DNA methylation mediates BmDeaf1-regulated tissue- and stage-specific expression of BmCHSA-2b in the silkworm, Bombyx mori
Accurate regulation of tissue- and stage-specific expression of genes is prerequisite for normal development in organisms. DNA methylation plays an important role in modulating gene expression in mammals and plants. However, there is no direct evidence showing how DNA methylation regulates gene transcription in insects.
During the development of Bombyx mori wing, the expression level of DNA methyltransferase 1 (BmDnmt1) gradually declined and became stationary at pupal stage, resulting in a lower methylation rate of the intragenic promoter of the mid-pupal wing-specific gene BmCHSA-2b, an epidermal chitin synthase controlling mid-pupal wing development in B. mori. The higher methylation rate of the promoter in the pupal epidermis was decreased and BmCHSA-2b transcription was significantly increased by the treatment with the DNA methylation inhibitor, 5-azacytidine-2′-deoxycytidine, suggesting that DNA methylation regulates the tissue-specific expression of BmCHSA-2b. Pupa-specific transcription factor BmDEAF1 bound to the unmethylated intragenic promoter and activated the BmCHSA-2b transcription in the mid-pupal wing. BmDnmt1 and BmDeaf1 influenced the BmCHSA-2b transcription by binding competitively to the CpG island in the promoter.
All the data together demonstrate that the cooperation between the down-regulation of BmDnmt1 and increased stage-specific expression of BmDeaf1 enhances BmCHSA-2b tissue- and stage-specific transcription to ensure mid-wing development in B. mori. This study highlights an elaborate regulation mechanism how tissue- and stage-specific gene expression is regulated through promoter methylation in insect development.
KeywordsDNA methylation Intragenic promoter Transcriptional regulation Chitin synthase Wing development
Bovine serum albumin
deformed epidermal autoregulatory factor 1
DNA methyltransferase 1
ethylene diamine tetraacetic acid
ethylene glycol bis(2-aminoethyl ether)tetraacetic acid
electrophoretic mobility shift assay
fetal bovine serum
phosphate buffer saline
sodium dodecyl sulfate
Tris-buffered saline tween-20
DNA methylation is a covalent modification that targets the fifth carbon of the pyrimidine ring of cytosines, which is catalyzed by DNA methyltransferase to give rise to 5-methylcytosine (5-mC) in genomic DNA [1, 2]. DNA methylation has been studied extensively in mammals and plants . In mammals, about 60–90% of CpGs are methylated across entire genomes  and DNA methylation-mediated transcriptional regulation usually occurs at promoter regions and telomeres [5, 6] to create the binding sites for specific transcription factors to activate the expression of some tissue-specific genes  or inhibit the transcription factor binding to the promoter, resulting in altered transcriptional activity of the gene. DNA methylation is involved in genomic imprinting, X-chromosome inactivation, silencing of transposons and other repetitive DNA sequences, in particular, the inhibitory regulation of gene expression .
In invertebrates, the study of DNA methylation is rudimentary, compared to that in mammals and plants . In insects, DNA methylation in the model insect fruit fly is rather elusive [10, 11] and overall extremely low levels of DNA methylation were observed in silkworm and honeybee [12, 13]. Bioinformatics analyses revealed that different methylation rates were associated to specific phenotypes, such as wing differentiation in Sogatella furcifera , caste differentiation  and long-term memory formation in Apis mellifera . It is speculated that the DNA methylation occurs mainly in gene body regions and enhances gene transcription while promoter methylation is often considered not to be involved in the regulation of gene transcription because of its lower methylation rate in insects . Recently, it is observed that DNA methylation in the gene promoter of the invertebrate, Ciona intestinalis, was tissue- and/or cell-type specific , similar to those identified in mammals. In Drosophila S2 cells, up-regulated promoter methylation rate inhibited the promoter activity of steroidogenic enzyme , suggesting the regulatory functionality of DNA methylation in the promoter of insect. However, the direct experimental evidence for the regulatory mechanism of DNA methylation has not been reported in insects.
