The collagen VI related muscular dystrophies (COL6-RD), Ullrich congenital muscular dystrophy (UCMD) and Bethlem myopathy (BM) are among the most common congenital muscular dystrophies and are characterized by distal joint laxity and a combination of distal and proximal joint contractures. Inheritance can be dominant negative (DN) or recessive depending on the type and location of the mutation. DN mutations allow incorporation of abnormal chains into secreted tetramers and are the most commonly identified mutation type in COL6-RD. Null alleles (nonsense, frameshift, and large deletions) do not allow incorporation of abnormal chains and act recessively. To better define the pathways disrupted by mutations in collagen VI, we have used a transcriptional profiling approach with RNA-Seq to identify differentially expressed genes in COL6-RD individuals from controls.
RNA-Seq allows precise detection of all expressed transcripts in a sample and provides a tool for quantification of expression data on a genomic scale. We have used RNA-Seq to identify differentially expressed genes in cultured dermal fibroblasts from 13 COL6-RD individuals (8 dominant negative and 5 null) and 6 controls. To better assess the transcriptional changes induced by abnormal collagen VI in the extracellular matrix (ECM); we compared transcriptional profiles from subjects with DN mutations and subjects with null mutations to transcriptional profiles from controls.
Differentially expressed transcripts between COL6-RD and control fibroblasts include upregulation of ECM components and downregulation of factors controlling matrix remodeling and repair. DN and null samples are differentiated by downregulation of genes involved with DNA replication and repair in null samples.
Citation: Butterfield RJ, Dunn DM, Hu Y, Johnson K, Bönnemann CG, Weiss RB (2017) Transcriptome profiling identifies regulators of pathogenesis in collagen VI related muscular dystrophy. PLoS ONE 12(12): e0189664. https://doi.org/10.1371/journal.pone.0189664
Editor: Florence Ruggiero, Ecole normale superieure de Lyon, FRANCE
Received: June 22, 2017; Accepted: November 29, 2017; Published: December 15, 2017
This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication.
Data Availability: The data, including raw sequence files for each subject, have been deposited in NCBI’s Gene Expression Omnibus and are accessible through GEO Series accession number GSE103270 (https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE103270).
Funding: CureCMD and NIH 1K08NS097631-01 to RJB; Intramural Research Program of the NIH, NINDS to CGB. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: Russell J. Butterfield is supported by NIH grant 1K08NS097631-01 and CureCMD. He is receiving funding via contracts for clinical trials from PTC Therapeutics, Sarepta Therapeutics, Pfizer, Marathon, Biogen, Summit Therapeutics, Santhera Pharmaceuticals, and aTyr Pharmaceuticals. Dr. Butterfield serves on scientific advisory boards for Sarepta Therapeutics, Biogen, PTC Therapeutics, and Wave Life Sciences. Diane M. Dunn has no competing interests. Ying Hu has no competing interests. Kory Johnson has no competing interests. Carsten G. Bönnemann no competing interests. Robert B. Weiss has no competing interests. This does not alter our adherence to PLOS ONE policies on sharing data and materials.
The collagen VI related muscular dystrophies (COL6-RD), Ullrich congenital muscular dystrophy (UCMD) and Bethlem myopathy (BM) are inherited disorders of collagen VI characterized by distal joint laxity and a combination of distal and proximal joint contractures [1, 2]. COL6-RD are increasingly recognized disorders accounting for up to 30% of patients with congenital muscular dystrophy (CMD) phenotypes.[2, 3] COL6-RD are unusual among the muscular dystrophies in that both muscle and connective tissue are significantly affected. Patients have muscle weakness and atrophy attributable to a defect in the muscle, but also have severe joint contractures, joint laxity, keratosis pilaris, and a predilection to keloid formation attributable to a connective tissue defect. Children with COL6-RD have life-long neurologic, orthopedic, and pulmonary complications necessitating complex, multispecialty care. Despite increased recognition of these disorders, there are no treatments.
