Torsin A, the gene linked to early-onset dystonia, is upregulated by the dopaminergic toxin MPTP in mice

R. Kuner, Peter Teismann, A. Trutzel, J. Naim, A. Richter, N. Schmidt, A. Bach, B. Ferger, A. Schneider

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Abstract

Early-onset torsion dystonias are caused by a mutation in TorsinA, a protein widely expressed in the nervous system. Here we report the cloning of the murine TorsinA cDNA and a mRNA in situ hybridization analysis of the expression patterns of TorsinA over developmental periods relevant to the etiology of early-onset dystonias. Several studies have demonstrated a functional involvement of the nigrostriatal dopaminergic system in pathological mechanisms underlying dystonia. In this study, we show that the expression of TorsinA is significantly increased in the brain within hours of treatment with the dopaminergic toxin, 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine in mice, suggesting that the TorsinA gene is regulated by cellular stress. These results provide insights into the pathophysiology of early-onset dystonia and strengthen links between the dopaminergic system and dystonia. (C) 2003 Elsevier Ireland Ltd. All rights reserved.

Original languageEnglish
Pages (from-to)126-130
Number of pages4
JournalNeuroscience Letters
Volume355
Issue number1-2
DOIs
Publication statusPublished - Jan 2004

Keywords

  • torsion dystonia
  • substantia nigra
  • striatum
  • development
  • movement disorder
  • DYT1 mutation
  • lewy bodies
  • human brain
  • expression

Cite this

Kuner, R., Teismann, P., Trutzel, A., Naim, J., Richter, A., Schmidt, N., Bach, A., Ferger, B., & Schneider, A. (2004). Torsin A, the gene linked to early-onset dystonia, is upregulated by the dopaminergic toxin MPTP in mice. Neuroscience Letters, 355(1-2), 126-130. https://doi.org/10.1016/j.neulet.2003.10.069