Abstract
Expanded polyglutamine repeats have been proposed to cause neuronal degeneration in Huntington's disease (HD) and related disorders, through abnormal interactions with other proteins containing short polyglutamine tracts such as the transcriptional coactivator CREB binding protein, CBP. We found that CBP was depleted from its normal nuclear location and was present in polyglutamine aggregates in HD cell culture models, HD transgenic mice, and human HD postmortem brain. Expanded polyglutamine repeats specifically interfere with CBP-activated gene transcription, and overexpression of CBP rescued polyglutamine-induced neuronal toxicity. Thus, polyglutamine-mediated interference with CBP-regulated gene transcription may constitute a genetic gain of function, underlying the pathogenesis of polyglutamine disorders.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Animals
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Brain / metabolism
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CREB-Binding Protein
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Cell Nucleus / metabolism
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Cell Survival
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Cells, Cultured
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Humans
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Huntingtin Protein
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Huntington Disease / genetics
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Huntington Disease / metabolism*
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Mice
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Mice, Transgenic
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Mutation
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Nerve Tissue Proteins / chemistry
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Nerve Tissue Proteins / genetics
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Nerve Tissue Proteins / metabolism*
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Neurons / cytology
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Neurons / metabolism*
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Nuclear Proteins / chemistry
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Nuclear Proteins / genetics
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Nuclear Proteins / metabolism*
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Peptides / chemistry
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Peptides / metabolism*
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Repetitive Sequences, Amino Acid
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Trans-Activators / chemistry
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Trans-Activators / metabolism*
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Transcription, Genetic*
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Transfection
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Tumor Cells, Cultured
Substances
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HTT protein, human
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Htt protein, mouse
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Huntingtin Protein
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Nerve Tissue Proteins
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Nuclear Proteins
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Peptides
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Trans-Activators
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atrophin-1
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polyglutamine
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CREB-Binding Protein
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CREBBP protein, human
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Crebbp protein, mouse