In most CMD phenotypes the molecular defect results in a direct disruption of the stability sarcolemmal membrane and its linkages between the cytoskeleton and extracellular matrix (ECM). In COL6-RD, the pathogenic mechanisms are less well understood. While components of the ECM in muscle, including collagens I, III, and V, are produced by both the myofiber and muscle connective tissue (MCT) fibroblasts, collagen VI in the muscle is produced primarily by MCT fibroblasts.[5, 6] It is not clear how a defect in collagen VI results in a defect in the muscle.[4, 7] COL6-RD may constitute a “non-cell autonomous” disorder whereby the cell causing disease (MCT fibroblast) is different from the cell where disease is expressed (myofiber). The mechanisms whereby a disruption of collagen VI in the ECM of muscle results in pathologic phenotype on the myofiber are not yet understood.[4, 7]
To better define the pathways disrupted by mutations in COL6-RD, we have used a transcriptional profiling approach with RNA-Seq to identify differentially expressed genes in cultured dermal fibroblasts from COL6-RD subjects and controls. Computational analysis of read count data from RNA-Seq experiments provide estimations of transcript isoforms and abundance on a genomic scale.[8, 9] To better assess the transcriptional changes induced by the presence abnormal collagen VI in the extracellular matrix (ECM) (as compared to its absence from the ECM); we have compared transcriptional profiles from subjects with dominant negative mutations and subjects with null mutations to transcriptional profiles from controls.
Materials and methods
Thirteen COL6-RD subjects and 6 control subjects were included in the study. (Table 1) All patients included in the study have clinical features typical of UCMD including early onset hypotonia with proximal contractures, distal hyperlaxity, and hyperkeratosis pilaris with loss of ambulation or trajectory toward loss of ambulation by teenage years. Dominant negative (DN) mutations including glycine substitutions and exon skipping mutations in the triple helical (TH) region of any of the collagen VI genes are the most common mutational mechanism in COL6-RD. DN mutations allow residual, abnormal collagen VI in the ECM, while null mutations produce no collagen VI in the ECM. We selected eight subjects with dominant negative mutations, 4 with the glycine substitution p.Gly284Arg or p.G281Arg in the TH domain in COL6A1 and 4 with exon skipping mutations involving exon 16 of the COL6A3 gene, thus representing the most common DN mutations. Five subjects with COL6-RD due to recessive, null mutations were also included. This study was approved by the Institutional Review Board of the National Institute of Neurological Disorders and Stroke, National Institutes of Health and the University of Utah (IRB registrations: 30923, Utah; 12N0095, NIH). Written informed consent and appropriate assent were obtained from all participating subjects.
Fibroblasts derived from skin biopsy samples were grown in Dulbecco’s modified Eagle medium with 10% FBS and 1% Penicillin/Streptomycin in a 6-well plate in 5% CO2 at 37°C until 80% confluence. Cells were continuously cultured in the presence of 25ug/ml L-ascorbic acid phosphate (Wako, Osaka, Japan) for 72 hours and then changed to medium without L-ascorbic acid phosphate for 16 hours before the RNA extraction using RNeasy Mini Kit (QIAGEN, cat# 74106).
Total RNA was obtained from previously existing dermal fibroblast cell lines from COL6-RD individuals with dominant negative or null mutations and from existing control fibroblast cell lines. Poly-A purified sequencing libraries were produced from total RNA using the Illumina TruSeq RNA Sample Prep Kit (Illuminia, Inc., San Diego, CA) according to the manufacturer’s protocol. Sequencing was performed using the Illumina HiSeq 2000 instrument with a 50 cycle single-end protocol at the University of Utah Microarray and Genomic Analysis Core. Sequenced reads were processed for quality using FASTX toolkit version 0.0.13 (http://hannonlab.cshl.edu/fastx_toolkit/) to clip adapter sequences and filter for minimum quality score of 15 or greater in 80% of bases per read.