The wing disks of the silkworm, B. mori, an important economic and model insect of Lepidoptera, undergo dramatic morphological changes and structural evagination to form pupal wings during larva–pupa transition . Recently, a B. mori chitin synthase (BmCHSA) was characterized, which catalyzes the synthesis of chitin, a major component of wings and epidermis consisting of polymers of N-acetylglucosamine [21, 22]. Two alternative splicing variants of BmCHSA, BmCHSA-2a and BmCHSA-2b were up-regulated in the beginning and middle of pupal wing, driven by two different promoters, respectively. BmCHSA-2b RNAi resulted in the undeveloped wing . The intragenic promoter that activates the tissue- and stage-specific expression of BmCHSA-2b is located between exon 2a and exon 2b of BmCHSA . We hypothesized that intragenic promoter methylation mediates the tissue-specific expression of BmCHSA-2b.
In this study, we revealed that demethylation or unmethylation of CpG island 2 (CpGI2) of the intragenic promoter, as a consequence of DNA methyltransferase 1 (DNMT1) down-regulation, enhanced the binding of pupa-specific transcription factor BmDeaf1 to the unmethylated CpGI2 and activated BmCHSA-2b transcription in mid-pupal wing, thus demonstrating that intragenic promoter methylation plays an important role in mediating tissue and stage-specific expression of genes in insects.
The CpGI2 of BmCHSA-2b promoter is differentially methylated between the pupal wings and epidermis
BmDnmt1 suppresses the BmCHSA-2b transcription
To further confirm whether or not the methylation of CpGI2 is related to BmDnmt1 that directly binds to the CpGI2, electrophoretic mobility shift assay (EMSA) was performed with the biotin-labeled CpGI2 probe and purified BmDnmt1 protein. The results showed that the BmDnmt1 protein bound to the CpGI2 fragment (Fig. 2d, lane 2). The addition of 100 × or 200 × non-labeled probe (cold probe) resulted in the disappearance of the BmDnmt1-bound band (Fig. 2d, lane 3 and 4). However, the mutated unlabeled CpGI2 probe could not compete off the labeled probe (Fig. 2d, lane 5), suggesting that the binding of BmDnmt1 to the CpGI2 was specific. Transfecting BmDnmt1 into Bm12 cells resulted in the overexpression and accumulation of BmDnmt1 in nuclei (Additional file 3: Fig. S3), and the inhibition of the transcriptional activity of the CpGI2 (Fig. 2e). When BmDnmt1 was knocked down by RNAi (Additional file 4: Fig. S4), the transcriptional activity of the CpGI2 was enhanced (Fig. 2f). The transcriptional activity of the mutated CpGI2 was not affected by either BmDnmt1 overexpression or RNAi. These results suggest that BmDnmt1 suppresses the transcription of BmCHSA-2b by directly binding to the CpGI2 site.
BmDeaf1 activates the BmCHSA-2b transcription
BmDeaf1 directly binds to the unmethylated CpGI2 of BmCHSA-2b
To confirm whether or not BmDeaf1 protein binds in vivo to the unmethylated CpGI2 in the wings, the nuclear proteins were extracted from the wings of 3-day-old pupae and used for EMSA. The similar result was also obtained (Fig. 4d). A nuclear protein that bound to the labeled unmethylated CpGI2 probe was detected and the binding could be competed off with the unlabeled probe but not with the mutated unlabeled probe (Fig. 4d). A supershifted band appeared after BmDeaf1 antibody was added (Fig. 4d), suggesting that this nuclear protein bound to the unmethylated CpGI2 probe is BmDeaf1. Thus, all of these results from the pull-down assay and EMSA with BmDeaf1 protein demonstrated that in the Bm12 cells and the pupal wings, BmDeaf1 bound directly to the unmethylated (but not the methylated) CpGI2.
The cooperation of BmDnmt1 and BmDeaf1 regulates the stage-specific expression of BmCHSA-2b
Bombyx mori BmCHSA-2b is a tissue- and stage-specifically expressed gene and expressed only in the pupal wings, not in the epidermis . What controls this high specificity is extremely important for the development progress and, therefore, is interesting. DNA methylation is an epigenetic regulation mechanism for gene expression in specific tissues and at particular stages [27, 28, 29]. Many studies have demonstrated that DNA methylation in the promoter region up-stream of the starting site of transcription can regulate the gene transcription [30, 31, 32, 33]. Regulation mechanism of gene transcription by DNA methylation in the intragenic promoter for different transcript variants that are tissue- and stage-specifically expressed has been reported in mammals , but not in insects. In this study, DNA methylation in the intragenic promoter of BmCHSA-2b is involved in the regulation of the tissue- and stage-specific expression of the gene in B. mori was strongly supported by the critical evidences. The different levels of BmDnmt1 expression in the wing and epidermis at the mid-pupal stage resulted in the different methylation rates in the CpGI2 of BmCHSA-2b promoter in both tissues and affected the binding of the transcription factor BmDeaf1 to the CpGI2 and finally leaded to the differential expression of gene in both tissues. Thus, our data demonstrated that DNA methylation in the intragenic promoter controls the tissue-specific gene transcription in B. mori, in a way similar to that found in mammals .
