A heterozygous 21-bp deletion inCAPN3causes dominantly inherited limb girdle muscular dystrophy
| Autor: | K. Dahlbom, J. Hudson, Christoffer Jonsrud, Morten Duno, Christoph M Wahl, Hanns Lochmüller, Volker Straub, Lise Gammelgaard, Rita Barresi, Snjolaug Arnardottir, Marijke Van Ghelue, Nanna Witting, Laurence A. Bindoff, John Vissing |
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| Rok vydání: | 2016 |
| Předmět: |
0301 basic medicine
Genetics medicine.medical_specialty Weakness Muscle biopsy medicine.diagnostic_test biology Muscle weakness Calpain Dominant-Negative Mutation medicine.disease 03 medical and health sciences Gastrocnemius muscle 030104 developmental biology 0302 clinical medicine Endocrinology Internal medicine medicine biology.protein Neurology (clinical) medicine.symptom Myopathy 030217 neurology & neurosurgery Limb-girdle muscular dystrophy |
| Zdroj: | Vissing, J, Barresi, R, Witting, N, Van Ghelue, M, Gammelgaard, L, Bindoff, L A, Straub, V, Lochmuller, H, Hudson, J, Wahl, C M, Arnardottir, S, Dahlbom, K, Jonsrud, C & Duno, M 2016, ' A heterozygous 21-bp deletion in CAPN3 causes dominantly inherited limb girdle muscular dystrophy ', Brain, vol. 139, no. 8, pp. 2154-2163 . https://doi.org/10.1093/brain/aww133 |
| ISSN: | 1460-2156 0006-8950 |
| Popis: | Limb girdle muscular dystrophy type 2A is the most common limb girdle muscular dystrophy form worldwide. Although strict recessive inheritance is assumed, patients carrying a single mutation in the calpain 3 gene (CAPN3) are reported. Such findings are commonly attributed to incomplete mutation screening. In this investigation, we report 37 individuals (age range: 21-85 years, 21 females and 16 males) from 10 families in whom only one mutation in CAPN3 could be identified; a 21-bp, in-frame deletion (c.643_663del21). This mutation co-segregated with evidence of muscle disease and autosomal dominant transmission in several generations. Evidence of muscle disease was indicated by muscle pain, muscle weakness and wasting, significant fat replacement of muscles on imaging, myopathic changes on muscle biopsy and loss of calpain 3 protein on western blotting. Thirty-one of 34 patients had elevated creatine kinase or myoglobin. Muscle weakness was generally milder than observed in limb girdle muscular dystrophy type 2A, but affected the same muscle groups (proximal leg, lumbar paraspinal and medial gastrocnemius muscles). In some cases, the weakness was severely disabling. The 21-bp deletion did not affect mRNA maturation. Calpain 3 expression in muscle, assessed by western blot, was below 15% of normal levels in the nine mutation carriers in whom this could be tested. Haplotype analysis in four families from three different countries suggests that the 21-bp deletion is a founder mutation. This study provides strong evidence that heterozygosity for the c.643_663del21 deletion in CAPN3 results in a dominantly inherited muscle disease. The normal expression of mutated mRNA and the severe loss of calpain 3 on western blotting, suggest a dominant negative effect with a loss-of-function mechanism affecting the calpain 3 homodimer. This renders patients deficient in calpain 3 as in limb girdle muscular dystrophy type 2A, albeit in a milder form in most cases. Based on findings in 10 families, our study indicates that a dominantly inherited pattern of calpainopathy exists, and should be considered in the diagnostic work-up and genetic counselling of patients with calpainopathy and single-allele aberrations in CAPN3. |
| Databáze: | OpenAIRE |
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