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From the Scientific Institute "Eugenio Medea",*
Conegliano Research Centre, Conegliano, and the Neuromuscular
Center,
Department of Neurology, University of
Padova, Padova, Italy
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Abstract |
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Introduction |
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TopAbstractIntroductionMaterials and MethodsResultsDiscussionReferences |
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The molecular basis of McArdle's disease has been linked to several mutations, either nonsense or missense, in the PYGM gene, which codes for M-GP.4,5 The most common mutation is the nonsense mutation at codon 49 (R49X), accounting for up to 60% of the alleles. Many patients, however, defy even an extensive search for mutations.6,7
Muscle biopsies of McArdle's patients are characterized by subsarcolemmal storage of normal glycogen and by absent stain with the histochemical phosphorylase reaction. In some patients, however, it is possible to find scattered fibers with positive phosphorylase staining.8,9 The identity of the glycogen phosphorylase isoform expressed in those phosphorylase-positive fibers has been a matter of debate. After the initial report describing the reappearance of phosphorylase activity in myophosphorylase-deficient patients,8 subsequent studies supported the assumption that those fibers, similarly to cultured immature myotubes, express non-muscle-specific (ie, fetal) isoforms.10,11 Later studies on cultured muscle in which differentiation was more advanced due to different culture techniques or innervation showed that M-GP was indeed expressed, albeit in small proportion, in both control and patients' myotubes in vitro.12,13
In this paper we assessed the frequency of phosphorylase-positive fibers in a consecutive series of 27 muscle biopsies of 25 McArdle's patients. We found phosphorylase-positive fibers in 19% of our muscle biopsies. Virtually all positive fibers are regenerating fibers. We show that the isoform expressed in phosphorylase-positive fibers differs according to the genetic background of the patient: in patients with no detected mutation in at least one allele of the PYGM gene, the muscle-specific isoform is transcribed and translated, whereas it is neither transcribed nor translated in patients with mutations identified in both alleles of the gene.
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Materials and Methods |
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A total of 27 muscle biopsies of 25 patients with Mc-Ardle's disease were screened for scattered phosphorylase positivity. The biopsies showing at least one positive fiber were further studied by immunohistochemistry and in situ hybridization.
All patients presented clinical and laboratory findings typical of
McArdle's disease, with muscle glycogen storage and severely reduced
glycogen phosphorylase activity. Clinical, biochemical, and molecular
data for patients whose biopsy showed phosphorylse positive fibers are
summarized in Table 1
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Cultured myoblasts were expanded from muscle explants obtained from patient and control biopsies as previously described.13 Myoblasts were allowed to fuse in myotubes, and selected dishes were innervated with rat fetal spinal cord explants as described.13 Aneural and innervated cultured muscle from patients and control were harvested, and the total RNA was extracted as described below.
Molecular Characterization
Total RNA and DNA were extracted from muscle biopsies or cultured muscle with the TRI-zol reagent according to the manufacturer's instructions (Gibco BRL, Gaithersburg, MD). Northern analysis for M-GP mRNA was carried out as described.13 The following mutations known to be associated with McArdle's disease were searched in all patients with described methods4,5 : R49X, G204S, L291P, L396P, K542T, E654K, del708, 1778del67 (splice junction mutation at the 5' end of intron 14), delG510, A to G transition in the translation initiation codon, frameshift mutation in exon 1, R575X, G685R, and delA753.
In addition, in those patients in whom none of the above mutations could be detected, we directly sequenced the entire PYGM cDNA.
