- Research article
- Open Access
Functional conservation between rodents and chicken of regulatory sequences driving skeletal muscle gene expression in transgenic chickens
© McGrew et al; licensee BioMed Central Ltd. 2010
Received: 7 August 2009
Accepted: 25 February 2010
Published: 25 February 2010
Regulatory elements that control expression of specific genes during development have been shown in many cases to contain functionally-conserved modules that can be transferred between species and direct gene expression in a comparable developmental pattern. An example of such a module has been identified at the rat myosin light chain (MLC) 1/3 locus, which has been well characterised in transgenic mouse studies. This locus contains two promoters encoding two alternatively spliced isoforms of alkali myosin light chain. These promoters are differentially regulated during development through the activity of two enhancer elements. The MLC3 promoter alone has been shown to confer expression of a reporter gene in skeletal and cardiac muscle in transgenic mice and the addition of the downstream MLC enhancer increased expression levels in skeletal muscle. We asked whether this regulatory module, sufficient for striated muscle gene expression in the mouse, would drive expression in similar domains in the chicken.
We have observed that a conserved downstream MLC enhancer is present in the chicken MLC locus. We found that the rat MLC1/3 regulatory elements were transcriptionally active in chick skeletal muscle primary cultures. We observed that a single copy lentiviral insert containing this regulatory cassette was able to drive expression of a lacZ reporter gene in the fast-fibres of skeletal muscle in chicken in three independent transgenic chicken lines in a pattern similar to the endogenous MLC locus. Reporter gene expression in cardiac muscle tissues was not observed for any of these lines.
From these results we conclude that skeletal expression from this regulatory module is conserved in a genomic context between rodents and chickens. This transgenic module will be useful in future investigations of muscle development in avian species.
The development of an organism entails the precise expression of lineage and tissue-specific gene products in a temporally-regulated manner during embryogenesis. The information for a cell to respond to external signals by differentiating down a particular developmental pathway is 'hardwired' into the regulatory regions surrounding these developmentally regulated genes [reviewed in ]. These conserved regulatory regions or modules drive spatial gene expression patterns in the forming tissues of the developing organism. Changes in the cis-regulatory elements of regulatory modules are hypothesized to be the predominant mechanism behind evolutionary changes in pattern formation .
Many expression modules have been shown to be functionally conserved in vertebrate species. For example, regulatory regions from several hox genes from fish and chicken are capable of driving some aspects of the spatial expression patterns of the paralogous murine gene in transgenic mice [3–6]. Examples of conserved regulatory modules have been shown for the processes of neurogenesis [7–9], limb morphogenesis  and haematopoiesis [11, 12], amongst many other examples.
We, and others, have previously shown that lentiviral vectors can be used to generate transgenic chickens and that cis-regulatory regions incorporated into these vectors will drive ubiquitous or tissue-specific expression in this species [13–16]. In this report we investigate the possibility of utilising rodent regulatory elements to drive transgene expression in skeletal muscle of chickens. To achieve this we investigated the transcriptional activity of the rat MLC regulatory domains in transgenic chickens. This locus encodes two alkali myosin light chains expressed from two promoters that are differentially regulated during development. The MLC1 isoform is expressed at embryonic stages of development and in the fast fibres of skeletal muscles of the adult. The MLC3 isoform is expressed at fetal stages and in the atria of the mouse heart [17, 18]. The construct we used consists of the rat MLC3 promoter, which is transcriptionally active in all striated muscle in mouse transgenic models [18, 19], and a downstream rat MLC enhancer which augments skeletal muscle expression and confers expression at embryonic stages of development [20, 21]. We show that a putative MLC enhancer is present in the chicken MLC locus. Using the rat MLC regulatory elements, we show that these elements support transgene expression in skeletal muscle of chickens. Cardiac transgene expression was not detected. These results indicate a functional conservation of the MLC regulatory elements exist between rodents and chickens in the skeletal muscle lineage. This demonstration is significant not only for the use of the chicken as a model organism for studies in developmental biology but also because poultry are an economically important food source.
Results and Discussion
Examination of the chicken locus at an analogous position for the MLC enhancer enabled us to identify a region of homology shared with human, rat, mouse, and opossum (Fig. 1bottom). A closer examination of this region revealed a putative enhancer module containing regulatory elements that closely resemble the core myosin light chain enhancer as defined in mouse, rat and human [19, 27, 28]. This core enhancer contains three canonical E boxes (CANNTG) that bind to the myogenic factors, myf-5, MRF4, myoD, and myogenin and an A/T rich region containing a sequence matching the consensus binding site of MEF2 . All four regulatory motifs are present in this DNA sequence as indicated in Fig. 1. These data suggest that the structure of the MLC1/3 locus is highly conserved between mammals and chicken.
