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Evaluation of the effect of a floxed Neo cassette within the dystroglycan (Dag1) gene
BMC Research Notesvolume 10, Article number: 601 (2017)
Dystroglycan (DG) is an adhesion complex formed by two subunits, α-DG and β-DG. In skeletal muscle, DG is part of the dystrophin-glycoprotein complex that is crucial for sarcolemma stability and it is involved in a plethora of muscular dystrophy phenotypes. Due to the important role played by DG in skeletal muscle stability as well as in a wide variety of other tissues including brain and the peripheral nervous system, it is essential to investigate its genetic assembly and transcriptional regulation.
Herein, we analyze the effect of the insertion of a floxed neomycin (Neo) cassette within the 3′ portion of the universally conserved IG1-intron of the DG gene (Dag1). We analyzed the transcription level of Dag1 and the expression of the DG protein in skeletal muscle of targeted mice compared to wild-type and we did not find any alterations that might be attributed to the gene targeting. However, we found an increase of the cross-sectional areas of tibialis anterior that might have some physiological significance that needs to be assessed in the future. Moreover, in targeted mice the skeletal muscle morphology and its regeneration capacity after injury did not show any evident alterations. We confirmed that the targeting of Dag1 with a floxed Neo-cassette did not produce any gross undesired effects.
Dystroglycan (DG) is a widely expressed adhesion complex encoded by a single gene (Dag1) as a unique precursor that undergoes post-translational cleavage to generate two interacting subunits: the extracellular and highly glycosylated α-DG and the transmembrane β-DG [1, 2].
DG is crucial for cell membrane stability connecting the actin cytoskeleton to extracellular matrix (ECM) proteins . Whenever the DG/ECM axis is perturbed, severe muscular dystrophy phenotypes do arise [4, 5].
Extensive genetic work has been carried out in order to analyze the function of DG in several tissues . It was shown that the knockout of Dag1 in mice is embryonic lethal . This result is in line with what was observed in some human patients, in which a homozygous loss-of-function mutation in Dag1 results in the absence of DG that leads to early postnatal lethality .
Conditional knockouts of Dag1 in several tissues have confirmed the importance of DG for tissue stability. In those studies, no apparent effects of the inserted floxed Neo cassette have been reported [9,10,11]. Moreover, the knock-in mouse carrying the pathological mutation T190M showed an evident muscular dystrophy phenotype and possible effects arising from the presence of the exogenous genetic elements might have been covered up . On the other hand, in the knock-in mouse Y890F the floxed-Neo cassette had been already removed in the chimeric mice and no effect arising from the presence of the remaining LoxP element has been reported .
Interestingly, the insertion of a floxed Neo-cassette can lead to a significantly reduced expression of the target gene and can also downregulate the transcription of genes located at a distance of several kilobases from it [14,15,16,17,18,19,20,21,22].
Considering the lack of experimental data on the effects of the floxed Neo cassette on Dag1 expression, we have decided to assess whether the presence of a floxed Neo cassette or single floxed site in the Dag1 allele might have per se some evident functional consequences for Dag1 expression in skeletal muscle.
