- Research article
- Open Access
- Open Peer Review
Identification of a deep intronic mutation in the COL6A2 gene by a novel custom oligonucleotide CGH array designed to explore allelic and genetic heterogeneity in collagen VI-related myopathies
- Matteo Bovolenta†1,
- Marcella Neri†1,
- Elena Martoni1,
- Anna Urciuolo2,
- Patrizia Sabatelli3,
- Marina Fabris1,
- Paolo Grumati2,
- Eugenio Mercuri4,
- Enrico Bertini5,
- Luciano Merlini1, 6,
- Paolo Bonaldo2,
- Alessandra Ferlini1 and
- Francesca Gualandi1Email author
© Bovolenta et al; licensee BioMed Central Ltd. 2010
- Received: 4 September 2009
- Accepted: 19 March 2010
- Published: 19 March 2010
Molecular characterization of collagen-VI related myopathies currently relies on standard sequencing, which yields a detection rate approximating 75-79% in Ullrich congenital muscular dystrophy (UCMD) and 60-65% in Bethlem myopathy (BM) patients as PCR-based techniques tend to miss gross genomic rearrangements as well as copy number variations (CNVs) in both the coding sequence and intronic regions.
We have designed a custom oligonucleotide CGH array in order to investigate the presence of CNVs in the coding and non-coding regions of COL6A1, A2, A3, A5 and A6 genes and a group of genes functionally related to collagen VI. A cohort of 12 patients with UCMD/BM negative at sequencing analysis and 2 subjects carrying a single COL6 mutation whose clinical phenotype was not explicable by inheritance were selected and the occurrence of allelic and genetic heterogeneity explored.
A deletion within intron 1A of the COL6A2 gene, occurring in compound heterozygosity with a small deletion in exon 28, previously detected by routine sequencing, was identified in a BM patient. RNA studies showed monoallelic transcription of the COL6A2 gene, thus elucidating the functional effect of the intronic deletion. No pathogenic mutations were identified in the remaining analyzed patients, either within COL6A genes, or in genes functionally related to collagen VI.
Our custom CGH array may represent a useful complementary diagnostic tool, especially in recessive forms of the disease, when only one mutant allele is detected by standard sequencing. The intronic deletion we identified represents the first example of a pure intronic mutation in COL6A genes.
- Comparative Genomic Hybridization
- Club Foot
- COL6 Gene
- Comparative Genomic Hybridization Array
- COL6A2 Gene
Mutations in the genes encoding collagen VI (COL6A1, COL6A2 and COL6A3) result in two major phenotypes: Bethlem myopathy [BM, OMIM #158810] and Ullrich congenital muscular dystrophy [UCMD, OMIM #254090]. Despite BM being classically reported as an autosomal dominant condition due to heterozygous COL6 mutations [1, 2], we and others have recently described autosomal recessive BM patients [3, 4]. In contrast, the allelic form UCMD was initially considered to be an autosomal recessive disorder, with homozygous or compound heterozygous mutations occurring in all three COL6 genes , although a few double heterozygous mutations in two different COL6 genes have also been described . Recently, however, up to 50% of UCMD cases have been found to carry only one mutated allele, indicating autosomal dominant inheritance [5–7]. Thus far, roughly 100 different mutations in COL6 genes have been associated with either UCMD or BM and most of them are confined to single families [5, 8].
The distribution of mutations along COL6 genes is rather uniform and lacks mutation hot spots, therefore these patients require extensive genotyping, which is currently performed by genomic or cDNA sequencing [1, 5]. Nevertheless, a relevant proportion of patients clinically diagnosed as having a collagen-VI related myopathy still lack molecular characterization. In fact, with currently available diagnostic tools, the detection rate of mutations of COL6 genes varies from 60-65% in BM cases and 75-79% in UCMD patients . The majority of these mutations are small variations like missense, frame-shifting, ins-del or point mutations which lead to a splicing defect. Large, multi-exon deletions of the COL6A1 gene, involving both exonic and intronic regions and thus detectable by mRNA analysis, have been reported as causative mutations in three patients [9, 10]. One limitation of PCR-based genome analysis techniques is their inability to detect gross CNVs, as well as atypical mutations, which could account for a significant proportion of undetected COL6 mutations. On the other hand, the relatively low rate of mutation detection in COL6 genes could be due to the genetic heterogeneity of these diseases. Thus, mutations in genes functionally related to collagen VI could theoretically underlie UCMD and BM phenocopies and/or be responsible for secondary collagen VI defects . In order to test this hypothesis, we selected 12 UCMD/BM patients who were found to be negative upon extensive sequence analysis of the three COL6 genes, and two patients carrying only one mutation, deemed insufficient to explain the clinical phenotype, it being inherited from a healthy parent.
The occurrence of both allelic and genetic heterogeneity was explored in these patients by using an innovative oligonucleotide array-based comparative genomic hybridization (CGH) approach able to detect CNVs in COL6 genes, as well as in other genes functionally related to collagen VI.
A deep intronic deletion in the COL6A2 gene was discovered in one BM patient, with a single mutation inherited from the healthy mother identified at sequencing analysis. Subsequently, the functional effect of the identified mutation was demonstrated via RNA studies. In the remaining patients, only non pathogenic CNVs were identified.
