Channelpedia

PubMed 19191339


Referenced in Channelpedia wiki pages of: none

Automatically associated channels: ClvC2 , ClvC4



Title: Two novel CLCN2 mutations accelerating chloride channel deactivation are associated with idiopathic generalized epilepsy.

Authors: Cécile Saint-Martin, Grégory Gauvain, Georgeta Teodorescu, Isabelle Gourfinkel-An, Estelle Fedirko, Yvonne G Weber, Snezana Maljevic, Jan-Peter Ernst, Jennie Garcia-Olivares, Christoph Fahlke, Rima Nabbout, Eric LeGuern, Holger Lerche, Jean Christophe Poncer, Christel Depienne

Journal, date & volume: Hum. Mutat., 2009 Mar , 30, 397-405

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/19191339


Abstract
Heterozygous mutations in the CLCN2 gene encoding the voltage-gated chloride channel CLC2 have been identified in patients with idiopathic generalized epilepsy (IGE). Yet the involvement of CLCN2 in epilepsy remains controversial. To investigate the involvement of CLCN2 in another independent sample, we screened 52 unrelated patients from IGE families and 23 patients with Doose syndrome for mutations in CLCN2. No mutations were found in patients with Doose syndrome. In three unrelated IGE families, we identified two novel missense mutations, p.Arg235Gln and p.Arg577Gln, which were absent in large ethnically-matched control populations, and one novel p.Arg644Cys variant, which was also found in five Indian controls. Functional characterization of mutant channels using heterologous expression in mammalian cells and whole-cell patch-clamp recordings revealed faster deactivation kinetics as the major phenotype of both missense mutations. This finding predicts a loss of function that may contribute to intracellular chloride accumulation or neuronal hyperexcitability. However, the incomplete segregation of the mutations among affected members and the transmission by unaffected parents suggests that these CLCN2 mutations alone are not sufficient to induce epilepsy. They may instead represent susceptibility factors among other so far undetected genetic alterations in the respective families.