A novel mutation of myelin protein zero associated with an axonal form of Charcot-Marie-Tooth disease

L. Santoro, F. Manganelli, E. Di Maria, D. Bordo, D. Cassandrini, F. Ajmar, P. Mandich, E. Bellone

Research output: Contribution to journalArticlepeer-review

Abstract

Objective: To report a new mutation in the MPZ gene which encodes myelin protein zero (P0), associated with an axonal form of Charcot-Marie-Tooth disease (CMT). Methods: Three patients from an Italian family with a mild, late onset axonal peripheral neuropathy are described clinically and electrophysiologically. To detect point mutation in MPZ gene the whole coding sequence was examined. The structure of the mutated protein was investigated using the three dimensional model of P0. Results: All patients showed a relatively mild CMT phenotype characterised by late onset and heterogeneity of the clinical and electrophysiological features. Molecular analysis demonstrated a novel heterozygous T/A transversion in the exon 3 of MPZ gene that predicts an Asp109Glu amino acid substitution in the extracellular domain of the P0. Asp109 is found at the protein surface, on β strand E, in the interior of the P0 tetramer. Conclusions: The identification of Asp109Glu mutation confirms the pivotal role of P0 in axonal neuropathies and stresses the phenotypic heterogeneity associated with MPZ mutations. This study suggests the value of screening for MPZ mutations in CMT family members with minor clinical and electrophysiological signs of peripheral neuropathy.

Original languageEnglish
Pages (from-to)262-265
Number of pages4
JournalJournal of Neurology, Neurosurgery and Psychiatry
Volume75
Issue number2
Publication statusPublished - Feb 2004

ASJC Scopus subject areas

  • Neuropsychology and Physiological Psychology
  • Neuroscience(all)
  • Psychiatry and Mental health

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