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Nat Genet. 1995 Jul;10(3):301-6.

The mouse dystonia musculorum gene is a neural isoform of bullous pemphigoid antigen 1.

Author information

1
Institut du cancer de Montréal, Centre de Recherche L.-C. Simard, Québec, Canada.

Abstract

Dystonia musculorum (dt) is a hereditary neurodegenerative disease in mice that leads to a sensory ataxia. We describe cloning of a candidate dt gene, dystonin, that is predominantly expressed in the dorsal root ganglia and other sites of neurodegeneration in dt mice. Dystonin encodes an N-terminal actin binding domain and a C-terminal portion comprised of the hemidesmosomal protein, bullous pemphigoid antigen 1 (bpag1). dt and bpag1 are part of the same transcription unit which is partially deleted in a transgenic strain of mice, Tg4, that harbours an insertional mutation at the dt locus, and in mice that carry a spontaneous dt mutation, dtAlb. We also demonstrate abnormal dystonin transcripts in a second dt mutant, dt24J. We conclude that mutations in the dystonin gene are the primary genetic lesion in dt mice.

PMID:
7670468
DOI:
10.1038/ng0795-301
[Indexed for MEDLINE]

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