Genome sequence analysis
Patients' genomic DNA was extracted from peripheral blood lymphocytes after informed consent and approval by the local ethics committee was obtained (approval number 7/2009). PCR primers (sequences are available upon request) were designed to amplify all the 107 exons of the COL6 genes, as well as their flanking intronic regions. Amplified fragments were directly sequenced using a BigDye Terminator v3.1 Cycle sequencing system on the automated ABI 3130 Genetic Analyzer (Applied Biosystems, Foster City, CA).
Micro-array design, hybridization and data analysis
COL6-CGH array design was performed using the high-density aCGH search function of the web-based Agilent eArray database, version 4.5 .
Genes, corresponding genomic regions and protein products included in the COL6-CGH micro-array design.
Chromosomal Coordinates (NCBI Build 35)
Heparan sulfate proteoglycan 2
Collagen, type VI, alpha-3 chain
Collagen, type XXIX, alpha 1
Collagen type VI alpha 6
Integrin, alpha 1
Integrin, alpha 2
Integrin, beta 1
Integrin, alpha 5;
Integrin, alpha 7
Chondroitin sulfate proteoglycan 4
Collagen, type VI, alpha 1 chain Collagen, type VI, alpha 2 chain
The array format utilized was 8 × 15K, made up of eight identical 15K arrays on a single slide, thereby permitting simultaneous analysis of eight different samples. Genomic DNA was extracted from the patients' whole blood or cultured fibroblasts by a Nucleon™ BACC Genomic DNA Extraction Kit (GE Healthcare). Labeling and hybridization were performed following the protocols provided by Agilent (Agilent Oligonucleotide Array-Based CGH for Genomic DNA Analysis protocol v5.0). The array was analyzed with the Agilent scanner and the Feature Extraction software (v9.1). A graphical overview and analysis of the data were obtained using the CGH analytics software (v3.5). For identifying duplications and deletions we used the statistical calculations based on ADM-2 algorithm provided by the CGH analytics software. According to this set-up and in the case of autosomal genes, deletions are visualized with values of -1 if in heterozygosity and with values of minus infinite (-4 in CGH analytics) if in homozygosity. For three copies, the value would be approximately +0.6 and for four copies the value would be +1.
The platform informations have been submitted to the online data repository Gene Expression Omnibus (GEO) , under accession number GPL9972.
Ad hoc Real-Time PCR assays were designed for the COL6A2 intron 1A deletion and the CNVs identified within the ITGB1 and ITGA5/ITGA genomic regions (Table 1 and Additional file 1). For confirming COL6A2 intron 1A deletion, a TaqMan assay was firstly used; MGB probe and primer design was performed by Primer Express Software 2.0 (Applied Biosystems) (FW TTGGTCACAGGTTATGCAACA, Rev GGTGAGTTTCACAGCTTCAAGGA; Probe 6-FAM-AACAAGTTAAATAGCATGAAGTG) (see Additional file 2)
Real-Time PCR was performed in triplicate in 96-well plates using 50 ng genomic DNA and default parameters on the Applied Biosystems Prism 7300 system. For relative quantification, the ΔΔCT Method (Applied Biosystems User Bulletin #2) was utilized. CFTR exon 15 was employed as a reference gene, and three control DNAs were used as calibrators for each experiment. Specific assays based on SYBR-green chemistry were also employed in order to further verify the intron 1A deletion and to confirm the CNVs identified in the ITGB1 and ITGA5/ITGA7 genomic regions, (Chr10_FW CGTGGAGATGGGATTAGTGTG, Chr10_Rev TTTGTTGGGAATTTACTTGGTG; Chr12_FW AATTTGCTGTTGCTGGGTCT, Chr12_Rev TCCCATACTCTCCATTGTCC; Chr21_FW GCCTGTCTGCCTCTTCCA, Chr21_Rev TGTTGCATAACCTGTGACCAA) (see Table 1 and Additional file 2).
Transcript analysis in BM Patient 1
Total RNA was isolated from confluent fibroblasts by using an RNeasy Kit (QIAGEN, Chatsworth, CA), and reverse transcribed using a High Capacity cDNA Reverse Transcription Kit (Applied Biosystem, Foster City CA). RT-PCR was performed with a forward primer within COL6A2 exon 25 and a reverse primer within the 5' of exon 28, as well as with a forward primer within exon 26 and a reverse within the 3' of exon 28, as previously described . The sequence of primers employed is available upon request.