In mammals and plants, the distribution of DNA methylation in genes may appears in two areas: in some cases DNA methylation accumulates in intragenic region; in the others, it appears in the promoter region. DNA methylation in the promoter up-stream of the transcription starting site usually functions as a transcriptional repressor while the methylation in gene body enhances gene transcription [35, 36, 37]. In insects, however, the gene body is methylated in much higher rates than the promoter region . The promoter of BmCHSA-2b is intragenically located in the intron between two parts of the alternative splicing exon 2 of BmCHSA (Fig. 1a) and, like the up-stream promoter methylation in mammals, its methylation inhibited the BmCHSA-2b expression as indicated by results of DNA methylation inhibitor treatment (Fig. 2), BmDnmt1 RNAi and BmDnmt1 overexpression (Fig. 2). To investigate whether the DNA methylation in BmCHSA-2b promoter, which is the intron of BmCHSA-2a, affects BmCHSA-2a transcription, BmCHSA-2a mRNA level was determined after DNA methylation inhibitor treatment and the result showed that BmCHSA-2a expression was not affected (Additional file 2: Fig. S2), suggesting that the intragenic DNA methylation does not regulate the expression of alternative splicing variant BmCHSA-2a, instead, as a factor influencing the activity of intragenic promoter and regulating the expression of BmCHSA-2b. This is similar to the DNA methylation in the intragenic promoters in mammals . In human and mouse SHANK3 gene, two transcripts (22t and 32t) encode a full-length SHANK3 protein, but they have their own promoters and the shared first exon . The methylation inhibitor treatment only resulted in the increase in 32t transcription. Thus, probably in both insects and mammals, DNA methylation in the intragenic promoter functions as a suppressor to control tissue-specific gene expression. This different effect of intragenic DNA methylation on BmCHSA-2a and BmCHSA-2b transcription is coincidence with their expression patterns: BmCHSA-2a is expressed in pupal wings as well as epidermis while BmCHSA-2b is specifically expressed in pupal wings . Similar CHSA gene structure was also found in other Lepidoptera, for example, Spodoptera litura SlCHSA . SlCHSA-2b expression was up-regulated in the mid-pupal wing (Additional file 8: Fig. S8) and was enhanced by methyltransferase inhibitor treatment (Additional file 9: Fig. S9) like BmCHSA-2b (Additional file 7: Fig. S7). Thus, the DNA methylation occurring in the intragenic promoter probably is one of the mechanisms for regulating the tissue- and stage-specific expression of specific transcripts of an insect gene.
Deaf-1, known as an important transcriptional regulator [38, 39], is ubiquitously expressed and appears to be constitutively localized in nuclei . In this study, BmDeaf1 enhanced BmCHSA-2b transcription by binding to the unmethylated CpGI2 of BmCHSA-2b promoter (Fig. 4), as demonstrated using chromatin immunoprecipitation, EMSA and pull-down assays (Fig. 4). Methylated or mutant core sequence TTCG  of Deaf1 CRE in the CpGI3 could not be recognized by BmDeaf1 (Fig. 3). The change of the sequence TTCG into TTAG resulted in the decrease in BmDnmt1 binding (Fig. 2) and increased DNA methylation by BmDnmt1 inhibited the BmDeaf1 enhancement of the BmCHSA-2b transcriptional activity (Fig. 3), suggesting that BmDnmt1 competes for the same binding site in the CpGI2 with BmDeaf1. However, the methylation inhibitor treatment did not affect BmDeaf1 expression in the pupal wings and increased the mRNA level of BmCHSA-2b only in the mid-pupal wings (Additional files 6, 7: Fig. S6 and S7). Furthermore, BmDeaf1 expression was up-regulated in the pupal epidermis (Additional file 5: Fig. S5) besides in the pupal wing, when the methylation rate in CpGI2 was decreased in the mid-pupal wings but not in the mid-pupal epidermis (Fig. 1), suggesting that the stage-specific expression of BmDeaf1 controls the BmCHSA-2b expression at the pupal stage by binding to the demethylated CpGI2 site of the BmCHSA-2b promoter. Deaf-1 was reported to be involved in the development regulation of early embryo, eye and wing in Drosophila  and could interact with transcriptional regulators LMO4 and NLI to mediate embryonic pattern formation and cell fate, including neuronal differentiation [42, 43]. This transcription factor also regulated immune gene expression, such as Mtk and Drs genes . In B. mori, BmCHSA-2b affects the mid-pupal wing development . In this study, it is demonstrated that BmDeaf1 is involved in the regulation of wing development by competing with BmDnmt1 for binding to the CpGI2 of the BmCHSA-2b promoter.