Differential expression analysis
Read mapping and differential expression analysis were performed using the TopHat-Cufflinks pipeline using a reference transcriptome based on (GRCv37 / UCSC hg19) reference genome. Alignment of filtered/clipped reads to the reference sequence was performed using Tophat2 (v2.0.10) with default parameters. Transcript abundances were estimated and normalized for transcript length and for read depth and reported as fragments per kb (in the transcript model) per million reads mapped (FPKM) using Cufflinks (v2.2.1). Differential expression was determined using Cuffdiff2 with pairwise comparisons for 1) control vs. dominant negative mutants, 2) control vs. null mutants, and 3) dominant negative mutants vs. null mutants. Our analysis used the –G option to restrict the analysis to the reference genome, -u to correct for multi-reads, and–b option to implement the fragment bias correction algorithm. Genes were considered differentially expressed and included in ontology and pathway analysis when the FDR-adjusted p-value was <0.05. We identified enriched gene ontology categories and KEGG pathways among differentially expressed genes using GOSeq, an algorithm specifically designed for RNA-Seq data. Gene ontology terms were considered significantly enriched if the FDR adjusted p-value was <0.01. Redundant gene ontology categories were parsed using Revigo, an online tool to identify redundant GO terms. GO terms with frequency > 1%, dispensability >0.2, and uniqueness <0.5 were filtered from the list of enriched terms. The data, including raw sequence files for each subject have been deposited in NCBI’s Gene Expression Omnibus and are accessible through GEO Series accession number GSE103270 (https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE103270).
Mapping and differential expression analysis
RNA sequencing (RNA-Seq) was completed for 13 COL6-RD samples and 6 control samples. Average sequencing depth was 32.8 million reads per sample (range 24.5–47.6 million). Filtering adaptor sequences and poor quality reads removed a mean 7.5% reads per sample. Mapping using TopHat was successful for a mean of 90.7% of total reads. There were no significant differences in sequencing depth or mapping efficiency between samples by mutation group (control vs. DN vs. null) or by gender (M vs. F).
Expression values were normalized to library size and transcript length using Cufflinks and reported as fragments per kilobase of transcript per million reads mapped (FPKM). As expected, the most highly expressed genes were ECM components including collagen I, fibronectin and vimentin. The three genes forming collagen VI (COL6A1, COL6A2, and COL6A3) were all in the top 100 highly expressed genes. Expression of COL6A3 was about 1/3 the level of expression of COL6A1 and COL6A2. As expected, collagen VI null samples had decreased expression for their null alleles compared to controls, while the expression of the non-mutated collagen VI genes does not appear to be increased in compensation for absence of the null allele (Table 2). Expression was not completely ablated by the null allele in subject 15 with an expression of COL6A3 of 26% of the control level. Residual expression of the mutant COL6A3 transcript in this sample suggests that some mutant transcripts may escape nonsense-mediated decay. Absence of collagen VI in cultured fibroblasts from this sample suggests that these transcripts do not produce significant amounts of collagen VI (S1 Fig). Expression of the COL6A4P1, COL6A4P2, COL6A5 and COL6A6 genes was below detection levels. Multidimensional scaling analysis based on estimated expression levels demonstrates that dominant negative samples are distinct from null and control samples (S2 Fig). Clustering of control and null samples is less distinct, but suggestive that groups are different from each other.
Differential expression analysis was performed using Cufflinks2. We identified 586 differentially expressed genes (FDR-adjusted p-value <0.05) in comparison of DN to Control samples, and 341 differentially expressed genes in Null vs. Control samples. Comparison of DN to Null samples revealed 868 differentially expressed (DE) genes. When considering all affected samples together, (DN and null compared to control) 171 genes were differentially expressed. Taken together we identified 1246 genes differentially expressed in one or more comparisons (Fig 1). A complete list of differentially expresses genes for each comparison (DN vs. control, Null vs. control, DN vs. Null, and any mutation vs. control) is included in electronic format including test statistics and an estimation of fold change (S1 File).
Gene ontology and pathway analysis
We identified 329 enriched GO terms in the DN vs. control group, 311 in the Null vs. control group, and 196 in the DN vs. null group. After parsing GO terms for redundancy, 76 GO terms remained in the DN vs. control group, 61 in the Null vs. control group, and 53 in the DN vs. Null group. The top enriched non-redundant GO terms in dominant negative vs. control fibroblasts came from categories centered on three primary themes, extracellular matrix, adhesion, and immune response (Table 3, S2 File). A similar pattern of enriched GO terms was seen in enrichment of DE genes in control vs. null fibroblasts. In contrast, enriched GO ontologies in DN vs. Null fibroblasts centered on DNA replication/repair and proliferation.
