Constitutive rat multidrug-resistance protein 2 gene transcription is down-regulated by Y-box protein 1

被引:24
作者
Geier, A
Mertens, PR
Gerloff, T
Dietrich, CG
En-Nia, A
Kullak-Ublick, GA
Karpen, SJ
Matern, S
Gartung, C [1 ]
机构
[1] Univ Hosp, Dept Internal Med 3, Aachen, Germany
[2] Univ Hosp, Dept Internal Med 2, Aachen, Germany
[3] Humboldt Univ, Dept Clin Pharmacol, Berlin, Germany
[4] Univ Hosp, Dept Internal Med, Zurich, Switzerland
[5] Baylor Coll Med, Dept Pediat, Houston, TX 77030 USA
关键词
gene regulation; transcription factor; promoter study; organic anion transport;
D O I
10.1016/j.bbrc.2003.08.041
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
Background/Aims: Molecular mechanisms underlying transcriptional rat multidrug-resistance protein 2 (Mrp2, Abcc2) gene regulation are mostly unclear. Given the presence of putative binding sites for the Y-box binding protein YB-1 in the regulatory sequence, its trans-regulatory influence was analyzed. Methods: Reporter assays in HepG2 cells with various Mrp2 deletion constructs in the absence and presence of co-transfected YB-1 were performed. DNA binding studies with recombinant YB-1 protein and nuclear extracts obtained from HepG2 cells and rat liver tissue were carried out. Results: The minimal promoter sequence was confined to the proximal 186 bp. A YB-1 responsive element, Mrp2 YRE-1, was mapped at -186/-157, which exhibits specific YB-1 binding. YB-1 acts as a potent repressor of Mrp2 promoter activity in vitro. Conclusions: Constitutive Mrp2 gene expression is conferred through the proximal -186 bp. YB-1 acts as a repressor in vitro by specific binding to a defined element in the proximal promoter sequence. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:612 / 618
页数:7
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