In this study, we upregulated insulin-like growth factor-1 (IGF1) expression specifically in skeletal muscle by engineering an enhancer into its non-coding regions and verified the expected phenotype in a mouse model. To select an appropriate site for introducing a skeletal muscle-specific myosin light chain (MLC) enhancer, three candidate sites that exhibited the least evolutionary conservation were chosen and validated in C2C12 single-cell colonies harbouring the MLC enhancer at each site. IGF1 was dramatically upregulated in only the site 2 single-cell colony series, and it exhibited functional activity leading to the formation of extra myotubes. Therefore, we chose site 2 to generate a genetically modified (GM) mouse model with the MLC enhancer incorporated by CRISPR/Cas9 technology. The GM mice exhibited dramatically elevated IGF1 levels, which stimulated downstream pathways in skeletal muscle. Female GM mice exhibited more conspicuous muscle hypertrophy than male GM mice. The GM mice possessed similar circulating IGF1 levels and tibia length as their WT littermates; they also did not exhibit heart abnormalities. Our findings demonstrate that genetically modifying a non-coding region is a feasible method to upregulate gene expression and obtain animals with desirable traits.
Many genetically modified (GM) animals with desirable phenotypes have been generated for agricultural and biomedical applications. However, most traditional methods for creating transgenic animals usually involve the random insertion of the coding cassette into the genome1,2,3,4,5. Although this technique seems straightforward, the copy number and insertion locus cannot be accurately controlled, leading to unstable gene expression6,7. Site-specific incorporation of the expressing construct is an improved option, but this approach is very arduous, particularly when the genomic DNA sequences of genes that span large genomic regions are used. Although cDNA can be used as a substitute, it may lack the complex non-coding regulatory elements that remain undefined but substantially contribute to expression, rendering cDNAs unfavourable for high expression levels in most cases8,9,10.
Naturally occurring mutations in the regulatory regions of genes can have large effects on phenotypic variation11,12,13,14. For example, a single-nucleotide polymorphism substitution in intron 3 of the insulin-like growth factor (IGF)-2 gene in pigs causes a three-fold increase in its mRNA levels in skeletal muscle, generating a 3–4% increase in meat production12,13. Moreover, a G to A transition in the 3′ untranslated region of the myostatin gene in Texel sheep creates a target site for mir1 and mir206, inhibiting translation of the myostatin gene and subsequently contributing to muscular hypertrophy14. However, most studies focus on naturally occurring mutations, and reports of artificially editing non-coding genomic sequences to improve production traits in live animals are rare.
As key components of non-coding regions, enhancers stimulate gene expression in a spatiotemporal-specific manner independent of the orientation or distance to the promoter. Moreover, enhancers are active in heterologous sequence contexts15,16. Thus, we speculated that the site-specific insertion of a tissue-specific enhancer might upregulate target gene expression physiologically and spatiotemporally, consequently preserving its original regulatory network and decreasing the abnormalities induced by the forced transgene expression.
IGF1 is a key factor regulating skeletal muscle development and growth, and the muscle-specific upregulation of IGF1 leads to muscle hypertrophy17,18,19,20,21. Until recently, Igf1 transgenic mice have not been generated using the entire genomic DNA sequence, which is >70 kb. To our knowledge, the existing Igf1 transgenic mouse models have all been created by randomly inserting a cDNA construct encoding either different isoforms of the pre-pro-peptide21,22,23 or the mature form24,25,26.
Here, we used the Igf1 gene as an example in this proof-of-concept report. We asked whether Igf1 expression was upregulated by including an enhancer in the non-coding regions upstream of its transcriptional start site. In addition, we investigated whether this genetic modification generates the expected phenotype in the mouse model.
A screen for an efficient candidate enhancer by luciferase reporter assays
The MLC (myosin light chain)27,28,29,30 and MCK (muscle creatine kinase)31,32,33,34 enhancers are extensively characterized muscle-specific enhancers; therefore, we chose them as candidates for insertion into the upstream regions of the Igf1 transcriptional start site. The two enhancers exert their functions in differentiated myotubes rather than undifferentiated myoblasts28,33. To evaluate the effects of the MLC and MCK enhancers on the Igf1 promoter, we performed luciferase reporter assays.