Histochemistry (HC) and Immunohistochemistry (IHC)
Serial cryostat sections (6 µm thick) were placed on slices pretreated with 0.25% gelatin, 0.025% chrome alum (Merck, Darmstadt, Germany), and processed separately. One section was used for histochemical phosphorylase stain. As marker of muscle regeneration, we used a monoclonal antibody against fetal myosin heavy chain (Novocastra, Newcastle, UK), diluted 1:100 in PBS and incubated for 1 hour at room temperature. The expression of M-GP was studied using sheep anti-M-GP antiserum.13 To block nonspecific staining, sections were incubated with 5% bovine serum albumin (BSA) in PBS for 1 hour. Anti-M-GP antiserum diluted 1:25 in 1% BSA/PBS was incubated overnight at 4°C and for one additional hour at room temperature on a shaker. The specific labeling was developed by an immunofluorescence method using appropriate biotinylated antibodies (Amersham, Little Chalfont, UK) for 30 minutes at 1:200 dilution and streptavidin-Texas red (Amersham) for 30 minutes at 1:100 dilution.
M-GP Ribonucleic Probes
A 232-bp stretch of the 3' end of the M-GP cDNA (bp 3243 to 3475) in which the divergence among muscle- and non-muscle-specific isoforms was maximal was subcloned in the SmaI/ApaI site of Bluescript KS+. Orientation was checked by direct sequencing. RNA probes were synthesized using [35S]UTP (1300 Ci/mmol) using T3 (antisense) and T4 (sense) polymerase following the supplier's instructions.
In Situ Hybridization (ISH)
ISH was performed as described14 on 10-µm cryostat muscle sections. Transverse sections were fixed 30 minutes at room temperature in 4% paraformaldehyde, treated for 7.5 minutes with proteinase K (20 µg/ml) in Tris/HCl (50 mmol/L), pH 7.2, and EDTA (5 mmol/L), acetylated in 0.5% acetic anhydride in 0.1 mol/L triethanolamine, pH 8.0, for 10 minutes, and dehydrated. The probe (108 cpm/ml) was applied directly to dried sections in hybridization buffer (50% deionized formamide, 0.3 mol/L NaCl, 20 mmol/L Tris/HCl, pH 7.4, 5 mmol/L EDTA, 10 mmol/L NaPO4, pH 8.0, 10% dextran sulfate, 1X Denhardt's, 50 µg/ml yeast RNA). Hybridization was carried out for 16 hours at 52°C in a humid chamber. The slides were washed 30 minutes at 42°C in 5X SSC (1X SSC contains 0.15 mol/L NaCl, 0.015 mol/L sodium citrate), 10 mmol/L dithiothreitol (DTT); 20 minutes at 65°C in 50% formamide, 2X SSC, 10 mmol/L DTT; 30 minutes at 37°C in 0.5 mol/L NaCl, 0.05 mmol/L NaP04, pH 7.0, 20 µg/ml RNAse; 15 minutes at 37°C in 1X SSC; and 15 minutes at 37°C in 0.1X SSC. The slices were rapidly dehydrated, processed for autoradiography using Kodak NBT-2 emulsion, exposed for 10 days at 4°C, and developed according to the manufacturer's directions.
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Results |
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TopAbstractIntroductionMaterials and MethodsResultsDiscussionReferences |
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There was complete overlapping between fibers positive with HC for
phosphorylase and fibers positive with IHC for fetal myosin (Figure 1)
, confirming their regenerating status.
In one case (patient 3), however, we observed four faintly stained,
normal-sized fibers, which were IHC fetal myosin negative.
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, indicating in
these patients localized re-expression of the defective enzyme.
In situ hybridization with the M-GP riboprobe showed diffuse
subsarcolemmal positivity in control, scattered patchy positivity in
the patients with IHC M-GP-positive fibers, and no specific signal in
the patients with regenerating IHC M-GP-negative fibers (Figure 2
; Table 2
). M-GP mRNA accumulation therefore
positively correlates with M-GP expression.
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Discussion |
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TopAbstractIntroductionMaterials and MethodsResultsDiscussionReferences |
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The relatively low frequency of patients with HC-positive fibers in our series is in agreement with previous reports,6,9 in which only single or very few patients were presented. Recent myonecrosis, as suggested in our cases by high serum creatine kinase and reported myoglobinuria, correlates with the presence of regenerating phosphorylase-positive fibers.