In animals, DNA methylation is mainly catalyzed by a family of Dnmts, which are classified into Dnmt1, Dnmt2 and Dnmt3 sub-groups. Dnmt3 is primarily responsible for de novo methylation to increase the new methylation sites; the function of Dnmt1 is to maintain the existing methylation . In B. mori and Schistocerca gregaria, however, Dnmt3 gene is missing and, instead, Dnmt1 enzyme plays a dual function of de novo methylation and the maintenance of methylation in B. mori [46, 47]. Binding of BmDnmt1 to 69-mer oligonucleotide duplex containing five CpG sites was also found in B. mori . In this study, BmDnmt1 protein directly bound to the 38-mer oligonucleotide duplex containing the 5th, 6th and 7th CpG sites in the CpGI2 promoter of BmCHSA-2b (Fig. 2d). The 5th CpG region also contains a BmDeaf1 binding site. Thus, overexpression of BmDnmt1 prior to BmDeaf1 inhibited the binding of BmDeaf1 to the CpGI2 and then the BmDeaf1-activated BmCHSA-2b transcription (Fig. 3). In vivo, BmDnmt1 levels in the wing disk gradually declined from the fifth instar larvae to mid-pupae (Fig. 5). In contrast, the expression of BmDeaf1 was increased so that it bound to the CpGI2 of the BmCHSA-2b promoter and specifically activated the expression of the gene. This cooperation between BmDnmt1 and BmDeaf1 regulates the tissue- and stage-specific expression of BmCHSA-2b, as well as the developmental progress. On the other hand, the similar expression profiles of Dnmt1, Deaf1 and CHSA-2b in Lepidoptera S. litura were also observed (Additional file 8: Fig. S8), suggesting that this regulation mechanism of intragenic promoter methylation in B. mori pupal wing may be suitable in other insects such as S. litura.
Insects and cell line
Bombyx mori strain Dazao was obtained from the Research and Development Center of the Sericultural Research Institute of the Academy of Agricultural Sciences of Guangdong Province, China. Larvae were reared on fresh mulberry leaves at 25 °C and a photoperiod of 12 h light:12 h darkness.
For methylation inhibitor treatments, 5-aza-dC (Sigma) was dissolved in 1X phosphate buffered saline (PBS). Two microliters of 5-aza-dC at the concentration of 10 μg/μL was injected into the hemolymph in the thoracic region of larvae at the second day of wandering stage (W2), the wings of 2 or 3 day-old pupa (PD2 and PD3) after 5-aza-dC injection were collected for RNA isolation. The same volume of 1× phosphate buffer saline (PBS) was injected as control. All data included three biological replicates, each with three technical repeats.
A B. mori cell line DZNU-Bm-12 (Bm12) originally developed from ovarian tissues  was maintained at 28 °C in Grace medium (Invitrogen) supplemented with 10% fetal bovine serum (FBS) (Hyclone).
Bisulfite conversion and bisulfite sequencing analysis
Genomic DNA of B. mori was extracted from pupal wings. Unmethylated cytosines were converted into uracil by using MethylDetector™ (Active Motif, Carlsbad, CA, USA), whereas methylated cytosines remain unchanged. Polymerase chain reaction (PCR) was then performed with primers designed on sequence of CpG islands. Compared to mammals, insects have far lower CpG frequencies. In this study, the region of more than 100 bp with GC% > 50%, Obs/Exp > 0.6 was defined as a CpG island. PCR products were sequenced in order to quantify the level of DNA methylation, which was done by aligning with the sequence of unconverted gDNA using DNAMAN software (Lynnon Biosoft). All data included three biological replicates, each with nine technical repeats.