For luciferase reporter vector construction, we used the Igf1 mini-gene, which contains exon 1, intron 1, exon 2, intron 2, and part of exon 3, as the promoter. In addition, an IRES element was used to connect the luciferase gene and the Igf1 mini-gene, which gave rise to several polypeptides (Fig. 1a).
The luciferase expression of the IGF1-basic construct was regarded as background level (Fig. 1a), and the SV40 enhancer was chosen as a positive control (Fig. 1a). In the differentiated C2C12 myotubes, the MLC enhancer dramatically increased luciferase expression by 12 to 20-fold above that of the background level in both orientations (Fig. 1b). The activity of the MLC enhancer in the 5′-3′ orientation was low but significant in C2C12 myoblasts (Fig. 1b), a result that may be explained by a small quantity of differentiated myotubes. The MLC enhancer was essentially inactive in Hepa1–6 cell lines (Fig. 1b). Compared with the background expression level, the MCK enhancer showed a small but significant increase in luciferase expression in differentiated C2C12 myotubes but no difference in either C2C12 myoblasts or the Hepa1–6 cell line (Fig. 1b). Hence, we selected the MLC enhancer for subsequent experiments.
A screen for the candidate insertion site and further validation in C2C12 single-cell colonies
To search for an appropriate integration site for the MLC enhancer, we divided the region 100 kb upstream the Igf1 transcriptional start site into non-overlapping 50 bp windows, and calculated average PhastCons score from the UCSC database for each window35. We chose the three candidate sites with the lowest PhastCons scores, or say the least evolutionarily conserved sites, to avoid functional cis-regulatory elements that are generally evolutionarily conserved36.
To evaluate the candidate sites for incorporation and to further investigate the MLC enhancer in the C2C12 cell line, we designed nine sgRNAs targeting the three candidate sites (three for each), which are located at distances of 1.5 kb, 6 kb, and 20 kb from the Igf1 transcriptional start site, respectively (Fig. 2a). A high cleavage efficiency of the sgRNAs targeting the three candidate sites was detected in C2C12 cells by T7EN1 assays (Fig. 2b). Then, successful homologous recombination in each of the three candidate sites was confirmed in a pool of cells co-transfected with the donor vector, a plasmid expressing the Cas9 protein and the sgRNAs targeting each respective site, and a green fluorescent protein (GFP)-expressing vector, which was used to enrich GFP+ cells by flow cytometry (Fig. 3a and Supplementary Fig. S1).
To obtain C2C12 single-cell colonies that incorporated the MLC enhancer for further investigation, we co-transfected the donor vector, a plasmid expressing the Cas9 protein and the sgRNAs targeting each respective site. Then, single-cell colonies were generated through a limiting dilution technique and examined for 5′ and 3′ integration by PCR. For the site 1, 4 out of 55 C2C12 single-cell colonies showed correct integration, whereas no positive C2C12 single-cell colonies were obtained for the site 2 and site 3. Therefore, to enrich for targeted cells, a GFP-coding cassette was added to the original Cas9 and sgRNA expressing vectors for flow cytometry sorting of GFP+ cells (Supplementary Fig. S2). The results showed that 11 out of 96 single-cell colonies tested for site 2 and 5 out of 48 single-cell colonies tested for site 3 were successfully targeted. The insertion of the MLC enhancer into site 2 was further confirmed by Southern blot analysis (Fig. 3a and b). Then, we examined the off-target effects in four single-cell colonies of site 2, and no mutations were detected in the ten most likely off-target sites by Sanger sequencing (Supplementary Fig. S3).