Immunohistochemistry, electron microscopy and Western Blot in BM Patient 1
Unfixed frozen sections of the tibialis anterior muscle from BM Patient 1 and control were labeled with anti-collagen VI antibody (Chemicon MAB1944) diluted 1:100, followed by FITC-conjugated anti-mouse antibody (DAKO); sections were double-labeled with anti-perlecan antibody (Chemicon) diluted 1:100, and revealed with a TRITC conjugated anti-rat antibody (SIGMA). Muscle sections were also labeled with anti-caveolin 3 (BD-Transduction), collagen IV, laminin α2 and laminin β1 chains (Chemicon), followed by FITC-conjugated secondary antibody, while fibronectin (Sigma) and alpha-dystroglycan (Upstate Biotechnologies) were followed by TRITC-conjugated antibody (Sigma, MO). The fibroblast cultures from Patient 1 and from a control were obtained by mechanical means from bioptic skin fragments and set up as previously described . A mouse monoclonal anti-collagen VI antibody (MAB1944, Chemicon) was employed, and the resulting immunoreaction was detected with a secondary FITC-conjugated anti-mouse antibody (DAKO). For immunoelectron microscopy analysis, cells were incubated with a monoclonal anti-collagen VI antibody (Chemicon) diluted 1:25 with Dulbecco's modified Eagle's medium and with 5 or 15-nm colloidal gold-labeled IgG (Amersham). Rotary shadowing electron microscopy was performed as described .
Samples derived from skin fibroblast cultures and muscle biopsies were prepared for Western Blot analysis as previously described . Collagen VI was detected by immunoblotting with antibodies recognizing either all collagen VI chains (Fitzgerald 70XR95) or the α1(VI) chain (Santa Cruz sc-20649) alone. Antibodies recognizing AKT (Cell Signaling) and myosin (Sigma) were used for cell culture loading and muscle samples.
Patient selection and COL6-CGH array validation
Summary of clinical and genomic data in the analyzed BM/UCMD patients.
Age at review, yr
Max motor ability
Creatine kinase level*
(% of predicted)
Collagen VI SKM
1 (BM) 
c.2947_2952del 6 het (mat)
3 yrs, difficulty in running & climbing stairs
Walked 15 mo-present
Neck, elbows, fingers, knees, ankles
Rough skin, dystrophic nails, cheloids
Mildly reduced at BM of several muscle fibers
chr21 g.(46352739-46352798) _ (46354892-46354936) del
c.350 C>T het p.V117A (pat)
Birth, hip dislocation
Able to walk
4 UL and 3,4 LL
3 yrs, difficulty in running & climbing stairs
Walked 13 mo-present
Neck, elbows, fingers, ankles
3 yrs, unable to collect objects from the floor
Walked 12 mo-present
Neck, elbows, fingers, knees, ankles
Mildly reduced at BM of some muscle fibers
chr10 g:(33176784_33176843) _(33178291_33178350)del
5 (BM) 
18 yrs, reduced stamina
Walked 12 mo-present
Neck, fingers, knees, ankles
Normal amount and localization
chr12 g:(54068784_54068843) _(54070617_54070676)dup
5 yrs, difficulty in bending forward
Walked 12 mo-14 yrs
Neck, trunk, elbows, fingers, hips, knees, ankles
Normal amount and localization
30 yrs, easily fatigued, falls
Walked 12 mo-present
Normal amount and localization
5 yrs, contractures
Walked 12 mo-present
Shoulders, elbows, fingers, hips
Birth with pes talus
Walked 14 mo-present
Reduced at BM of muscle fibers
10 (UCMD) 
Birth with delay in motor milestones
Able to walk
4 UL and LL
Reduced at BM of muscle fibers
2 yrs, hyperlaxity and hyperCK
Able to walk
1 hip flex - 3 knees ext
Fingers, hip, knees, ankles
18 mo, unable to walk
Able to walk 24 mo-12 yrs
Neck, trunk, elbows, fingers, hips, knees, ankles
Normal amount and localization
Walked 18 mo-present
Fingers, knees, ankles
Reduced at the BM of muscle fibers
Able to walk at 3 yrs
One BM patient (Patient 1) had previously been described by Demir et al. (# 10, Family 8), who linked the disease in this family to chromosome 21q22.3 . This patient carries a heterozygous small deletion in exon 28 of the COL6A2 gene (NM_001849, c. 2947_2952del6, p.Asp983_Val984del) inherited from the healthy mother. Patient 2 (UCMD) bears a heterozygous missense alteration (NM_001848, c.350 C>T, V117A) within COL6A1 exon 3, inherited from the unaffected father. The V117A substitution noted in this patient had not previously been described, so in order to evaluate the pathogenic effect of this missense variation, polymorphism phenotyping predictions were obtained by PolyPhen  and SIFT  with contrasting results: PolyPhen predicted a benign variation whereas SIFT foresaw a harmful effect of the V117A substitution. Subsequently, amino acid conservation of V117 was analyzed, and sequence alignment between distant species showed high conservation of the residue in the VWFA1 domain (data not shown). The screening of 200 control chromosomes excluded it as a common polymorphism.
The COL6-CGH array was designed to cover the regions of genes COL6A1-A2-A3-A5 and -A6 and a group of genes functionally related to collagen VI (Table 1). Ten possible candidate genes were considered on the basis of the following criteria: either i) their direct interaction with collagen VI, as in the case of HSPG2 , ITGA1, ITGA2, ITGB1 , DNC and BGN ; ii) their secondary involvement in collagen VI-deficient tissues, as in NG2-proteoglycan [16, 17], ITGA5 and ITGA7 [18, 19], or iii) their mutations causing an overlapping phenotype with collagen VI-related myopathies, as in TNXB . COL6A5 (COL29A1) and COL6A6, which are expressed in skeletal muscle, were also included since collagen VI alpha1-deficient mice do not express collagen VI alpha 5 or alpha 6 chains .
