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Deletion of Dystrophin In-Frame Exon 5 Leads to a Severe Phenotype: Guidance for Exon Skipping Strategies

  • Zhi Yon Charles Toh,

    Affiliations: Western Australian Neuroscience Research Institute, Perth, Australia, University of Western Australia, Perth, Australia

  • May Thandar Aung-Htut,

    Affiliation: Centre for Comparative Genomics, Murdoch University, Perth, Australia

  • Gavin Pinniger,

    Affiliation: School of Anatomy, Physiology and Human Biology, University of Western Australia, Perth, Australia

  • Abbie M. Adams,

    Affiliations: Western Australian Neuroscience Research Institute, Perth, Australia, University of Western Australia, Perth, Australia, Centre for Comparative Genomics, Murdoch University, Perth, Australia

  • Sudarsan Krishnaswarmy,

    Affiliation: University of Western Australia, Perth, Australia

  • Brenda L. Wong,

    Affiliation: Department of Paediatrics, Department of Neurology, Cincinnati Children’s Hospital Medical Center, Cincinnati, Ohio, United States of America

  • Sue Fletcher,

    Affiliations: Western Australian Neuroscience Research Institute, Perth, Australia, University of Western Australia, Perth, Australia, Centre for Comparative Genomics, Murdoch University, Perth, Australia

  • Steve D. Wilton

    swilton@ccg.murdoch.edu.au

    Affiliations: Western Australian Neuroscience Research Institute, Perth, Australia, University of Western Australia, Perth, Australia, Centre for Comparative Genomics, Murdoch University, Perth, Australia

Deletion of Dystrophin In-Frame Exon 5 Leads to a Severe Phenotype: Guidance for Exon Skipping Strategies

  • Zhi Yon Charles Toh, 
  • May Thandar Aung-Htut, 
  • Gavin Pinniger, 
  • Abbie M. Adams, 
  • Sudarsan Krishnaswarmy, 
  • Brenda L. Wong, 
  • Sue Fletcher, 
  • Steve D. Wilton
PLOS
x

Abstract

Duchenne and Becker muscular dystrophy severity depends upon the nature and location of the DMD gene lesion and generally correlates with the dystrophin open reading frame. However, there are striking exceptions where an in-frame genomic deletion leads to severe pathology or protein-truncating mutations (nonsense or frame-shifting indels) manifest as mild disease. Exceptions to the dystrophin reading frame rule are usually resolved after molecular diagnosis on muscle RNA. We report a moderate/severe Becker muscular dystrophy patient with an in-frame genomic deletion of DMD exon 5. This mutation has been reported by others as resulting in Duchenne or Intermediate muscular dystrophy, and the loss of this in-frame exon in one patient led to multiple splicing events, including omission of exon 6, that disrupts the open reading frame and is consistent with a severe phenotype. The patient described has a deletion of dystrophin exon 5 that does not compromise recognition of exon 6, and although the deletion does not disrupt the reading frame, his clinical presentation is more severe than would be expected for classical Becker muscular dystrophy. We suggest that the dystrophin isoform lacking the actin-binding sequence encoded by exon 5 is compromised, reflected by the phenotype resulting from induction of this dystrophin isoform in mouse muscle in vivo. Hence, exon skipping to address DMD-causing mutations within DMD exon 5 may not yield an isoform that confers marked clinical benefit. Additional studies will be required to determine whether multi-exon skipping strategies could yield more functional dystrophin isoforms, since some BMD patients with larger in-frame deletions in this region have been reported with mild phenotypes.

Introduction

Duchenne and Becker muscular dystrophy (DMD and BMD) are X-linked recessive muscle-wasting diseases arising from mutations in the massive dystrophin gene (DMD) that leads to degeneration of muscle. DMD is the most prevalent and severe form of childhood muscle wasting with a cited incidence of 1 in 3,500 live-male births, whereas BMD is a clinically milder form of the disease with slower disease progression [1, 2]. BMD mutations may present with a spectrum of phenotypes, depending upon the nature and location of the DMD lesion, as BMD mutations do not usually disrupt the reading frame, thereby allowing production of an internally shortened but functional dystrophin. BMD patients remain ambulant until at least 16 years of age but, in some mild or asymptomatic cases, may only be diagnosed by accident or late in life [3, 4]. Conversely, intermediate muscular dystrophy has been used to describe “mildly affected” DMD patients (those whose genetic structure would predict prematurely truncated dystrophin and loss of ambulation by 12 years of age) or “severely affected” BMD cases (those who would be expected to produce some functional dystrophin and therefore remain ambulant after 16 years of age). In 1989, Dubowitz stated that ‘Intermediate DMD patients are defined as patients with a dystrophinopathy with onset of symptoms (of motor difficulties) by about 5 years of age, similar to the classical DMD patients but with a slower rate of disease progression, with loss of ambulation between 13 and 16 years of age.” [5]. Children of the same age vary widely in clinical presentation, and patients that appear to have a milder dystrophinopathy have also been termed "outliers." [6]

In over 90% of DMD cases, correlation between the disease phenotype and the genotype is obvious. However, there are exceptions to the reading frame rule, where an in-frame deletion may result in a severe phenotype, or conversely, some out-of-frame gene rearrangements or nonsense mutations present with relatively mild symptoms, consistent with a diagnosis of BMD [7, 8].

The pathogenic basis of particular in-frame dystrophin deletions reflects the number of exons lost, where deletions of 34 or more exons are usually associated with severe pathology [9], or secondary effects on pre-mRNA processing. Other in-frame deletions may have severe consequences, due to the loss of a crucial functional domain within dystrophin, eg the actin or beta-dystroglycan binding regions. Mutations in the 5’ region of the DMD gene frequently manifest as exceptions to the reading frame rule [10], and various mechanisms have been proposed to impact on the consequences of these mutations, including re-initiation of translation [11] and splicing perturbations [12].

Gualandi and colleagues reported that the loss of DMD exon 5 compromised pre-mRNA processing and selection of exon 6, consistent with a severe dystrophic phenotype [13]. Here, we describe another patient carrying a genomic deletion of DMD exon 5 who manifests with moderate/severe a phenotype, despite detectable dystrophin as demonstrated by immunofluorescence. We show that the DMD transcript from this patient is missing only exon 5, and the genomic loss of this exon does not obviously alter the recognition and splicing of exon 6.

Only a small number of patients missing DMD exon 5 have been described, therefore opportunities to explore phenotypic variation and perhaps understand the basis for more severe than expected disease are limited. In order to further evaluate a dystrophin isoform lacking the actin binding domain encoded by exon 5, we induced a transient dystrophinopathy model by skipping Dmd exon 5 in wild-type mice. Analysis of dystrophin, components of the dystrophin-associated glycoprotein complex, muscle architecture and isolated muscle function, reveals moderate dystrophic changes in diaphragm, intermediate between mdx and wild-type phenotypes. Excision of Dmd exon 5 greatly reduced dystrophin expression in mouse diaphragm and compromised muscle function.