RNA isolation and quantitative real-time PCR (qRT-PCR)
Total RNA was extracted from tissue or cell samples using Trizol reagent (TaKaRa), and cDNAs were synthesized by using the First Strand cDNA Synthesis Kit (TaKaRa) following the manufacturer’s protocol. qRT-PCR was performed by using 2 × SYBR Premix EXTaq™ Kit (TaKaRa). The relative mRNA level of gene expression was normalized to the expression level of a house-keeping gene ribosomal protein 49 (Rp49) (GenBank accession no.: AB048205) and analyzed by the 2−ΔΔCt method . All data included three biological replicates.
Cell culture, transfection and promoter activity determination
Bm12 cells at logarithmic growth phase were used for transfection. Plasmid DNAs were mixed with Lipfectamine 2000 (Invitrogen) and added to cells in each well of 12-well culture plates with Grace medium (Invitrogen). To normalize the firefly luciferase activity, the renilla luciferase vector, pRL-SV40, was co-transfected with each of the pGL3-drived vectors containing tested promoters. After 6-h post transfection, the old medium was replaced with fresh Grace medium containing 10% FBS. The cells were cultured for additional 48 h at 28 °C before promoter activity assay. The cells were washed once with filtered PBS and then lysed in 200 μL Passive Lysis Buffer (Promega). Luciferase activity of the supernatant was analyzed using the Dual-Luciferase Assay System (Promega) according to the manufacturer’s instruction with a luminometer (IBA7300, Veritas, Turner Biosystems). All assays were conducted three times.
Nuclear protein preparation and electrophoretic mobility shift assay (EMSA)
Tissues or cells were harvested and washed three times with PBS. Nuclear protein was extracted according to the instruction of NE-PER Nuclear and Cytoplasmic Extraction Kit (Thermo Scientific, Waltham, USA). EMSA was conducted using the LightShift Chemiluminescent EMSA Kit (Thermo Scientific). The oligonucleotides conjugated with biotin at 5′end or methylated to cytosine were synthesized by Invitrogen. Oligonucleotide probes were heated at 95 °C for 10 min and then slowly cooled to room temperature.
Binding assays were performed according to the manufacture’s protocol of EMSA Kit (Thermo Scientific). Briefly, nuclear extracts (proteins) were incubated for 20 min at room temperature with 20 μL binding buffer containing 50 ng of poly (dI-dC), 2.5% glycerol, 0.05% NP-40, 50 mM potassium chloride, 5 mM magnesium chloride, 4 mM EDTA and 20 fmol of a biotinylated end-labeled double-stranded probe. Different concentrations of cold probes (unlabeled) were added into the binding mixture as competitors. Two micrograms of BmDeaf1 antiserum or 2 μg of normal rabbit IgG (control) was added to detect the supershift bands. Polyacrylamide gels (6%) were run at 100 volts for 1.5 h on ice. After electrophoresis, the proteins were blotted onto positively charged nylon membranes (Hybond Nþ; Amersham Biosciences) and the bands were visualized by using the LightShift Chemiluminescent EMSA Kit according to the manufacturer’s protocol.
DNA–protein pull-down assays
Single-stranded probes were heated at 95 °C for 10 min and then slowly cooled to room temperature to obtain the double-stranded probes. To minimize non-specific interactions, the oligo-bead complexes were incubated for 30 min with a blocking buffer (0.25% albumin from bovine serum (BSA), 10 mM HEPES, 10 mM glutamate potassium, 2.5 mM DTT, 10 mM magnesium acetate, 5 mM EGTA, 3.5% glycerine, 0.003% NP-40, 0.5% PVP-K30). Immobilized double-stranded probes were incubated with 20 μg of nuclear extract for 4 h at 4 °C with constant rotation in a 400 μL of protein binding buffer (10 mM HEPES, 100 mM glutamate potassium, 80 mM potassium chloride, 2.5 mM DTT, 10 mM magnesium acetate, 5 mM EGTA, 3.5% glycerine, 0.001% NP-40). Protein-DNA complexes were then washed three times with wash buffer (10 mM HEPES, 100 mM glutamate potassium, 2.5 mM DTT, 10 mM magnesium acetate, 5 mM EGTA, 3.5% glycerine, 0.05% BSA, 0.05% NP-40). Proteins bound to the probe were eluted with 20 μL of denaturing Laemmli sample loading buffer (50 mM Tris–HCl, 100 mM DTT, 2% SDS, 0.1% bromophenol blue, 10% glycerine) at 37 °C for 15 min. The target proteins in the supernatant were identified by Western blot with antibody at 1:2000 dilution and the color depth of protein bands was transferred to data by using Image J software (National Institutes of Health, USA).