Enrichment of KEGG pathways reflected similar themes with significant enrichment of the ECM-receptor interaction pathway (hsa04512) and the cytokine-cytokine receptor interaction pathway (hsa04060) in the DN vs. control and DN vs Null groups (S1 Table). Structural ECM components such as collagens were increased generally, with significant upregulation of COL11A1 and COL5A3 in DN vs. control fibroblasts and COL11A1, COL4A1 and COL4A2 in null vs. control samples (Fig 2). While not a part of the hsa04512 pathway other collagen genes were also significantly upregulated: COL14A1, COL15A1, COL7A1, and COL8A2 in DN vs. control fibroblasts and COL14A1, COL15A1, COL8A2 in null vs. control fibroblasts. In contrast, integrins and other signaling/adhesion components of the matrix were downregulated, including: ITGA2, ITGA3, ITGA6 and LAMB3 in DN vs. control and ITGA3, ITGA6, and LAMB3 in null vs. control.
Differential expression of genes in the ECM-receptor interaction pathway (hsa04512) for control vs. dominant negative mutation (upper panel) and control vs null mutation (lower panel). Log2 fold change is plotted for each gene in the pathway. Genes with significant differential expression (FDR-adjusted p-value was <0.05) are marked with an *. COL6A1 and COL6A2 (marked with + in the lower panels) are decreased in null samples as expected due to their null allele.
DE genes in the cytokine-cytokine interaction pathway (hsa04060) include downregulation of a cluster of ELR (glutamic acid-leucine-arginine)-positive CXC chemokines, including: CXCL2, CXCL3, CXCL5, and CXCL6 in both the DN vs. control and the Null vs. control groups (Fig 3). IL8, another ELR-positive CXC chemokine is also significantly downregulated. Other notable DE genes in this pathway include upregulation of ACVR2A and down regulation of IL1B and IL24 in the DN vs. control group and upregulation of FLT1, IL6, NGFR, and TNFSF4 in the Null vs. control group. PRLR is significantly downregulated in the Null vs. control group, but not differentially expressed in the DN vs. control group.
Differential expression of genes in the cytokine-cytokine receptor interaction pathway (hsa04060) for control vs. dominant negative mutation (upper panel) and control vs. null mutation (lower panel). Log2 fold change is plotted for each gene in the pathway. Genes with significant differential expression (FDR-adjusted p-value was <0.05) are marked with an *.
Enrichment of KEGG pathways in comparing the DN vs. null group cluster strongly around a single theme: proliferation and cell division. Enriched pathways include both cell cycle (hsa04110) and DNA replication (hsa03030) pathways (Fig 4). In both pathways, null samples show downregulation of almost all genes compared to DN including clusters of cyclin genes, polymerases, and minichromosome maintenance complex (MMC) genes. CDKN1B and TGFB1 were upregulated in the null compared to DN; however, consistent with the effects from other genes in the pathway, both TGFB1 and CDKN1B are negative regulators of proliferation. Mismatch repair (hsa03430), pyrimidine metabolism (hsa00240), and nucleotide excision repair (hsa03420) pathways all showed similar findings (S1 Table).
Differential expression of genes in the cell cycle pathway (hsa04110, upper panel) and DNA replication (hsa03030, lower panel) for COL6-RD dominant negative vs. null (lower panel). Log2 fold change is plotted for each gene in the pathway (positive values reflect increased expression in the dominant negative mutants). Genes with significant differential expression (FDR-adjusted p-value was <0.05) are marked with an *.
COL6-RD are the paradigmatic disorders of the extracellular matrix of muscle and are unique among the CMD in that both muscle and connective tissue are affected. Since collagen VI is produced by resident interstitial fibroblasts, the downstream pathological effects on muscle cells are cell non-autonomous. Thus the effect of mutant collagen VI on fibroblasts is critical to understanding the mechanisms whereby a disruption of collagen VI in the muscle ECM confers pathologic consequences on the myofiber. To approach this question, we used a transcriptome profiling approach with RNA-Seq in cultured dermal fibroblasts from individuals with COL6-RD. While transcriptional analysis in muscle connective tissue fibroblasts may be preferable given the muscle phenotype, they are not readily available. Patients with COL6-RD also have significant clinical findings in the skin including keloid scarring and hyperkeratosis pilaris making skin fibroblasts a valuable tool for both the diagnosis and study of pathogenies of COL6-RD. We anticipate that key transcriptional pathways regulating both muscle and skin fibroblast phenotypes can be identified with our approach. Differentially expressed genes between COL6-RD subjects (with either DN or null mutations) and controls centered on two themes: an increase in expression of genes in the extracellular matrix and a decrease in expression of genes involved with inflammation and immune response. Matrix-related genes including multiple collagens are upregulated in COL6-RD samples, while multiple integrin and ECM signaling genes are downregulated (Fig 2). Inflammatory regulators including Il1B, IL24 and multiple ELR+ CXC chemokines (most notably CXCL5 and Il8) are downregulated (Fig 3). Since collagen VI is retained intracellularly in fibroblasts from individuals with DN mutations,[6, 16] we hypothesized that the retained collagen VI may induce ER stress; however, genes associated with ER stress were not differentially expressed.
