Genetic Manipulation of MicroRNAs in the Silk Gland of Silkworm, Bombyx Mori
MicroRNAs (miRNAs) are a class of non-coding RNAs with important post-transcriptional regulatory functions. To reveal the function of miRNAs in vivo, the critical step is to change their expression levels in the tissues or organs. In this work, we explored the application of several important genetic techniques in altering the expression of silk gland-specific miR-274 of silkworm (Bombyx mori).
Injection of synthesized microRNA mimics and antagomirs exerted no effect on the expression of miR-274 in the silk gland, miR-274 sponge specifically absorbed miR-274 and down-regulated its expression, transgenic overexpression of miR-274 precursor significantly up-regulated miR-274, and finally tissue-specific CRISPR/Cas9 system achieved deletion of miR-274.
A practical technical system was established for studying the functions of miRNAs in silk gland of Bombyx mori. Our research provides methodological support for the functional study of miRNAs and other noncoding RNAs in the silk gland and more organs in other species.
KeywordsBombyx mori Silk gland microRNA Functional study Knockout CRISPR/Cas9
Anterior silk gland
Clustered regularly interspersed palindromic repeats
CRISPR-associated protein 9
- D3 IL5
Day 3 of the fifth instar
Middle silk gland
Antagomir, negative control antagomir
Negative control mimics
Protospacer adjacent motif
Polymerase chain reaction
Posterior silk gland
Real-time fluorescent quantitative polymerase chain reaction
Silkworm is not only an important economic insect, but also a model insect for molecular biology research . Silk gland of silkworm can be divided into three divisions according to its morphology and function . Anterior silk gland (ASG) is the site where liquid silk protein is assembled into silk fibers, middle silk gland (MSG) consists of three segments and synthesizes different sericin proteins, posterior silk gland (PSG) is a coiled long tube and synthesizes silk fibroin proteins. The division-specific structures and functions are highly related to the expression patterns of genes [2, 3]. Therefore, silk gland is an ideal organ for studying gene regulation and tissue remodeling .
MicroRNA (MiRNA) is a kind of non-coding RNA post-transcriptionally regulating almost all important life processes [4, 5]. As early as 2010, we identified miRNAs in the MSG and PSG of silkworm at day 3 of the fifth instar (D3 IL5) [6, 7], and confirmed that miR-274 is silk gland-specifically expressed . In 2018, Qin et al. identified the miRNAs related to silk protein synthesis by sequencing the silk glands of three silk-producing strains . So far, however, studies on silk gland miRNAs still mainly focus on the validation of miRNAs and their targets [9, 10], and very few reports are available on their roles in the silk gland, which is mainly due to the lack of effective techniques compatible with this specialized organ.
The techniques for the functional study of miRNAs can be divided into two main categories. One is the strategy of gain of function using miRNA mimics, recombinant virus overexpression vector and transgenic overexpression vector. MiRNA mimic is a chemically synthesized double-stranded RNA to up-regulate miRNAs at cellular and individual levels [11, 12]. Both recombinant viral and transgenic methods are adopted to overexpress the miRNA precursor, which is then successively cleaved by host nucleases to form mature sequences [13, 14]. The second is the strategy of loss of function by means of miRNA antagomir, miRNA sponge and miRNA knockout. MiRNA antagomir is a chemically synthesized sequence reverse complementary to the miRNA and chemical modifications are needed to enhance the stability and transmission efficiency . MiRNA sponge contains tandem repetitive sequences reverse complementary to the miRNA and can reduce the chance of Ago protein in cleaving the target mRNA . CRISPR/Cas9 is an evolved defense mechanism acquired by bacteria and archaea to resist the invasion of viruses or exogenous DNA [17, 18]. Endogenous or artificial gRNA guides Cas9 endonuclease to cleave the double strand DNA at a fixed point in the genome, and in the process of non-homologous end-repair, code-shifting mutations probably happen in coding genes . However, knockout of miRNAs cannot be realized through code-shifting mutation [20, 21, 22]. Taking the silk gland-specific miR-274 as an example, here we aim to explore the genetic tools that can effectively manipulate miRNAs in the silk gland, and hopefully provide technical support for the functional study of miRNAs in silk glands.