The full coding region of all selected genes was included, together with intronic sequences and 100 kb at the 5' and 3' of the first and last exons, respectively. The array was technically validated before commencing by using DNA from 8 normal controls; no CNVs were detected.
Two novel CNVs were identified in BM patients 4 and 5 (Table 1 and Additional File 2). The first was a 1.4 Kb deletion, located 35 Kb downstream the ITGB1 gene and the second was a 1.7 Kb duplication in the intergenic region between ITGA5 and ITGA7. Both CNVs were confirmed by Real-Time PCR analysis (data not shown), but the occurrence of both variations in unaffected family members and healthy controls from the general population permitted exclusion of their pathogenic significance (see Additional File 2).
The complete CGH datasets have been submitted to the online data repository Gene Expression Omnibus , under accession number GSE20025.
Identification of a pure intronic deletion in intron 1A of the COL6A2 gene in BM patient 1
In early infancy, Patient 1 (BM) (Table 2) attained normal motor milestones and walked at 15 months of age. However, aged 3 and a half, she began to have difficulty running. Creatine kinase was 3.5 times the upper limit of normal, and examination at age 21 revealed a short stature, excessive weight and bilateral club foot. The patient was able to walk and climb stairs without support, but was unable to run. Mild facial and limb/girdle weakness and moderate axial and distal weakness were noted. The patient was unable to bury the eyelashes completely or to flex neck against gravity, and digitorum extension weakness was evident. The patient suffered contractures of the neck, elbows, fingers, knees and ankles, combined with finger extension hypermobility when the wrist was flexed. Her skin was rough and cheloidal, and nails were dystrophic. Forced vital capacity was 52%, and cardiac examination evidenced no abnormality. Examination at age 30 years revealed a relatively stable condition, with only the ability to get up from the floor having been further compromised.
In BM Patient 1, CGH analysis revealed the presence of a deletion within intron 1A of the COL6A2 gene (NM_001849). This deletion was detected by two overlapping probes which covered 95 base pairs: the 5'-deleted probe lying 12.237 nucleotides from exon 1A, and the 3'-deleted probe located 999 nucleotides from exon 2. The two flanking probes, which showed normal hybridization levels, were localized respectively, 1900 nucleotides from the proximal 5'-deleted probe and 194 nucleotides from the distal 3'-deleted probe. Thus, the identified deletion spans a maximum theoretical region of 2094 bp, and is located 1 kb upstream of the first COL6A2 coding exon (exon 2). Comparative sequence analysis using the two deleted probes identified a genomic region lying adjacent to a cluster of repetitive elements (Figure 1A) .
Real-Time PCR analysis performed using two different assays, one based on SYBR-green and the other on TaqMan chemistries, confirmed the occurrence of the deletion, which was inherited from the healthy father (see Additional File 3). Analysis of 100 control subjects from the normal population by Real-Time PCR failed to identify the COL6A2 intron deletion.
Genotypic analysis of the proband's parents showed the intronic deletion and the exon 28 small mutations in trans, denoting autosomal recessive transmission.
An attempt to amplify by junction PCR the deletion breakpoint with primers outside the maximum theoretical deleted region was unsuccessful, and sequencing analysis of the PCR products obtained using different sets of primers failed to identify the mutated allele. This suggests the possibility of a complex rearrangement/inversion of the involved genomic region (Figure 1A).
Occurrence of monoallelic COL6A2 transcription in BM Patient 1 fibroblasts
In order to strengthen the case for a relationship between the identified intronic deletion and the transcriptional behavior, RNA analysis was performed on cultured skin fibroblasts from the patient's father. The two exon 26 polymorphisms (Ala698Ala; Gly699Gly) were found to be heterozygous at the genomic level, although their transcription was strongly imbalanced. The nucleotide variant of the polymorphisms (c.2094 G>A - A698A; C.2097 C>T - G699G) that was completely undetectable in the proband's RNA (G and C, respectively), was only barely visible in cells from the father (Figure 2).
Collagen VI expression in muscle and cell cultures from BM Patient 1
Molecular genotyping of UCMD and BM patients is currently performed by extensive sequencing of COL6A1, A2 and A3 genes. Unfortunately, however, the PCR-based techniques used in routine screening miss gross rearrangements as well as CNVs which exceed the dimensional limitations of PCR amplification. Furthermore, molecular analysis fails to identify the causative mutation in a significant percentage of patients, ranging from 20-25% in UCMD to 35-40% in BM . This relatively low detection rate of current molecular approaches in collagen VI myopathies could be ascribed to allelic heterogeneity (linked to the abovementioned limitations of PCR-based techniques) and/or genetic heterogeneity. This latter hypothesis implies that UCMD/BM phenocopies could occur, due to mutations in different, still unidentified genes.
