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Spinocerebellar ataxia type 6 knockin mice develop a progressive neuronal dysfunction with age-dependent accumulation of mutant CaV2.1 channels.

Spinocerebellar ataxia type 6 (SCA6) is a neurodegenerative disorder caused by CAG repeat expansions within the voltage-gated calcium (Ca(V)) 2.1 channel gene. It remains controversial whether the mutation exerts neurotoxicity by changing the function of Ca(V)2.1 channel or through a gain-of-function mechanism associated with accumulation of the expanded polyglutamine protein. We generated three strains of knockin (KI) mice carrying normal, expanded, or hyperexpanded CAG repeat tracts in the Cacna1a locus. The mice expressing hyperexpanded polyglutamine (Sca6(84Q)) developed progressive motor impairment and aggregation of mutant Ca(V)2.1 channels. Electrophysiological analysis of cerebellar Purkinje cells revealed similar Ca(2+) channel current density among the three KI models. Neither voltage sensitivity of activation nor inactivation was altered in the Sca6(84Q) neurons, suggesting that expanded CAG repeat per se does not affect the intrinsic electrophysiological properties of the channels. The pathogenesis of SCA6 is apparently linked to an age-dependent process accompanied by accumulation of mutant Ca(V)2.1 channels.

Pubmed ID: 18687887

Authors

  • Watase K
  • Barrett CF
  • Miyazaki T
  • Ishiguro T
  • Ishikawa K
  • Hu Y
  • Unno T
  • Sun Y
  • Kasai S
  • Watanabe M
  • Gomez CM
  • Mizusawa H
  • Tsien RW
  • Zoghbi HY

Journal

Proceedings of the National Academy of Sciences of the United States of America

Publication Data

August 19, 2008

Associated Grants

  • Agency: NINDS NIH HHS, Id: NS24607
  • Agency: Howard Hughes Medical Institute, Id:

Mesh Terms

  • Aging
  • Alternative Splicing
  • Animals
  • Calcium Channels, N-Type
  • Disease Progression
  • Electrophysiology
  • Exons
  • Gene Expression
  • Mice
  • Mice, Transgenic
  • Mutant Proteins
  • Mutation
  • Nervous System Diseases
  • Phenotype
  • Spinocerebellar Ataxias
  • Transgenes