To test the ability of each of the three candidate sites to support IGF1 expression, we evaluated the Igf1 mRNA expression levels in the three series of single-cell colonies. Compared with the WT control, only the site 2 series of single-cell colonies exhibited a 4-fold higher Igf1 expression level, whereas the Igf1 expression level in both the site 1 and site 3 series was downregulated (Fig. 3c), thus suggesting a disruption of important cis-regulatory elements. A significant increase in IGF1 protein levels was also detected in three separate single-cell colonies of the site 2 series compared with the levels in the WT C2C12 controls (Fig. 3d). To determine whether the elevated IGF1 amplified the IGF1/Akt pathway, which is closely related to muscle hypertrophy, we examined the phosphorylation levels of Akt. Both the phosphorylation levels of Akt (Ser473) and Akt (Thr308) were higher in most of the site 2 series of single-cell colonies compared with the WT C2C12 cells (Fig. 3e). Moreover, the site 2 series of single-cell colonies more readily differentiated into myotubes (Supplementary Fig. S5), and more myotubes were detected by immunofluorescence staining of myosin heavy chain (MHC) (Fig. 4).
Together, these results showed that site 2 was an ideal site for incorporation of the MLC enhancer to drive Igf1 expression in C2C12 cells.
Generation of GM mice with the MLC enhancer incorporated in site 2
To extend our study from cell lines to a whole animal context, we generated genetically modified mice by injecting Cas9 mRNA, sgRNA targeting site 2 and the circular donor plasmid into mouse zygotes (Table 1). The successful incorporation of the MLC enhancer was confirmed in F0 mice by PCR across the 3′ and 5′ junctions (Table 1) and was confirmed in their offspring by Southern blot analysis (Figs 3a and 5a). The efficiency of homologous recombination was 37.50% (Table 1). The integration observed in the eight positive founders that were chosen for offspring production were transmitted through the germline to the F1 progeny.
Upregulation of Igf1 expression and the stimulation of downstream signal pathway in skeletal muscle
To investigate whether the incorporation of the MLC enhancer increased Igf1 transcription and thus increased protein accumulation in vivo, Igf1 mRNA and protein expression levels were examined in two-month-old mice. In the gastrocnemius (GA) muscle, the Igf1 mRNA levels in both male and female GM mice showed a significant increase relative to the levels in their WT littermates (Fig. 5b). Two-way ANOVA analysis demonstrated that the genotype factor significantly affected the results (P < 0.0001), while the sex factor did not (P = 0.7959), and the interaction of the two factors also showed no significant effects (P = 0.3234). Then, we further examined the IGF1 protein levels, which also sharply increased in both male and female GM mice compared with their sex-matched WT littermates (Fig. 5c). Interestingly, the IGF1 protein levels increased by a greater extent in the female GM mice than the male GM mice, as compared with their sex-matched WT littermates (Fig. 5c). However, the male WT mice demonstrated greater endogenous IGF1 protein levels compared with those of the female WT mice (P < 0.00000001) (Fig. 5c). Two-way ANOVA analysis demonstrated that the genotype factor significantly affected the results (P < 0.0001), but the sex factor had no significant effects on the results (P = 0.1743). However, the interaction of the two factors showed significant effects on the results (P < 0.05).
Significantly increased levels of the phosphorylation of Akt (Ser473) and Akt (Thr308) were detected at one month in the GA muscles of female GM mice (Fig. 5d), but not at two months (Supplementary Fig. S4). This result was consistent with a previous report showing that a growth stimulus is required for the Akt activation in respond to elevated IGF123. Besides, a higher phosphorylation level of Akt (Ser473) in the GA muscle of 1-month-old male GM mice was also detected (Supplementary Fig. S6).
Furthermore, the results demonstrated that in the GA muscle of both male and female GM mice, the phosphorylation levels of mTOR (Ser2448), P70S6K (Thr389), and S6 (Ser240/244) were increased, and the phosphorylation levels of 4E-BP1 (Ser65) were decreased. Thus, the IGF1/Akt pathway was stimulated (Supplementary Fig. S6).
Elevated IGF1 leads to skeletal muscle hypertrophy in female GM mice
At the age of three months, the homozygous female GM mice demonstrated a significantly heavier body weight and carcass weight compared with that of sex-matched WT mice; in contrast, no differences were detected for the male mice (Fig. 6a).
