) and cooperates with the steroid 20-hydroxyecdysone (20E) that is synthesized and released from the prothoracic glands to orchestrate insect molting, growth, metamorphosis, via stage-specific changes in the titers of these two endocrine hormones (Dubrovsky, 2005). JH activity is elevated early in each larval instar to maintain larval shape and characteristics, whereas the titer of 20E is always increased at the end of each larval instar to trigger the transition instar from larva to larva (Bownes and Rembold, 1987; Riddiford, 1994; Wyatt and Davey, 1996; Futahashi and Fujiwara, 2008). In the final larval instar, the JH titer is remarkably decreased and the 20E titer is increased to a very high level enough to initiate a metamorphic transition from larva to pupa. In addition, JH has been showed to regulate aging and reproduction in insects (Riddiford, 2012; Yamamoto et al., 2013; Zou et al., 2013).

The dynamic change in JH titer is mainly modulated through biosynthetic and metabolic pathways that are catalyzed by different sets of endogenous enzymes (Li et al., 2004; Minakuchi et al., 2006; Noriega et al., 2006; Kinjoh et al., 2007). As summarized in Figure S1, JH biosynthesis involves the mevalonate (MVA) pathway and the isoprenoid branch. The MVA pathway includes eight enzymatic steps and uses acetyl-CoA to generate farnesyl diphosphate (FPP) as a JH precursor. Then, the isoprenoid branch converts the FPP into JH through several continuous steps of oxidization and epoxidation (Kinjoh et al., 2007). In addition, allatotropin (AT) and allatostatin (AS), which belong to the neuropeptide hormone family, promotes and inhibits, respectively, the JH biosynthesis by affecting CA activity (Kataoka et al., 1989; Kramer et al., 1991; Bogus and Scheller, 1996). Furthermore, proper nutritional signals can affect the release of AT and AS by the brain and further results in the activation or inhibition of JH biosynthesis (Noriega, 2004). Moreover, the decrease in JH titer is controlled through its metabolism, which is mainly catalyzed by JH esterase (JHE), JH epoxide hydrolase (JHEH), and JH diol kinase (JHDK). Particularly, several genes involved in JH biosynthesis, metabolism, and signaling have been previously analyzed in insects (Noriega et al., 2006; Kinjoh et al., 2007; Hua-Jun et al., 2011).

Deciphering JH signaling in insects has been attracting increasing attention worldwide. Although the nature of JH signaling has not been completely uncovered, some molecules have been demonstrated to be involved in JH signaling, including JH binding protein (JHBP), methoprene-tolerant (Met), the 20E receptor EcR, Ultraspiracle (USP), Krüppel homolog 1 (Kr-h1), FKBP39, and Chd64 (Riddiford, 2008; Jindra et al., 2013). Notably, Met protein is a bHLH-PAS transcription factor and has been confirmed as a potential JH receptor in some insect species (Jindra et al., 2013). In Drosophila melanogaster and Bombyx mori, Met paralog, germ-cell expressed (Gce) or Met2 protein functions as a partner of Met in modulating JH signaling (Abdou et al., 2011; Guo et al., 2012).

Intriguingly, there are eight types of natural JHs characterized in insects, including JH0, JHI, JHII, JHIII, JHIII skipped bisepoxide (JHSB3), JHIII bisepoxide (JHB3), methyl farnesoate (MF), and iso JH0 (Minakuchi et al., 2006; Daimon and Shinoda, 2013). Currently, only JHIII is ubiquitous in all insects. The other four JH variants, including JH0, iso JH0, JHI, and JHII, have been found exclusively in Lepidoptera (Furuta et al., 2013). JHSB3 and JHB3 are specific to Hemiptera and Diptera, respectively. MF is found to be present in both Diptera and Coleoptera. However, little is known about how genes involved in JH biosynthesis, metabolism, and signaling vary among insects.

As noted above, some of the genes (referred to as JH-related genes) participating in JH-related pathways (biosynthesis, metabolism, and signaling) have been characterized in various insect species. However, with the availability of whole-genome sequence, the number, structure, and evolution of all JH-related genes have not yet been investigated and compared systematically at a genome-wide level among insects. The silkworm (B. mori) belongs to the order Lepidoptera. In this study, based on the current B. mori genome assembly (Xia et al., 2008), we performed a genome-wide identification of genes involved in JH bio-synthesis, metabolism, and signaling in B. mori; we then evolutionarily compared the B. mori genes with their orthologs in other insects.

Materials and Methods

Gene identification and phylogenetic analysis

The B. mori genome sequences and the predicted proteins were downloaded from the SilkDB database and were used in our analysis. The predicted protein sets for D. melanogaster, Anopheles gambiae, Apis mellifera, Tribolium castaneum, and Danaus plexippus were downloaded from NCBI, Ensembl, or specific databases such as FlyBase for D. melanogaster, BeeBase for A. mellifera (Munoz-Torres et al., 2011), MonarchBase for D. plexippus (Zhan and Reppert, 2013), and the Butterfly Genome Database for Heliconius melpomene (Heliconius Genome, 2012).

We used protein sequences or conserved domains of known JH-related genes to query against the predicted protein sets of B. mori and of other insects, using the BLAST program with an E-value threshold of less than 1e-6. In addition, an online SMART program was used to search for the functional domains of predicted proteins. Multiple candidate members of a JH-related gene were identified on the basis of agreement with both the E-value threshold and the existence of typical domains. Regarding the nomenclature, candidate genes were defined with an original name if the biological properties (such enzymatic activities) had been confirmed or if the genes had only one copy in each insect surveyed. If a JH-related gene had multiple copies and no functional attributes, we refer them as original-like genes.

The chromosomal distribution of JH-related genes in B. mori was determined using a B. mori genetics linkage map constructed using single-nucleotide polymorphism (SNP) markers (Yamamoto et al., 2008). The multiple alignments of the complete amino acid sequences or functional domains of JH-related genes were performed using ClustalX (Thompson et al., 1997). Based on the multiple sequence alignment results, neighbor-joining phylogenetic trees for JH-related genes from all surveyed insects were constructed using MEGA4.0 (Tamura et al., 2007) with a bootstrap of 1000 replicates.

