Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis

Sir, A recent study by Bannwarth and colleagues has shown that variation in the CHCHD10 gene is a cause of familial amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) (Bannwarth et al., 2014). The study identified a c.176C > T (p.Ser59Leu, NM_213720.1) missense mutation in a multi-generational kindred. In the present study, we performed genome sequencing of four affected individuals from a large ALS family (USALS#5). This identified a G to T transversion at position c.44 (chr22:24,109,778, hg19) that segregated with disease within this pedigree and leads to a p.R15L amino acid change in exon two of the CHCHD10 mitochondrial protein. Previous attempts to identify the causative mutation in this family using an exome sequencing approach failed to identify this variant due to poor sequence coverage in this genomic region. The variant was not described as a human polymorphism in the Single Nucleotide Polymorphism (SNP) database (http://www.ncbi.nlm.nih.gov/SNP/, build 141) and was not found in 1158 control individuals of the Exome Sequencing Project (http://snp.gs.washington.edu/SeattleSeqAnnotation138/). To further assess the mutation burden in patients, we Sanger sequenced all exons of CHCHD10 in an additional series of 84 patients diagnosed with familial ALS according to the El Escorial criteria (Brooks, 1994). These samples did not carry the C9orf72 hexanucleotide repeat expansion or known mutations in ALS genes including SOD1, TARDBP, FUS, VCP, PFN1, UBQLN1, MATR3, SQSTM1, OPTN, and HNPNPA2B1 (Renton et al., 2014). The ethical review boards at each institution approved the study, and all participants provided informed consent. Our mutational screening of CHCHD10 identified the same p.R15L mutation discovered in the USALS#5 family in two additional familial ALS cases (www.coriell.org, ND10928 and ND11809). Analysis of genome-wide SNP chip data indicates that all six patients carrying the p.R15L variant share a 6.2 Mb haplotype across the gene. Our data demonstrate that mutations in CHCHD10 are a relatively common cause of familial ALS and that pathogenic variants are concentrated in exon 2. This represents the first time, to our knowledge, that genome sequencing has been applied to familial ALS. The primary advantage of this methodology is improved coverage of protein-coding regions of the genome, particularly in GC-rich regions that may not be effectively captured by the oligonucleotide baits that are central to exome sequencing. It is also noteworthy that patients in the pedigree reported by Bannwarth and colleagues had reliable evidence of mitochondrial myopathy. Two other ALS genes, VCP and MATR3, have been associated with clinical myopathy (Johnson et al., 2010, 2014), suggesting that muscle involvement may be more common in familial ALS than previously appreciated. DNA samples for this study were obtained in part from the National Institute of Neurological Disorders and Stroke (NINDS) repository at the Coriell Cell Repositories (http://www.coriell.org/). We thank the patients and research subjects who contributed samples for this study. This work was supported in part by the Intramural Research Programs of the US National Institutes of Health (NIH), National Institute on Ageing (Z01-AG000949-02) and NINDS. The work was also supported by the Packard Centre for ALS Research at Johns Hopkins, ALS Association, Muscular Dystrophy Association, Ontario Research Fund, Italian Health Ministry, Fondazione Vialli e Mauro Onlus, Federazione Italiana Giuoco Calcio, Compagnia di San Paolo, Adelis Foundation, European Community’s Health Seventh Framework Programme (FP7/2007-2013) under grant agreements 259867.

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