Targeted exon skipping is emerging as a promising therapy to treat DMD, and at this time, the focus has been on exclusion of exons that flank frame shifting-deletions in order to re-frame the transcript. Similarly, removing an in-frame exon carrying an intra-exonic protein truncating mutation [14, 15], or a duplicated in-frame exon [16], would allow synthesis of functional dystrophin isoforms. The rationale is that re-framing the DMD transcript will produce a BMD-like isoform and reduce disease severity. Examination of BMD phenotype:genotype correlations can indicate DMD transcript structures most likely to generate functional dystrophin isoforms and therefore inform exon skipping strategies [17, 18]. We propose that removal of DMD exon 5 alone is unlikely to provide significant clinical benefit, and alternative exon skipping strategies or treatments should be considered for dystrophinopathy patients with mutations within exon 5, or those with duplications of exon 5.

Materials and Methods

Patient clinical summary

The patient showed normal development until 2nd grade. He had slightly enlarged calves and also presented with an unusual muscle atrophy involving the paraspinal muscles and quadriceps. DNA testing revealed a de novo in-frame deletion of dystrophin exon 5. A muscle biopsy was performed and the tissue analysed by a diagnostic laboratory for the expression of dystrophin and associated proteins. DNA testing revealed a de novo in-frame deletion of dystrophin exon 5.

Cell culture and MyoD mediated myogenic conversion of fibroblasts

De-identified patient and normal human skin fibroblasts were obtained after informed consent (University of Western Australia Human Research Ethics Committee approval RA/4/1/2295). The fibroblasts were cultured in DMEM (Life Technologies, Melbourne, Australia) supplemented with 20% foetal calf serum (FCS) (Serana, Bunbury Australia), 1% GlutaMax-I (Gibco Life Technologies, Melbourne, Australia), 10 U/mL penicillin (Invitrogen), 10 mg/ML streptomycin (Life Technologies) and 250 ng/mL amphotericin B (Sigma-Aldrich, Sydney, Australia). Fibroblasts were transformed into the myogenic lineage by transfection with an adenoviral construct expressing MyoD (Ad5.f5.0.AdApt.MyoD) at a multiplicity of infection of 200 (The Native Antigen Company, Oxford, UK) [19]. These cells were then differentiated in low serum media (5% HS-DMEM) for 3–4 days as described by Harding et al [20]. The 24 well plates were pre-coated with 50 μg/mL poly D-lysine (Sigma) and 100 μg/mL Matrigel (VWR, Brisbane, Australia) for 1 hour each, respectively. The patient and normal fibroblasts were seeded at 3 x 104 cells/well in the pre-prepared 24 well plates.

Splice switching antisense oligomers

An antisense oligomer, composed of 2’-O-methyl modified bases on a phosphorothioate backbone, was synthesized on an Expedite 8909 Nucleic Acid synthesizer using reagents from Azco Biotech (Ca, USA). Designed to induce DMD exon 6 skipping, the AO (5’-UAC GAG UUG AUU GUC GGA CCC AG-3’) annealed to bases 69–91 in exon 6, and had been shown to induce specific exon 6 skipping [21].

A panel of splice switching AOs was developed to excise mouse dystrophin exon 5, targeting similar coordinates used to excise human dystrophin exons 5 (Table 1). The 2’-O-methyl modified oligomer 5’ UAU GAU UUC CAU CCA CUA UGU CAG UGC UUC 3’ (Table 1, underlined) annealing to bases 20–49 in mouse dystrophin exon 5, was identified to efficiently remove the target exon 5 in vitro. This sequence was synthesized as a phosphorodiamidate morpholino oligomer coupled to the cell penetrating peptide k [22] (PPMO) for in vivo experiments.

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Table 1. Sequence of splice switching 2’-O-methyl modified AOs to induce skipping of mouse Dmd exon 5.

The underlined sequence (M5A(+20+49) was synthesised as a phosphorodiamidate morpholino oligomer coupled to the cell penetrating peptide k [22].

http://dx.doi.org/10.1371/journal.pone.0145620.t001

Transfection of myogenic cells, RNA extraction and RT-PCR

The myogenic cells were transfected, 3 days after the initiation of myogenic differentiation, with the 23mer AO complexed with Lipofectamine 2000® (1:1 w/w) in Opti-MEM media (Gibco) as per the manufacturer’s instructions. AO concentrations of 2.5, 5, 10, 25, 50 and 100 nM were used and the cells were then incubated at 37°C for 3 days before RNA extraction.

The total RNA was extracted using Trizol® (Life Technologies) according to the manufacturer’s instructions and the RNA pellet resuspended in 30 μL of sterile water (Baxter Healthcare, Australia). Approximately 100 ng of total RNA was used as template for the initial reverse transcriptase PCR reaction (55°C for 30 minutes), using Superscript® III One-step RT-PCR (35 cycles) of 94°C, 55°C and 72°C for 0.5, 1 and 2 minutes respectively to amplify DMD exons 1 to 10. A 1 μL aliquot from the primary reaction was then used as template for nested PCR using AmpliTaq Gold (Applied Biosystems, Melbourne, Australia) amplifying across DMD exons 1 to 10 with the inner primer set for 30 cycles. Obtained from (Geneworks, Thebarton, Australia), the outer and inner primer sets spanning DMD exons 1–10 described by Roberts et al. [23] were used for the amplifications. Forced myogenic conversion of the fibroblasts is not an efficient process and whilst adequate for RNA studies, the degree of myogenic differentiation of the cultures makes detailed protein studies challenging.

Deletion breakpoint mapping in DMD introns 4 and 5

Normal and patient fibroblasts were propagated, trypsinised and genomic DNA harvested using the Pure Link Genomic DNA kits (Life Technologies). PCR primers were designed to generate amplicons of approximately 3kb across introns 4 (~21.4 kb) and 5 (~6.6kb) to localize the breakpoints in the flanking introns. Long range PCR was performed on ~60 ng of genomic DNA using TaKaRa LA Taq polymerase (TAKARA Biotechnology (Dalian) Co., LTD, Japan) with LA and GC rich amplification buffer according to the manufacturer’s instructions. Primer sequences are shown in Table 2. The PCR amplicons from the normal and exon 5-deleted dystrophin genes were fractionated on 2% agarose gels and the images captured on a Fusion FX gel documentation system (Vilber Lourmat, Marne-la-Vallée, France). The approximate locations of breakpoints in introns 4 and 5 were identified by comparison of amplification product sizes, generated from normal and patient DNA. Additional primers (Table 3) were designed to sequence the intron 4:5 junction using BigDye sequencing chemistry, with analysis by the Australian Genome Research Facility, Perth, Australia.