Microarray-based gene expression analysis

The spatio-temporal expression patterns of JH-related genes in B. mori were first surveyed using the microarray method. Microarray gene expression data of multiple larval tissues from B. mori larvae at the third day of the fifth instar and related analytical methods from our previous report (Xia et al., 2007) were used to profile the tissue-specific expression of JH-related genes. In nine larval tissues, including the A/MSG (anterior/median silk gland), PSG (posterior silk gland), testis, ovary, fat body, midgut, integument, hemocyte, Malpighian tubule, and head (containing the brain and the associated glands in the retrocerebral complex, corpora allata (CA), corpus cardiacum (CC)), a total of 10,393 genes (transcripts) have been estimated to be activated based on an intensity threshold of 400 (Xia et al., 2007). We retrieved the microarray data for B. mori JH-related genes from the active gene selection to examine their tissue expression profiles.

The developmental expression pattern was analyzed using microarray data of B. mori gene expression during metamorphosis (unpublished data), including 19 developmental time points during the larva-pupa-adult transitions, namely, V4 (fourth day of the fifth larval instar), V5, V6, V7, W0 (beginning of wandering), W12 (12 hours after wandering), W24, W36, W48 (completing spinning), W60 (immediately after pupation), W72, W96, W120, W144, W168, W192, W216, W240, and adulthood. Gene expression in B. mori larvae at V3 (third day of the fifth larval instar) was set as the common reference. The ratio between the experimental and reference intensities for a JH-related gene was used to evaluate expression changes during the larva-pupa-adult transitions of B. mori. The related analytical method was based on our previous reports (Xia et al., 2007; Huang et al., 2009). Tissue and developmental expression patterns from the microarray analysis were visualized using the GeneCluster2.0 program (Reich et al., 2004).

Real-time quantitative RT-PCR examination of gene expression

We also used a real-time quantitative RT-PCR approach to examine expression patterns of JH-related genes during the larval growth of B. mori. The B. mori strain Dazao was reared under a temperature of 25 °C. B. mori larvae were collected at ten time points during the larval feeding and molting stages from the fourth instar to the fifth instar, including IV0 (0 hour after the third larval molt, namely, the beginning of the fourth instar), IV1 (day 1 after the third molt), IV2 (day 2 after the third molt), IV3 (day 3 after the third molt), IV4 (day 4 after the third molt), IVM (just initiating the fourth larval molt), V0 (0 hours after the fourth molt, namely, the beginning of the fifth instar), and V1 (day 1 of the fifth instar).

Total RNA was extracted using TRIzol reagent (Invitrogen, USA) and was reverse transcribed into cDNA with M-MLV reverse transcriptase (Promega, USA). Real-time RT-PCR was conducted as described in our previous study (Wang et al., 2008). The B. mori ribosomal protein L3 (RpL3) was used as an internal control. All primers used are listed in Table S1.

Results

Inventory of genes involved in JH biosynthesis, metabolism, and signaling in B. mori and other insects

We used the amino acid sequences of known insect JH-related genes to search against the predicted B. mori proteins using the BLAST program. Initially, 55 JH-related genes were identified, including 34 for JH biosynthesis, 13 for JH metabolism, and eight for JH signaling (Table 1). Several JH-related genes exhibited multiple copies, including farnesyl diphosphate synthase (FPPS), farnesyl phosphatase (FPPase), aldehyde dehydrogenase (ALDH), JH acid methyltransferase (JHAMT), farnesoic acid O-methyltransferase (FAMeT), JHE, JHEH, and JHDK. All JH-related genes for B. mori mapped to different chromosomes except for the FPPase gene and allatostatin receptor (ASR) gene (Figure 1 and Table 1). Intriguingly, the copies of several JH-related gene with multiple copies were distributed on the same chromosome in a tandem manner, for example, FPPS on chromosome 12, JHDK on chromo-some 3, FAMeT on chromosomes 5 or 6, JHAMT on chromosome 12, JHE on chromosome 25, and JHEH on chromosome 28.

Table 1.

Inventory of JH-related genes in the B. mori genome.

