These authors contributed equally to this study.
Exome sequencing detection of two untranslated GFPT1 mutations in a family with limb-girdle myasthenia
Version of Record online: 11 MAR 2013
© 2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd
Volume 85, Issue 2, pages 166–171, February 2014
How to Cite
Maselli, R.A., Arredondo, J., Nguyen, J., Lara, M., Ng, F., Ngo, M., Pham, J.M., Yi, Q., Stajich, J.M., McDonald, K., Hauser, M.A. and Wollmann, R.L. (2014), Exome sequencing detection of two untranslated GFPT1 mutations in a family with limb-girdle myasthenia. Clinical Genetics, 85: 166–171. doi: 10.1111/cge.12118
Nothing to declare.
- Issue online: 13 JAN 2014
- Version of Record online: 11 MAR 2013
- Manuscript Revised: 1 FEB 2013
- Manuscript Accepted: 1 FEB 2013
- Manuscript Received: 22 OCT 2012
- NIH. Grant Number: 5R01NS049117-03
- The Myasthenia Gravis Foundation of California
- The Muscular Dystrophy Association. Grant Numbers: MDA 4090, MDA 186447
- congenital myasthenic syndromes;
- limb-girdle myasthenia;
- neuromuscular junction;
- whole-exome sequencing
The term ‘limb-girdle myasthenia’ (LGM) was first used to describe three siblings with proximal limb weakness without oculobulbar involvement, but with EMG decrement and responsiveness to anticholinesterase medication. We report here that exome sequencing in the proband of this family revealed several sequence variations in genes linked to proximal limb weakness. However, the only mutations that cosegregated with disease were an intronic IVS7-8A>G mutation and the previously reported 3′-UTR c.*22C>A mutation in GFPT1, a gene linked to LGM. A minigene assay showed that IVS7-8A>G activates an alternative splice acceptor that results in retention of the last seven nucleotides of intron 7 and a frameshift leading to a termination codon 13 nucleotides downstream from the new splice site. An anconeus muscle biopsy revealed mild reduction of the axon terminal size and postsynaptic fold simplification. The amplitudes of miniature endplate potentials and quantal release were also diminished. The DNA of the mildly affected father of the proband showed only the intronic mutation along with sequence variations in other genes potentially relevant to LGM. Thus, this study performed in the family originally described with LGM showed two GFPT1 untranslated mutations, which may cause disease by reducing GFPT1 expression and ultimately impairing protein glycosylation.