HUMAN CARBONYL REDUCTASE (CBR) LOCALIZED TO BAND-21Q22.1 BY HIGH-RESOLUTION FLUORESCENCE INSITU HYBRIDIZATION DISPLAYS GENE DOSAGE EFFECTS IN TRISOMY-21 CELLS

被引:30
作者
LEMIEUX, N
MALFOY, B
FORREST, GL
机构
[1] CITY HOPE NATL MED CTR,BECKMAN RES INT,DIV BIOL,1450 E DUARTE RD,DUARTE,CA 91010
[2] UNIV MONTREAL,FAC MED,DEPT PATHOL,MONTREAL H3C 3J7,QUEBEC,CANADA
[3] INST CURIE,BIOL SECT,CNRS,URA 620,F-75231 PARIS 05,FRANCE
关键词
D O I
10.1006/geno.1993.1024
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Human carbonyl reductase (CBR) belongs to a group of NADPH-dependent enzymes called aldo-keto reductases. The enzyme can function as an aldo-keto reductase or as a quinone reductase with potential for modulating quinone-mediated oxygen free radicals. The CBR gene was mapped by high-resolution fluorescence in situ hybridization to band 21q22.12, very close to the SOD1 locus at position 21q22.11. CBR displayed gene dosage effects in trisomy 21 human lymphoblasts at the DNA and mRNA levels. Lymphoblasts with increasing chromosome 21 ploidy also showed increased aldo-keto reductase activity and increased quinone reductase activity. Both aldo-keto reductase activity and quinone reductase activity have been shown to be associated with carbonyl reductase. The location of CBR near SOD1 and the increased enzyme activity and potential for free radical modulation in trisomy 21 cells implicate CBR as a candidate for contributing to the pathology of certain diseases such as Down syndrome and Alzheimer disease. © 1993 Academic Press, Inc.
引用
收藏
页码:169 / 172
页数:4
相关论文
共 28 条
[11]  
FORREST GL, 1991, MOL PHARMACOL, V40, P502
[12]  
FOURNEY RM, 1988, FOCUS, V10, P5
[13]   AN EFFICIENT METHOD FOR SELECTING UNIQUE-SEQUENCE CLONES FROM DNA LIBRARIES AND ITS APPLICATION TO FLUORESCENT STAINING OF HUMAN CHROMOSOME-21 USING INSITU HYBRIDIZATION [J].
FUSCOE, JC ;
COLLINS, CC ;
PINKEL, D ;
GRAY, JW .
GENOMICS, 1989, 5 (01) :100-109
[14]  
HURWITZLIEMAN J, 1982, P NATL ACAD SCI USA, V79, P2808
[15]   POLYCYCLIC AROMATIC HYDROCARBON QUINONE-MEDIATED OXIDATION REDUCTION CYCLING CATALYZED BY A HUMAN PLACENTAL NADPH-LINKED CARBONYL REDUCTASE [J].
JARABAK, J .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1991, 291 (02) :334-338
[16]  
KALLIONIEMI A, 1992, CYTOGENET CELL GENET, V40, P668
[17]  
KITTUR SD, 1985, CYTOGENET CELL GENET, V40, P668
[18]  
LANDEGENT JE, 1987, HUM GENET, V77, P336
[19]   A SIMPLE METHOD FOR SIMULTANEOUS R-BANDING OR G-BANDING AND FLUORESCENCE INSITU HYBRIDIZATION OF SMALL SINGLE-COPY GENES [J].
LEMIEUX, N ;
DUTRILLAUX, B ;
VIEGASPEQUIGNOT, E .
CYTOGENETICS AND CELL GENETICS, 1992, 59 (04) :311-312
[20]   DELINEATION OF INDIVIDUAL HUMAN-CHROMOSOMES IN METAPHASE AND INTERPHASE CELLS BY INSITU SUPPRESSION HYBRIDIZATION USING RECOMBINANT DNA LIBRARIES [J].
LICHTER, P ;
CREMER, T ;
BORDEN, J ;
MANUELIDIS, L ;
WARD, DC .
HUMAN GENETICS, 1988, 80 (03) :224-234