MiR-274 is Exclusively Highly Expressed in the Silk Gland of Silk Worm
MiRNA Mimics and Antagomir Failed in Changing the Expression of MiR-274 in the Silk Gland
The silk gland was collected at 48 h post injection of functional reagents for qPCR assay, but both miR-274 mimic and miR-274 antagomir failed in changing the expression of miR-274 in the silk gland (Fig. 1c and d). We tried different concentrations and doses, but still observed no significant changes of miR-274 expression. Further, both miR-274 mimic and antagomir exerted no clear effect in the three divisions of silk glands (Fig. 1e-j). We also injected the functional reagents of some other miRNAs but did not found significant changes in their expressions in the silk gland. For example, the mimic of aae-miR-1175, which significantly changed the expression of miR-1175 in the midgut of mosquitoes , also failed in the silk gland of silkworm (Fig. 1e-g). These exogenous molecules might not enter the highly specialized silk gland, or, there possibly exist a special mechanism in the silk gland cells reducing the efficacy of these reagents. Therefore, it is not feasible to study the functions of miRNAs in silk glands by injecting exogenous miRNA mimics and antagomirs.
Down-regulation of MiR-274 in Silk Gland by Transgenic MiRNA Sponge
The designed miR-274 sponge sequence (Fig. 1k) was cloned into pSL1180 [Hr3/A4-Luc] vector to form the expression cassette of [Hr3/A4–274-sponge] (Fig. 1l). The expression cassette was digested with Asc I, and cloned into the vector backbone piggyBac [3 × P3-EGFP] to form the transgenic plasmid piggyBac [3 × P3-EGFP, Hr3/A4–274-sponge] (Fig. 1m). The positive F1 individuals were screened under fluorescence microscopy by identifying the green light in the eyes of day 6 embryos (Fig. 1n). The positive F2 generation was obtained from the oviposition of F1 (Fig. 1o). The silk glands of F2 were collected at D3 IL5 for RNA extraction and qPCR assay. The results showed that the expression of miR-274 was down-regulated by about 20% in the [miR-274-Sponge] strain (Fig. 1p), and as a control, the expression of miR-274-3p remained unchanged (Fig. 1q). Therefore, miRNA sponge adsorption technique can be explored to down-regulate miR-274 in silk glands, whereas the extent of down-regulation needs to be improved by using more effective promoters.
Transgenic Overexpression of MiR-274 in Different Divisions of Silk Gland
Knockout of MiR-274 in PSG Using RNA-guided CRISPR/Cas9 System
The synthesized gRNA1 and gRNA2 spacer sequences were sequentially annealed and ligated to pUC57[U6-2gRNA] to form pUC57[U6-miR-274-2gRNA] vector. The expression cassette [U6-miR-274-2gRNA] was cloned into the transgenic vector piggyBac[3 × P3-EGFP], generating the transgenic 2gRNA expression plasmid, piggyBac[3 × P3-EGFP,U6-miR-274-2gRNA] (Fig. 3b), which was then injected into the eggs for hatching. The positive 2gRNA-expressing transgenic individuals (miR-274-2gRNA) were screened at embryonic and adult stages according to the green light in the eyes (Fig. 3c and d). The adults of miR-274-2gRNA were crossed with those of PSG-specific Cas9 to obtain F1 generation, which had four different light-emitting forms in the eyes (Fig. 3e). The larvae of each group were cultivated to D3 IL5, when the PSGs were collected to extract the total RNA and genome DNA. The q-PCR results showed that miR-274 was successfully knocked out by CRISPR/Cas9 system, and its expression decreased by about 54% in the PSG (Fig. 3f). Through TA cloning and sequencing, it was found that CRISPR/Cas9 system mainly mediated base deletion at target sites of gRNAs, ranging from 7 bp to 50 bp at gRNA1 (Fig. 3g) and from 3 bp to 68bp at gRNA2 (Fig. 3h), respectively. In all examined sequencing results, we noticed some base deletions by two gRNAs, but the fragment deletions between the two gRNAs were not observed.
