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J Peripher Nerv Syst. 2015 Dec;20(4):380-6. doi: 10.1111/jns.12145.

Mutational mechanisms in MFN2-related neuropathy: compound heterozygosity for recessive and semidominant mutations.

Author information

1
Department of Clinical Neurosciences, Clinic of Central and Peripheral Degenerative Neuropathies Unit, IRCCS Foundation, C. Besta Neurological Institute, Milan, Italy.
2
Department of Diagnostics and Applied Technology, Unit of Genetics of Neurodegenerative and Metabolic Disease, IRCCS Foundation, C. Besta Neurological Institute, Milan, Italy.
3
Department of Diagnostics and Applied Technology, Neurophysiopathology and Epilepsy Centre, IRCCS Foundation, C. Besta Neurological Institute, Milan, Italy.

Abstract

Mitofusin-2 (MFN2) mutations are the most common cause of autosomal dominant axonal Charcot-Marie-Tooth disease (CMT, type 2A), sometimes complicated by additional features such as optic atrophy (CMT6) and upper motor neuron involvement (CMT5). Several pathogenic mutations are reported, mainly acting in a dominant fashion, although few sequence variants behaved as recessive or semidominant in rare homozygous or compound heterozygous patients. We describe a 49-year-old woman with CMT5 associated with compound heterozygosity for two MFN2 variants, one already reported missense mutation (c.748C>T, p.R250W) and a novel nonsense sequence change (c.1426C>T, p.R476*). Her mother, carrying the p.R250W variant, had very late-onset minimal axonal neuropathy, whilst the father harboring the nonsense sequence change had neither clinical nor electrophysiological neuropathy. The missense mutation is likely pathogenic according to in silico analyses and a previous report, while the nonsense variant is predicted to behave as a null allele. The p.R250W variant behaves as semidominant by causing only a mild, almost subclinical, neuropathy when heterozygous; the nonsense mutation in the father was phenotypically silent, suggesting that haploinsufficiency for MFN2 is not disease causative, but was deleterious in the daughter who had only one active mutated MFN2 allele.

KEYWORDS:

Charcot-Marie-Tooth disease; mitochondrial dynamic; mitochondrial fusion; mitofusin-2

PMID:
26306937
DOI:
10.1111/jns.12145
[Indexed for MEDLINE]

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