PubMed 19015483

Referenced in Channelpedia wiki pages of: none

Automatically associated channels: Nav1.4 , Slo1

Title: A novel dominant mutation of the Nav1.4 alpha-subunit domain I leading to sodium channel myotonia.

Authors: S Petitprez, L Tiab, L Chen, L Kappeler, K M Rösler, D Schorderet, H Abriel, J-M Burgunder

Journal, date & volume: Neurology, 2008 Nov 18 , 71, 1669-75

PubMed link:

Mutations in SCN4A may lead to myotonia.Presentation of a large family with myotonia, including molecular studies and patch clamp experiments using human embryonic kidney 293 cells expressing wild-type and mutated channels.In a large family with historic data on seven generations and a clear phenotype, including myotonia at movement onset, with worsening by cold temperature, pregnancy, mental stress, and especially after rest after intense physical activity, but without weakness, the phenotype was linked with the muscle sodium channel gene (SCN4A) locus, in which a novel p.I141V mutation was found. This modification is located within the first transmembrane segment of domain I of the Na(v)1.4 alpha subunit, a region where no mutation has been reported so far. Patch clamp experiments revealed a mutation-induced hyperpolarizing shift (-12.9 mV) of the voltage dependence of activation, leading to a significant increase (approximately twofold) of the window current amplitude. In addition, the mutation shifted the voltage dependence of slow inactivation by -8.7 mV and accelerated the entry to this state.We propose that the gain-of-function alteration in activation leads to the observed myotonic phenotype, whereas the enhanced slow inactivation may prevent depolarization-induced paralysis.