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Table 2. Primers used for long range PCR to amplify DMD exon 4 to exon 6 from genomic DNA to identify the patient’s deletion breakpoint.

The predicted amplicon size is estimated according to the reference sequence NG_012232.1.

http://dx.doi.org/10.1371/journal.pone.0145620.t002

Agarose gel electrophoresis

PCR products were resolved on 2% agarose gels in 1xTAE buffer as indicated, and the images captured using the Vilber Lourmat Fusion FX gel documentation system.

Transient induction of a ‘Dmd exon 5 deletion’ mouse model

All experiments performed on animals were approved by the University of Western Australia Animal Experimentation Committee (approval number RA4/100/702) and carried out in strict accordance with the recommendations in the National Health and Medical Research Council Australian code for the care and use of animals for scientific purposes 8th edition (2013).

A phosphorodiamidate morpholino oligomer conjugated to a cell penetrating peptide (5-PPMOk) [22] targeting dystrophin exon 5; M5A(+20+49), (5’ UAU GAU UUC CAU CCA CUA UGU CAG UGC UUC 3’) was injected via the intraperitoneal route into C57BL/10ScSn (C57BL/10) mice (n = 5) to induce a dystrophin isoform missing the amino acids encoded by exon 5. The 5-PPMOk peptide conjugate, supplied by AVI Biopharma Inc. Bothell, Oregon, (now Sarepta Therapeutics) was re-suspended in sterile normal saline and pre-warmed to 37°C before injection [24, 25]. Over an 8-week period, beginning at 3–4 days of age, the C57BL/10 mice were given twice weekly intraperitoneal (IP) injections of 5-PPMOk at 20 mg/kg. Mice assigned to the control groups, C57BL/10 (n = 5) and C57BL/10ScSnDmd mdx (mdx) mice (n = 4), received sham treatment containing an equal volume of normal saline. The mice were anaesthetised (IP, sodium pentobarbitone 40mg/kg) a week after completing the treatment regimen, sampled for physiological testing and then killed via cervical dislocation before further analysis. Diaphragm muscles were snap-frozen in liquid nitrogen-cooled isopentane and stored at -80°C for molecular, histological and immunofluorescence studies.

End point analysis and tissue sampling was performed under sodium pentobarbital anesthesia, and all efforts were made to minimize suffering.

Western blot analysis

Approximately 30 mg of tissue was homogenized in 600 μl of 125 mM Tris-HCl (pH 6.8), 15% SDS (w:v), 10% glycerol (v:v), 0.5 mM phenylmethylsulfonyl fluoride and 1 μl protease inhibitors cocktail (Sigma Aldrich, Sydney, Australia) per 9μg of tissue. Western blots were carried out essentially as described by Cooper [26]. Briefly, 5 μl of diluted aliquots of protein extract (7.5μg total protein) were separated on NuPAGE 4–12% Bis-Tris gels (Life Technologies, Mulgrave, Australia) and stained with 0.2% Coomassie blue and destained with 0.7% acetic acid. Gel densitometry was used to estimate relative myosin expression to ensure equal protein loading on subsequent gels for western blotting.

Samples (5 μl containing 7.5μg total protein per lane) were loaded onto a 3% - 10% gradient SDS–polyacrylamide electrophoresis (PAGE) gel with a 3% stacking gel and run at 30 mA for 2h, with C57BL/10ScSn and mdx muscle samples used as positive and negative controls respectively. Fractionated proteins were then electro-blotted onto a nitrocellulose membrane (Amersham Pharmacia Biotech, Sydney, Australia) overnight at 290 mA in transfer buffer (25 mM Tris-HCl, pH 8.3, 192mM glycine, 20% methanol, 0.075% SDS). The transfer was performed with cooling water circulating at 18°C. Dystrophin and beta-dystroglycan were detected by probing the membrane with NCL-DYS2 monoclonal anti-dystrophin (1:100 Novocastra Laboratories, Newcastle-Upon-Tyne, UK) and beta-dystroglycan primary monoclonal antibody (1:4000 Santa Cruz Biotechnology), respectively. The signals were developed using WesternBreeze® Chemiluminescent protein detection Kit (Life Technologies). Immunodetection was performed according to the manufacture’s protocol. Images were obtained using a Vilber Lourmat Fusion FX Gel document system and band intensities determined using the Bio-1D software (Vilber Lourmat). The band intensities obtained from the treatment groups were analysed and compared to the positive and negative controls.

Histology and immunostaining on muscle

Diaphragm samples from sham treated mdx and C57BL/10 control mice, and the 5-PPMOk treated C57BL/10ScSn were snap frozen in liquid nitrogen-cooled isopentane. Immunochemistry was performed on unfixed serial cryosections (7μm thick) from all the mice, stained with either monoclonal or polyclonal antibodies diluted in PBST containing 10% normal goat serum. Collagen staining with picro-sirius red is based on the method described by Puchtler, 1973 [27].

The following antibodies were used: monoclonal antibodies, NCL-DYS2 (Novocastra), against dystrophin carboxy terminal domain, (NCL-MHCd) (Novocastra) against developmental myosin heavy chain, and the polyclonal rabbit antibodies, AB 782259 (1:300, Santa Cruz) against anti-beta-dystroglycan and AB 310722, anti-neuronal nitric oxide synthase (nNOS) (1:1000, Millipore Upstate). Monoclonal antibody detection was performed using the Zenon Alexa fluor 488 labelling kit (Life Technologies) according to the manufacturer’s recommendation, without fixation, until after immunofluorescence staining was completed. Both NCL-DYS2 and NCL-MHCd primary antibodies were used at 1:10 dilution with a molar ratio of 4.5:1. Mouse IgG1 anti Aspergillus niger cytochrome oxidase (DakoCytomation code X093101) (AB 577451) was used as an isotype negative control antibody (data not shown).

Goat-anti-rabbit IgG Alexa Fluor 594 (1:400) (Molecular Probes) was used as secondary antibody to detect the rabbit polyclonal antibodies against beta-dystroglycan (1:300) and neuronal nitric oxide synthase (1:1000). Cryosections were incubated at room temperature for 1.5 hours before washing in PBST and incubation with the secondary antibody at room temperature for an hour, washed in PBST and mounted under a coverslip in anti-fade aqueous mountant after washing in PBS. As above, negative controls were prepared by substituting the primary antiserum with PBST containing rabbit immunoglobulin fraction (DakoCytomation X0936), diluted to match final immunoglobulin concentration on duplicate serial sections. An Olympus IX-70 inverted microscope was used to examine the sections. Images were captured on an Olympus DP70 digital camera (Olympus Australia Pty Ltd, Sydney, Australia) and photographed at 10x and 20x magnification. Each set of serial sections were photographed in batches and exposed under the same settings to allow valid comparison.

