Genomic structure, gene expression, and promoter analysis of human multidrug resistance-associated protein 7

被引:14
作者
Kao, HH
Chang, MS [1 ]
Cheng, JF
Huang, JD
机构
[1] Natl Cheng Kung Univ, Coll Med, Grad Inst Biochem, Tainan 701, Taiwan
[2] Natl Cheng Kung Univ, Dept Food Nutr, Chung Hwa Coll Med Technol, Tainan 701, Taiwan
[3] Natl Cheng Kung Univ, Grad Inst Pharmacol, Tainan 701, Taiwan
[4] Lawrence Berkeley Natl Lab, Berkeley, CA USA
关键词
multidrug resistance; ABC transporter; MRP7; genomic organization; promoter analysis;
D O I
10.1159/000068078
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The multidrug resistance-associated protein (MRP) subfamily transporters associated With anticancer drug efflux are attributed to the multidrug-resistance of cancer cells. The genomic organization of human multidrug resistance-associated protein 7 (MRP7) was identified. The human MRP7 gene, consisting of 22 exons and 21 introns, greatly differs from other members of the human MRP subfamily. A splicing variant of human MRP7, MRP7A, expressed in most human tissues, was also characterized. The 1.93-kb promoter region of MRP7 was isolated and shown to support luciferase activity at a level 4- to 5-fold greater than that of the SV40 promoter. Basal MRP7 gene expression was regulated by 2 regions in the 5'-flanking region at -1,780-1,287 bp, and at -611 to -208 bp. In Madin-Darby canine kidney (MDCK) cells, MRP7 promoter activity was increased by 226% by genotoxic 2-acetylaminofluorene and 347% by the histone deacetylase inhibitor, trichostatin A. The protein was expressed in the membrane fraction of transfected MDCK cells. Copyright (C) 2003 National Science Council, ROC and S. Karger AG, Basel.
引用
收藏
页码:98 / 110
页数:13
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