To determine whether the increased body weight resulted from increased muscle mass, we dissected out the GA, soleus (Sol), extensor digitorum longus (EDL), and tibialis anterior (TA) muscles from the male and female mice at three months of age. The homozygous female GM mice showed a significant increase in TA (11.86%), GA (9.23%), Sol (11.68%) and EDL (16.75%) muscle weights compared with those of the sex-matched WT littermates (Fig. 6b). In addition, compared with the WT littermates, a similarly increasing trend was observed in the weights of the TA (4.18%), GA (3.55%), Sol (5.74%) and EDL (8.02%) muscles in homozygous male GM mice, though these results were not statistically significant (Fig. 6b). One possible explanation for the less conspicuous phenotype of male GM mice may be that the smaller increase fold of IGF1 protein in male GM mice than that in the female GM mice compared with sex-matched WT littermates (Fig. 5c).
To determine whether increased muscle mass was due to the hyperplasia and/or hypertrophy of myofibres, we examined the total number of myofibres in the tibialis anterior (TA) muscle but detected no differences between GM mice and their WT littermates (Supplementary Figure S7). Then, we measured the cross-sectional area (CSA) of the TA and GA muscles in three-month-old GM mice and their WT littermates. Compared with sex-matched WT littermates, the average CSA of the TA muscle increased by 18.6% and 17.8% in male and female GM mice, respectively (Fig. 6c). An increase in the CSA of the GA muscle in GM mice was also observed. The CSA distribution for the TA muscle demonstrated that the relative proportion of larger myofibres in the GM mice was greater, and very large myofibres, which were not ordinarily found in WT littermates, were also detected (Fig. 6d).
To examine whether elevated IGF1 levels exhibited fibre-type-specific effects on muscle hypertrophy, we performed immunofluorescence by staining for MHCI, MHCIIa and MHCIIb and measured the CSA of each fibre type. We found that the CSA of MHC type IIb fibres exhibited a significant increase in the muscles of GM mice; however the CSA of MHC I and MHC IIa type fibres exhibited only a minor increase (Supplementary Figure S8). To examine whether fibre-type-specific hypertrophy was driven by fibre-type-specific IGF1 pathway stimulation, we dissected the EDL muscle, a typical fast-twitch muscle, and the Sol muscle, a slow-twitch muscle, to examine S6 phosphorylation (Ser240/244) in each muscle individually. Higher levels of S6 phosphorylation (Ser240/244) were detected in the EDL muscle of GM mice, whereas no significant differences were detected in the Sol muscle of the mice (Supplementary Figure S9). The increased S6 activation (Ser240/244) in the EDL muscle of GM mice might have resulted from higher Igf1 expression in fast-twitch fibres, because the MLC enhancer is active predominately in fast IIb fibres21.
Assessment of the systemic effect of elevated IGF1 in skeletal muscle
To investigate whether the increased levels of IGF1 in skeletal muscle had a systemic effect, we detected the circulating IGF1 levels and examined the heart and bone, which are closely related to skeletal muscle.
There were no differences in the circulating levels of IGF1 between the GM mice and their sex-matched WT littermates (Fig. 7a). In the GM mice, no differences in the weight and size of the heart were detected, and the hearts showed no pathological changes (Fig. 7b and c). The tibia lengths were measured, and no differences were detected in either male or female GM mice compared with their sex-matched WT littermates (Fig. 7d).
Together, these results showed that the increase in IGF1 expression was restricted to skeletal muscle, and the effect of the increased IGF1 in the skeletal muscle did not cause systemic perturbations in the GM mice.
In our study, we established a method for altering gene expression that affects traits via the genomic editing of a non-coding sequence. By incorporating the MLC enhancer into the site 2 upstream of the Igf1 promoter, IGF1 was successfully upregulated in both the C2C12 cell line and in the skeletal muscle of GM mice. The GM mice developed normally and exhibited skeletal muscle hypertrophy with no systemic perturbations.
In our mouse model, we circumvented the disadvantages of the lack of important cis-regulatory elements not included in cDNA sequences and addressed the difficulties of site-specifically incorporating a large genomic sequence (>70 kb) when generating transgenic animals. By exploiting the endogenous regulatory mechanisms of Igf1, the addition of a skeletal muscle-specific enhancer simply and elegantly increased expression in a physiological and spatiotemporal manner.