Results

Clinical details

Clinical summary at presentation, age 9 ½ years.

The patient, aged 9-years, 6-months was noted at around 5 years of age to have enlarged calves, associated with a slow run, difficulty climbing stairs and using a Gower’s manoeuvre to rise from the floor. Around 6 years of age concerns regarding his inability to keep up with his peers were communicated to his parents and he was referred for further investigation. His CK was elevated (19,000 U/Dl), genetic testing showed a deletion of DMD exon 5 and he was diagnosed with Becker’s muscular dystrophy at the age of 8-years. He had a baseline cardiac evaluation with normal echocardiogram and pulmonary evaluation.

Although the patient has an in-frame deletion of DMD exon 5 that predicts a Becker’s muscular dystrophy diagnosis, his signs and symptoms of prominent pelvic girdle weakness (full timed Gower’s in 3.2 seconds); plantigrade stance; run with increased upper extremity swings and a waddle; unable to extend his hips fully against gravity for the table top manoeuvre; rising from a chair by turning his body, followed by hand push off the chair and waddling gait with lordosis with a heel-toe progression warranted further investigation. The diagnostic laboratory undertook analysis of limb girdle muscular dystrophy (LGMD) genes and found no sequence variants for CAPN3; the autosomal recessive LGMD genes, FKRP, DYSF, TCAP, TRIM32, TTN, SGCA, SGCB, SGCE and SGCG. A heterozygous change was found in ANO5 exon 15 (undocumented variant of uncertain clinical significance).

The patient phenotype was considered to be more consistent with a severe Becker muscular dystrophy and the diagnosis was revised accordingly at age nine and a half years. In view of the findings of the more severe phenotype, steroid therapy was recommended.

The patient profile since diagnosis of his DMD exon 5 deletion is summarised in Table 4.

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Table 4. DMD exon 5 deletion patient data obtained at diagnosis and follow up visits.

http://dx.doi.org/10.1371/journal.pone.0145620.t004

Histology and dystrophin analysis.

A muscle biopsy from the patient was analysed and indicated dystrophic changes, including fibre size variation. Immunofluorescence using NCL-DYS 1 (dystrophin rod domain) and DYS-2 (carboxy-terminus) showed reduced intensity, while that for NCL-DYS 3 (amino-terminus) was almost undetectable (Fig 1a). Very low levels of dystrophin were detected by western blot, less than 10% relative to the level in normal healthy muscle (Fig 1b). Spectrin immunostaining of the sarcolemma (Fig 1a) shows muscle fibres of irregular size, with some very large diameter fibres and many mononuclear cells in the patient section, while normal muscle section shows muscle fibres of very regular size and shape, typical of healthy muscle. The diagnostic laboratory reported that the staining intensity for alpha-sarcoglycan, merosin, alpha-dystroglycan, collagen VI, dysferlin, caveolin, lamin A/C and emerin appeared normal (data not shown).

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Fig 1. Dystrophin and spectrin expression in patient and normal muscle.

(a) Dystrophin immunofluorescence using Novocastra Laboratories antibodies, NCL DYS-1 (upper row, specific for the rod domain) NCL DYS-2 (upper middle row, specific for the carboxy-terminus) and NCL-DYS 3 (lower middle row, specific for the amino-terminus) and spectrin (lower row) on patient (left panel) and normal human muscle (right panel) cryosections. Nuclei are stained with DAPI. (Bar = 100μm). (b) Western blot using NCL-DYS 1 to detect dystrophin in normal and patient muscle sample. (c) Sequencing of the DMD RT-PCR exon 1–10 amplicon from the exon 5-deletion patient showing the junction of DMD exons 4 and 6.

http://dx.doi.org/10.1371/journal.pone.0145620.g001

Confirmation of DMD exon 5 deletion and breakpoint mapping in patient cells.

RT-PCR across dystrophin exons 1–10 on total RNA extracted from patient myogenic cells indicated that the patient DMD transcript is missing only exon 5. Sequencing of the dystrophin RT-PCR product confirmed the loss of exon 5, with precise splicing of exon 4 to exon 6 (Fig 1c).

The deletion breakpoints in introns 4 and 5 were identified by generating 3 kb amplicons across the introns and identifying sets of reactions that failed when patient DNA was used as the template. DNA from a normal individual was included in the analysis for comparison. Amplification with primer combinations HIn4 F4-R5 to HIn5 F1-R2 (Table 3) failed to generate a signal from the patient DNA, whereas the normal DNA generated products of the expected size, indicating that the intron 4 breakpoint was between 6.3 to 9.3kb upstream of exon 5, while the intron 5 breakpoint was more than 3.7 kb downstream of that exon Subsequent amplification of patient DNA with HIn4 F4 and the reverse primer targeted to exon 6 (HEx6ROuter) generated an amplicon of about 5.4 kb, while long range PCR of the normal dystrophin gene using these primers generated a product in excess of 16 kb (Fig 2a). Although efficient amplification of the patient-specific amplicon was achieved with both the TAKARA LA and GC buffers, use of the later buffer improved amplification of the larger dystrophin gene product. The 5.4 kb patient-derived amplicon was used as a DNA sequencing template with primers shown in Table 4. Comparison to the reference sequence NG_012232.1 showed that the entire genomic deletion in this patient was 10,864 bp, with two ‘T’s common to introns 4 and 5 at the breakpoint junction (Fig 2b). The position of the 10.8kb genomic deletion is shown, relative to two other exon 5 deletions that were reported to lead to DMD [13] (Fig 2c).

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Fig 2. DMD deletion breakpoint characterization.

(a) Amplification of patient and normal DNA with HIn4 F4 and the reverse primer targeted to exon 6 (HEx6ROuter), across the predicted DMD breakpoint location. A 1 kb DNA ladder was used as a marker to estimate amplicon sizes. (b) Alignment of nucleotide sequences from introns 4 and 5 showing the precise deletion breakpoint in the DMD exon 5 deletion patient. The size of the deletion is estimated, relative to the reference sequence NG_012232.1. (c) Representation of three DMD exon 5 deletions, showing deletion breakpoints. The patient described in the current study has the largest genomic deletion, 10.8 kb and the breakpoint downstream of exon 5 is located between the breakpoints in previously reported individuals, with 3.4 and 7.78 kb deletions [13].

http://dx.doi.org/10.1371/journal.pone.0145620.g002

The predominant amplicon after RT-PCR of patient muscle RNA across DMD exons 1–10 was missing only exon 5, and there was no evidence of any DMD transcripts missing exon 6 in the patient cells (Fig 3). Normal and patient fibroblasts, forced into the myogenic lineage after transfection with the adenovirus construct expressing MyoD, were transfected with an AO designed to excise DMD exon 6 to ascertain if recognition of the exon by the splicing machinery was compromised by the patient deletion. As shown in Fig 3, the efficiency of exon 6 skipping after transfection was similar in both cell strains.

