COMPARISON BETWEEN MEDIUM-CHAIN ACYL-COA DEHYDROGENASE MUTANT PROTEINS OVEREXPRESSED IN BACTERIAL AND MAMMALIAN-CELLS

被引:19
作者
JENSEN, TG [1 ]
BROSS, P [1 ]
ANDRESEN, BS [1 ]
LUND, TB [1 ]
KRISTENSEN, TJ [1 ]
JENSEN, UB [1 ]
WINTHER, V [1 ]
KOLVRAA, S [1 ]
GREGERSEN, N [1 ]
BOLUND, L [1 ]
机构
[1] AARHUS UNIV HOSP,CTR MED MOLEC BIOL,DK-8200 AARHUS N,DENMARK
关键词
FOLDING MUTANTS; CHAPERONES; EXPRESSION SYSTEMS; RESIDUAL ACTIVITY;
D O I
10.1002/humu.1380060305
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency is a potentially lethal inherited defect in the beta-oxidation of fatty acids. By comparing the behaviour of five missense MCAD mutant proteins expressed in COS cells and in Escherichia coli, we can define some of these as ''pure folding mutants.'' Upon expression in E. coli, these mutant proteins produce activity levels in the range of the wild-type enzyme only if the chaperonins GroESL are co-overproduced. When overexpressed in COS cells, the pure folding mutants display enzyme activities comparable to the wild-type enzyme. The results suggest that the MCAD mutations can be modulated by chaperones, a phenomenon that may influence the manifestation of the MCAD disease. (C) 1995 Wiley Liss, Inc.
引用
收藏
页码:226 / 231
页数:6
相关论文
共 25 条
  • [1] ANDRESEN BS, 1994, AM J HUM GENET, V54, P975
  • [2] ANDRESEN BS, 1993, AM J HUM GENET, V53, P730
  • [3] Beinert H., 1963, ENZYMES, P447
  • [4] CHARACTERIZATION OF WILD-TYPE HUMAN MEDIUM-CHAIN ACYL-COA DEHYDROGENASE (MCAD) AND MUTANT ENZYMES PRESENT IN MCAD-DEFICIENT PATIENTS BY 2-DIMENSIONAL GEL-ELECTROPHORESIS - EVIDENCE FOR POSTTRANSLATIONAL MODIFICATION OF THE ENZYME
    BROSS, P
    JENSEN, TG
    ANDRESEN, BS
    KJELDSEN, M
    NANDY, A
    KOLVRAA, S
    GHISLA, S
    RASCHED, I
    BOLUND, L
    GREGERSEN, N
    [J]. BIOCHEMICAL MEDICINE AND METABOLIC BIOLOGY, 1994, 52 (01): : 36 - 44
  • [5] 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
    BROSS, P
    ANDRESEN, BS
    WINTER, V
    KRAUTLE, F
    JENSEN, TG
    NANDY, A
    KOLVRAA, S
    GHISLA, S
    BOLUND, L
    GREGERSEN, N
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1993, 1182 (03) : 264 - 274
  • [6] BROSS P, 1992, NEW DEV FATTY ACID O, P473
  • [7] DEFECTIVE INTRACELLULAR-TRANSPORT AND PROCESSING OF CFTR IS THE MOLECULAR-BASIS OF MOST CYSTIC-FIBROSIS
    CHENG, SH
    GREGORY, RJ
    MARSHALL, J
    PAUL, S
    SOUZA, DW
    WHITE, GA
    ORIORDAN, CR
    SMITH, AE
    [J]. CELL, 1990, 63 (04) : 827 - 834
  • [8] IMMUNOCHEMICAL CHARACTERIZATION OF VARIANT MEDIUM-CHAIN ACYL-COA DEHYDROGENASE IN FIBROBLASTS FROM PATIENTS WITH MEDIUM-CHAIN ACYL-COA DEHYDROGENASE-DEFICIENCY
    COATES, PM
    INDO, Y
    YOUNG, D
    HALE, DE
    TANAKA, K
    [J]. PEDIATRIC RESEARCH, 1992, 31 (01) : 34 - 38
  • [9] PROCESSING OF MUTANT CYSTIC-FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR IS TEMPERATURE-SENSITIVE
    DENNING, GM
    ANDERSON, MP
    AMARA, JF
    MARSHALL, J
    SMITH, AE
    WELSH, MJ
    [J]. NATURE, 1992, 358 (6389) : 761 - 764
  • [10] LOW-DENSITY-LIPOPROTEIN RECEPTOR POINT MUTATION RESULTS IN EXPRESSION OF BOTH ACTIVE AND INACTIVE SURFACE FORMS OF THE SAME MUTANT RECEPTOR
    FOURIE, AM
    COETZEE, GA
    GEVERS, W
    VANDERWESTHUYZEN, DR
    [J]. BIOCHEMISTRY, 1992, 31 (51) : 12754 - 12759