Upregulation of matrix components and downregulation of inflammatory mediators in both DN and null samples compared to controls may be reflected in a dysregulation of normal wound healing processes in absence of normal collagen VI. Wound healing is a complex process including an intial inflammatory response and recruitment of fibroblasts and inflammatory cells, production and deposition of extracellular matrix, and matrix organization and remodeling. This combination of upregulation of matrix components and downregulation of genes controlling matrix remodeling may result in disruption of the balance of matrix production and remodeling and result in overproduction of matrix leading to fibrosis. In this respect collagen VI is thought to be a significant regulator of matrix assembly and composition.
Prior analyses of transcriptional changes in COL6-RD using microarray in both muscle and dermal fibroblast samples both described upregulation of ECM genes, and disruption or ECM remodeling.[18, 19] These authors identified an upregulation of both IGF-1 and follistatin genes in muscle samples from COL6-RD subjects. In our study, IGFBP2 (Insulin-Like Growth Factor Binding Protein 2) is one of the most significantly upregulated genes with log2 fold change of +4.0 in control vs. DN and +3.3 in control vs. null samples. IGFBP2 is thought to be an important regulator of wound healing by its effect promoting proliferation and differentiation of fibroblasts and myoblasts.[20, 21] In agreement with previous findings that FST (follistatin) is upregulated in muscle biopsy samples form COL6-RD individuals, in our study, FST in dermal fibroblasts is significantly upregulated (log2 fold change +1.4 in DN and +1.2 in Null). FST is of particular interest since follistatin is a natural myostatin antagonist and has been proposed as a target for treatment of muscular dystrophy by promotion of muscle growth and decreasing fibrosis.[22, 23] Upregulation of FST in COL6-RD subjects may reflect an active response to progressing fibrosis.
COL6-RD are unusual in that inheritance can be either dominant or recessive. In most cases, dominant mutants produce an abnormal, dysfunctional matrix, while recessive mutations result in absent collagen VI in the matrix. While similar in many respects, DN and null subjects have key differences in DE genes compared to controls. THBS4 (thrombospondin 4, log2 fold change +3.1) and TNXB (tenascin XB, log2 fold change +1.5) were markedly upregulated in DN vs. control samples but not null vs. control samples, perhaps reflecting the role of abnormal collagen VI in the ECM of DN fibroblasts which is not present in null fibroblasts. Thrombospondins, including THBS4 are secreted proteins that are embedded in the ECM and play a role in angiogenesis and wound healing, and may play a role in regulation of the composition of the ECM in skeletal muscle. Overexpression of mouse Thbs4 induces an ATF6-dependent endoplasmic reticulum stress response after cardiac injury that induces one branch of the UPR gene expression program, including increasing the protein levels of BiP (Grp78), Sdf2l1, Creld2, Calr, Armet, Hyou1, Mthfd2, and PDI. In our study, only SDF2L1 from this pathway was differentially expressed in the DN vs. control comparison, although the decreased expression level in DN fibroblast suggests this was not an ER stress-induced response. It has also been suggested that Thbs4 may facilitate the trafficking of ECM proteins through the vesicular secretory pathway. Therefore, THBS4 upregulation in both DN and null fibroblast may also reflect a change in the regulation of intracellular trafficking in response to unbalanced collagen VI levels in the secretory pathway. TNXB is a glycoprotein in the ECM with significant role in matrix maturation and wound healing. Biallelic mutations in TNXB are associated with classical-like Ehlers-Danlos syndrome, and share many symptoms with COL6-RD.[27–30] COMP (cartilage oligomeric matrix protein) is another thrombospondin family gene (thrombospondin 5) with a role in bridging ECM structures and fibrosis. COMP is one of the most significant DE genes with log2 fold change of +1.7 in DN vs. control fibroblasts but no significant difference between null and control fibroblasts.