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Fig 3. Antisense oligomer induced skipping of DMD exon 6 in patient and normal myogenic cells.

Normal and DMD exon 5 deletion patient fibroblasts, forced into the myogenic lineage by transfection with the MyoD expressing adenovirus, were transfected with an AO designed to excise DMD exon 6. Dystrophin exons 1–10 were amplified from RNA prepared from control and oligomer (H6A(+69+91))-treated normal and patient RNA samples by nested RT-PCR. The full-length amplicon is 1157 bp, the amplicon derived by RT-PCR of patient RNA, missing exon 5, is 1064 bp. The induced amplicons missing exon 6 (normal) are 984 bp and 891 (patient). The RT-PCR generating the amplicons from the 100 nM transfection of patient cells was not efficient due to low RNA yields, but both full-length and skipped products are evident.

http://dx.doi.org/10.1371/journal.pone.0145620.g003

Induction of an exon 5 deletion dystrophin isoform in wild type mice

An AO (2’-O-methyl modified bases on a phosphorothioate backbone), designed to anneal to mouse dystrophin exon 5 bases 20 to 49, was identified in a panel of overlapping oligomers as efficiently skipping this exon after in vitro transfection in primary mouse myogenic cells (data not shown). This sequence was synthesized as a PMO conjugated to a cell penetrating peptide for in vivo studies in wild type mice, with the aim to generate a transient Dmd exon 5 deletion in vivo model. A dystrophic phenotype, induced by skipping of Dmd exon 5 was evident in the diaphragms, although the dystrophic pathology was quite as marked as for the sham treated mdx mice. Immunostaining using the antibody, NCL-DYS2 to detect the carboxy terminus of dystrophin reflected patchy and greatly reduced staining in the diaphragm of 5-PPMOk treated C57BL/10 mice, compared to sham treated control C57BL/10 mice (Fig 4a, top row), and western blotting indicated that dystrophin levels were reduced to less than 10% of wild-type levels (data not shown). The reduced dystrophin staining was associated with reduced β-dystroglycan and nNOS expression in diaphragm of treated mice (Fig 4a, left panel), compared to levels in sham-treated control C57BL/10 mice (Fig 4a, central panel), whereas expression in mdx mouse diaphragm is very low. A modest degree of muscle regeneration in the diaphragm from 5-PPMOk- treated mice is indicated by the presence of developmental myosin heavy chain (dMHC) in muscle fibres (Fig 4a). Neither muscle regeneration nor fibrosis is evident in diaphragm from sham-treated C57BL10 mice, whereas abundant dMHC staining, fibrosis revealed by Picro-sirius Red staining and central nucleation is apparent in the 5-PPMOk treated C57BL10 and in the sham treated mdx mice, and is consistent with a moderate dystrophic muscle phenotype.

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Fig 4. AO-mediated induction of Dmd exon 5 deletion dystrophin isoform in wild type mice.

(a) Cryosections from diaphragm of 5-PPMOk and sham treated C57BL10 mice, and sham treated mdx mice were stained to reveal dystrophin carboxy terminus (NCL DYS-2), β-dystroglycan (β-Dys), neuronal nitric oxide synthase (nNOS) and developmental myosin heavy chain (NCL-MHCd). Picro sirius red was used to stain collagen, as an indicator of fibrosis, and muscle architecture is revealed by hematoxylin and eosin (H&E) staining. (Bar = 200μm) (b) RT-PCR across Dmd exons 1–7 on RNA extracted from diaphragm of 5-PPMOk (n = 5) and sham treated C57BL10 mice, and sham treated mdx mice. The percentage of induced amplicon (exon 5 deleted) as a percentage of the total transcript product is indicated. (c) Western blot on protein extracts (7.5μg total protein per lane) from diaphragm of 5-PPMOk (n = 5) and sham treated C57BL10 mice, and sham treated mdx mice. Dystrophin was detected using NCL-Dys2 (Novocastra Laboratories) and Western Breeze (Life Technologies/Thermo Fisher Scientific). The percentage of dystrophin, relative to the wild type control, was assessed by densitometry after normalization to myosin heavy chain expression.

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RT-PCR across Dmd exons 1–7 on RNA extracted from diaphragm of 5-PPMOk (n = 5) and sham treated C57BL10 mice, and sham treated mdx mice showed efficient skipping of exon 5, varying from 68–96% of the total Dmd transcript product, as determined by densitometry. (Fig 4b). Western blot analysis on protein extracts from diaphragm of 5-PPMOk treated C57BL10 mice showed greatly reduced dystrophin expression, relative to the sham-treated wild type control (Fig 4c). The percentage of dystrophin, relative to the wild type control, was assessed by densitometry after normalization to myosin heavy chain expression and correlated with analysis of the Dmd transcript shown in Fig 4b.

Discussion

The dystrophin reading frame rule holds true for over 90% of DMD and BMD deletion cases, [28] [29] determined by DNA molecular diagnoses [30], [31]. Detailed examination of causative mutations in cases that are ‘reading frame exceptions’ have revealed several mechanisms that account for a discrepancy between DMD genotype and clinical phenotype. In-frame exonic deletions may result in a severe phenotype if the deletion involves more than 25 exons in [32]) or results in the loss of a crucial functional motif, eg that encoding the beta-dystroglycan binding domain or the first 20 exons [32]. Protein truncating mutations in the 5’ region can lead to re-initiation of translation in exons 5, 6 or 8 and synthesis of a functional dystrophin [11] [33]. Secondary RNA processing events, not apparent by analysis of the DNA, may influence exon selection and processing of the transcript. Nonsense mutations in some of the in-frame exons encoding the dystrophin rod domain manifest with a milder than expected phenotype due to natural skipping of the mutated and splice compromised exon [34] [35].

Single exon deletions in the DMD N-terminal region are relatively uncommon, with 8 entries in the Leiden database (http://www.dmd.nl) describing deletion of only exon 5. Although clinical details on these patients are minimal, three were listed as having DMD and the remaining five were recorded as having Intermediate MD. Interestingly, there were seven entries for a duplication of DMD exon 5, with five records reporting a BMD phenotype and one entry each listed as having DMD or Intermediate MD.

