Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethonin (original) (raw)
- Letter
- Published: February 2000
- Tim J. Wiltshire3,
- Georgine Faulkner4,
- Antje Nilforoushan5,
- Mariz Vainzof1,6,
- Oscar T. Suzuki1,2,
- Giorgio Valle7,
- Roger Reeves3,
- Mayana Zatz1,2,
- M. R. Passos-Bueno1,2 &
- …
- Dieter E. Jenne5
Nature Genetics volume 24, pages 163–166 (2000)Cite this article
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Abstract
Autosomal recessive limb-girdle muscular dystrophies (AR LGMDs) are a genetically heterogeneous group of disorders that affect mainly the proximal musculature1. There are eight genetically distinct forms of AR LGMD, LGMD 2A–H (refs 2–10), and the genetic lesions underlying these forms, except for LGMD 2G and 2H, have been identified. LGMD 2A and LGMD 2B are caused by mutations in the genes encoding calpain 3 (ref. 11) and dysferlin12, respectively, and are usually associated with a mild phenotype11,12,13. Mutations in the genes encoding γ-(ref. 14), α-(ref. 5), β-(refs 6,7) and δ (ref. 15)-sarcoglycans are responsible for LGMD 2C to 2F, respectively. Sarcoglycans, together with sarcospan, dystroglycans, syntrophins and dystrobrevin, constitute the dystrophin-glycoprotein complex16,17 (DGC). Patients with LGMD 2C–F predominantly have a severe clinical course4,5,6,7,8,13,14,15,18,19,20. The LGMD 2G locus maps to a 3-cM interval in 17q11–12 in two Brazilian families with a relatively mild form of AR LGMD (ref. 9). To positionally clone the LGMD 2G gene, we constructed a physical map of the 17q11–12 region and refined its localization to an interval of 1.2 Mb. The gene encoding telethonin, a sarcomeric protein, lies within this candidate region. We have found that mutations in the telethonin gene cause LGMD 2G, identifying a new molecular mechanism for AR LGMD.
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Acknowledgements
We thank the family members for their constant collaboration; C. Urbani for secretarial assistance; A.A.F.C. Ribeiro, A.L. Sertié, A.M.P. Cerqueira, B. Birren, M. Canovas, W. Caldeira, H. Reimann and E. Stegmann for support and technical assistance; and R.C. Pavanello, I. Pavanello and S.K. Marie for clinical assessment. This research has been supported by grants from the Fundação de Amparo a Pesquisa do Estado de São Paulo (FAPESP), Conselho Nacional de Pesquisa e Desenvolvimento (CNPq) and the Programa dos Núcleos de Excelência (PRONEX). D.J. is supported by the Sonderforschungsbereich 469, project A5, of the German Research Council and the European commission (BMH4-98-3865). G.F. and G.V. are supported by the Italian Telethon Foundation, grant 1023 and B41. M.R.P.B. is supported in part by an International Research Scholars grant from the Howard Hughes Medical Institute.
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Authors and Affiliations
- Centro de Estudos do Genoma Humano, Universidade de São Paulo, São Paulo, Brazil
Eloisa S. Moreira, Mariz Vainzof, Oscar T. Suzuki, Mayana Zatz & M. R. Passos-Bueno - Departamento de Biologia, Instituto de Biociências, Universidade de São Paulo, São Paulo, Brazil
Eloisa S. Moreira, Oscar T. Suzuki, Mayana Zatz & M. R. Passos-Bueno - Johns Hopkins University School of Medicine, Baltimore, Maryland, USA
Tim J. Wiltshire & Roger Reeves - International Centre for Genetic Engineering and Biotechnology , Trieste, Italy
Georgine Faulkner - Department of Neuroimmunology, Max-Planck Institute of Neurobiology, Martinsried, Germany
Antje Nilforoushan & Dieter E. Jenne - Departamento de Neurologia, FMUSP,
Mariz Vainzof - CRIBI, University of Padua, Padua, Italy
Giorgio Valle
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Moreira, E., Wiltshire, T., Faulkner, G. et al. Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethonin.Nat Genet 24, 163–166 (2000). https://doi.org/10.1038/72822
- Received: 15 October 1999
- Accepted: 10 January 2000
- Issue Date: February 2000
- DOI: https://doi.org/10.1038/72822