Mutations in the MTM1 gene implicated in X-linked myotubular myopathy

Jocelyn Laporte, Christophe Guiraud-Chaumeil, Marie Claire Vincent, Jean Louis Mandel, Stephan M. Tanner, Sabina Liechti-Gallati, Carina Wallgren-Pettersson, Niklas Dahl, Wolfram Kress, Pieter A. Bolhuis, Michel Fardeau, Françoise Samson, Enrico Bertini

Research output: Contribution to journalArticle

Abstract

X-linked recessive myotubular myopathy (XLMTM) is characterized by severe hypotonia and generalized muscle weakness, with impaired maturation of muscle fibres. The gene responsible, MTM1, was identified recently by positional cloning, and encodes a protein (myotubularin) with a tyrosine phosphatase domain (PTP). Myotubularin is highly conserved through evolution and defines a new family of putative tyrosine phosphatases in man. We report the identification of MTM1 mutations in 55 of 85 independent patients screened by single-strand conformation polymorphism for all the coding sequence. Large deletions were observed in only three patients. Five point mutations were found in multiple unrelated patients, accounting for 27% of the observed mutations. The possibility of detecting mutations and determining carrier status in a disease with a high proportion of sporadic cases is of importance for genetic counselling. More than half of XLMTM mutations are expected to inactivate the putative enzymatic activity of myotubularin, either by truncation or by missense mutations affecting the predicted PTP domain. Additional mutations are missenses clustered in two regions of the protein. Most of these affect amino acids conserved in the homologous yeast and Caenorhabditis elegans proteins, thus indicating the presence of other functional domains.

Original languageEnglish
Pages (from-to)1505-1511
Number of pages7
JournalHuman Molecular Genetics
Volume6
Issue number9
DOIs
Publication statusPublished - Sep 1997

ASJC Scopus subject areas

  • Genetics

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    Laporte, J., Guiraud-Chaumeil, C., Vincent, M. C., Mandel, J. L., Tanner, S. M., Liechti-Gallati, S., Wallgren-Pettersson, C., Dahl, N., Kress, W., Bolhuis, P. A., Fardeau, M., Samson, F., & Bertini, E. (1997). Mutations in the MTM1 gene implicated in X-linked myotubular myopathy. Human Molecular Genetics, 6(9), 1505-1511. https://doi.org/10.1093/hmg/6.9.1505