Detailed DMD transcript studies by Gualandi and colleagues reported that exon 6, present in the genomes of their exon 5 deletion patients was absent from the dystrophin mRNA, indicating that these genomic deletions compromised exon 6 recognition by the splicing machinery [13]. The loss of exons 5 and 6 from the DMD transcript would disrupt the dystrophin reading frame, consistent with a severe pathology. The patient that we describe had a genomic deletion of only exon 5, and RNA analysis indicated that only that exon was missing from the DMD mRNA. We hypothesize that the size and/or location of this particular in frame deletion, 10.8kb compared to the 7.78 and 3.84 kb deletions identified in the other exon 5 deletion patients [13], may have contributed to the processing of dystrophin exons during splicing. Gualandi and colleagues [13] proposed that a 2.1 kb block of sequence, immediately upstream of exon 6 and common to both DMD exon 5 deletion patients, influences splice site selection and the novel fusion introns favour exon 6 skipping. This possibility no longer seems likely since the deletion breakpoint in our patient is located between those in the DMD exon 5 deleted patients reported by Gualandi and colleagues [13].

It is possible that novel sequence at the 10.8 kb deletion breakpoint may have strengthened exon 6 recognition compared to other DMD exon 5 deletions. Clearly, genomic rearrangements and the subsequent fusion of normally non-contiguous sequences can have unexpected consequences [36]. However, we were able to demonstrate that AO induced skipping of exon 6 in myogenic cells from our exon 5 deletion patient occurred at a similar efficiency to that induced in normal myogenic cells, suggesting that this 10.8 kb deletion does not compromise dystrophin exon 6 recognition and processing. Since the deletion of exon 5 does not disrupt the reading frame, but nevertheless the relative amounts of dystrophin were low as assessed by western blotting and immunofluorescence, it must be assumed that the quality of a dystrophin isoform lacking the amino acids encoded by exon 5 is compromised.

In order to further explore the functionality of the dystrophin isoform, missing the domain encoded by exon 5, we used an AO designed to exclude exon 5 from the mature Dmd transcript in wild-type mice, essentially creating a transient dystrophinopathy mouse model. Dystrophin expression and localisation, and muscle architecture in the patient’s muscle is reflected by the analysis of 5-PPMOk treated mouse diaphragm. Dystrophin expression is greatly reduced, beta-dystroglycan and nNOS are somewhat reduced, developmental myosin expression is readily detectable in numerous muscle fibres and the muscle shows increased collagen staining, fibre size variation and the presence of central nuclei, indicating active muscle regeneration. These features are not quite as marked as those in mdx mouse diaphragm, in which dystrophin is undetectable apart from occasional revertant fibres. Although Dmd exon 5 is small and in-frame, exclusion of this exon removes the entire second actin binding sequence and appears to severely compromise function of the dystrophin isoform, leading to a more severe muscle phenotype.

The three dystrophin primary actin binding sites (ABS 1-2-3), specifically amino acids 18–27, 88–116 and 131–147, are encoded by DMD exons 2, 5 and 6. Since pathogenic missense mutations have been identified in this region: L54R in exon 3, A168D and A171P in exon 6, and Y231N in exon 8, the loss of in-frame dystrophin exon 5 encoding the entire ABS2 could impact on dystrophin binding to F actin [37].

The issue is further complicated when other in frame deletion dystrophin isoforms are considered. The deletion of dystrophin exons 3–9 removes ABS 2 and 3, but caused only mild symptoms in a patient diagnosed with BMD after the age of 60 years [38]. Although this suggests that only ABS1 is needed for functional actin binding, Amann and colleagues [3941] reported a cluster of basic repeats in the rod domain, amino acids 1416–1880 encoded by exons 31 to 40 also bound F-actin, and this secondary binding site contributed to the milder phenotype. Since the secondary binding domain would also be present in the DMD exon 5 deleted individuals, it is conceivable that the spatial disruption of the remaining ABS 1 and 3 compromises actin binding.

Multi-exon frame-shifting deletions in the 5’ end of DMD are more common than small in-frame deletions, and this is most likely due to intron length and also the number of SINES, LINES, Alu repeats and microsatellite blocks [42]. However, the few reports of single in-frame exon deletions in the primary actin-binding domain indicate that such changes have variable consequences. Two brothers with a deletion of DMD exon 3, showed early onset dystrophy and loss of ambulation, but stabilised in early adulthood and did not have respiratory or cardiac insufficiency [29]. A Japanese male, diagnosed as autistic at age 3 years was subsequently found to have a DMD deletion of exon 4. He was reported to have mild pseudo-hypertrophy, modestly elevated CK, but with otherwise normal muscle strength [43, 44]. His three affected brothers were found to have similar severe mental retardation and also did not exhibit any muscle weakness. One can only speculate if the autism was related to the dystrophin isoform in this one family.

The dystrophin isoform encoded by the transcript missing exon 5 appears to have reduced function, and therefore clinical application of exon 5 skipping to overcome intra-exonic mutations may be of limited benefit. Consequently, the simplest exon skipping strategy, that is, skipping exon 5 may not offer the best outcome for patients with intra-exonic mutations in this region of the gene. A deletion of DMD exons 3–9 is reported to be associated with a mild BMD phenotype [38], and further investigations on patients with other in-frame deletions in the DMD amino terminal region may help to define better functional dystrophin isoforms that could be induced by AO mediated exon selection.

Acknowledgments

The 5-PPMOk used in this study was kindly provided by Sarepta Therapeutics, Cambridge, MA.

Author Contributions

Conceived and designed the experiments: SF SDW. Performed the experiments: ZYCT MTAH GP AMA SK SF. Analyzed the data: ZYCT GP SF BLW SDW. Contributed reagents/materials/analysis tools: GP BLW SF SDW. Wrote the paper: ZYCT BLW SF SDW.

