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Characterization of mouse Clpp protease cDNA, gene, and protein.

作者信息

Andresen B S, Corydon T J, Wilsbech M, Bross P, Schroeder L D, Hindkjaer T F, Bolund L, Gregersen N

机构信息

Research Unit for Molecular Medicine, Aarhus University Hospital and Faculty of Health Science, Skejby Sygehus, Denmark.

出版信息

Mamm Genome. 2000 Apr;11(4):275-80. doi: 10.1007/s003350010052.

Abstract

Mutations that cause accumulation or rapid degradation owing to protein misfolding are a frequent cause of inherited disease in humans. In Escherichia coli, Clpp protease is one of the components of the protein quality control system that handles misfolded proteins. In the present study, we have characterized the mouse Clpp cDNA sequence, the organization of the mouse gene, the chromosomal localization, and the tissue-specific expression pattern. Moreover. the cellular localization and processing of mouse Clpp was studied by overexpression in transfected eukaryotic cells. Our results indicate that mouse and human Clpp have similar roles, and they provide the molecular basis for establishing a Clpp knockout mouse and to study its phenotype, thereby shedding light on a possible role of Clpp in human disease.

摘要

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