In the last few years, novel genomic-based technologies have been reported as an efficient and improved alternative to PCR in molecular diagnosis. Oligonucleotide array-based CGH was initially developed to detect major changes in chromosomal copy number , and since then both commercial and custom arrays have been also used to discern these changes in selected genomic regions of interest [31, 32]. The DMD gene was a perfect candidate to test the validity of this approach, due to the large size and high number of gross copy number variations apparent in this condition. Moreover, different custom arrays have already been validated for the exploration of both coding  and non-coding regions of the gene [34–36]. For COL6 genes, the possibility that genomic dosage imbalance or large CNVs occur with significant frequency in UCMD/BM patients still remains untested.
With the aim of increasing the sensitivity of molecular diagnosis in collagen VI-related disorders, a custom oligonucleotide-based CGH array able to detect CNVs in coding and non-coding regions of the COL6A1, A2, A3, and the A5 and A6 genes recently discovered to encode novel collagen VI chains [21, 37] was designed. Moreover, in order to investigate genetic heterogeneity, the genomic regions of other genes selected on the basis of their known or hypothetical functional relationship with collagen VI were also included in the design, as all these genes potentially represent candidates for mutations that could underlie phenocopies of collagen VI-related diseases [38, 39, 13, 15, 40–42].
By testing our array in 14 selected UCMD/BM patients, we identified a deep intronic deletion in the COL6A2 gene in a BM patient occurring in compound heterozygosity with a small exonic mutation previously detected by sequencing. Despite not definitively proven, due to the failure to amplify the deletion breakpoint, nevertheless the pathogenic potential of this intronic mutation is supported by the transcriptional impairment of the mutated allele that was demonstrated both in the proband and in her healthy carrier father. The COL6A2 gene is characterized by a first-coding exon (exon 2) separated from two alternatively spliced 5'-untranslated exons (exon 1 and 1a) by a huge 12 kb intron (intron 1A) .
Deletion of this intron may abolish cis-acting elements and/or the binding of trans-acting factors involved in the regulation of COL6A2 gene expression. Alternatively, the deletion itself might be the marker for a complex genomic rearrangement occurring in the COL6A2 gene that inverts or scrambles the entire genomic configuration. The failure of PCR to amplify the deletion junction seems to support this hypothesis.
This study documents an additional case of a BM patient with a compound heterozygous genotype for recessive COL6A2 mutations. Interestingly, both of the autosomal recessive BM cases we previously described carried a peculiar allele combination consisting of a truncating mutation partnered by missense changes within the α2(VI) C2 region . Despite different (null mutation/in-frame deletion), the allelic configuration of BM Patient 1 also indicates the presence of a mutated α2(VI) C2 domain, derived from a single allele, similar to the recessive BM cases previously described . The findings in this patient also substantiate the observation that recessive BM mutations, unlike the classical dominant cases, affect collagen VI expression in skeletal muscle , as attested by immunohistochemical and biochemical analyses showing a decreased amount of this protein.
In the twelve patients who tested negative upon genomic sequence analysis, no CNVs were identified in COL6 genes using the CGH array. Even though the limited size of the analyzed patient cohort hampered definitive estimations, our results did exclude a relevant incidence of CNVs within COL6 genes, thereby supporting UCMD/BM genetic heterogeneity. Likewise, no pathogenic CNVs were identified among the other genomic regions potentially harboring candidate BM/UCMD genes that were explored in the array. Nevertheless, these results do not rule out the possibility that genetic heterogeneity could account for some COL6A1-3-negative patients and suggest that high-throughput sequencing technologies could represent more appropriate future approaches for detection of point mutations. In fact, these innovative tools could allow significant enlargement of the spectrum of functionally related collagen VI genes to be explored sequentially via CNV identification and re-sequencing for detection of point mutations.
The described COL6-CGH array could represent a useful complementary diagnostic test, useful for increasing the sensitivity of molecular analysis in patients with a clinical diagnosis of collagen VI-related disorders. The limited size of the patient cohort we analyzed hampered estimation of copy number variation frequency, but analysis of larger populations could well permit conclusions to be drawn. In fact, this novel tool allowed us for the first time to identify a COL6A2 mutation affecting gene transcription deeply located within an intronic region, and thus undetectable with all other techniques currently available. Furthermore, in recent years specific genetic diagnosis has become mandatory for a patient to be eligible for upcoming therapeutic trials , and thus the lack of molecular diagnosis in a large percentage of patients with collagen-VI related phenotypes makes the search and the validation of novel diagnostic tools an ever-more pressing issue.
This study was supported by the Italian Telethon Foundation grants GUP07004 (to GF). The Telethon grant GGP08107 (awarded to AF and PB) and the TREAT-NMD Network of Excellence of EU FP7 (awarded 036825 to LM and Telethon-Italy), are also acknowledged.