Generation of targeting vector
Genomic DNA from V6.4 murine ES (embryonic stem) cells, (genotype C57BL/6J × 129/SvJae), was used as a template to amplify the right and left hand arms of the DG targeting construct. The 5′ arm of the construct consisted of 3.2 kb of intronic sequences amplified from the Dag1 intron using the following primers: forward 5′-GAGTAAGACTTTGTCTATAAAACA-3′ and reverse 5′-AAACCCCAACAACTACGGTCCTCA-3′. The 3′ arm was 4 kb in length, consisted of the exon 3 region, harboring four mutations, flanked by intronic sequences and the 3′-UTR, respectively, was amplified using the following primers: forward 5′-GAGAAGTGGGATTCATTTAGACAG-3′ and reverse 5′GAATGTAATCTTTAGCTACTGTT-3′. To allow the linearization of the targeting vector that is necessary for the recombination and integration of the construct into the ES cells genome, site-directed mutagenesis was used to mutate a XhoI site in the 5′ arm using the QuikChange site-directed mutagenesis kit (Stratagene®) and the following primers: forward 5′-AGTTCCTTCCTGCCTAGAGTGGGTGTTCCCT-3′ and reverse 5′-AGGGAACACCCACTCTAGGCAGGAAGGAACT-3′ (mutated nucleotides in bold). Both the right and left hand arms were initially cloned into separate TOPO vectors (Invitrogen) and then sub-cloned into the final targeting vector, a modified pBluescript KS vector containing a floxed neomycin cassette under the PGK promoter (Fig. 1a). The 5′ and 3′ arms were cloned within a BamHI and HindIII sites respectively. Both enzymes (New England Biolabs® Inc) were incubated at 37 °C for 1.5 h. The Herpes simplex thymidine kinase (HSVtk) cassette acts as a negative selection marker. The targeting vector was used at the Core Facility for Conditional Mutagenesis, Dibit-San Raffaele Scientific Institute, Milan to electroporate and analyze murine ES cells by Southern blot. One homologous recombinant ES clone was microinjected into blastocysts from 129 J mice. The resulting chimeras were then bred with C57BL6 mice to generate germ line-transmitted heterozygous mice (Dag1 Neo/+). Dag1 Neo/+ mice were backcrossed into the C57BL/6 background for ten generations and then used to create the experimental colonies. Mice from different colonies were crossbred to generate wild-type (Dag1 +/+), heterozygous (Dag1 Neo/+) and homozygous mice (Dag1 Neo/Neo).
To remove the Neo cassette, homozygotes were crossbred with male transgenic mice expressing the transgene Cre under the CMV promoter (Jackson Laboratories) to generate Dag1 Neo/+ mice. Female F1 animals were bred again with homozygous Dag1 Neo/Neo mice to generate Dag1 ΔNeo/ΔNeo mice.
Creatine kinase assay
Fresh serum was collected by retro-orbital bleeding. The creatine kinase (CK) level was determined according to the International Federation of Clinical Chemistry with commercial reagents on the Cobas 8000/c701® (Roche Diagnostics).
Histological and immunofluorescence analysis
All the analyses described below were not performed blind. Tibialis anterior (TA) and gastrocnemius (GA) muscles of 5 months-old female mice (n = 4 per genotype) were embedded in Jung tissue freezing medium and frozen in liquid nitrogen-cooled isopentane. Frozen sections (7 μm) were stained with hematoxylin and eosin (HE) using standard methods . Fiber cross-sectional areas (CSA) of muscle sections were counted manually using ImageJ (NIH, Bethesda, MD) from 6 to 12 randomly selected fields per section. At least 150 fibres per mouse from three mice per genotype were counted.
For the immunofluorescences analysis, TA muscle frozen sections of 5 months-old female mice were incubated with the following antibodies diluted in PBS containing 1% BSA (Sigma-Aldrich): mouse monoclonal anti-α-DG IIH6 (Millipore, code 05–593) (1:100), rabbit polyclonal anti-β-DG (Abcam, code ab43125) (1:300) and rat monoclonal anti-laminin-α2 clone 4H8-2 (Sigma-Aldrich, code L0663) (1:100). The primary antibodies were followed by the appropriate secondary goat anti-mouse IgM (for IIH6), goat anti mouse, anti rat or anti rabbit IgG antibodies conjugated with Alexa®488 or Alexa®633 fluorophores (1:500) (Invitrogen-Thermo Fisher Scientific). Muscle sections incubated with the only secondary antibody were used as control to validate the primary antibody specificity. Sections were viewed with a Leica SP2 microscope and all images were analyzed using ImageJ software (NIH).
TA muscles of female 5 months-old mice (four mice per group) were injured along the entire length of the muscle with cardiotoxin (CTX) (LATOXAN SAS, code L8102) injections, 5 μL of 10 μM CTX in saline solution. These conditions ensured muscle damage a uniform manner. The muscles were harvested 10 days after cardiotoxin-induced damage. Frozen sections were processed for histological analysis. Contralateral intact muscles were used as a control. In our previous study, regeneration was fully active at 7 days after injury . Sections were viewed with a Leica SP2 microscope and all images were analyzed using ImageJ software (NIH).