Pathway Gene Symbol Gene ID ORF (aa) Scaffold Chromosome
MVA pathway of JH biosynthesis Acetoacetyl CoA thiolase Acat BGIBMGA011029 405 nscaf3015 23
Hydroxymethylglutaryl-CoA synthase HMGS BGIBMGA004001 456 nscaf2767 19
Hydroxymethylglutaryl-CoA reductase HMGR BGIBMGA003229 785 nscaf2623 2
Mevalonate kinase MevK BGIBMGA013075 410 nscaf3058 16
Phosphomevalonate kinase MevPK BGIBMGA001556 186 nscaf2136 21
Diphosphomevalonate decarboxylase MevPPD BGIBMGA007459 383 nscaf2886 3
Isopentenyl-diphosphate delta-isomerase IPPI BGIBMGA004904 251 nscaf2822 25
Farnesyl diphosphate synthase 1 FPPS1 BGIBMGA001926 427 nscaf2204 19
Farnesyl diphosphate synthase 2 FPPS2 BGIBMGA001927 382 nscaf2204 19
Farnesyl diphosphate synthase 3 FPPS3 BGIBMGA014635* 385 nscaf2204 19
Isoprenoid branch of JH biosynthesis Farnesyl phosphatase-like protein 1 FPPase-l1 BGIBMGA011595 251 nscaf3028 -
Farnesyl phosphatase-like protein 2 FPPase-l2 BGIBMGA011596 247 nscaf3028 -
Farnesol dehydrogenase FOHSDR BGIBMGA005248 254 nscaf2827 8
Aldehyde dehydrogenase-like protein 1 ALDH-l1 BGIBMGA001966 750 nscaf2204 19
Aldehyde dehydrogenase-like protein 2 ALDH-l2 BGIBMGA001965 440 nscaf2204 19
Juvenile hormone acid methyltransferase JHAMT BGIBMGA010391 250 nscaf2993 12
Juvenile hormone acid methyltransferase-like protein 1 JHAMT-l1 BGIBMGA008032 136 nscaf2889 9
Juvenile hormone acid methyltransferase-like protein 2 JHAMT-l2 BGIBMGA010392 266 nscaf2993 12
Juvenile hormone acid methyltransferase-like protein 3 JHAMT-l3 BGIBMGA010393 168 nscaf2993 12
Juvenile hormone acid methyltransferase-like protein 4 JHAMT-l4 BGIBMGA010563 137 nscaf2993 12
Juvenile hormone acid methyltransferase-like protein 5 JHAMT-l5 BGIBMGA010564 121 nscaf2993 12
Juvenile hormone acid methyltransferase-like protein 6 JHAMT-l6 BGIBMGA014014 267 nscaf3099 28
Farnesoic acid O-methyltransferase-like protein 1 FAMeT-l1 BGIBMGA002604 443 nscaf2529 5
Farnesoic acid O-methyltransferase-like protein 2 FAMeT-l2 BGIBMGA002314 248 nscaf2330 26
Farnesoic acid O-methyltransferase-like protein 3 FAMeT-l3 BGIBMGA006513 229 nscaf2853 6
Farnesoic acid O-methyltransferase-like protein 4 FAMeT-l4 BGIBMGA002684 206 nscaf2529 5
Farnesoic acid O-methyltransferase-like protein 5 FAMeT-l5 BGIBMGA002605 338 nscaf2529 5
Farnesoic acid O-methyltransferase-like protein 6 FAMeT-l6 BGIBMGA006319 224 nscaf2852 6
Farnesoic acid O-methyltransferase-like protein 7 FAMeT-l7 BGIBMGA006318 829 nscaf2852 6
Cytochrome P450 15C1 Cyp15 C1 BGIBMGA011708 288 nscaf3031 11
Neuropeptide regulation of JH biosynthesis Allototropin AT BGIBMGA011850 291 nscaf3031 11
Allatostatin AS BGIBMGA014377 150 scaffold416 14
Allatotropin receptor ATR BGIBMGA004429 255 nscaf2795 20
Allatostatin receptor ASR BGIBMGA005708 362 nscaf2830 -
JH metabolism Juvenile hormone esterase JHE BGIBMGA000772 567 nscaf1705 25
Juvenile hormone esterase-like protein 1 JHE-l1 BGIBMGA000774 566 nscaf1705 25
Juvenile hormone esterase-like protein 2 JHE-l2 BGIBMGA000775 560 nscaf1705 25
Juvenile hormone esterase-like protein 3 JHE-l3 BGIBMGA000776 572 nscaf1705 25
Juvenile hormone epoxide hydrolase JHEH BGIBMGA013930 461 nscaf3099 28
Juvenile hormone epoxide hydrolase-like protein 1 JHEH-l1 BGIBMGA011468 401 nscaf3027 23
Juvenile hormone epoxide hydrolase-like protein 2 JHEH-l2 BGIBMGA009211 510 nscaf2943 14
Juvenile hormone epoxide hydrolase-like protein 3 JHEH-l3 BGIBMGA013994 637 nscaf3099 28
Juvenile hormone epoxide hydrolase-like protein 4 JHEH-l4 BGIBMGA013793 395 nscaf3097 28
Juvenile hormone epoxide hydrolase-like protein 5 JHEH-l5 BGIBMGA013929 355 nscaf3099 28
Juvenile hormone diol kinase JHDK BGIBMGA008814 183 nscaf2925 3
Juvenile hormone diol kinase-like protein 1 JHDK-l1 BGIBMGA008813 182 nscaf2925 3
Juvenile hormone diol kinase-like protein 2 JHDK-l2 BGIBMGA008815 179 nscaf2925 3
JH signaling Juvenile hormone binding protein JHBP BGIBMGA011549 243 nscaf3027 23
FKBP39 FKBP39 BGIBMGA001490 402 nscaf2136 21
Chd64 Chd64 BGIBMGA007092 174 nscaf2865 17
Methoprene-tolerant 1 Met1 BGIBMGA005416 455 nscaf2828 8
Methoprene-tolerant 2 Met2 BGIBMGA000657 661 nscaf1690 1
Ecdysone receptor EcR BGIBMGA006767 496 nscaf2855 10
Ultraspiracle USP BGIBMGA006183 270 nscaf2847 4
Kruppel homolog 1 Kr-h1 BGIBMGA003160 348 nscaf2589 4
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Note:

*

indicates new gene assembly.

–

indicates unknown.

Figure 1.

Figure 1

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Chromosomal distribution of JH-related genes in B. mori. Based on the assembly of the whole-genome sequence and single-nucleotide polymorphism (SNP) markers linkage map for B. mori, a total of 52 JH-related genes were mapped on the different chromosomes of B. mori. Several different copies of each of the JH-related genes with multiple copies are clustered in tandem on the chromosomes.

To determine comprehensively the evolution of JH-related genes among insects, we further identified JH-related genes in other insects, namely, 35 in D. melanogaster, 35 in A. gambiae, 36 in A. mellifera, 47 in T. castaneum, and 44 in D. plexippus (Table 2, Table S2). Some JH-related genes in these five insects had at least two copies, including three genes (Farnesol dehydrogenase (FOHSDR), JHE, and JHEH) in D. melanogaster, three (FOHSDR, JHE, and JHEH)in A. gambiae, four (FPPase, FOHSDR, FAMeT, and JHE)in A. mellifera, five (FPPase, FOHSDR, ALDH, JHAMT, and JHEH) in T. castaneum, and six (FPPS, FPPase, ALDH, FAMeT, JHEH, and JHDK) in D. plexippus. Moreover, the copies of several JH-related genes in these insects were distributed in tandem on a chromosome, including the JHEHs in D. melanogaster; the JHEHs and FOHSDRs in A. gambiae; the JHAMTs and JHEHs in T. castaneum; and the FPPSs, FPPases, FAMeTs, JHEHs, and JHDKs in D. plexippus. On the basis of these and similar observations in B. mori, we speculate that the JH-related genes with multiple copies were duplicated during the evolution of B. mori and other insects.

Table 2.

Copy number of JH-related genes in B. mori and the other insects.

