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Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias.

作者信息

Trottier Y, Lutz Y, Stevanin G, Imbert G, Devys D, Cancel G, Saudou F, Weber C, David G, Tora L

机构信息

Institut de Génétique et de Biologie Moléculaire et Cellulaire (GBMC), CNRS, INSERM, Illkirch, France.

出版信息

Nature. 1995 Nov 23;378(6555):403-6. doi: 10.1038/378403a0.

DOI:10.1038/378403a0
PMID:7477379
Abstract

A polyglutamine expansion (encoded by a CAG repeat) in specific proteins causes neurodegeneration in Huntington's disease (HD) and four other disorders, by an unknown mechanism thought to involve gain of function or toxicity of the mutated protein. The pathological threshold is 37-40 glutamines in three of these diseases, whereas the corresponding normal proteins contain polymorphic repeats of up to about 35 glutamines. The age of onset of clinical manifestations is inversely correlated to the length of the polyglutamine expansion. Here we report the characterization of a monoclonal antibody that selectively recognizes polyglutamine expansion in the proteins implicated in HD and in spinocerebellar ataxia (SCA) 1 and 3. The intensity of signal depends on the length of the polyglutamine expansion, and the antibody also detects specific pathological proteins expected to contain such expansion, in SCA2 and in autosomal dominant cerebellar ataxia with retinal degeneration, whose genes have not yet been identified.

摘要

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