References

  1. 1. Worton RG, Thompson MW. Genetics of Duchenne muscular dystrophy. Annu Rev Genet. 1988;22:601–29. Epub 1988/01/01. doi: 10.1146/annurev.ge.22.120188.003125 pmid:3071259.
  2. 2. Muntoni F, Torelli S, Ferlini A. Dystrophin and mutations: one gene, several proteins, multiple phenotypes. Lancet Neurol. 2003;2(12):731–40. Epub 2003/11/26. S1474442203005854 [pii]. pmid:14636778. doi: 10.1016/s1474-4422(03)00585-4
  3. 3. Flanigan KM, von Niederhausern A, Dunn DM, Alder J, Mendell JR, Weiss RB. Rapid direct sequence analysis of the dystrophin gene. Am J Hum Genet. 2003;72(4):931–9. pmid:12632325. doi: 10.1086/374176
  4. 4. Witting N, Duno M, Vissing J. Becker muscular dystrophy with widespread muscle hypertrophy and a non-sense mutation of exon 2. Neuromuscul Disord. 2012. Epub 2012/09/04. S0960-8966(12)00556-1 [pii] doi: 10.1016/j.nmd.2012.07.004 pmid:22939275.
  5. 5. Dubowitz V. The Duchenne dystrophy story: from phenotype to gene and potential treatment. J Child Neurol. 1989;4(4):240–50. pmid:2677113. doi: 10.1177/088307388900400402
  6. 6. Brooke MH, Fenichel GM, Griggs RC, Mendell JR, Moxley R, Miller JP, et al. Clinical investigation in Duchenne dystrophy: 2. Determination of the "power" of therapeutic trials based on the natural history. Muscle Nerve. 1983;6(2):91–103. Epub 1983/02/01. doi: 10.1002/mus.880060204 pmid:6343858.
  7. 7. Gangopadhyay SB, Sherratt TG, Heckmatt JZ, Dubowitz V, Miller G, Shokeir M, et al. Dystrophin in frameshift deletion patients with Becker muscular dystrophy. Am J Hum Genet. 1992;51(3):562–70. Epub 1992/09/01. pmid:1496988; PubMed Central PMCID: PMC1682710.
  8. 8. Malhotra SB, Hart KA, Klamut HJ, Thomas NS, Bodrug SE, Burghes AH, et al. Frame-shift deletions in patients with Duchenne and Becker muscular dystrophy. Science. 1988;242(4879):755–9. pmid:3055295. doi: 10.1126/science.3055295
  9. 9. Nevo Y, Muntoni F, Sewry C, Legum C, Kutai M, Harel S, et al. Large in-frame deletions of the rod-shaped domain of the dystrophin gene resulting in severe phenotype. Isr Med Assoc J. 2003;5(2):94–7. Epub 2003/04/05. pmid:12674656.
  10. 10. Gualandi F, Rimessi P, Trabanelli C, Spitali P, Neri M, Patarnello T, et al. Intronic breakpoint definition and transcription analysis in DMD/BMD patients with deletion/duplication at the 5' mutation hot spot of the dystrophin gene. Gene. 2006;370:26–33. Epub 2006/01/28. S0378-1119(05)00698-0 [pii] doi: 10.1016/j.gene.2005.11.002 pmid:16439068.
  11. 11. Wein N, Vulin A, Falzarano MS, Szigyarto CA, Maiti B, Findlay A, et al. Translation from a DMD exon 5 IRES results in a functional dystrophin isoform that attenuates dystrophinopathy in humans and mice. Nat Med. 2014;20(9):992–1000. doi: 10.1038/nm.3628 pmid:25108525; PubMed Central PMCID: PMC4165597.
  12. 12. Fletcher S, Adkin CF, Meloni P, Wong B, Muntoni F, Kole R, et al. Targeted exon skipping to address "leaky" mutations in the dystrophin gene. Mol Ther Nucleic Acids. 2012;1:e48. Epub 2013/01/25. doi: 10.1038/mtna.2012.40 pmid:23344648; PubMed Central PMCID: PMC3499695.
  13. 13. Gualandi F, Trabanelli C, Rimessi P, Calzolari E, Toffolatti L, Patarnello T, et al. Multiple exon skipping and RNA circularisation contribute to the severe phenotypic expression of exon 5 dystrophin deletion. J Med Genet. 2003;40(8):e100. Epub 2003/08/16. pmid:12920092. doi: 10.1136/jmg.40.8.e100
  14. 14. Fragall CT, Adams AM, Johnsen RD, Kole R, Fletcher S, Wilton SD. Mismatched single stranded antisense oligonucleotides can induce efficient dystrophin splice switching. BMC Med Genet. 2011;12:141. Epub 2011/10/22. 1471-2350-12-141 [pii] doi: 10.1186/1471-2350-12-141 pmid:22013876; PubMed Central PMCID: PMC3213239.
  15. 15. Mann CJ, Honeyman K, Cheng AJ, Ly T, Lloyd F, Fletcher S, et al. Antisense-induced exon skipping and synthesis of dystrophin in the mdx mouse. Proc Natl Acad Sci U S A. 2001;98(1):42–7. pmid:11120883. doi: 10.1073/pnas.98.1.42
  16. 16. Greer KL, Lochmuller H, Flanigan K, Fletcher S, Wilton SD. Targeted exon skipping to correct exon duplications in the dystrophin gene. Mol Ther Nucleic Acids. 2014;3:e155. doi: 10.1038/mtna.2014.8 pmid:24643206; PubMed Central PMCID: PMC3982197.
  17. 17. Beroud C, Tuffery-Giraud S, Matsuo M, Hamroun D, Humbertclaude V, Monnier N, et al. Multiexon skipping leading to an artificial DMD protein lacking amino acids from exons 45 through 55 could rescue up to 63% of patients with Duchenne muscular dystrophy. Hum Mutat. 2007;28(2):196–202. pmid:17041910. doi: 10.1002/humu.20428
  18. 18. Wilton SD, Veedu RN, Fletcher S. The emperor's new dystrophin: finding sense in the noise. Trends Mol Med. 2015;21(7):417–26. doi: 10.1016/j.molmed.2015.04.006 pmid:26051381.
  19. 19. Lattanzi L, Salvatori G, Coletta M, Sonnino C, Cusella De Angelis MG, Gioglio L, et al. High efficiency myogenic conversion of human fibroblasts by adenoviral vector-mediated MyoD gene transfer. An alternative strategy for ex vivo gene therapy of primary myopathies. J Clin Invest. 1998;101(10):2119–28. pmid:9593768. doi: 10.1172/jci1505
  20. 20. Harding PL, Fall AM, Honeyman K, Fletcher S, Wilton SD. The influence of antisense oligonucleotide length on dystrophin exon skipping. Mol Ther. 2007;15(1):157–66. Epub 2006/12/14. 6300006 [pii] doi: 10.1038/sj.mt.6300006 pmid:17164787.
  21. 21. Wilton SD, Fall AM, Harding PL, McClorey G, Coleman C, Fletcher S. Antisense Oligonucleotide-induced Exon Skipping Across the Human Dystrophin Gene Transcript. Mol Ther. 2007;15(7):1288–96. pmid:17285139. doi: 10.1038/sj.mt.6300095
  22. 22. Jearawiriyapaisarn N, Moulton HM, Buckley B, Roberts J, Sazani P, Fucharoen S, et al. Sustained Dystrophin Expression Induced by Peptide-conjugated Morpholino Oligomers in the Muscles of mdx Mice. Mol Ther. 2008;16(9):1624–9. Epub 2008/06/12. mt2008120 [pii] doi: 10.1038/mt.2008.120 pmid:18545222.
