Dominantly inherited myotonia congenita resulting from a mutation that increases open probability of the muscle chloride channel CLC-1

David P Richman, Yawei Yu, Ting Ting Lee, Pang Yen Tseng, Wei Ping Yu, Ricardo A Maselli, Chih Yung Tang, Tsung-Yu Chen

Research output: Contribution to journalArticle

8 Citations (Scopus)

Abstract

Myotonia congenita-inducing mutations in the muscle chloride channel CLC-1 normally result in reduced open probability (Po) of this channel. One well-accepted mechanism of the dominant inheritance of this disease involves a dominant-negative effect of the mutation on the function of the common-gate of this homodimeric, doublebarreled molecule. We report here a family with myotonia congenita characterized by muscle stiffness and clinical and electrophysiologic myotonic phenomena transmitted in an autosomal dominant pattern. DNA sequencing of DMPK and ZNF9 genes for myotonic muscular dystrophy types I and II was normal, whereas sequencing of CLC-1 encoding gene, CLCN1, identified a single heterozygous missense mutation, G233S. Patch-clamp analyses of this mutant CLC-1 channel in Xenopus oocytes revealed an increased Po of the channel's fast-gate, from ̃0.4 in the wild type to>0.9 in the mutant at -90 mV. In contrast, the mutant exhibits a minimal effect on the Po of the commongate. These results are consistent with the structural prediction that the mutation site is adjacent to the fast-gate of the channel. Overall, the mutant could lead to a significantly reduced dynamic response of CLC-1 to membrane depolarization, from a fivefold increase in chloride conductance in the wild type to a twofold increase in the mutant-this might result in slower membrane repolarization during an action potential. Since expression levels of the mutant and wild-type subunits in artificial model cell systems were unable to explain the disease symptoms, the mechanism leading to dominant inheritance in this family remains to be determined.

Original languageEnglish (US)
Pages (from-to)328-337
Number of pages10
JournalNeuroMolecular Medicine
Volume14
Issue number4
DOIs
StatePublished - Dec 2012

Fingerprint

Myotonia Congenita
Chloride Channels
Muscles
Mutation
Electrophysiological Phenomena
Myotonia
Artificial Cells
Myotonic Dystrophy
Membranes
Muscular Dystrophies
Missense Mutation
Xenopus
DNA Sequence Analysis
Genes
Action Potentials
Oocytes
Chlorides

Keywords

  • Chloride channel
  • CLCN1
  • Dominant
  • Gain of function
  • Muscle
  • Myotonia congenita

ASJC Scopus subject areas

  • Cellular and Molecular Neuroscience
  • Molecular Medicine
  • Neurology

Cite this

Dominantly inherited myotonia congenita resulting from a mutation that increases open probability of the muscle chloride channel CLC-1. / Richman, David P; Yu, Yawei; Lee, Ting Ting; Tseng, Pang Yen; Yu, Wei Ping; Maselli, Ricardo A; Tang, Chih Yung; Chen, Tsung-Yu.

In: NeuroMolecular Medicine, Vol. 14, No. 4, 12.2012, p. 328-337.

Research output: Contribution to journalArticle

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abstract = "Myotonia congenita-inducing mutations in the muscle chloride channel CLC-1 normally result in reduced open probability (Po) of this channel. One well-accepted mechanism of the dominant inheritance of this disease involves a dominant-negative effect of the mutation on the function of the common-gate of this homodimeric, doublebarreled molecule. We report here a family with myotonia congenita characterized by muscle stiffness and clinical and electrophysiologic myotonic phenomena transmitted in an autosomal dominant pattern. DNA sequencing of DMPK and ZNF9 genes for myotonic muscular dystrophy types I and II was normal, whereas sequencing of CLC-1 encoding gene, CLCN1, identified a single heterozygous missense mutation, G233S. Patch-clamp analyses of this mutant CLC-1 channel in Xenopus oocytes revealed an increased Po of the channel's fast-gate, from ̃0.4 in the wild type to>0.9 in the mutant at -90 mV. In contrast, the mutant exhibits a minimal effect on the Po of the commongate. These results are consistent with the structural prediction that the mutation site is adjacent to the fast-gate of the channel. Overall, the mutant could lead to a significantly reduced dynamic response of CLC-1 to membrane depolarization, from a fivefold increase in chloride conductance in the wild type to a twofold increase in the mutant-this might result in slower membrane repolarization during an action potential. Since expression levels of the mutant and wild-type subunits in artificial model cell systems were unable to explain the disease symptoms, the mechanism leading to dominant inheritance in this family remains to be determined.",
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