1. Nonsense mutations in alpha-II spectrin in three families with juvenile onset hereditary motor neuropathy.
- Author
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Beijer, Danique, Deconinck, Tine, Bleecker, Jan L De, Dotti, Maria Teresa, Malandrini, Alessandro, Urtizberea, J Andoni, Zulaica, Miren, Munain, Adolfo López de, Asselbergh, Bob, Jonghe, Peter De, Baets, Jonathan, De Bleecker, Jan L, López de Munain, Adolfo, and De Jonghe, Peter
- Subjects
NONSENSE mutation ,LEBER'S hereditary optic atrophy ,SPECTRIN ,MOTOR neurons ,SENSORY neurons ,NEUROPATHY - Abstract
Distal hereditary motor neuropathies are a rare subgroup of inherited peripheral neuropathies hallmarked by a length-dependent axonal degeneration of lower motor neurons without significant involvement of sensory neurons. We identified patients with heterozygous nonsense mutations in the αII-spectrin gene, SPTAN1, in three separate dominant hereditary motor neuropathy families via next-generation sequencing. Variable penetrance was noted for these mutations in two of three families, and phenotype severity differs greatly between patients. The mutant mRNA containing nonsense mutations is broken down by nonsense-mediated decay and leads to reduced protein levels in patient cells. Previously, dominant-negative αII-spectrin gene mutations were described as causal in a spectrum of epilepsy phenotypes. [ABSTRACT FROM AUTHOR]
- Published
- 2019
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