TA muscle proteins from 5 months-old mice were extracted with PBS 1% Triton-X100 containing protease inhibitors. 20 μg of soluble proteins were analyzed in Western blot as described elsewhere  using the following antibodies: anti mouse α-DG IIH6 (Millipore) (1:1000), anti rabbit β-DG (Abcam) (1:1000) and anti-tubulin HRP-conjugated (Abcam) antibodies.
RNA was isolated from frozen muscle using the RNeasy Fibrous Tissue Mini Kit. Reverse Trascriptase PCR reactions were carried out using 3 μg of RNA. Quantitative RT-PCR was performed in triplicate using a standard TaqMan® PCR protocol on a StepOne Real time PCR System (Applied Biosystems). Probes were specific for mouse Dag1 and mouse Gadph genes. Data analysis was performed as described elsewhere .
Data were expressed as mean ± standard error of the mean (SE). Comparisons among groups were performed using an analysis of variance (One-way ANOVA) followed by a Bonferroni’s post hoc multiple comparison test to determine statistical significance of the differences among the four experimental mice groups; p value of < 0.05 was considered to be statistically significant. Statistical analyses were performed with SPSS software (version 17.0, Chicago, IL, US).
Results and discussion
Insertion of the floxed Neo cassette into Dag1 and removal by Cre recombinase: the Dag1 Neo/Neo and Dag1 ΔNeo/ΔNeo mouse lines
In an attempt to produce a novel DG knock-in mouse line harboring four mutations at the α/β-DG interface , an incomplete homologous recombination at the 3′ arm (Fig. 1) prevented the generation of the desired mutated mouse line. Indeed, we generated and studied a mouse line with a Dag1 allele in which a Neo cassette, flanked by two LoxP sites, was inserted into the second intron (Dag1 Neo allele) (Fig. 1).
The Neo cassette was introduced in the second intron (also termed IG1-intron since it interrupts the structure of the IG1 domain within the structurally autonomous N-terminal region of α-DG ). In addition, we have also crossbred our mice with a mouse line that expresses the Cre recombinase under a CMV-promoter and results in Cre-mediated recombination in germ line. This resulted in the Cre-driven excision of the floxed Neo cassette in the targeted Dag1 (Dag1 ΔNeo allele, Fig. 1a, b).
Histological and molecular analysis of skeletal muscle
Animals with two wild-type alleles are denoted by “Dag1 +/+”, mouse lines in which one allele carries the floxed Neo cassette are designated “Dag1 Neo/+”, whilst their homozygous counterpart is denoted by “Dag1 Neo/Neo”. Finally, “Dag1 ΔNeo/ΔNeo” indicates the mouse line obtained upon the excision of the Neo cassette by Cre recombinase.
At 5 months of age, body weights of Dag1 Neo/+ (male 31.5 g ± 2.3; female 25 g ± 1.7), Dag1 Neo/Neo (male 31.7 g ± 2.6; female 24.5 g ± 1.5) and Dag1 ΔNeo/ΔNeo (male 31.8 g ± 2.2; female 26 g ± 1.1) mice were not significantly different from wild-type controls (male 31.8 g ± 2.5; female 25 g ± 1.5).
Histology of tibialis anterior (TA) and gastrocnemius (GA) muscles of 5 months-old female mice, derived from crosses between heterozygotes (intercross) belonging to different colonies, examined by HE staining did not show any gross morphological sign indicating skeletal muscle alterations in Dag1 Neo/+, Dag1 Neo/Neo, and Dag1 ΔNeo/ΔNeo mice compared to Dag1 +/+ controls (Fig. 2). In all the Dag1 targeted mice, the levels of serum CK, a marker for skeletal muscle damage, did not significantly differ from those of wild-type animals (female: Dag1 +/+ 366 U/L ± 0.8; Dag1 Neo/+ 370 U/L ± 0.8; Dag1 Neo/Neo 355 U/L ± 0.7; Dag1 ΔNeo/ΔNeo 360 U/L ± 0.85). CK was measured in 3 and 5-months old mice. Immunofluorescence analysis showed the expected localization of the two DG subunits as well as of the DG major skeletal muscle binding partner laminin to the cell membrane and cell surface, respectively (Fig. 3). Western blot analysis confirmed that the DG precursor is correctly cleaved into its two subunits and that α-DG is highly glycosylated in all the lines (Fig. 4a). The levels of α- and β-DG were similar compared to wild-type mice (data not shown).