In our mouse model, the IGF1 expression was not as high as in previous reports. Two possible explanations for this outcome are (1) different genetic mouse backgrounds might affect the phenotype differently37,38; and (2) previous studies have used multiple copies of the expression cassette, whereas in our study, only a single copy of the MLC enhancer was used. To increase IGF1 upregulation, combinations of natural enhancers or powerful, synthetic artificial enhancers can be used. Furthermore, the gene expression pattern can be accurately and predictably adjusted by substituting enhancers with different tissue specificity and potency; this strategy is both versatile and flexible.
Both male and female GM mice exhibited significant upregulation of Igf1 mRNA and IGF1 protein in skeletal muscle, demonstrating that we achieved the goal of our research. However, the Igf1 mRNA and the IGF1 protein showed a greater increase in female GM mice than male GM mice compared with their sex-matched WT littermates. Moreover, female GM mice exhibited clear muscle hypertrophy, and although male GM mice exhibited a similar trend toward increased muscle weight and muscle hypertrophy, the differences were not statistically significant.
Two non-exclusive explanations might account for the differences between male and female GM mice. First, it has been reported that testosterone stimulates IGF1 expression in skeletal muscle39,40,41, and a previous report identified two androgen response elements within the human IGF1 upstream promoter that in cis activate IGF1 expression42. Using TF-Scan to screen the ∼800 bp of sequence flanking site 2, we did not detect any defined androgen response elements. Thus, we inferred that some uncharacterized skeletal muscle-specific androgen response elements potentiating the expression of Igf1 exist in site 2 but may have been disrupted by insertion of the MLC enhancer. However, the positive effect of including the MLC enhancer might have predominated, compensating for the loss of potential androgen response element activity and leading to compromised upregulation of Igf1. The above speculation is supported by the fact that the Igf1 mRNA levels in homozygous female GM mice were roughly 10-fold higher than sex-matched WT littermates, whereas the Igf1 mRNA levels in homozygous male GM mice were about 7-fold higher. Second, in our study, we found that IGF1 protein levels were significantly higher in the muscles of WT male mice than WT female mice (P < 0.00000001) and inferred that the IGF1 signalling pathway may already be maximally stimulated in the intact male WT mice, making them resistant to further IGF1 upregulation and insensitive to the growth-promoting effects of IGF1.
Although the male GM mice did not exhibit conspicuous muscle hypertrophy, the pathway downstream of IGF1 was highly stimulated, similar to female GM littermates. We inferred that the lower expression of IGF1 protein would exhibit a delay exerting its function in male GM muscle, which might be less sensitive to IGF1 compared with female GM mice. In our subsequent research, we will re-examine the phenotype of male GM mice at a later time point.
With additional investigation into non-coding sequences and the development of genomic editing tools, the ability to create precise genetic modifications in animals to generate desired traits is becoming routine. As a proof-of-concept study in a mouse model, our strategy might provide insights into the production of livestock for agricultural and biomedical purposes.
All animal experiments in the present study were approved by the Animal Care and Use Committee of China Agricultural University (approval number: SKLAB-2012–01–08). All experimental procedures were performed in accordance with the guidelines for the Care and Use of Laboratory Animals of China Agricultural University.
Construction of the Luciferase Reporter Vectors
We cloned the Igf1 mini-gene containing exon 1, intron 1, exon 2, intron 2, and part of exon 3, 920 bp of the MLC enhancer28, 206 bp of the 5′ MCK enhancer32 and the SV40 enhancer by PCR. The results were confirmed by sequencing. We linked the Igf1 mini-gene sequence to the luciferase gene in the PGL3 basic plasmid via an IRES element; the vector was named IGF1-basic and was used as the parent vector for the construction of other vectors. Starting with the IGF1-basic vector, we linked the MLC enhancer, the MCK enhancer, and the SV40 enhancer in either the 5′-3′ or 3′-5′ orientation.
