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A locus on chromosome 15q for a dominantly inherited nemaline myopathy with core-like lesions

Gommans, I.M.P., Davis, M., Saar, K., Lammens, M., Mastaglia, F., Lamont, P., van Duijnhoven, G., ter Laak, J., Reis, A., Vogels, O.J.M., Laing, N., van Engelen, B.G.M. and Kremer, H. (2003) A locus on chromosome 15q for a dominantly inherited nemaline myopathy with core-like lesions. Brain, 126 (7). pp. 1545-1551.

Link to Published Version: http://dx.doi.org/10.1093/brain/awg162
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Abstract

Nemaline myopathy is a congenital neuromuscular disorder characterized by muscle weakness and the presence of nemaline rods. Five genes have now been associated with nemaline myopathy: α‐tropomyosin‐3 (TPM3), α‐actin (ACTA1), nebulin (NEB), β‐tropomysin (TPM2) and troponin T (TNNT1). In addition, mutations in the ryanodine receptor gene (RYR1) have been associated with core‐rod myopathy. Here we report linkage in two unrelated families, with a variant of nemaline myopathy, with associated core‐like lesions. The clinical phenotype consists of muscle weakness in addition to a peculiar kind of muscle slowness. A genome‐wide scan revealed a locus for nemaline myopathy with core‐like lesions on chromosome 15q21–q23 for both families. Combining the two families gave a two‐point LOD score of 10.65 for D15S993. The α‐tropomyosin‐1 gene (TPM1) located within this region is the strongest candidate gene. However, no mutations were found in the protein‐coding region of TPM1, although small deletions or mutations in an intron cannot be excluded. The critical region contains few other candidate genes coding for muscle proteins and several genes of unknown function, and has not yet been sequenced completely. The novel phenotype of nemaline myopathy in the two presented families corresponds to an also novel, as yet uncharacterized, genotype.

Publication Type: Journal Article
Publisher: Oxford University Press
Copyright: 2003 Guarantors of Brain
URI: http://researchrepository.murdoch.edu.au/id/eprint/25777
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