Pathway Gene Symbol B. mori (Lepidoptera) D. melanogaster (Diptera) A. gambiae (Diptera) A. mellifera (Hymenoptera) T. castaneum (Coleoptera) D. plexippus (Lepidoptera)
MVA pathway of JH biosynthesis Acetoacetyl CoA thiolase ACAT 1 1 1 1 1 1
Hydroxymethylglutaryl-CoA synthase HMGS 1 1 1 1 1 1
Hydroxymethylglutaryl-CoA reductase HMGR 1 1 1 1 1 1
Mevalonate kinase MevK 1 1 1 1 1 1
Phosphomevalonate kinase MevPK 1 1 1 1 1 1
Diphosphomevalonate decarboxylase MevPPD 1 1 1 1 1 1
Isopentenyl-diphosphate delta-isomerase IPPI 1 1 1 1 1 1
Farnesyl diphosphate synthase FPPS 3 1 1 6 1 2
Isoprenoid branch of JH biosynthesis Farnesyl phosphatase FPPase 2 1 1 2 3 2
Farnesol dehydrogenase FOHSDR 1 6 6 2 7 1
Aldehyde dehydrogenase ALDH 2 1 1 1 6 2
Juvenile hormone acid methyltransferase JHAMT 7 1 1 1 3 1
Farnesoic acid
O-methyltransferase		 FAMeT 7 1 1 2 1 5
Cytochrome P450 15A1 Cyp15A1 - - - 1 1 -
Cytochrome P450 15C1 Cyp15C1 1 - - - - 1
Neuropeptide regulation of JH biosynthesis Allototropin AT 1 - 1 - 1 1
Allatostatin AS 1 1 1 1 1 1
Allototropin receptor ATR 1 1 1 1 1 1
Allatostatin receptor ASR 1 1 1 1 1 1
JH metabolism Juvenile hormone esterase JHE 4 2 2 2 1 1
Juvenile hormone epoxide hydrolase JHEH 6 3 3 1 5 8
Juvenile hormone diol kinase JHDK 3 1 1 1 1 2
JH signaling Juvenile hormone binding protein JHBP 1 1 1 1 1 1
FKBP39 FKBP39 1 1 1 1 1 1
Chd64 Chd64 1 1 1 1 1 1
Methoprene-tolerant/Methoprene-tolerant 1 Met/Met1 1 1 1 1 1 1
Germ cell expressed/Methoprene-tolerant 2 Gce/Met2 1 1 - - - 1
Ecdysone receptor EcR 1 1 1 1 1 1
Ultraspiracle USP 1 1 1 1 1 1
Kruppel homolog 1 Kr-h1 1 1 1 1 1 1
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Note: - represents no identification.

The MVA pathway of JH biosynthesis

The upstream mevalonate (MVA) pathway of JH biosynthesis is responsible for producing the JH precursor farnesyl diphosphate (FPP). As shown in Figure S1, the MVA pathway involved eight enzymatic steps. Interestingly, each of the enzyme-encoding genes involved in the first seven steps of the MVA pathway, which produce the FPP precursor isopentenyl diphosphate (IPP), existed as a single copy in B. mori and five other surveyed insects and showed a 1:1:1:1:1:1 orthologous relationship (Table 2).

Farnesyl diphosphate synthase (FPPS) catalyzes the final reaction of the MVA pathway, converting IPP into the JH precursor FPP. Three transcripts of the FPPS gene have been identified in B. mori (Kinjoh et al., 2007). We noted that only two FPPS transcripts matched well with two predicted genes for B. mori, namely, FPPS1 for BGIBMGA001926 and FPPS2 for BGIBMGA001927. We further used the complete cDNA sequence of the FPPS3 transcript to search against the B. mori genome assembly using the BLASTn algorithm. In this search, we found that the FPPS3 transcript matched the downstream genomic region of the FPPS2 gene; therefore, we defined FPPS3 as BGIBMGA014635 for a supplement of the B. mori predicted genes. Strikingly, a comparative analysis revealed a copy number variation in the FPPS genes among the surveyed insects. In addition to three copies in B. mori, there were six copies in A. mellifera, two in D. plexippus, and one each in D. melanogaster, A. gambiae, and T. castaneum. From the phylogenetic tree of the FPPS and FPPS-like genes that were identified here and collected from online resources for other insects (Figure 2), we observed that all FPPS and FPPS-like genes from B. mori and other lepidopterans, including D. plexippus, Heliconius melpomene, Choristoneura fumiferana, Mythimna unipuncta, and Agrotis ipsilon, clustered into two groups, and different copies from each insect were separately grouped, indicating that the FPPS duplication in lepidopterans may have occurred after their separation from other insect species and before their separation from each other. However, all six FPPS-like genes in A. mellifera grouped well together, suggesting that the FPPS genes from A. mellifera may have been duplicated after the separation of A. mellifera from other insects. The FPPS genes from other five insect species, including Aedes aegypti, Culex quinquefasciatus, Anthonomus grandis, Dendroctonus jeffreyi, and Nasonia vitripennis, also existed as a single copy and clustered together with the FPPS genes from D. melanogaster, A. gambiae, and T. castaneum.

Figure 2.

Figure 2

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Phylogenetic tree of the FPPS genes from B. mori and other insects. Based on the multiple alignments of the amino acid sequences of FPPS proteins from B. mori and other insects, a phylogenetic tree was constructed using the neighbor-joining method with 1000bootstrap replicates after removing the highly divergent sequences at the N- or C-terminus. Bootstrap values > 60% are marked. Bm, Bombyx mori; Dm, Drosophila melanogaster; Aga, Anopheles gambiae; Am, Apis mellifera; Tc, Tribolium castaneum; Dp, Danaus plexippus; Cf, Choristoneura fumiferana; Hm, Heliconius melpomene; Mu, Mythimna unipuncta; Agi, Agrotis ipsilon; Aa, Aedes aegypti; Cq, Culex quinquefasciatus; Agr, Anthonomus grandis; Dj, Dendroctonus jeffreyi; Nv, Nasonia vitripennis.

The isoprenoid branch of JH biosynthesis

The downstream isoprenoid branch pathway of JH biosynthesis converts FPP to JH (Minakuchi et al., 2006). Recently, in insects, three types of catalytic enzymes, including farnesyl pyrophosphate phosphatase (FPPase), farnesol dehydrogenase (FOHSDR), and aldehyde dehydrogenase (ALDH), have been successfully identified as being responsible for the sequential conversion of FPP into farnesol, farnesal, and farnesoic acid (FA) (Mayoral et al., 2009; Nyati et al., 2013; Rivera-Perez et al., 2013). In addition to the previous prediction of these genes in several insects, we identified two FPPase-like genes, one FOHSDR gene, and two ALDH-like genes in D. plexippus. Although each of these genes exhibited a different number of copies among the surveyed insects, the copy number of each gene was the same in B. mori and D. plexippus as well as in D. melanogaster and A. gambiae (Table 2 and Table S2).

The conversion of FA into JH is completed via two catalytic reactions in insects, namely, epoxidation and methyl esterification. Notably, this conversion can occur in two ways (Figure S1). One involves FA oxidation by Cyp15C1 to form JH acid (JHA), after which JHA is methylated by juvenile hormone acid methyltransferase (JHAMT) to synthesize JH. Another way is that FA is methylated to form methyl farnesoate (MF) by farnesoic acid O-methyltransferase (FAMeT), after which MF is oxidized by Cyp15A1 to produce JH.