Next, we examined the muscle fiber cross-sectional areas (CSA) by sampling a set of muscle fiber size in TA (Fig. 5a) and GA (Fig. 5b) muscle within the four experimental groups (four mice per group). Overall, we found a significant difference of the medians of fiber CSAs between the groups (lines) of mice (p < 0.001) whereas in GA we did not find any difference (p = 0.998). In particular, in TA muscle the CSA in mouse line Dag1 ΔNeo/ΔNeo (mean 1826 μm2 ± 37) was significantly increased when compared with Dag1 +/+ mice (mean 1609 μm2 ± 36) (p < 0.001). At present, we cannot rule out that the observed variability in TA might have significant physiological repercussions. Further investigations will be required to better clarify this point.
The increase of TA muscle fibers was not mirrored by an increase either in DG protein levels or in Dag1 transcription (see below) (Figs. 4, 6). The Dag1 transcription levels were measured by Real Time PCR experiments that monitor the changes in mRNA levels of Dag1 Neo/Neo, and Dag1 ΔNeo/ΔNeo mice relative to Dag1 +/+ littermates and no significant change was detected (p = 0.707) (Fig. 6).
Cardiotoxin-induced skeletal muscle regeneration
Dystroglycan is essential for postnatal muscle growth, stability and regeneration [9, 28]. To further analyze the possible presence of skeletal muscle defects of the regenerative process, we analyzed the TA muscles of Dag1 Neo/+, Dag1 Neo/Neo, and Dag1 ΔNeo/ΔNeo 5-months old female mice compared to Dag1 +/+ mice, 10 days after CTX-induced damage. HE staining revealed that, although CTX injection caused muscle necrosis with the accumulation of mononucleated infiltrating cells, the regeneration response occurred in all the analysed muscles, as demonstrated by the amount of central nucleated fibers present (p = 0.559) (Fig. 7).
The targeting of Dag1 with a floxed Neo cassette did not produce any strong undesired skeletal muscle phenotype. The increase of CSA that we observed in TA of Dag1 ΔNeo/ΔNeo mice might be due to some degree of variability between the analyzed mice, but must be further analyzed. Dag1 second intron is large (10 Kb) and this justifies the absence of relevant effects on Dag1 mRNA upon the introduction of the floxed Neo-cassette .
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Conceived and designed the experiments: FS, AB. Performed the experiments: FS, BMS, GS, MGB, BT, MB. Analysed the data: FS, BMS, FL GS, BG, SB, AB. Wrote the paper: FS, AB. All authors reviewed and contributed to the various draft versions of the manuscript. All authors read and approved the final manuscript.
We gratefully acknowledge Massimo Aquilina and Fabrizio Fiore from the animal facility of the Catholic University of Rome for their skillful assistance, and Alexandra Joyner, Memorial Sloan Kettering Cancer Center New York, for the PGK-Neo plasmid.
The authors declare that they have no competing interests.
Availability of data and materials
The datasets used and analyzed during the current study are available from the corresponding author on reasonable request.
Consent for publication
Ethics approval and consent to participate
All animal procedures were approved by the Ethics Committee of the Animal Facility of the Università Cattolica del Sacro Cuore (UCSC, Roma, Prot. Sf 11100/13 and Prot. CE 20353/14 06_01) and by the Italian Ministry of Health, Direzione Generale della Sanità Animale e dei Farmaci Veterinari (196/2015-PR).
This work was supported by a Wellcome Trust Career Re-entry fellowship to MGB and by an AFM post-doctoral fellowship to FS. This work was in part supported by a PRIN 20109MXHMR_001 Grant to BG.
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