Functional characterization of ClC-1 mutations from patients affected by recessive myotonia congenita presenting with different clinical phenotypes

• Published in: Experimental neurology 2013-10, Vol.248, p.530-540
• Main Authors: Desaphy, Jean-François, Gramegna, Gianluca, Altamura, Concetta, Dinardo, Maria Maddalena, Imbrici, Paola, George, Alfred L., Modoni, Anna, LoMonaco, Mauro, Conte Camerino, Diana
• Format: Article
• Language: English
• Subjects: Acetazolamide; Action Potentials - physiology; Chloride channel mutation; Chloride Channels - genetics; Chloride Channels - metabolism; ClC-1 chloride channel; Genotype–phenotype relationship; HEK293 Cells; Humans; Muscle, Skeletal - metabolism; Muscle, Skeletal - physiopathology; Mutation; Myotonia congenita; Myotonia Congenita - genetics; Myotonia Congenita - metabolism; Myotonia Congenita - physiopathology; Non-dystrophic myotonia; Patch-clamp; Phenotype; Transitory weakness
• ISSN: 0014-4886; 1090-2430
• DOI: 10.1016/j.expneurol.2013.07.018

Myotonia congenita (MC) is caused by loss-of-function mutations of the muscle ClC-1 chloride channel. Clinical manifestations include the variable association of myotonia and transitory weakness. We recently described a cohort of recessive MC patients showing, at a low rate repetitive nerves stimulation protocol, different values of compound muscle action potential (CMAP) transitory depression, which is considered the neurophysiologic counterpart of transitory weakness. From among this cohort, we studied the chloride currents generated by G190S (associated with pronounced transitory depression), F167L (little or no transitory depression), and A531V (variable transitory depression) hClC-1 mutants in transfected HEK293 cells using patch-clamp. While F167L had no effect on chloride currents, G190S dramatically shifts the voltage dependence of channel activation and A531V reduces channel expression. Such variability in molecular mechanisms observed in the hClC-1 mutants may help to explain the different clinical and neurophysiologic manifestations of each ClCN1 mutation. In addition we examined five different mutations found in compound heterozygosis with F167L, including the novel P558S, and we identified additional molecular defects. Finally, the G190S mutation appeared to impair acetazolamide effects on chloride currents in vitro. •Myotonia congenita is a muscle disorder due to mutations in ClC-1 chloride channel.•Eight ClC-1 channel mutants were studied using patch-clamp technique.•Mutations induce a variety of molecular defects in ClC-1 channel function.•We discuss the relationship between genotype and clinical phenotype.