Phosphorylase expression is mostly restricted to regenerating fibers, as was shown by morphological criteria in previous studies.8,9 However, few normal-sized fibers that were fetal myosin negative showed faint phosphorylase positivity in one patient. In those fibers, the regeneration process could be just completed, and consequently, the expression of fetal myosin and possibly M-GP could have been already shut down.
The results of IHC and ISH indicate that regenerating fibers in patients in whom at least one allele of the PYGM gene does not carry an identified mutation express M-GP. This finding is in agreement with previous in vitro studies showing re-expression of the defective enzyme in aneural12 and innervated13 cultured muscle of patients with McArdle's disease. In aneural and innervated cultured muscle from myophosphorylase-deficient patients, the deleterious mutations identified in the adult muscle were retained; therefore, we can exclude gene reversion as the explanation for the observed phenomenon. The similarity between in vitro and in vivo behavior of regenerating muscle cells from myophosphorylase-deficient patients suggests that the same conclusion could be applied to our in vivo observations.
The present work provides the first evidence that re-expression of M-GP can occur also in vivo, and correlates this finding with the molecular basis of the defect. Patients with mutation identified in both alleles, and with absent or grossly reduced M-GP mRNA, did not express M-GP, despite the presence of regenerating fibers (almost 7% in patient 4).
IHC and ISH could identify in patients 1 and 2 M-GP as the GP isoform expressed. The same was not possible for the other patients. From what is known of GP gene regulation we can hypothesize that the observed GP activity in IHC M-GP-negative fibers is due to a fetal isoform. In vivo regenerating rat muscle grafts do not express non-M-GP, in contrast to primary rat skeletal muscle explants in vitro.15 In vivo regenerating muscle from non-myophosphorylase-deficient patients (eg, Duchenne muscular dystrophy patients) shows intense staining for M-GP IHC in fetal-myosin-positive fibers (data not shown), suggesting that M-GP is the prevalent isoform expressed in regenerating human muscle in vivo.
The mechanism leading to the activation of M-GP expression in regenerating fibers and to its suppression in mature fibers is not known. Possible explanations are: 1) activation in regenerating cells of a PYGM pseudogene normally silent, 2) mRNA editing with correction, in regenerating fibers, of deleterious mutations, as described for transcripts with GAGAG motifs in neurons,16 and 3) use of an alternative promoter or enhancer in poorly differentiated muscle fibers, leading to reversion in the dividing cells of a transcriptional or translational block preventing expression in mature myotubes.
The striking sequence homology among the genes coding for the three GP
isozymes suggests that they have evolved through duplication and
translocation events,17
although no
PYGM-related sequences have been spotted in mapping studies
covering the whole genome.18
Several GAGAG islands are
present in the second half of the coding sequence of the
PYGM gene, although none is the site of a known
mutation,4,5
and none were found to be mutated in our
patients after direct sequencing. There are conflicting reports on the
presence in rat and human muscle of alternative spliced M-GP
transcripts15,19
; alternative splicing and transcript
processing is a common feature in muscle-specific isoforms of
glycolytic enzymes such as aldolase A, phosphofructokinase, and
phosphorylase kinase-
.20-22
This last hypothesis would
imply that in some patients with McArdle's disease the defect is due
to a reversible impairment of PYGM transcription or
translation. If confirmed, this mechanism could be exploited for a
novel form of gene therapy, which would take advantage of the
self-healing potential of the diseased gene itself.
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Acknowledgements |
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Footnotes |
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Supported by Telethon of Italy grant 855 to A. Martinuzzi.
Accepted for publication March 6, 1999.
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References |
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TopAbstractIntroductionMaterials and MethodsResultsDiscussionReferences |
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-skeletal actins are early markers for myogenesis in the mouse embryo. Development 1988, 104:155-164[Abstract]
M and L subunits is a hotspot of differential mRNA processing and molecular evolution. J Biol Chem 1993, 268:23208-23214
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