Abstract
The mutations responsible for several human neurodegenerative disorders are expansions of translated CAG repeats beyond a normal size range. To address the role of repeat context, we have introduced a 146-unit CAG repeat into the mouse hypoxanthine phosphoribosyltransferase gene (Hprt). Mutant mice express a form of the HPRT protein that contains a long polyglutamine repeat. These mice develop a phenotype similar to the human translated CAG repeat disorders. Repeat containing mice show a late onset neurological phenotype that progresses to premature death. Neuronal intranuclear inclusions are present in affected mice. Our results show that CAG repeats do not need to be located within one of the classic repeat disorder genes to have a neurotoxic effect.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, Non-P.H.S.
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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 / enzymology
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Brain / pathology*
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Cell Nucleus / enzymology
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Cell Nucleus / pathology
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Cell Nucleus / ultrastructure
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Crosses, Genetic
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Exons
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Female
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Homozygote
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Humans
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Hypoxanthine Phosphoribosyltransferase / analysis
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Hypoxanthine Phosphoribosyltransferase / deficiency
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Hypoxanthine Phosphoribosyltransferase / genetics*
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Inclusion Bodies / enzymology
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Inclusion Bodies / pathology
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Inclusion Bodies / ultrastructure
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Male
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Mice
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Mice, Neurologic Mutants / genetics*
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Peptides
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Phenotype
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Trinucleotide Repeats*
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Ubiquitins / analysis
Substances
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Peptides
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Ubiquitins
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polyglutamine
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Hypoxanthine Phosphoribosyltransferase