- Lampe AK, Bushby KM: Collagen VI related muscle disorders. J Med Genet. 2005, 42: 673-85. 10.1136/jmg.2002.002311.View ArticlePubMedPubMed CentralGoogle Scholar
- Bertini E, Pepe G: Collagen type VI and related disorders: Bethlem myopathy and Ullrich scleroatonic muscular dystrophy. Eur J Paediatr Neurol. 2002, 6: 193-198. 10.1053/ejpn.2002.0593.View ArticlePubMedGoogle Scholar
- Gualandi F, Urciuolo A, Martoni E, Sabatelli P, Squarzoni S, Bovolenta M, Messina S, Mercuri E, Franchella A, Ferlini A, Bonaldo P, Merlini L: Autosomal recessive Bethlem myopathy. Neurology. 2009, 73 (22): 1883-91. 10.1212/WNL.0b013e3181c3fd2a.View ArticlePubMedGoogle Scholar
- Foley AR, Hu Y, Zou Y, Columbus A, Shoffner J, Dunn DM, Weiss RB, Bönnemann CG: Autosomal recessive inheritance of classic Bethlem myopathy. Neuromuscul Disord. 2009, 19: 813-7. 10.1016/j.nmd.2009.09.010.View ArticlePubMedPubMed CentralGoogle Scholar
- Lampe AK, Dunn DM, von Niederhausern AC, Hamil C, Aoyagi A, Laval SH, Marie SK, Chu ML, Swoboda K, Muntoni F, Bonnemann CG, Flanigan KM, Bushby KM, Weiss RB: Automated genomic sequence analysis of the three collagen VI genes: applications to Ullrich congenital muscular dystrophy and Bethlem myopathy. J Med Genet. 2005, 42: 108-20. 10.1136/jmg.2004.023754.View ArticlePubMedPubMed CentralGoogle Scholar
- Baker NL, Morgelin M, Peat R, Goemans N, North KN, Bateman JF, Lamande SR: Dominant collagen VI mutations are a common cause of Ullrich congenital muscular dystrophy. Hum Mol Genet. 2005, 14: 279-93. 10.1093/hmg/ddi025.View ArticlePubMedGoogle Scholar
- Giusti B, Lucarini L, Pietroni V, Lucioli S, Bandinelli B, Sabatelli P, Squarzoni S, Petrini S, Gartioux C, Talim B, Roelens F, Merlini L, Topaloglu H, Bertini E, Guicheney P, Pepe G: Dominant and recessive COL6A1 mutations in Ullrich scleroatonic muscular dystrophy. Ann Neurol. 2005, 58: 400-10. 10.1002/ana.20586.View ArticlePubMedGoogle Scholar
- Leiden Pages. [http://www.dmd.nl/]
- Pepe G, Lucarini L, Zhang RZ, Pan TC, Giusti B, Quijano-Roy S, Gartioux C, Bushby KM, Guicheney P, Chu ML: COL6A1 genomic deletions in Bethlem myopathy and Ullrich muscular dystrophy. Ann Neurol. 2006, 59: 190-5. 10.1002/ana.20705.View ArticlePubMedGoogle Scholar
- Pan TC, Zhang RZ, Sudano DG, Marie SK, Bonnemann CG, Chu ML: New molecular mechanism for Ullrich congenital muscular dystrophy: a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype. Am J Hum Genet. 2003, 73: 355-69. 10.1086/377107.View ArticlePubMedPubMed CentralGoogle Scholar
- Petrini S, D'Amico A, Sale P, Lucarini L, Sabatelli P, Tessa A, Giusti B, Verardo M, Carrozzo R, Mattioli E, Scarpelli M, Chu ML, Pepe G, Russo MA, Bertini E: Ullrich myopathy phenotype with secondary ColVI defect identified by confocal imaging and electron microscopy analysis. Neuromuscul Disord. 2007, 17: 587-96. 10.1016/j.nmd.2007.04.010.View ArticlePubMedGoogle Scholar
- Agilent Technologies eArray. [https://earray.chem.agilent.com/earray]
- Tillet E, Wiedemann H, Golbik R, Pan TC, Zhang RZ, Mann K, Chu ML, Timpl R: Recombinant expression and structural and binding properties of alpha 1(VI) and alpha 2(VI) chains of human collagen type VI. Eur J Biochem. 1994, 221: 177-85. 10.1111/j.1432-1033.1994.tb18727.x.View ArticlePubMedGoogle Scholar
- Pfaff M, Aumailley M, Specks U, Knolle J, Zerwes HG, Timpl R: Integrin and Arg-Gly-Asp dependence of cell adhesion to the native and unfolded triple helix of collagen type VI. Exp Cell Res. 1993, 206: 167-76. 10.1006/excr.1993.1134.View ArticlePubMedGoogle Scholar
- Wiberg C, Hedbom E, Khairullina A, Lamandé SR, Oldberg A, Timpl R, Mörgelin M, Heinegård D: Biglycan and decorin bind close to the n-terminal region of the collagen VI triple helix. J Biol Chem. 2001, 276: 18947-52. 10.1074/jbc.M100625200.View ArticlePubMedGoogle Scholar
- Petrini S, Tessa A, Stallcup WB, Sabatelli P, Pescatori M, Giusti B, Carrozzo R, Verardo M, Bergamin N, Columbaro M, Bernardini C, Merlini L, Pepe G, Bonaldo P, Bertini E: Altered expression of the MCSP/NG2 chondroitin sulfate proteoglycan in collagen VI deficiency. Mol Cell Neurosci. 2005, 30: 408-17. 10.1016/j.mcn.2005.08.005.View ArticlePubMedGoogle Scholar
