ASSIGNMENT OF THE HUMAN UDP GLUCURONOSYLTRANSFERASE GENE (UGT1A1) TO CHROMOSOME REGION 2Q37

被引:55
作者
VANES, HHG
BOUT, A
LIU, J
ANDERSON, L
DUNCAN, AMV
BOSMA, P
ELFERINK, RO
JANSEN, PLM
CHOWDHURY, JR
SCHURR, E
机构
[1] KINGSTON GEN HOSP,KINGSTON K7L 2V7,ONTARIO,CANADA
[2] UNIV AMSTERDAM,ACAD MED CTR,DEPT GASTROENTEROL,1105 AZ AMSTERDAM,NETHERLANDS
[3] YESHIVA UNIV ALBERT EINSTEIN COLL MED,LIVER RES CTR,BRONX,NY 10461
[4] MCGILL UNIV,DEPT MED,MONTREAL H3A 2T5,QUEBEC,CANADA
[5] TNO,INST APPL RADIOBIOL & IMMUNOL,DEPT GENE THERAPY,RIJSWIJK,NETHERLANDS
来源
CYTOGENETICS AND CELL GENETICS | 1993年 / 63卷 / 02期
关键词
D O I
10.1159/000133513
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
UDP glucuronosyltransferases (UGTs) comprise a multigene family of drug-metabolizing enzymes. The subfamily of UGTs that conjugate bilirubin and phenolic compounds with glucuronic acid has been termed UGT1A1. In man, UGT1A1 isoforms are encoded by a single gene, UGT1A1. Protein isoforms encoded by UGT1A1 originate by alternative splicing. In the present study, we used the cDNA of UGT1A1*4, a bilirubin-conjugating isoform, to localize the UGT1A1 locus in the human genome. The UGT1A1 gene was assigned by in situ hybridization to chromosome region 2q37.
引用
收藏
页码:114 / 116
页数:3
相关论文
共 22 条
[1]  
BEESON D, 1989, CYTOGENET CELL GENET, V51, P960
[2]   MECHANISMS OF INHERITED DEFICIENCIES OF MULTIPLE UDP-GLUCURONOSYLTRANSFERASE ISOFORMS IN 2 PATIENTS WITH CRIGLER-NAJJAR SYNDROME, TYPE-I [J].
BOSMA, PJ ;
CHOWDHURY, JR ;
HUANG, TJ ;
LAHIRI, P ;
ELFERINK, RPJO ;
VANES, HHG ;
LEDERSTEIN, M ;
WHITINGTON, PF ;
JANSEN, PLM ;
CHOWDHURY, NR .
FASEB JOURNAL, 1992, 6 (10) :2859-2863
[3]   SEQUENCE OF EXONS AND THE FLANKING REGIONS OF HUMAN BILIRUBIN-UDP-GLUCURONOSYLTRANSFERASE GENE-COMPLEX AND IDENTIFICATION OF A GENETIC MUTATION IN A PATIENT WITH CRIGLER-NAJJAR SYNDROME, TYPE-I [J].
BOSMA, PJ ;
CHOWDHURY, NR ;
GOLDHOORN, BG ;
HOFKER, MH ;
ELFERINK, RPJO ;
JANSEN, PLM ;
CHOWDHURY, JR .
HEPATOLOGY, 1992, 15 (05) :941-947
[4]   THE UDP GLUCURONOSYLTRANSFERASE GENE SUPERFAMILY - SUGGESTED NOMENCLATURE BASED ON EVOLUTIONARY DIVERGENCE [J].
BURCHELL, B ;
NEBERT, DW ;
NELSON, DR ;
BOCK, KW ;
IYANAGI, T ;
JANSEN, PLM ;
LANCET, D ;
MULDER, GJ ;
CHOWDHURY, JR ;
SIEST, G ;
TEPHLY, TR ;
MACKENZIE, PI .
DNA AND CELL BIOLOGY, 1991, 10 (07) :487-494
[5]  
CHOWDHURY JR, 1991, J BIOL CHEM, V266, P18294
[6]  
COHENHAGUENAUER O, 1987, CYTOGENET CELL GENET, V46, P595
[7]  
Dutton GJ, 1980, GLUCURONIDATION DRUG, P1
[8]   CLONING AND SUBSTRATE-SPECIFICITY OF A HUMAN PHENOL UDP-GLUCURONOSYLTRANSFERASE EXPRESSED IN COS-7 CELLS [J].
HARDING, D ;
FOURNELGIGLEUX, S ;
JACKSON, MR ;
BURCHELL, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (22) :8381-8385
[9]   CHROMOSOMAL MAPPING OF A HUMAN PHENOL UDP-GLUCURONOSYLTRANSFERASE, GNT1 [J].
HARDING, D ;
JEREMIAH, SJ ;
POVEY, S ;
BURCHELL, B .
ANNALS OF HUMAN GENETICS, 1990, 54 :17-21
[10]  
HARDING D, 1988, P NATL ACAD SCI USA, V54, P17