Cyp15C1 and Cyp15A1, the two genes involved in FA epoxidation, belong to the Cyp15 subfamily of cytochrome P450 enzymes. The Cyp15C1 gene has been identified in B. mori and D. plexippus, and the Cyp15A1 gene has been characterized in T. castaneum and A. mellifera (Daimon et al., 2012; Daimon and Shinoda 2013). No Cyp15C1 or Cyp15A1 was identified in D. melanogaster. We performed a BLASTp search against the genome of H. melpomene (Lepidoptera) and identified a homolog of the B. mori Cyp15C1 gene, namely, HMEL006305, further indicating that Cyp15C1 may be Lepidoptera-specific.

JHAMT and FAMeT are considered two catalytic enzymes for the methyl esterification of FA. One authentic JHAMT enzyme was first characterized in B. mori (Shinoda and Itoyama, 2003). As listed in Table 1, the gene (BGIBMGA010391) encoding the authentic JHAMT and six JHAMT-like genes (from JHAMT-l1 to JHAMT-l6) were found in the B. mori genome, and each contains a methyltransf_12 domain. Furthermore, three JHAMT copies (including authentic JHAMT, JHAMT-l1, and JHAMT-l2) were predicted in T. castaneum, whereas only one copy of JHAMT gene was identified in four other insects (Table 2 and Table S2). A phylogenetic tree revealed that the different copies of the JHAMT gene in B. mori and D. plexippus grouped well together, and that the three JHAMT copies in T. castaneum also grouped into a clade (Figure S2), suggesting that the JHAMT gene in B. mori or T. castaneum was duplicated after their separation from other insect species.

FAMeT has been found to exist in insects and crustaceans (Hui et al., 2010), and evidence from D. melanogaster has suggested that FAMeT has a minor role in JH biosynthesis, but it may play a major role in JH signaling (Burtenshaw et al., 2008; Zhang et al., 2010). Our data revealed that in the B. mori genome, there are seven FAMeT-like genes, each of which contains two typical Methyltransf_FA and DM9 domains. Comparatively, FAMeT exists as a single copy in T. castaneum as well as in two Diptera insects but as two copies in A. mellifera and five copies in D. plexippus (Table 2 and Table S2). A phylogenetic tree of insect FAMeT or FAMeT-like genes was constructed using their coding sequences containing two functional domains (Figure S2). In this tree, with the exception of A. mellifera, one copy of the FAMeT gene from each of the five remaining insects grouped into a clade. Other copies of the FAMeT gene from B. mori, A. mellifera, and D. plexippus grouped together into an additional clade in an irregular manner. This phylogenetic relationship indicates that the duplication of the different FAMeT copies may have occurred after insect radiation and subsequently undergone a rapid sequence diversification during insect evolution.

Neuropeptide regulation of JH biosynthesis

Insect JH biosynthesis is also modulated by two neuropeptides, namely, allatotropin (AT) and allatostatin (AS). AT and AS play antagonistic roles during JH bio-synthesis, with the former being a stimulator and the later being an inhibitor of CA activity (Stay, 2000). As listed in Table 1, from the B. mori genome, we retrieved four genes that respectively encode AT, AS, the AT receptor (ATR), and the AS receptor (ASR), which have been previously reported in other insects (Secher et al., 2001; Park et al., 2002; Roller et al., 2008; Yamanaka et al., 2008; Horodyski et al., 2011). In addition, AS, ASR, and ATR were all identified in five other insects, whereas AT gene was predicted only in A. gambiae, T. castaneum, and D. plexippus in our analysis. Notably, each of the identified genes related to the neuropeptide regulation of JH bio-synthesis appears to exist as a single copy in B. mori and the other surveyed insects (Table 2).

Enzymes involved in JH metabolism

The metabolic degradation of JH contributes to the reduction of JH titer and is catalyzed by three enzymes, namely, JHE, JHEH, and JHDK. As shown in Figure S1, JHE catalyzes the conversion of JH into JH acid (JHa) or the conversion of JH diol (JHd) into JH acid diol (JHad). A previous report characterized one JHE gene encoding an authentic JHE enzyme in B. mori (Hirai et al., 2002). Here, in addition to the known JHE gene, three JHE-like genes (namely, JHE-l1, JHE-l2, and JHE-l3) were identified from the B. mori genome (Table 1). Moreover, we retrieved different copies of the JHE gene in five other insects, namely, 2, 2, 2, 1, and 1 for D. melanogaster, A. gambiae, A. mellifera, T. castaneum, and D. plexippus, respectively (Table 2 and Table S2). All the identified JHE genes contain a COesterase domain. A phylogenetic analysis showed that the JHE genes in Lepidoptera, Hymenoptera, Diptera, or Coleoptera separately grouped well together (Figure S3), consistent with the classical phylogeny of these insect species. Notably, different copies of the JHE gene in D. melanogaster grouped first together, as did those in A. gambiae and A. mellifera, suggesting that JHE duplication in these three species occurred after their separation. Nevertheless, in Lepidoptera, JHE from B. mori grouped first with JHE from D. plexippus and then with the grouping clade of JHE-l1 and JHE-l2 from B. mori, suggesting that JHE in both B. mori and D. plexippus may have a common ancestor, and the other three JHE-like genes in B. mori may have undergone a great sequence diversification after their duplication from JHE.

JHEH catalyzes the conversion of JH into JHa or the conversion of JHa into JHad. According to previous reports in B. mori (Zhang et al., 2005; Seino et al., 2010),in addition to an authentic JHEH, there are five JHEH-like genes in the B. mori genome (Table 1). The copy numbers of the JHEH genes vary, with three in D. melanogaster, three in A. gambiae, one in A. mellifera, five in T. castaneum, and seven in D. plexippus (Table 2 and Table S2). On the phylogenetic tree of the JHEH genes (Figure S3), different copies of the JHEH gene from each of four insect species (D. melanogaster, A. gambiae, A. mellifera, and T. castaneum) grouped first together, indicating that the JHEH gene from these four species may have undergone species-specific duplication after their separation from the other insects. Moreover, the copies of the JHEH genes from two lepidopterans, B. mori and D. plexippus, grouped into four clades, and each clade contained different copies from both of these species, suggesting that JHEH duplication in Lepidoptera may have occurred before their radiation.

JHDK is required for the conversion of JHd into JH diol phosphate (JHdp). To date, JHDK has been functionally characterized in two Lepidoptera insects, namely, B. mori and Manduca sexta (Maxwell et al., 2002; Li et al., 2005). Here, three copies of the JHDK gene were identified in the B. mori genome (Table 1), including one authentic JHDK and two JHDK-like genes, each of which contains an EF-hand domain. Furthermore, as listed in Table 2 and Table S2, there were two copies of the JHDK gene in another lepidopteran, D. plexippus, but only one copy was identified in four other surveyed insects. Phylogenetic analysis showed that the JHDK copies from Lepidoptera grouped into two clades, and the JHDK genes from other insects grouped well together (Figure S3), suggesting that JHDK duplication in Lepidoptera may have also occurred before their separation.