- Higashi K, Higuchi I, Niiyama T, Uchida Y, Shiraishi T, Hashiguchi A, Saito A, Horikiri T, Suehara M, Arimura K, Osame M: Abnormal expression of proteoglycans in Ullrich's disease with collagen VI deficiency. Muscle Nerve. 2006, 33: 120-6. 10.1002/mus.20449.View ArticlePubMedGoogle Scholar
- Hu J, Higuchi I, Shiraishi T, Suehara M, Niiyama T, Horikiri T, Uchida Y, Saito A, Osame M: Fibronectin receptor reduction in skin and fibroblasts of patients with Ullrich's disease. Muscle Nerve. 2002, 26: 696-701. 10.1002/mus.10250.View ArticlePubMedGoogle Scholar
- Pepe G, Bertini E, Bonaldo P, Bushby K, Giusti B, de Visser M, Guicheney P, Lattanzi G, Merlini L, Muntoni F, Nishino I, Nonaka I, Yaou RB, Sabatelli P, Sewry C, Topaloglu H, Kooi van der A: Bethlem myopathy (BETHLEM) and Ullrich scleroatonic muscular dystrophy: 100th ENMC international workshop 2001, 23-24 November Naarden, The Netherlands. Neuromuscul Disord. 2002, 12: 984-93. 10.1016/S0960-8966(02)00139-6.View ArticlePubMedGoogle Scholar
- Voermans NC, Jenniskens GJ, Hamel BC, Schalkwijk J, Guicheney P, van Engelen BG: Ehlers-Danlos syndrome due to tenascin-X deficiency: muscle weakness and contractures support overlap with collagen VI myopathies. Am J Med Genet A. 2007, 143A: 2215-9. 10.1002/ajmg.a.31899.View ArticlePubMedGoogle Scholar
- Gara SK, Grumati P, Urciuolo A, Bonaldo P, Kobbe B, Koch M, Paulsson M, Wagener R: Three novel collagen VI chains with high homology to the alpha3 chain. J Biol Chem. 2008, 283: 10658-70. 10.1074/jbc.M709540200.View ArticlePubMedGoogle Scholar
- Gene Expression Omnibus. [http://0-www.ncbi.nlm.nih.gov.brum.beds.ac.uk/geo/]
- Merlini L, Martoni E, Grumati P, Sabatelli P, Squarzoni S, Urciuolo A, Ferlini A, Gualandi F, Bonaldo P: Autosomal recessive myosclerosis myopathy is a collagen VI disorder. Neurology. 2008, 71: 1245-53. 10.1212/01.wnl.0000327611.01687.5e.View ArticlePubMedGoogle Scholar
- Martoni E, Urciuolo A, Sabatelli P, Fabris M, Bovolenta M, Neri M, Grumati P, D'Amico A, Pane M, Mercuri E, Bertini E, Merlini L, Bonaldo P, Ferlini A, Gualandi F: Identification and characterization of novel collagen VI non-canonical splicing mutations causing ullrich congenital muscular dystrophy. Hum Mutat. 2009, 30: E662-72. 10.1002/humu.21022.View ArticlePubMedGoogle Scholar
- Zhang RZ, Sabatelli P, Pan TC, Squarzoni S, Mattioli E, Bertini E, Pepe G, Chu ML: Effects on collagen VI mRNA stability and microfibrillar assembly of three COL6A2 mutations in two families with Ullrich congenital muscular dystrophy. J Biol Chem. 2002, 277: 43557-64. 10.1074/jbc.M207696200.View ArticlePubMedGoogle Scholar
- Demir E, Ferreiro A, Sabatelli P, Allamand V, Makri S, Echenne B, Maraldi M, Merlini L, Topaloglu H, Guicheney P: Collagen VI status and clinical severity in Ullrich congenital muscular dystrophy: phenotype analysis of 11 families linked to the COL6 loci. Neuropediatrics. 2004, 35: 103-12. 10.1055/s-2004-815832.View ArticlePubMedGoogle Scholar
- Polyphen. [http://genetics.bwh.harvard.edu/pph/]
- SIFT. [http://sift.jcvi.org/www/SIFT_chr_coords_submit.html]
- Repeat Masker. [http://www.repeatmasker.org/]
- Lu X, Shaw CA, Patel A, Li J, Cooper ML, Wells WR, Sullivan CM, Sahoo T, Yatsenko SA, Bacino CA, Stankiewicz P, Ou Z, Chinault AC, Beaudet AL, Lupski JR, Cheung SW, Ward PA: Clinical implementation of chromosomal microarray analysis: summary of 2513 postnatal cases. PLoS One. 2007, 2: e327-10.1371/journal.pone.0000327.View ArticlePubMedPubMed CentralGoogle Scholar
- Wong LJ, Dimmock D, Geraghty MT, Quan R, Lichter-Konecki U, Wang J, Brundage EK, Scaglia F, Chinault AC: Utility of oligonucleotide array-based comparative genomic hybridization for detection of target gene deletions. Clin Chem. 2008, 54: 1141-8. 10.1373/clinchem.2008.103721.View ArticlePubMedGoogle Scholar
