Characterization of mouse Clpp protease cDNA, gene, and protein

被引:6
作者
Andresen, BS [1 ]
Corydon, TJ
Wilsbech, M
Bross, P
Schroeder, LD
Hindkjær, TF
Bolund, L
Gregersen, N
机构
[1] Aarhus Univ Hosp, Res Unit Mol Med, DK-8200 Aarhus N, Denmark
[2] Skejby Sygehus, Fac Hlth Sci, DK-8200 Aarhus, Denmark
[3] Aarhus Univ, Inst Human Genet, DK-8000 Aarhus C, Denmark
关键词
D O I
10.1007/s003350010052
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
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页码:275 / 280
页数:6
相关论文
共 22 条
[1]  
Andresen BS, 1996, HUM MOL GENET, V5, P1390
[2]   Cloning and characterization of human very-long-chain acyl-CoA dehydrogenase cDNA, chromosomal assignment of the gene and identification in four patients of nine different mutations within the VLCAD gene [J].
Andresen, BS ;
Bross, P ;
VianeySaban, C ;
Divry, P ;
Zabot, MT ;
Roe, CR ;
Nada, MA ;
Byskov, A ;
Kruse, TA ;
Neve, S ;
Kristiansen, K ;
Knudsen, I ;
Corydon, MJ ;
Gregersen, N .
HUMAN MOLECULAR GENETICS, 1996, 5 (04) :461-472
[3]   The molecular basis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in compound heterozygous patients: Is there correlation between genotype and phenotype? [J].
Andresen, BS ;
Bross, P ;
Udvari, S ;
Kirk, J ;
Gray, G ;
Kmoch, S ;
Chamoles, N ;
Knudsen, I ;
Winter, V ;
Wilcken, B ;
Yokota, I ;
Hart, K ;
Packman, S ;
Harpey, JP ;
Saudubray, JM ;
Hale, DE ;
Bolund, L ;
Kolvraa, S ;
Gregersen, N .
HUMAN MOLECULAR GENETICS, 1997, 6 (05) :695-707
[4]   Clear correlation of genotype with disease phenotype in very-long-chain acyl-CoA dehydrogenase deficiency [J].
Andresen, BS ;
Olpin, S ;
Poorthuis, BJHM ;
Scholte, HR ;
Vianey-Saban, C ;
Wanders, R ;
Ijlst, L ;
Morris, A ;
Pourfarzam, M ;
Bartlett, K ;
Baumgartner, ER ;
deKlerk, JBC ;
Schroeder, LD ;
Corydon, TJ ;
Lund, H ;
Winter, V ;
Bross, P ;
Bolund, L ;
Gregersen, N .
AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 64 (02) :479-494
[5]   TRANSCRIPTION TERMINATION AND 3' PROCESSING - THE END IS IN SITE [J].
BIRNSTIEL, ML ;
BUSSLINGER, M ;
STRUB, K .
CELL, 1985, 41 (02) :349-359
[6]   Protein processing: A role in the pathophysiology of genetic disease [J].
Brooks, DA .
FEBS LETTERS, 1997, 409 (02) :115-120
[7]   Human ClpP protease: CDNA sequence, tissue-specific expression and chromosomal assignment of the gene [J].
Bross, P ;
Andresen, BS ;
Knudsen, I ;
Kruse, TA ;
Gregersen, N .
FEBS LETTERS, 1995, 377 (02) :249-252
[8]  
Bross P, 1998, PROG NUCLEIC ACID RE, V58, P301
[9]   CO-OVEREXPRESSION OF BACTERIAL GROESL CHAPERONINS PARTLY OVERCOMES NONPRODUCTIVE FOLDING AND TETRAMER ASSEMBLY OF E-COLI-EXPRESSED HUMAN MEDIUM-CHAIN ACYL-COA DEHYDROGENASE (MCAD) CARRYING THE PREVALENT DISEASE-CAUSING K304E MUTATION [J].
BROSS, P ;
ANDRESEN, BS ;
WINTER, V ;
KRAUTLE, F ;
JENSEN, TG ;
NANDY, A ;
KOLVRAA, S ;
GHISLA, S ;
BOLUND, L ;
GREGERSEN, N .
BIOCHIMICA ET BIOPHYSICA ACTA, 1993, 1182 (03) :264-274
[10]  
Bross P, 1999, HUM MUTAT, V14, P186, DOI 10.1002/(SICI)1098-1004(1999)14:3<186::AID-HUMU2>3.0.CO