The mature sequence of miR-30 accumulates in mammalian cells when pol II promoter was used to overexpress the precursor of miR-30 . Here in this work, we realized the up-regulation of miR-274 in the MSG and PSG, through injection of transgenic overexpression plasmids overexpressing pre-miR-274, and it is beyond doubt that transgenic overexpression technology is an effective gain-of-function approach for miRNAs in silk gland (Fig. 4c). As competitive inhibitors, miRNA sponges are expressed under strong promoters and can strongly depress miRNA targets . Combined with UAS/Gal4 system, artificial sponges have been widely used to down-regulate tissue−/stage-specific miRNAs in different species to create loss-of-function phenotypes (Fig. 4d). In this study, the whole-body A4 promoter of silkworm was used to express the miR-274 sponge in silk gland, and only about 20% down-regulation was achieved in the silk gland (Fig. 1j), and the inhibition effect should be improved by using more efficient promoters or increasing the number of binding sites.
As the latest and most efficient genome editing technology, CRISPR/Cas9 system has been widely used in various organisms (Fig. 4e). Remarkable progress in genome editing of silkworm have been made by using CRIRSPR/Cas9 technology [26, 27, 28, 29]. Our laboratory researchers have also implemented genome editing in the silkworm and even knocked out some important protein coding genes in the silk gland by CRISPR/Cas9 technology [24, 30]. However, up to now, no reports are available on the use of CRISPR/Cas9 system to study miRNAs in the silk gland of silkworm. We designed two gRNAs expressed simultaneously to guide the cleavage, and diverse deletions of bases were found at each gRNA binding site, which were similar to single gRNA-mediated knockout, but no fragment deletions were observed within the precursor of miR-274. The deletion of the bases exhibited a strong directivity, occurring upstream of the PAM structure of gRNA in the genomic sequence, which is similar to the knockout of BmLMN . The CRISPR/cas9 targeting miR-274 vector is not injected for transient expression of the Cas9 protein in the silk gland. On the contrary, the strategy we used to knockout miRNA in silk glands can lead to the knockdown phenotypes for a long term because the positive strains of gRNAs and Cas9 protein can be steadily inherited, and the stable and simultaneous expression of gRNA and Cas9 is achieved by hybridization of the positive gRNA strain and the Cas9 strain, which stably expresses the Cas9 in the posterior silk gland during the whole larval stages of silkworm .
Silk gland of Bombyx Mori is an ideal organ for exploring gene regulation and tissue remodeling. However, functional study of silk gland miRNAs depends on techniques compatible with this specialized organ. In this work, a practical technical system for studying the function of miRNAs in silk gland was established, which provides an important technical reference for the functional study of miRNAs and other noncoding RNAs in silk gland of Bombyx mori. The technical system and research strategy of this study will also be valuable for studying the functions of noncoding RNA in other insect organs and tissues.
RNA Extraction and Real-time Fluorescent Quantitative PCR Assay
The total RNA of tissues of silkworm (Dazao) was extracted by TRIzol (Ambion, U.S.A), and the concentration was determined by spectrophotometer (NanoDrop 2000). DNase I (Promega, U.S.A) was used to digest the genome DNA at 37 °C for 30 min. MiRNA reverse transcription kit (Clontech, U.S.A) was used to synthesize the cDNA, and the expression of miRNA-274 was detected by real-time fluorescent quantitative PCR (qPCR) on the instrument, ABI 7500 fast. The primers for qRT-PCR include qmiR-274-5p, TTTGTGACCGTCACTAACGGGCA; qmiR-274-3p, TCGTTTTGGCGATCGCAAAATG; qmiR-1175, AAGTGGAGTAGTGGTCTCATCG.
Injection of MiRNA Mimics and Antagomirs
The mimics and antagomirs of miRNAs were synthesized in Dharmacon (U.S.A) and were dissolved with nuclease free water to 100 μM and 200 μM, respectively. To avoid repeatedly freezing and thawing, the dissolved reagents were packed into small tubes and stored at − 80 °C for use. Totally, each silkworm larva at D3 IL 5 was injected with 0.5 nmol miR-274 mimics or 1.0 nmol antagomir. The injection was carried out through the stomata on the surface of silkworm larvae. The non-injected larvae were set as the wild type control and those injected with NC mimic and NC antagomir served as negative control groups. All silkworms were fed with fresh mulberry leaves and the silk glands were collected about 48 h post injection for the extraction of total RNA and qPCR assay. The sequences of miRNA mimics and antagomirs injected here are: bmo-miR-274 mimic: UUUGUGACCGUCACUAACGGGCA; bmo-miR-274 antagomir, 5′ mU(*)mG(*)mCmCmCmGmUmUmAmGmUmGmAmCmGmGmUmCmA(*)mC(*)mA(*)mA(*)mA (3′-Chl); aae-miR-1175 mimic, AAGUGGAGUAGUGGUCUCAUCG.
