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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
1-2
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pubmed:dateCreated |
2004-1-19
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pubmed:abstractText |
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.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/1-Methyl-4-phenyl-1,2,3,6-tetrahydro...,
http://linkedlifedata.com/resource/pubmed/chemical/Carrier Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/DNA, Complementary,
http://linkedlifedata.com/resource/pubmed/chemical/Dyt1 protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Molecular Chaperones,
http://linkedlifedata.com/resource/pubmed/chemical/Neurotoxins,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger
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pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
0304-3940
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:day |
23
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pubmed:volume |
355
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
126-30
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pubmed:dateRevised |
2004-12-3
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pubmed:meshHeading |
pubmed-meshheading:14729251-1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine,
pubmed-meshheading:14729251-Age of Onset,
pubmed-meshheading:14729251-Animals,
pubmed-meshheading:14729251-Animals, Newborn,
pubmed-meshheading:14729251-Carrier Proteins,
pubmed-meshheading:14729251-DNA, Complementary,
pubmed-meshheading:14729251-Dopamine,
pubmed-meshheading:14729251-Dystonia Musculorum Deformans,
pubmed-meshheading:14729251-MPTP Poisoning,
pubmed-meshheading:14729251-Mice,
pubmed-meshheading:14729251-Mice, Inbred C57BL,
pubmed-meshheading:14729251-Molecular Chaperones,
pubmed-meshheading:14729251-Molecular Sequence Data,
pubmed-meshheading:14729251-Nerve Degeneration,
pubmed-meshheading:14729251-Neurons,
pubmed-meshheading:14729251-Neurotoxins,
pubmed-meshheading:14729251-Oxidative Stress,
pubmed-meshheading:14729251-RNA, Messenger,
pubmed-meshheading:14729251-Sequence Homology, Amino Acid,
pubmed-meshheading:14729251-Sequence Homology, Nucleic Acid,
pubmed-meshheading:14729251-Substantia Nigra,
pubmed-meshheading:14729251-Up-Regulation
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pubmed:year |
2004
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pubmed:articleTitle |
TorsinA, the gene linked to early-onset dystonia, is upregulated by the dopaminergic toxin MPTP in mice.
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pubmed:affiliation |
Pharmacology Institute, University of Heidelberg, Im Neunheimer Feld 366, 69120 Heidelberg, Germany. rohini.kuner@urz.uni-heidelberg.de
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pubmed:publicationType |
Journal Article
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