A comparison of transcriptional profiles between DN and null samples reveals a striking down-regulation of genes involved in cell division and proliferation pathways in null samples. While the upregulation of genes promoting production of ECM and downregulation of regulators of inflammation and tissue remodeling (wound healing) may not be surprising in a disorder such as COL6-RD, the down-regulation of cell division and proliferation pathways is less intuitive, and may reflect a role for collagen VI in regulating cell proliferation. In that regard, soluble collagen VI has been shown to stimulate cell proliferation and DNA synthesis in a variety of cell-culture systems. This effect is thought to be regulated through promotion of G1 to S phase by cyclins A, B, and D1. In our study, cyclins B1, B2 and D1 were all significantly downregulated in null samples which lack collagen VI in the ECM compared to DN (log2 fold change for CCNB1–0.61, CCNB2–0.68, and for CCND1–0.80). The difference in transcription of genes associated with proliferation and cell division between DN and null may reflect the absence of collagen VI in the matrix of null samples. Consistent with this idea, individuals with collagen VI null mutations lack a soluble cleavage product of the C5 domain of the collagen VI α3(VI) chain, referred to as endotrophin, which has been identified as a soluble regulator of tumor progression in several cancers and a mediator of metabolic regulation.[34–36]
Collagen VI is an important component of the extracellular matrix of many tissues including muscle, skin, tendon, cartilage, and adipose tissues, and has an important role in maintaining structural stability of tissues by anchoring the basement membrane to the extracellular matrix.[37–39] It is not yet clear how a defect in collagen VI, which is produced primarily by muscle connective tissue fibroblasts results in a defect in the muscle.[4, 6, 7] It has been suggested that the simultaneous presence of myofiber atrophy and regeneration seen in collagen VI myopathy may represent a failure of myogenesis and repair mechanisms that are dependent on interactions between the MCT fibroblasts and the satellite cell.[40, 41] Here we have identified differentially expressed genes in fibroblast samples form COL6-RD subjects that reflect the importance of pathways controlling inflammation and production of ECM as well as highlight the importance of collagen VI in regulating proliferation. Our results suggest that a defect in the balance of ECM synthesis and breakdown in COL6-RD may result in increased matrix deposition, leading to early fibrosis.
S1 Fig. Immunofluorescent staining of cultured fibroblasts from a COL6-RD individual (subject 15) with a homozygous null mutation in COL6A3 (p.S18*).
Staining for collagen VI in cultured fibroblasts from subject 15 shows absence of collagen VI in the ECM of patient fibroblasts compared to control. Collagen VI staining in the presence of TritonX-100 to permeablize the cell membrane demonstrates absence of intracellular retention of collagen VI that is typical samples with dominant negative mutations. Immunofluorescence analysis of cultured fibroblasts was performed as described by Lampe et al., Hum Mutat. 2008; 29:809–822. Fibroblasts were grown to 80% confluence and then treated with L-ascorbic acid (50ng/μl) for 5 days and then fixed in 4% parformaldehyde and blocked with 10% fetal bovine serum albumin with or without 0.1% TritonX-100. Staining for collagen VI was performed using anti-collagen VI monoclonal antibody MAB3303 (Chemicon, Temecula, CA) 1:2,500 dilution, and Alexa Fluor 488-conjugated goat anti-mouse immunoglobulin (Molecular Probes, Eugene, OR) 1:500 dilution. Images were obtained using a Nikon Eclipse Ti microscope.
S2 Fig. Multidimensional scaling analysis for differentially expressed genes in COL6-RD and control fibroblasts.
COL6-RD fibroblast samples with dominant negative mutations (n = 8), null mutations (n = 5), and controls (n = 6) showing clustering by mutation class based on gene expression levels.
S1 File. Significant Differentially Expressed Genes in control and COL6-RD fibroblasts with dominant negative or null mutations.
S2 File. Significant DE genes within enriched Gene Ontology categories.
We are grateful to the patients and families for their participation in the study. The research was supported by funds from Cure CMD to RJB, NIH/NINDS 1K08NS097631-01 to RJB, and by intramural funds of NINDS to CGB.
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