C2C12 and Hepa1–6 cells were maintained in growth medium consisting of Dulbecco’s Modified Eagle’s Medium (DMEM, Gibco), 10% fetal bovine serum (FBS, Gibco) and 1% penicillin-streptomycin. At a confluence of 60–70%, differentiation of the C2C12 cells was induced by replacement of the growth medium with differentiation medium (DMEM supplemented with 2% horse serum).
Three days after transfection, total DNA was extracted from C2C12 cells with a DNeasy Blood & Tissue Kit (Qiagen, Germany). The fragments flanking the Cas9 cutting sites were then PCR amplified. The primers used were shown in Supplementary Table S1. After annealing, the PCR products were digested with T7EN1 (NEB, cat. M0302S) at 37 °C for 1 h. PAGE electrophoresis was performed for fragment separation.
Construction of the donor plasmids for homologous recombination
Through Gibson assembly (NEB, cat. E2611S), we constructed three targeting donor vectors, which contained 920 bp of the MLC enhancer flanked by ~2–3 kb of the 5′ and ~1 kb of the 3′ homology arms adjacent to each of the three candidate loci.
Detection of homologous recombination in C2C12 single-cell colonies and mice by PCR
The primers used to detect positive C2C12 single-cell colonies were shown in Supplementary Table S2; to detect positive mice, the primers for amplifying across the 3′ junction of site 2 locus, across the 5′ junction of site 2 locus and across the MLC enhancer, were used.
Transfection and luciferase assay
Transient transfections were performed with FuGENE® HD Transfection Reagent (Promega, USA) according to the manufacturer’s instructions. The Firefly luciferase plasmids were co-transfected with The Renilla luciferase plasmid (phRL-TK) as an internal control for normalization. The luciferase assay was performed with a dual-luciferase reporter assay system (Promega, USA).
To perform immunofluorescence staining for myosin heavy chain, cells were fixed with 4% PFA for 20 min and permeabilized in 0.1% Triton X-100 for 10 min at room temperature. The cells were blocked with the immunostaining blocking buffer (Beyotime, China) for 1 h at room temperature, incubated with primary antibody against myosin heavy chain (1:1,000, Sigma-Aldrich, USA) at 4 °C overnight and then with Goat anti-Mouse IgG (H + L) Highly Cross-Adsorbed Secondary Antibody, Alexa Fluor 594 (1:400, Invitrogen, USA) for 1 h at room temperature. The cells were stained with DAPI for 5 min at room temperature to visualize the nuclei and were finally examined using a fluorescence microscope.
For muscle fibre-type experiments, tibialis anterior (TA) and soleus (Sol) muscle samples were dissected, embedded in optimum cutting temperature (OCT) compound, flash frozen in cold isopentane, and sectioned at 10 μm. Primary antibodies against MHCI, MHCIIa and MHCIIb were obtained from Developmental Studies Hybridoma Bank (DSHB). The following corresponding secondary antibodies were obtained from Thermo-Fisher: Alexa Fluor 594 anti-mouse IgG2b (A-21145), Alexa Fluor 594 anti-mouse IgG1 (A-21125) and Alexa Fluor 594 anti-mouse IgM (A-21044). The TA muscle was stained for MHCIIa and MHCIIb, and the Sol muscle was stained for MHCI.
To count the total number of myofibres, immunofluorescence staining for laminin was performed. The TA muscle was dissected, embedded in OCT compound, flash frozen in cold isopentane, and sectioned at 10 μm. The primary antibody against laminin (L9393) was obtained from Sigma, and the corresponding secondary antibody was Alexa Fluor 488 Goat Anti-Rabbit IgG (H + L) Antibody (A-11008), which was obtained from Invitrogen.
The immunofluorescent staining for MHCI, MHCIIa, MHCIIb and laminin was performed according to a previous report43.
Cas9 vector construction
Cas9 expression vectors were constructed according to a previous study44 and were then transfected into C2C12 cells using Nucleofector™ Kits for Mammalian Fibroblasts (Lonza, Germany).