Generation of a muscle-specific reporter cassette
Generation of transgenic chickens carrying the MLC-lacZtransgene
Transgene expression is limited to avian skeletal muscle
Unexpectedly, no β-galactosidase was detected in heart atria or ventricles of birds from any of the three expressing lines. In transgenic mice, the MLC3 promoter alone drove β-galactosidase expression in cardiac muscle of transgenic mice (3 of 3 mouse lines) . Addition of the MLC enhancer to the transgene construct inhibited expression in cardiac tissues of two out of three transgenic mouse lines. A similar effect was also reported by Zammit et al., . The lack of expression in cardiac tissue from the transgenic chickens mimicked the result obtained by transfection experiments into chicken cardiomyocytes and was also similar to the expression patterns observed in transgenic mice for constructs containing the MLC enhancer.
Tissues from the transgenic adult birds were stained for β-galactosidase activity to observe the spatial expression pattern in skeletal muscle. Non-muscle tissues and cardiac muscle did not stain for β-galactosidase (Fig. 4, bottom). Pectoral muscle of the breast was entirely stained for β-galactosidase. Immunofluorescence of chicken pectoral muscle with an antibody to chicken myosin light chain 1 and 3 revealed extensive expression throughout this tissue (Fig. 4C). In contrast to the pectoral musculature, staining of leg muscle displayed a cobbled expression pattern. Chicken pectoral muscle contains predominantly fast fibre muscle (white muscle) whereas leg musculature contains both fast and slow muscle fibres (red muscle) [29, 30]. This result suggests that the transgene is expressed extensively in the fast fibre tissue of the breast flight muscle and is restricted in expression in leg muscle which contains slow as well as fast muscle fibres.
To demonstrate that the transgene expression follows that of the endogenous MLC1/3 locus, a tissue section was stained for β-galactosidase and an adjacent section immunostained with an antibody to MLC1 and 3 isoforms (F310) (Fig. 5C, 5D) . Muscle fibres that are negative for β-galactosidase activity are immuno-negative for MLC1 and 3 indicating that the rat regulatory elements are expressed in a similar fibre type as the endogenous gene.
The MLCmodule drives early embryonic expression
These experiments are a further demonstration that the chicken can be used as an alternative model for transgenic analysis of gene regulation and of the use of lentivirus in avian transgenesis. These results indicate that the MLC regulatory module is functionally conserved for fast muscle fibre expression in mammals and birds and is developmentally regulated. Regulatory regions in the MLC enhancer are also conserved between mammals and chicken (Fig. 1). In contrast, sequences in the MLC3 promoter are divergent when compared to the MLC1 promoter [18, 25]. The GATA regulatory element of the rat MLC3 promoter, essential for cardiac expression in the rat, is not conserved in the chicken MLC3 promoter, yet there is expression from the endogenous MLC1/3 locus in the embryonic chicken heart (Fig. 6D), suggesting that regulatory modules for avian cardiac expression are divergent from those in mammals.
The construct described here will be useful as an expression module to drive skeletal muscle expression in avian species. This will have applications for the expression of proteins or RNAs in avian muscle tissue for studies of muscle differentiation and function. For example, the expression of microRNAs targeting genes involved in skeletal muscle myopathy in broiler chickens could be specifically targeted to skeletal muscle using this regulatory module . Additionally, similarly constructed transgenes will permit the analysis of candidate genes, identified by QTL mapping and expression analyses, implicated in control of muscle mass in chicken lines selected for increased muscle mass [35, 36]. Inherent difficulties still remain in the generation of transgenic chickens including the long period to sexual maturity (16 weeks) and the difficulties in generating high titre lentivirus for large and complex transgenes.
Lentivirus construction and packaging
The 628 bp MLC3 promoter was isolated from p628Luc920  using HindIII and subcloned into the HindIII site of the minimal EIAV lentiviral vector pONY8.45NCmcs . A lacZ reporter gene was isolated from pONY 8.45NCZ using Sph1 and Xho1 and subcloned into the Xho1 and Nru1 sites of the above plasmid to generate pONY8.45NCMLC3-Z. A residual CMV promoter was deleted from this vector by digestion with EcoR1 and SacII and re-ligation of the plasmid. Finally, a 920 bp MLC enhancer fragment was isolated from p628Luc920  using BamH1 and subcloned into the Not1 site upstream of the introduced promoter fragment to generate pONY8.45N-E-MLC3-Z (pONY-MLZ). The original direction of the enhancer was reversed in this construct. Packaged virus stocks were generated by FuGENE6 (Roche, Lewes, U.K.) transfection of HEK 293T cells plated on 10 cm dishes with 2 μg of vector plasmid, 2 μg of gag/pol plasmid (pONY3.1) and 1 μg of VSV-G plasmid (pRV67) . 36-48 hours after transfection supernatants were filtered (0.22 μm) and stored at -80°C. Concentrated viral preparations were made by initial low speed centrifugation at 6,000 × g for 16 hours at 4°C followed by ultracentrifugation at 50,500 × g for 90 minutes at 4°C. The virus was resuspended in formulation buffer (20 mM Tris, 100 mM NaCl, 10 mg/ml sucrose,10 mg/ml mannitol, pH 7.4) for 2-4 hours, aliquoted and stored at -80°C. Viral titre was estimated at 4.5 × 107 T.U./μl.