- Gunn SR, Robetorye RS, Mohammed MS: Comparative genomic hybridization arrays in clinical pathology: progress and challenges. Mol Diagn Ther. 2007, 11: 73-7.View ArticlePubMedGoogle Scholar
- Dhami P, Coffey AJ, Abbs S, Vermeesch JR, Dumanski JP, Woodward KJ, Andrews RM, Langford C, Vetrie D: Exon array CGH: detection of copy-number changes at the resolution of individual exons in the human genome. Am J Hum Genet. 2005, 76: 750-762. 10.1086/429588.View ArticlePubMedPubMed CentralGoogle Scholar
- Hegde MR, Chin EL, Mulle JG, Okou DT, Warren ST, Zwick ME: Microarray-based mutation detection in the dystrophin gene. Human mutation. 2008, 29: 1091-9. 10.1002/humu.20831.View ArticlePubMedPubMed CentralGoogle Scholar
- Saillour Y, Cossée M, Leturcq F, Vasson A, Beugnet C, Poirier K, Commere V, Sublemontier S, Viel M, Letourneur F, Barbot JC, Deburgrave N, Chelly J, Bienvenu T: Detection of exonic copy-number changes using a highly efficient oligonucleotide-based comparative genomic hybridization-array method. Human mutation. 2008, 29: 1083-90. 10.1002/humu.20829.View ArticlePubMedGoogle Scholar
- Bovolenta M, Neri M, Fini S, Fabris M, Trabanelli C, Venturoli A, Martoni E, Bassi E, Spitali P, Brioschi S, Falzarano MS, Rimessi P, Ciccone R, Ashton E, McCauley J, Yau S, Abbs S, Muntoni F, Merlini L, Gualandi F, Ferlini A: A novel custom high density-comparative genomic hybridization array detects common copy number variations as well as deep intronic mutations in dystrophinopathies. BMC genomics. 2008, 9: 572-10.1186/1471-2164-9-572.View ArticlePubMedPubMed CentralGoogle Scholar
- Fitzgerald J, Rich C, Zhou FH, Hansen U: Three novel collagen VI chains, alpha4(VI), alpha5(VI), and alpha6(VI). J Biol Chem. 2008, 283: 20170-80. 10.1074/jbc.M710139200.View ArticlePubMedGoogle Scholar
- Bonaldo P, Russo V, Bucciotti F, Doliana R, Colombatti A: Structural and functional features of the alpha 3 chain indicate a bridging role for chicken collagen VI in connective tissues. Biochemistry. 1990, 29: 1245-54. 10.1021/bi00457a021.View ArticlePubMedGoogle Scholar
- Bidanset DJ, Guidry C, Rosenberg LC, Choi HU, Timpl R, Hook M: Binding of the proteoglycan decorin to collagen type VI. J Biol Chem. 1992, 267: 5250-6.PubMedGoogle Scholar
- Merlini L, Villanova M, Sabatelli P, Malandrini A, Maraldi NM: Decreased expression of laminin beta 1 in chromosome 21-linked Bethlem myopathy. Neuromuscul Disord. 1999, 9: 326-9. 10.1016/S0960-8966(99)00022-X.View ArticlePubMedGoogle Scholar
- Sabatelli P, Bonaldo P, Lattanzi G, Braghetta P, Bergamin N, Capanni C, Mattioli E, Columbaro M, Ognibene A, Pepe G, Bertini E, Merlini L, Maraldi NM, Squarzoni S: Collagen VI deficiency affects the organization of fibronectin in the extracellular matrix of cultured fibroblasts. Matrix Biol. 2001, 20: 475-86. 10.1016/S0945-053X(01)00160-3.View ArticlePubMedGoogle Scholar
- Scacheri PC, Gillanders EM, Subramony SH, Vedanarayanan V, Crowe CA, Thakore N, Bingler M, Hoffman EP: Novel mutations in collagen VI genes: expansion of the Bethlem myopathy phenotype. Neurology. 2002, 58: 593-602.View ArticlePubMedGoogle Scholar
- Saitta B, Timpl R, Chu ML: Human alpha 2(VI) collagen gene. Heterogeneity at the 5'-untranslated region generated by an alternate exon. J Biol Chem. 1992, 267: 6188-96.PubMedGoogle Scholar
- Merlini L, Angelin A, Tiepolo T, Braghetta P, Sabatelli P, Zamparelli A, Ferlini A, Maraldi NM, Bonaldo P, Bernardi P: Cyclosporin A corrects mitochondrial dysfunction and muscle apoptosis in patients with collagen VI myopathies. Proc Natl Acad Sci USA. 2008, 105: 5225-9. 10.1073/pnas.0800962105.View ArticlePubMedPubMed CentralGoogle Scholar
- Merlini L, Morandi L, Granata C, Ballestrazzi A: Bethlem myopathy: early-onset benign autosomal dominant myopathy with contractures. Description of two new families. Neuromuscul Disord. 1994, 4: 503-11. 10.1016/0960-8966(94)90091-4.View ArticlePubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://0-www.biomedcentral.com.brum.beds.ac.uk/1471-2350/11/44/prepub
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.