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volume 13 number 2 page 196 
 
 
Expanded polyglutamine in the Machado-Joseph disease protein induces cell death in vitro and in vivo
Hanako Ikeda1, Masahiro Yamaguchi1, Satoshi Sugai2, Yoshiya Aze2, Shuh Narumiya1 & Akira Kakizuka1
 

Recently, we identified a novel gene, MJD1, which contains an expanded CAG triplet repeat in Machado-Joseph disease. Here we report the induction of apoptosis in cultured cells expressing a portion of the MJD1 gene that includes the expanded CAG repeats. Cell death occurs only when the CAG repeat is translated into polyglutamine residues, which apparently precipitate in large covalently modified forms. We also created ataxic transgenic mice by expressing the expanded polyglutamine stretch in Purkinje cells. Our results demonstrate the potential involvement of the expanded polyglutamine as the common aetiological agent for inherited neurodegenerative diseases with CAG expansions.


1Department of Pharmacology, Kyoto University Faculty of Medicine, Kyoto 606-01, Japan
2Fukui Institute for Safety Research, Ono Pharmaceutical, Mikuni, Fukui 913, Japan
H.I. and M.Y. contributed equally to this work.
Correspondence should be addressed to A.K.

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