Production and analysis of transgenic birds
Founder transgenic birds were generated by injection of viral particles into fertilised eggs at the new-laid egg stage, followed by culture of the embryos to hatch as described [13, 38]. The hatched chicks were raised to; sexual maturity and DNA extracted from semen from adult males was screened by PCR (13) to; identify cockerels that carried vector sequences in the germ line. One cockerel identified by this method was crossed to; stock hens and their offspring screened by PCR to; identify G1 hemizygous transgenic birds. All experiments, animal breeding, and care procedures were carried out under license from the U.K. Home Office.
The vector insertions in individual G1 birds were analyzed by Southern transfer. Genomic DNA (10 μg), extracted from whole blood, was digested with HindIII or Sph1 restriction endonucleases, resolved on a 0.7% agarose gel, and transferred to Hybond-N membrane (Amersham Biosciences, U.K.). These blots were analyzed by using a probe of the lacZ coding sequence, labelled with [32P]dCTP using a RediPrime II kit (Amersham Biosciences). Hybridization was in 500 mM sodium phosphate (pH 7.2)/7% SDS at 65°C and signal was detected by autoradiography.
Transfection of chicken primary cultures
The lentiviral plasmids described above were digested with Bgl II and Xba I and re-ligated to remove a 1.8 kb CMV enhancer/promoter fragment used for transcribing the lentiviral constructs during packaging and which could potentially transactivate the downstream MLC3 promoter (pONY-MLZ-del CMV constructs).
Skeletal or cardiac tissue was isolated from day 9 chicken embryos, macerated and dissociated in trypsin for 3 × 5 minutes with vigorous pipetting. The solution was spun at 1000 × g, 5 minutes, and re-suspended in plating media (10%FBS, 1% chick serum in DMEM, 1× NEAA). On day two of culture, cells were transfected using Fugene HD (Roche) with 5 ug of pONY-MLZ (del CMV) constructs and 1 ug of CAG-GFP in 35 mm tissue culture plates (Primaria, BD Biosciences). Culture media for skeletal muscle cultures was changed to differentiation media (2% chick serum in DMEM, 1× NEAA) after 24 hours. All plates were incubated for two additional days, photographed for GFP fluorescence, and stained for β-galactosidase activity as described below.
Analysis of β-galactosidase activity and processing of tissues
Selected tissues were snap-frozen and total protein extracted by homogenization in PBS containing protease inhibitors (complete mini, Roche). Protein concentration was determined by Bradford assay. ELISA was performed using β-gal Elisa kit (Roche). Elisa assays were carried out on two G1 birds for each integration event. The data shown in Fig. 4 are for one transgenic animal for each integration event.
Adult tissues were isolated, fixed for 30 min in 4% paraformaldehyde, 0.25% gluteraldehyde in phosphate buffered saline (PBS) and tissues cryo-embedded and sectioned at 14 μm. β-galactosidase activity was detected by incubating at 37°C in 5 mM potassium ferricyanide, 5 mM potassium ferrocyanide, 2 mM MgCl2, 0.5 mg/ml X-gal for 90 minutes, counterstained with eosin and mounted. Fast (F59) and slow (S58) fibre-type antibodies and an antibody against MLC1 and 3 isoforms (F310), developed by F.E. Stockdale, were obtained from the Developmental Studies Hybridoma Bank, University of Iowa, and used at 1:10 dilutions. The secondary antibodies used were TRITC conjugated goat anti-mouse IgG and FITC conjugated goat anti-mouse IgA (Sigma), and Alexa Fluoro 488 conjugated goat anti-mouse IgG respectively. Slides were counterstained with Hoechst, and mounted with Vectashield mounting media (Vector). Whole mount in situ hybridizations were carried out as described . The riboprobe to MLC1 and 3 transcripts was described in .
We are grateful to K. Mitrophanous and L. Elliot for valuable input on the project and to N. Rosenthal for providing the MLC regulatory module. We thank H. Gilhooley, M. Hutchison, R. Mitchell and F. Thomson for care of transgenic birds and processing of samples. This work was supported by the Biotechnology and Biological Sciences Research Council, U.K. and by Viragen Inc.
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