Genes involved in the JH signaling pathway

Recently, additional evidence has shown that the bHLH-PAS transcription factor Met is a potential receptor for JH signaling (Jindra et al., 2013). Met and its paralogous gene Gce were first identified in D. melanogaster (Wilson and Fabian, 1986; Baumann et al., 2010b), in which they were partially redundant in mediating JH signaling (Baumann et al., 2010a; Abdou et al., 2011). Two copies of the Met gene, Met1 and Met2, have been characterized in B. mori (Li et al., 2010; Guo et al., 2012; Kayukawa et al., 2012). Intriguingly, our analysis also identified two copies of the Met gene in two other lepidopteran insects, D. plexippus and H. melpomene, namely DpMet-l1 and DpMet-l2 in D. plexippus (Table 2 and Table S2) and HmMet-l1 (HMEL011931) and HmMet-l1 (HMEL009818) in H. melpomene. However, only one copy of the Met gene was identified in A. gambiae, A. mellifera, and T. castaneum (Table 2 and Table S2). Phylogenetic analysis revealed that Met and Gce from D. melanogaster grouped together (Figure 3). In Lepidoptera, Met1 and Met-l1 grouped into one clade, whereas Met2 and Met-l2 grouped into another, indicating that the Met duplication in Lepidoptera may have occurred before their separation.

Figure 3.

Figure 3

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Phylogenetic tree of the Met genes in B. mori and other insects. The amino acid sequences encoding by Met genes from seven insect species, including Bombyx mori (Bm), Drosophila melanogaster (Dm), Anopheles gambiae (Aga), Apis mellifera (Am), Tribolium castaneum (Tc), Danaus plexippus (Dp), and Heliconius melpomene (Hm), were used to build a phylogenetic tree. See Figure 2 for a detailed description of the approaches for constructing phylogenetic tree.

In addition, some molecules, including JHBP, FKBP39, Chd64, EcR, USP, and Kr-h1, have been demonstrated to be involved in JH signaling (Dubrovsky, 2005; Li et al., 2007; Jindra et al., 2013). Our results showed that each of these six genes was identified as having one copy in B. mori and five other insect species (Table 2 and Table S2).

Expression profiles of JH-related genes in multiple tissues of B. mori larvae

Using microarray data of gene expression in multiple tissues of B. mori larvae on the third day of the fifth instar when JH titer is present (Sakurai and Niimi, 1997; Xia et al., 2007), we investigated the tissue expression of JH-related genes. As a result, 36 of 55 JH-related genes were detected in at least one tissue (Figure 4). Among JH bio-synthesis-related genes, Acat, MevPK, IPPI, FPPS2, ALDH-l1, JHAMT-I6, FAMeT-I4, and Cyp15C1 were expressed in the head (mainly containing CA, CC, and brain), which may be directly involved in JH biosynthesis. In particular, several JH biosynthesis-related genes showed either high expression in other larval tissues or ubiquitous expression, such as Acat and MevPK in all surveyed tissues; FAMeT-l1, FAMeT-l5, and FAMeT-l7 in the midgut; and JHAMT-l4, JHAMT-l5, and JHAMT-l6 in the fat body and integument. This indicates that these genes may function in other biological processes.

Figure 4.

Figure 4

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Expression pattern of JH-related genes in multiple tissues from B. mori larvae. Microarray data of genome-wide gene expression in multiple tissues from B. mori larvae on the third day of the fifth instar were downloaded from the B. mori genome database. Each tissue sample was analyzed with at least two biological repeats. If a JH-related gene was estimated to have an average expression signal intensity of more than 400 in any tissue, it was considered to be expressed in that tissue. F, female; M, male. A/MSG, anterior/median silk gland; PSG, posterior silk gland.

Some genes involved in JH metabolism are mostly expressed in the midgut or Malpighian tubule (Figure 4). For example, five genes, namely, JHE-l1, JHEH, JHEH-l4, JHDK, and JHDK-l1, were expressed in both the midgut and Malpighian tubule. JHEH-l1 and JHDK-l2 were expressed in the midgut and Malpighian tubule, respectively. JHE-l3 and JHEH-l2 expression was enriched in both the A/MSG and PSG, whereas JHEH6 was highly expressed in all tissues with the exception of hemocytes. JHEH-l2 was specifically expressed in the A/MSG. In addition, among the genes involved in the JH signaling pathway, JHBP, Met1, EcR, FKBP39, and Chd64 were all weakly expressed in at least one larval tissue. In particular, FKBP39 and Chd64 were expressed in all analyzed tissues. However, from the microarray data, the expression of three genes, USP, Met2, and Kr-h1, was not observed in any tissue. It is possible that the expression levels for these three transcription factors may be too low at day 3 of the fifth larval instar and were therefore difficult to be detected.

Expression profiles of JH-related genes during B. mori metamorphosis

Based on microarray data for gene expression at 19 developmental points during B. mori metamorphosis (unpublished data), we found that 42 of 55 JH-related genes were expressed during at least one developmental point (Figure 5). Among the genes involved in the MVA pathway of JH biosynthesis the majority were highly expressed during the pupa-adult transition, with the exception of MevK, whose expression was detected in the female on the fourth day of the fifth larval instar (V4). In particular, Acat and IPP1 displayed a high expression in males, whereas FPPS1 and FPPS3 were highly expressed in females. Among the genes involved in the isoprenoid branch of JH biosynthesis, only ALDH-l1, Cyp15C1, and several copies of JHAMT and FAMeT were detected during metamorphosis, and they were highly expressed before wandering and during the pupa-adult transition (Figure 5). In particular, FAMeT-l2 and FAMeT-l4 exhibited a male-specific expression pattern during the pupa-adult transition. Further studies will be required to decipher the roles of these two FAMeT genes during the development of B. mori males.

Figure 5.

Figure 5

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Expression profiles of JH-related genes during metamorphosis in B. mori. The developmental expression profiles of JH-related genes for B. mori were analyzed using microarray data of genome-wide gene expressions at 19 time points during B. mori metamorphosis. The ratio was calculated by comparing the signal intensity of the mRNA expression level for each JH-related gene at each time point to that in the common reference of larvae on the third day of the fifth instar in B. mori. Subsequently, the expression change of each JH-related gene was evaluated by this expression ratio and visualized using the GeneCluster2.0 program. Plus and minus denote up- and down-regulation, respectively.

