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Polyglutamine pathogenesis Ross CA; Wood JD; Schilling G; Peters MF; Nucifora FC Jr; Cooper JK; Sharp AH; Margolis RL; Borchelt DRPhilos Trans R Soc Lond B Biol Sci 1999[Jun]; 354 (1386): 1005-11An increasing number of neurodegenerative disorders have been found to be caused by expanding CAG triplet repeats that code for polyglutamine. Huntington's disease (HD) is the most common of these disorders and dentatorubral-pallidoluysian atrophy (DRPLA) is very similar to HD, but is caused by mutation in a different gene, making them good models to study. In this review, we will concentrate on the roles of protein aggregation, nuclear localization and proteolytic processing in disease pathogenesis. In cell model studies of HD, we have found that truncated N-terminal portions of huntingtin (the HD gene product) with expanded repeats form more aggregates than longer or full length huntingtin polypeptides. These shorter fragments are also more prone to aggregate in the nucleus and cause more cell toxicity. Further experiments with huntingtin constructs harbouring exogenous nuclear import and nuclear export signals have implicated the nucleus in direct cell toxicity. We have made mouse models of HD and DRPLA using an N-terminal truncation of huntingtin (N171) and full-length atrophin-1 (the DRPLA gene product), respectively. In both models, diffuse neuronal nuclear staining and nuclear inclusion bodies are observed in animals expressing the expanded glutamine repeat protein, further implicating the nucleus as a primary site of neuronal dysfunction. Neuritic pathology is also observed in the HD mice. In the DRPLA mouse model, we have found that truncated fragments of atrophin-1 containing the glutamine repeat accumulate in the nucleus, suggesting that proteolysis may be critical for disease progression. Taken together, these data lead towards a model whereby proteolytic processing, nuclear localization and protein aggregation all contribute to pathogenesis.|*Trinucleotide Repeat Expansion[MESH]|Animals[MESH]|Atrophy[MESH]|Brain/*pathology[MESH]|Dentate Gyrus/pathology[MESH]|Globus Pallidus/pathology[MESH]|Humans[MESH]|Huntingtin Protein[MESH]|Huntington Disease/*genetics/pathology[MESH]|Inclusion Bodies/pathology[MESH]|Mice[MESH]|Nerve Tissue Proteins/*chemistry/*genetics/metabolism[MESH]|Neurodegenerative Diseases/genetics/pathology[MESH]|Nuclear Proteins/*chemistry/*genetics/metabolism[MESH]|Peptides/*genetics[MESH] |