Genomic DNA was extracted from C2C12 cells or mouse tail tissue and digested with HindIII (Takara, China) overnight at 37 °C. The digested genomic fragments were separated on a 0.8% agarose gel and transferred to a positively charged nylon membrane (Roche, Germany) for hybridization. The primers for amplifying the digoxigenin-labelled probe were as follows: F: 5′ CCA AAT TCT CTG CCT GGT GG 3′, R: 5′ GCT CCT CTG TGT TCC GTA GA 3′.
The hybridization and detection procedures were performed according to the manufacturer’s instructions (Roche, Germany).
Protein extraction and Western blot
The total protein was extracted from C2C12 myotubes and gastrocnemius muscle using cell lysis buffer for western blotting and IP (Beyotime, China) according to the manufacturer’s protocol. The quantification of total protein was measured with a BCA Protein Assay Kit (Beyotime, China) according to the manufacturer’s protocol.
The primary antibodies to Pan-Akt, P-Akt (Ser473), P-Akt (Thr308), mTOR, P-mTOR (Ser2448), S6, P-S6 (Ser240/244), P70S6K, P-P70S6K (Thr389), 4E-BP1, 4E-BP1 (Ser65) and GAPDH were all purchased from Cell Signaling Technology. Anti-rabbit IgG HRP (ZSGB-Bio, China) was used as a secondary antibody (1:10,000). The blots were visualized using SuperSignal West Dura Extended Duration Substrate (Thermo scientific, USA).
The amount of total IGF1 in C2C12 myotubes, mouse serum and gastrocnemius muscle were measured using a Mouse/Rat IGF-I Immunoassay kit (R&D systems, USA) according to the manufacturer’s protocol. The concentrations of total IGF1 in C2C12 myobtubes and gastrocnemius muscle were normalized to the total protein respectively.
Quantitative real-time polymerase chain reaction
Total RNA was extracted from C2C12 myotubes and the gastrocnemius muscles of mice by using TRIzol reagent (Invitrogen, USA). Reverse transcription was performed using 2 μg of RNA. The primers to detect the Igf1 mRNA expression levels and GAPDH levels are listed below; GAPDH was used as an internal control.
IGF1-F: 5′ GGA CCG AGG GGC TTT TAC TT 3′; IGF1-R: 5′ GTG GGG CAC AGT ACA TCT CC 3′. GAPDH-F: 5′ GTG CCG CCT GGA GAA ACC T 3′; GAPDH-R: 5′ AAG TCG CAG GAG ACA ACC 3′.
The relative expression levels of Igf1 mRNA in myotubes of single-cell colonies were displayed as fold changes relative to that in WT C2C12 myotubes using the 2−△△CT method. The relative expression levels of Igf1 mRNA in the gastrocnemius muscles were calculated using the 2−△CT method.
Haematoxylin and eosin staining (H&E)
The TA and GA were dissected out and fixed in 4% PFA for approximately five days. After dehydration, the samples were embedded in paraffin. Then, 5-μm-thick sections were made and stained with H&E. The CSA of more than 1,500 myofibres from at least five mice per group were measured using image J software.
Detection of potential off-target sites
Potential off-target sites were screened in the mouse genome using the CRISPR design tool (http://crispr.mit.edu/). The top 10 potential off targets for PCR amplification were shown in Supplementary Table S3, and then the PCR products were examined by Sanger sequencing. The primers for amplifying the potential off targets were shown in Supplementary Table S4.
Equipment and settings
Image processing including brightness and contrast adjustments, cropping, were performed with Adobe Photoshop software. And the brightness and contrast adjustments were applied equally across the entire image and were applied equally to controls.
All values are presented as means ± SEM. The student’s t test was used to determine p values. Statistical significance was defined as p < 0.05.
No datasets were generated or analysed during the current study.
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We wish to thank Yang Su, Mengxu Ge, Chuncheng Liu and Meng Wang for their technical help. This work was supported by the National High Technology Research and Development Program of China (2013AA102502).
The authors declare no competing interests.
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Zou, Y., Dong, Y., Meng, Q. et al. Incorporation of a skeletal muscle-specific enhancer in the regulatory region of Igf1 upregulates IGF1 expression and induces skeletal muscle hypertrophy. Sci Rep 8, 2781 (2018). https://doi.org/10.1038/s41598-018-21122-5