Microarray data of gene expression during B. mori metamorphosis also revealed that among the genes involved in JH metabolism, JHE and JHE-l1 were highly expressed during pupation. JHEH, JHEH-l2, JHEH-l4, JHEH-l5, JHDK-l1, JHDK, and JHDK-l2 were mainly expressed before wandering. JHEH-l1 and JHEH-l3 displayed a high expression in females during pupa-adult transition. Among the genes involved in JH signaling, JHBP, FKBP39, Chd64, and Met1 exhibited ubiquitous expression during B. mori metamorphosis. Met2 expression was detected only in males during pupa-adult transition, and EcR and USP were highly expressed before wandering. Kr-h1 presented a high expression during the late stage of the pupa-adult transition.

Because JH biosynthesis and JH metabolism are initiated during larval feeding and molting, respectively, we used real-time quantitative RT-PCR experiments to further check the consistency between JH titer and the expression profiles of several JH-related genes with multiple copies during B. mori larval growth. As shown in Figure 6, FPPS1 expression was highly during B. mori larval molting and gradually decreased during larval feeding, which was consistent with the changes in JH titer. Interestingly, FPPS1 expression at the beginning of the feeding stages was higher in the fifth instar larvae than in the fourth instar larvae. Several copies of the genes involved in the isoprenoid branch of JH biosynthesis, including JHAMT-l3, JHAMT-l4, FAMeT-l2, and FAMeT-l5, exhibited a high expression during larval feeding and subsequently decreased during larval molting, also indicating consistency with the changes in the JH titer. Moreover, four copies of the genes involved in JH metabolism, including JHE-l1, JHE-l3, JHDK, JHDK-l1, JHDK-l2, JHEH-l1, JHEH-l3, and JHEH-l5, showed an increased expression during larval feeding and were obviously decreased during larval molting. The expression of these genes was also consistent with the change in JH titer during B. mori larval feeding and molting.

Figure 6.

Figure 6

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Expression patterns of JH-related genes with multiple copies during larval growth and molting in B. mori. Quantitative analysis of the gene expression of JH-related genes with multiple copies during larval growth and molting in B. mori was performed by real-time RT-PCR. The B. mori ribosomal protein L3 (RpL3) gene was used as an internal control. IV0, immediately after completion of the third larval molting and the beginning of feeding in the fourth larval instar; IV1, one day after feeding in the fourth larval instar; IV2, two days after feeding in the fourth larval instar; IV3, three days after feeding in the fourth larval instar; IV4, four days after feeding in the fourth larval instar; IVM, the fourth larval molting; V0, immediately after completion of the fourth larval molting and the beginning of feeding in the fifth larval instar; V1, one day after feeding in the fifth larval instar.

Discussion

JH plays key roles in the regulation of various aspects of insect growth and development. Previous studies have reported the genome-wide identification of genes involved in JH biosynthesis, metabolic degradation, or signaling in several insect species, such as the JH biosynthesis-related genes in B. mori (Kinjoh et al., 2007; Xia et al., 2008), JHEs in A. aegypti (Bai et al., 2007), and JHEHs in T. castaneum (Seino et al., 2010). To understand comprehensively the evolutionary conservation and variation of JH-related genes in insects, we systematically identified and compared JH-related genes in B. mori and five other insect species whose whole genomes have been sequenced, including the recently completed D. plexippus (Lepidoptera) genome sequence.

The developmental changes in JH titer in insects are mainly controlled by the processes of biosynthesis in the CA and metabolic degradation in the targeting tissues. Here, we observed an evolutionary divergence of the genes involved in JH biosynthesis among B. mori and other insects. First, the genes related to the upstream seven steps of the MVA pathway of JH biosynthesis, which is responsible for producing IPP as FPP precursor, all existed as a single copy and displayed a rigorous orthologous relationship among the analyzed insects (Table 2 and Table S2), indicating that the process of IPP production was conserved during insect evolution. Second, the FPPS gene involved in the last step of the MVA pathway (production of JH precursor FPP) and all identified genes participating in the isoprenoid branch for producing JH showed a variation in copy number or gene class among B. mori and other insects (Table 2 and Table S2), which may be a consequence of gene duplication. In fact, JH types also varied between Lepidoptera and other insect orders, and more types of JH variants are present in Lepidoptera (Minakuchi et al., 2006; Riddiford, 2008; Goodman and Cusson, 2012; Daimon and Shinoda, 2013; Jindra et al., 2013). Thus, we speculate that the copy variation among the genes involved in the FPP production from IPP and in the isoprenoid branch may reflect the functional divergence of the associated gene products, and is likely linked to the diversity of JH types among insects. Our comparison raised two additional issues regarding the relationship between the variations in JH-related genes and in JH types. One issue is that FPPS genes from Lepidoptera may have undergone a species-specific divergence (Figure 2), which agrees with previous findings (Kinjoh et al., 2007). Therefore, we hypothesize that FPPS-mediated enzymatic reactions may be the first step leading to the diversity of JH types among insects. Undoubtedly, whether all the predicted FPPS genes are authentically involved in JH biosynthesis needs to be investigated by more enzymatic experiments. However, JHAMT and FAMeT, two enzymes involved in the methyl esterification of FA, were predicted in B. mori and other insects (Table 2 and Table S2). Previous studies in D. melanogaster have reported that FAMeT was likely not involved in JH biosynthesis (Burtenshaw et al., 2008; Zhang et al., 2010). However, another analysis speculated that FAMeT-mediated methyl esterification should exist in insects and crustaceans (Hui et al., 2010). Undoubtedly, more evidence is required to resolve the controversial functions of FAMeTs in JH biosynthesis. Furthermore, Cyp15C1 and Cyp15A1 were confirmed to be involved in two routes of FA epoxidation (Daimon and Shinoda, 2013). However, several surveyed insects do not contain either Cyp15C1 or Cyp15A1 (Table 2 and Table S2). Thus, additional experiments are needed to address whether both epoxidation routes occur in insects with no Cyp15C1 or no Cyp15A1 or whether other Cyp genes whose functions have yet to be identified catalyze one or the other route. Finally, all identified genes involved in neuropeptide regulation of JH biosynthesis existed as a single copy, implying that their regulatory mechanism is also conserved among insects.