Design of MiR-274 Sponge and Construction of Transgenic Vector
Six sequences reverse complementary to miR-274 were linked by fragment GAUCG (underlined in the sponge below) to synthesize the miR-274 sponge, within which the bases 9–12 after the seed of each mature sequence were mutated to form a protuberance. The pUC57 [miR-274 sponge] vector was synthesized at Beijing Genomics Institute (BGI) after adding the BamH I and Not I (TAKARA, Japan) sites at 5′ and 3′ end of the sponge sequence (highlighted in bold in the sponge sequence below), respectively. The recovered vector [miR-274 sponge] from digestion of BamH I and Not I was cloned into pSL1180 [Hr3/A4-Luc] to obtain pSL1180 [Hr3/A4-miR-274 sponge]. The recovered miR-274 expression cassette [Hr3/A4-miR-274 sponge] from Asc I (NEB, U.S.A) digestion was cloned into the piggyBac [3 × P3-EGFP] to construct the overexpression vector of miR-274 sponge, piggyBac [3 × P3-EGFP, Hr3/A4-miR-274 sponge] with the 3 × P3-activated green fluorescence as a screening marker. When verified by Asc I digestion, the sponge plasmids were extracted with QIAprep Spin Miniprep Kit (QIAGEN, Germany) and measured by spectrophotometer (NanoDrop 2000). The packed plasmids with a concentration of about 400 ng/μL and a A260/A280 ratio about 1.8 were stored at − 80 °C for use. The synthesized miR-274 sponge: CGGGATCCACUGCCCGUUGUGUGCCUCACAAACGAUCGACUGCCCGUUGUGUGCCUCACAAACGAUCGACUGCCCGUUGUGUGCCUCACAAACGAUCGACUGCCCGUUGUGUGCCUCACAAACGAUCGACUGCCCGUUGUGUGCCUCACAAACGAUCGACUGCCCGUUGUGUGCCUCACAAACGCGGCCGCAA.
Construction of transgenic miR-274 overexpression vector
The silkworm genome DNA served as the template to amplify the precursor sequence of miR-274 (miR-274-OE) with primers miR-274-OE-F: CGGGATCCTTTATCGTTTCCAGGGTGTCG (BamH I site underlined) and miR-274-OE-R: TTGCGGCCGCGCTCGCACCTTCCACCTTCT (Not I site underlined). The precursor fragment was cloned into pMD-19 T vector by TA cloning and verified by sequencing. After digestion with BamH I and Not I, the verified fragment was cloned into pSL1180[Hr3/Ser1-Red] and pSL1180[Hr3/FibH-EGFP], respectively, producing the recombinant plasmids pSL1180[Hr3/Ser1-miR-274-OE] and pSL1180[Hr3/FibH-miR-274-OE]. After digestion with Asc I, the expression cassettes [Hr3/Ser1-miR-274-OE] and [Hr3/FibH-miR-274-OE] were cloned into the transgenic vectors piggyBac[3 × P3-Red] and piggyBac[3 × P3-EGFP], respectively, generating the MSG-specific recombinant overexpression vector, piggyBac[3 × P3-Red,Hr3/Ser1-miR-274-OE] and the PSG-specific overexpression recombinant vector, piggyBac[3 × P3-EGFP, Hr3/FibH-miR-274-OE]. After digestion by Asc I, both plasmids were extracted QIAprep Spin Miniprep Kit (QIAGEN, Germany) and measured by spectrophotometer (NanoDrop 2000) and the packed plasmids with a concentration of over 400 ng/μL L and a A260/A280 ratio about 1.8 were stored at − 80 °C for use.