  23. 23. Roberts RG, Barby TF, Manners E, Bobrow M, Bentley DR. Direct detection of dystrophin gene rearrangements by analysis of dystrophin mRNA in peripheral blood lymphocytes. Am J Hum Genet. 1991;49(2):298–310. pmid:1867192.
  24. 24. Fletcher S, Honeyman K, Fall AM, Harding PL, Johnsen RD, Steinhaus JP, et al. Morpholino Oligomer-Mediated Exon Skipping Averts the Onset of Dystrophic Pathology in the mdx Mouse. Mol Ther. 2007;15(9):1587–92. pmid:17579573. doi: 10.1038/sj.mt.6300245
  25. 25. Moulton HM, Fletcher S, Neuman BW, McClorey G, Stein DA, Abes S, et al. Cell-penetrating peptide-morpholino conjugates alter pre-mRNA splicing of DMD (Duchenne muscular dystrophy) and inhibit murine coronavirus replication in vivo. Biochem Soc Trans. 2007;35(Pt 4):826–8. pmid:17635157. doi: 10.1042/bst0350826
  26. 26. Cooper ST, Lo HP, North KN. Single section Western blot: improving the molecular diagnosis of the muscular dystrophies. Neurology. 2003;61(1):93–7. Epub 2003/07/09. pmid:12847163. doi: 10.1212/01.wnl.0000069460.53438.38
  27. 27. Puchtler H, Waldrop FS, Valentine LS. Polarization microscopic studies of connective tissue stained with picro-sirius red FBA. Beitrage zur Pathologie. 1973;150(2):174–87. pmid:4129194. doi: 10.1016/s0005-8165(73)80016-2
  28. 28. Takeshima Y, Yagi M, Okizuka Y, Awano H, Zhang Z, Yamauchi Y, et al. Mutation spectrum of the dystrophin gene in 442 Duchenne/Becker muscular dystrophy cases from one Japanese referral center. J Hum Genet. 2010;55(6):379–88. doi: 10.1038/jhg.2010.49 pmid:20485447.
  29. 29. Winnard AV, Klein CJ, Coovert DD, Prior T, Papp A, Snyder P, et al. Characterization of translational frame exception patients in Duchenne/Becker muscular dystrophy. Hum Mol Genet. 1993;2(6):737–44. Epub 1993/06/01. pmid:8353493. doi: 10.1093/hmg/2.6.737
  30. 30. Tuffery-Giraud S, Beroud C, Leturcq F, Yaou RB, Hamroun D, Michel-Calemard L, et al. Genotype-phenotype analysis in 2,405 patients with a dystrophinopathy using the UMD-DMD database: a model of nationwide knowledgebase. Hum Mutat. 2009;30(6):934–45. Epub 2009/04/16. doi: 10.1002/humu.20976 pmid:19367636.
  31. 31. Aartsma-Rus A, Van Deutekom JC, Fokkema IF, Van Ommen GJ, Den Dunnen JT. Entries in the Leiden Duchenne muscular dystrophy mutation database: an overview of mutation types and paradoxical cases that confirm the reading-frame rule. Muscle Nerve. 2006;34(2):135–44. pmid:16770791. doi: 10.1002/mus.20586
  32. 32. Magri F, Govoni A, D'Angelo MG, Del Bo R, Ghezzi S, Sandra G, et al. Genotype and phenotype characterization in a large dystrophinopathic cohort with extended follow-up. J Neurol. 2011. Epub 2011/03/15. doi: 10.1007/s00415-011-5979-z pmid:21399986.
  33. 33. Gurvich OL, Maiti B, Weiss RB, Aggarwal G, Howard MT, Flanigan KM. DMD exon 1 truncating point mutations: amelioration of phenotype by alternative translation initiation in exon 6. Hum Mutat. 2009;30(4):633–40. Epub 2009/02/12. doi: 10.1002/humu.20913 pmid:19206170; PubMed Central PMCID: PMC2663021.
  34. 34. Magri F, Del Bo R, D'Angelo MG, Govoni A, Ghezzi S, Gandossini S, et al. Clinical and molecular characterization of a cohort of patients with novel nucleotide alterations of the Dystrophin gene detected by direct sequencing. BMC medical genetics. 2011;12:37. Epub 2011/03/15. doi: 10.1186/1471-2350-12-37 pmid:21396098; PubMed Central PMCID: PMC3061890.
  35. 35. Flanigan KM, Dunn DM, von Niederhausern A, Soltanzadeh P, Howard MT, Sampson JB, et al. Nonsense mutation-associated Becker muscular dystrophy: interplay between exon definition and splicing regulatory elements within the DMD gene. Human mutation. 2011;32(3):299–308. Epub 2011/10/06. doi: 10.1002/humu.21426 pmid:21972111.
  36. 36. Greer K, Mizzi K, Rice E, Kuster L, Barrero RA, Bellgard MI, et al. Pseudoexon activation increases phenotype severity in a Becker muscular dystrophy patient. Mol Genet Genomic Med. 2015;3(4):320–6. doi: 10.1002/mgg3.144 pmid:26247048; PubMed Central PMCID: PMCPMC4521967.
  37. 37. Norwood FL, Sutherland-Smith AJ, Keep NH, Kendrick-Jones J. The structure of the N-terminal actin-binding domain of human dystrophin and how mutations in this domain may cause Duchenne or Becker muscular dystrophy. Structure. 2000;8(5):481–91. pmid:10801490. doi: 10.1016/s0969-2126(00)00132-5
  38. 38. Heald A, Anderson LV, Bushby KM, Shaw PJ. Becker muscular dystrophy with onset after 60 years. Neurology. 1994;44(12):2388–90. pmid:7991131. doi: 10.1212/wnl.44.12.2388
  39. 39. Amann KJ, Renley BA, Ervasti JM. A cluster of basic repeats in the dystrophin rod domain binds F-actin through an electrostatic interaction. J Biol Chem. 1998;273(43):28419–23. pmid:9774469. doi: 10.1074/jbc.273.43.28419
  40. 40. Ervasti JM, Rybakova IN, Amann KJ. A multiple site, side binding model for the interaction of dystrophin with F-actin. Soc Gen Physiol Ser. 1997;52:31–44. pmid:9210218.
  41. 41. Rybakova IN, Amann KJ, Ervasti JM. A new model for the interaction of dystrophin with F-actin. J Cell Biol. 1996;135(3):661–72. pmid:8909541; PubMed Central PMCID: PMC2121071. doi: 10.1083/jcb.135.3.661
  42. 42. McNaughton JC, Broom JE, Hill DF, Jones WA, Marshall CJ, Renwick NM, et al. A cluster of transposon-like repetitive sequences in intron 7 of the human dystrophin gene. J Mol Biol. 1993;232(1):314–21. doi: 10.1006/jmbi.1993.1389 pmid:8392588.
  43. 43. Matsumura K, Imoto N. [Two long-living brothers of dystrophin-related muscular dystrophy with an in-frame deletion of exon 3 of the dystrophin gene—clinical features and diagnosis]. Rinsho Shinkeigaku. 1991;31(3):286–90. pmid:1893667.
  44. 44. Futamura N, Kawamoto K, Takahashi K, Funakawa I, Jinnai K. [Four siblings with becker muscular dystrophy (BMD) manifesting severe mental retardation]. Rinsho Shinkeigaku. 2006;46(1):62–5. pmid:16541798.