The metabolic degradation of JH is catalyzed mainly by JHE, JHEH, and JHDK. Our results showed that each of the genes encoding these three enzymes may have undergone duplication in Lepidoptera (Table 2 and Table S2). In particular, JHDK has multiple copies in Lepidoptera but one copy in the other surveyed insects. Given the existence of more JH types in Lepidoptera, we propose that, as was true of copy variation among several JH biosynthesis-related genes, the duplication and divergence of JH metabolism-related genes may also be a functionally adaptive evolution to the diversity of JH types in insects.

The nature of JH signaling has been the subject of an increasing number of experimental studies. To date, it has been confirmed that seven genes, namely, JHBP, FKBP39, Chd64, EcR, USP, Met, and Kr-h1, are implicated in JH signaling (Li et al., 2007; Suzuki et al., 2011: Jindra et al., 2013). Except for Met, each of the other genes existed as a single copy in B. mori and other surveyed insects (Table 2 and Table S2). The Met protein is a bHLH-PAS transcription factor and has been characterized as a JH receptor in insects (Wilson and Fabian, 1986; Jindra et al., 2013). Unlike the single copy of the Met gene in A. gambiae, A. mellifera, and T. castaneum, two copies of the Met gene have been identified previously in other insects, namely, Met and Gce in Drosophila (Baumann et al., 2010b) and Met1 and Met2 in B. mori (Li et al., 2010; Guo et al., 2012; Kayukawa et al., 2012). Our analysis also identified two copies (Met-l1 and Met-l2) of the Met gene in two other lepidopterans, D. plexippus and H. melpomene. Although current evidence is not sufficient to elucidate why Met was duplicated in these insects, two copies of the Met gene have been demonstrated to cooperatively modulate JH signaling via a protein-protein interaction in D. melanogaster (Baumann et al., 2010a; Abdou et al., 2011) and in B. mori (Guo et al., 2012; Kayukawa et al., 2012). Together with the findings from the phylogenetic tree of insect Met genes (Figure 3) and the functional redundancy of two copies of the Met gene, we propose that the JH signaling cascade is also evolutionarily conserved across insects.

Given that multiple copies were predicted for several genes involved in JH biosynthesis and metabolism, it was important to determine whether these copies were functional. Our microarray data and quantitative RT-PCR experiments in B. mori showed that some copies of the JH-related genes exhibited moderate expression in the head (mainly containing CA, CC, and brain) or in a dynamic manner that correlated with the temporal changes in JH titer, such as FPPS1, FPPS2, JHAMT-l3, JHAMT-l4, JHE-l1, JHEH-l5, JHDK, and JHDK-l2. Previous studies have confirmed the enzymatic activities or physiological functions of several JH-related genes in B. mori, such as JHAMT (Shinoda and Itoyama, 2003), JHE (Tan et al., 2005), JHEH (Seino et al., 2010), and JHDK (Li et al., 2005). One copy of the JHAMT gene has also been verified to be activated functionally in JH biosynthesis in T. castaneum (Minakuchi and Riddiford, 2008). Furthermore, most enzyme-encoding genes with multiple copies appear to be expressed in other larval tissues excluding head (mainly containing CA, CC, and brain), during developmental stages with no JH activities, or in one or other sex (Figures 4, 5 and 6). These observations indicate that the copies of the JH-related genes may play roles in other physiological processes. Nevertheless, further enzymatic activity assays are undoubtedly required to assess whether multiple copies of the JH-related genes encode authentic enzymes involved in JH biosynthesis and metabolism or encode proteins involved in other physiological processes.

In summary, we first performed a systematic identification of the genes involved in JH biosynthesis, metabolism, and signaling in insects, including two lepidopterans (B. mori and D. plexippus), two dipterans (D. melanogaster and A. gambiae), one hymenopteran (A. mellifera), and one coleopteran (T. castaneum). A comparative analysis concluded that the early steps of the MVA pathway and neuro-peptide regulation of JH biosynthesis, as well as JH signaling, are apparently conserved among B. mori and other surveyed insects. However, most genes involved in the last step of the MVA pathway and the isoprenoid branch of JH biosynthesis, as well as JH metabolism, seem to have undergone duplication, resulting in multiple copies in Lepidoptera. This duplication may be functionally and evolutionarily relevant to the variation of JH types among Lepidoptera and other insect species. Although some copies of several JH-related multi-copy genes show a specific spatio-temporal expression correlated to JH activity in B. mori, it remains to be confirmed whether their enzymatic activities are associated with JH biosynthesis and metabolism. Taken together, the results of our analysis provide new clues for understanding the genetic basis of JH bio-synthesis, metabolism, and signaling in insects.

Acknowledgments

This work was supported by grants from the National Basic Research Program of China (No. 2012CB114600), the National Hi-Tech Research and Development Program of China (No. 2011AA100306), the National Natural Science Foundation of China (No. 31172267 and No. 31272503), and the Municipal Natural Science Foundation of Chongqing (No. cstc2012jjA80023).

Footnotes

Associate Editor: Houtan Noushmehr

Supplementary Material

The following online material is available for this article:

Table S1 - RT-PCR Primers used in this study.

gmb-73-2-310-ts1.pdf (462.2KB, pdf)

Table S2 - JH-related genes in the other surveyed insects.

gmb-73-2-310-ts2.pdf (496.3KB, pdf)

Figure S1 - Summary of insect JH-related pathways.

gmb-73-2-310-fs1.pdf (1,011.8KB, pdf)

Figure S2 - Phylogenetic tree of the JHAMT and FAMeT genes.

gmb-73-2-310-fs2.pdf (881KB, pdf)

Figure S3 - Phylogenetic tree of the JHE, JHEH, and JHDK genes.

gmb-73-2-310-fs3.pdf (1.1MB, pdf)

This material is available as part of the online article from http://www.scielo.br/gmb.

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Internet Resources

  1. SMART program, http://smart.embl-heidelberg.de/.
  2. Microarray data in Bombyx mori genome database, http://www.silkdb.org/microarray/download.html.

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Table S1 - RT-PCR Primers used in this study.

gmb-73-2-310-ts1.pdf (462.2KB, pdf)

Table S2 - JH-related genes in the other surveyed insects.

gmb-73-2-310-ts2.pdf (496.3KB, pdf)

Figure S1 - Summary of insect JH-related pathways.

gmb-73-2-310-fs1.pdf (1,011.8KB, pdf)

Figure S2 - Phylogenetic tree of the JHAMT and FAMeT genes.

gmb-73-2-310-fs2.pdf (881KB, pdf)

Figure S3 - Phylogenetic tree of the JHE, JHEH, and JHDK genes.

gmb-73-2-310-fs3.pdf (1.1MB, pdf)

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