Injection of Transgenic Overexpression Vectors and Screening of Positive Individuals
Each transgenic overexpression plasmid above was mixed at a mole proportion of 1:1 with the plasmid pHA3PIG, an auxiliary vector of piggyBac transposase preserved in our laboratory. The mixture of plasmids was injected into D9L silkworm eggs with a microinjector within one hour after being laid and then the injection holes were sealed with non-toxic instant dry glue. The injected eggs were incubated at 25 °C and 90% relative humidity for hatching. After 9–10 days, fresh mulberry leaves were used to collect newly hatched silkworms. The larvae were cultivated to adults for intragroup mating to obtain eggs of the first filial generation (F1 generation). The eggs were incubated at 25 °C and 90% relative humidity for six days (the day when the green spot emerges), when the transgenic positive individuals were screened by using macro-electro-fluorescence microscopy MVX10 (Olympus, Tokyo, Japan). The EGFP marker was screened under blue light produced by excitation filter BP460-480HQ and barrier filter BA495-540HQ. The Red gene marker was screened under green light produced by excitation filter BP535-555HQ and barrier filter BA570-625HQ.
Design of GRNA and Construction of Transgenic GRNA Expression Vector
The sequence containing pre-miR-274 was input into the CCtop website (https://crispr.cos.uni-heidelberg.de/)  to determine the binding sites of gRNA with the structure G(N20)GG. The gRNAs with low off-target rate were screened at both ends of the precursor, and were named gRNA1 and gRNA2. After adding the terminal bases (in bold), the primers of gRNA1 and gRNA2 were synthesized in BGI. gRNA1-spacer-F: TGCAGCAGTAAGTGCGACGTGAGC, gRNA1-spacer-R: AAACGCTCACGTCGCACTTACTGC, gRNA2-spacer-F: TCCGGCGGCTCACGAGCGGGGGAG and gRNA2-spacer-R: AAACCTCCCCCGCTCGTGAGCCGC.
The gRNA spacer sequences were annealed to form double-stranded DNA. After digestion by Aar I (Thermo fisher, U.S.A), the gRNA1-spacer was ligated to pUC57 [U6-2gRNA] vector to generate the intermediate vector pUC57 [U6-miR-274-gRNA1], which was further verified by sequencing. After digestion by Bbs I (NEB, U.S.A), the gRNA2-spacer was ligated to the vector pUC57 [U6-miR-274-gRNA1] to form the vector, pUC57[U6-miR-274-2gRNA], which was then digested with Asc I (NEB, U.S.A) to recover the 2gRNA expression cassette, namely [U6-miR-274-2gRNA]. The purified expression cassette [U6-miR-274-2gRNA] was finally ligated to the transgenic vector piggyBac[3 × P3-EGFP], generating the transgenic 2gRNA overexpression vector piggyBac[3 × P3-EGFP, U6-miR-274-2gRNA].
Screening and Verification of MiR-274 Knockout Strains
The positive transgenic individuals of miR-274-2gRNA were cultivated to adults, which were then crossed with the PSG-specific Cas9 transgenic expression strain. Positive F1 individuals were screened under the macro-electro-fluorescence microscopy at day 6 embryo according to the light in the eyes: no light in wild type (WT), red light in the Cas9 expression line (PSG-Cas9), green light in the double gRNA expression line (miR-274-2gRNA), and both red and green light in the knockout line (△miR-274-PSG). The knockout line △miR-274-PSG and the controls were cultivated to D3 IL5, when the PSG was dissected out for the extraction of genomic DNA using the tissue DNA extraction kit (Omega, U.S.A). The sequence covering the knockout site of miR-274 was amplified with primers, pF: CCAGTAGCGTCCATTTCTTCC and pR: CATACTGTGAACTGGTGTCCCTA. All PCR products were submitted to TA cloning and sequencing, followed by analysis with software BioEdit.
The authors are very grateful to the two anonymous reviewers for their kindly comments and helpful suggestions. The authors wish to thank Dr. Sanyuan Ma (Southwest University) for the technical support and Dr. Yin Ling (Southwest University) for the silkworm eggs.
WW performed the experiments, analyzed and interpreted the data. XW, XL, QP, CL, LX and XP reared the silkworm and analyzed the data. SL designed the research and wrote the manuscript. All authors read and approved the final manuscript.
This work was supported by National Natural Science Foundation of China (31571334), State Key Program of National Natural Science of China (31530071), National Basic Research Program of China (2012CB114602) and Fundamental and Advanced Research Projects of Chongqing (cstc2014jcyjA00025). The academic funding has no commercial interest and is intended for research, purchase of reagents and equipment.
Ethics approval and consent to participate
Ethical approval for use of Bombyx mori as a model organism in this study was not necessary because the species was not covered by any ethical committee.
Consent for publication
The authors declare that they have no competing interests.
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