Chromatin immunoprecipitation (ChIP)
ChIP was performed in the Bm12 cells following the instruction of Pierce Magnetic ChIP Kit (Thermo Scientific). Briefly, approximately 4x106 cells were set up, then cross-linked with 1% formaldehyde for 10 min, and de-cross-linked with glycine. The cells were treated with MNase diluted in MNase Digestion Buffer for 15 min at 37 °C, and then nuclei were released from the cells by using ultrasonic breaking with several pulses and 20 s ice-cold interval. The protein-DNA complexes were immunoprecipitated using antibody, enriched by Magnetic Beads, and cross-linked reversely at 65 °C for 30 min with vigorous rotation. DNA was purified using the column method (Thermo Scientific), and detected by PCR or qPCR. Input (10%) was used as a control.
DNA methyltransferase activity assay
The nuclear protein at 10 μg extracted from the Bm12 cells was treated with 5-aza-dC or PBS (as control). DNA methyltransferase activity was analyzed using the EpiQuik DNA Methyltransferase Activity/Inhibition Assay Kit (Epigentek) following the manufacturer’s instructions. Pure mouse methyltransferase DNMT1 in the kit was used as a positive control. Methyltransferase activity is presented as the average absorbance at 450 nm.
Western blot analysis
Protein analysis was performed using SDS-PAGE gel and Western blot. Total 40 μg proteins extracted from tissues or Bm12 cells were denatured and then separated in 12% SDS-PAGE gel, followed by transferring to a nitrocellulose blotting membrane (GE healthcare). The membrane was blocked with Tris-buffered saline with Tween-20 (TBST) (20 mM Tris–HCl, 150 mM sodium chloride, 0.05% Tween-20, pH7.4) containing 3% (w/v) BSA for 2 h at room temperature, followed by hybridization overnight at 4 °C in TBST containing 1% BSA and primary antibody. The secondary antibody was a horseradish peroxidase (HRP)-conjugated antibody (Dingguo Biotechnology). Primary and secondary antibodies were diluted 1:1000 and 1:10,000 in TBST with 1% (w/v) BSA, respectively. Anti-tubulin antibody (Dingguo Biotechnology) was used to verify equal loading of the proteins on the gel.
The newly dissected silkworm tissues or Bm12 cells were fixed in 4% paraformaldehyde for 30 or 10 min at room temperature. Tissues or cells were blocked in PBS containing 5% BSA and 0.5% Triton-X (PBT) for 1–2 h, and then incubated with the primary antibody (diluted 1:200) at 4 °C overnight.
Tissues were washed three times for 1 h each in PBT and cells were washed three times for 10 min each. The samples were then incubated with Alexa Fluor™488 goat anti-rabbit IgG (diluted 1:200; Invitrogen) for 2 h. DAPI (Beyotime) was added to stain nucleus. The tissues or cells stained with antibody and DAPI were observed and imaged using a FV3000 confocal microscope (Olympus).
GFX conducted all the experiments, participated in the statistical analyses of the data and drafted the manuscript. JZ and HL participated in some experiments. HX helped bioinformatics analysis. QSS provided technical support and helped the drafting and revising the manuscript. QLF provided technical support and participated in discussion and revising the manuscript. SCZ conceived and designed the study, oversaw the research, and drafted and finalized the manuscript. All authors read and approved the final manuscript.
We thank Prof. Alexander Raikhel of University of California, Riverside, USA and Prof. Xiaoqiang Yu of South China Normal University for their help in the manuscript preparation.
The authors declare that they have no competing interests.
Availability of data and materials
The sequence of BmCHSA is available in the GeneBank.
Consent for publication
Ethics approval and consent to participate
This research was supported by the National Basic Research Program of China (No. 2012CB114603) and the National High Technology Research and Development Program of China (863 Program) (No. 2011AA10A204-3).
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