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Length of huntingtin and its polyglutamine tract influences localization and frequency of intracellular aggregates.

Authors
Martindale, D; Hackam, A; Wieczorek, A; Ellerby, L; Wellington, C; McCutcheon, K; Singaraja, R; Kazemi-Esfarjani, P; Devon, R; Kim, SU; Bredesen, DE; Tufaro, F; Hayden, MR
Citation
Nature genetics, 18(2):150-154, 1998
Journal Title
Nature genetics
ISSN
1061-40361546-1718
Abstract
It is unclear how polyglutamine expansion is associated with the pathogenesis of Huntington disease (HD). Here, we provide evidence that polyglutamine expansion leads to the formation of large intracellular aggregates in vitro and in vivo. In vitro these huntingtin-containing aggregates disrupt normal cellular architecture and increase in frequency with polyglutamine length. Huntingtin truncated at nucleotide 1955, close to the caspase-3 cleavage site, forms perinuclear aggregates more readily than full-length huntingtin and increases the susceptibility of cells to death following apoptotic stimuli. Further truncation of huntingtin to nucleotide 436 results in both intranuclear and perinuclear aggregates. For a given protein size, increasing polyglutamine length is associated with increased cellular toxicity. Asymptomatic transgenic mice expressing full-length huntingtin with 138 polyglutamines form exclusively perinuclear aggregates in neurons. These data support the hypothesis that proteolytic cleavage of mutant huntingtin leads to the development of aggregates which compromise cell viability, and that their localization is influenced by protein length.
MeSH terms
AnimalsCell AggregationCell LineCell SurvivalHaplorhiniHumansHuntington Disease/*geneticsMiceMice, TransgenicNerve Tissue Proteins/biosynthesis/*chemistry/*metabolismNeurons/cytology/metabolism/pathologyNuclear Proteins/biosynthesis/*chemistry/*metabolism*PeptidesRecombinant Proteins/biosynthesis/chemistry/metabolismTransfection
DOI
10.1038/ng0298-150
PMID
9462744
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Neurology
AJOU Authors
김, 승업
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