Role of GAC63 in transcriptional activation mediated by the aryl hydrocarbon receptor

被引:26
作者
Chen, YH
Beischlag, TV
Kim, JH
Perdew, GH
Stallcup, MR
机构
[1] Univ So Calif, Dept Biochem & Mol Biol, Los Angeles, CA 90089 USA
[2] Univ So Calif, Dept Pathol, Los Angeles, CA 90089 USA
[3] Penn State Univ, Ctr Mol Toxicol & Carcinogenesis, University Pk, PA 16802 USA
[4] Penn State Univ, Dept Vet & Biomed Sci, University Pk, PA 16802 USA
关键词
D O I
10.1074/jbc.M512537200
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
The aryl hydrocarbon receptor (AHR), a member of the basic helix-loop-helix/Per-Arnt-Sim (bHLH-PAS) gene family, binds a variety of polycyclic aromatic hydrocarbons and mediates their toxic effects. GAC63 has been shown to act as a coactivator in nuclear receptor-mediated gene transcription. In this report, we demonstrate that GAC63 interacts with AHR through its bHLH-PAS domain. Overexpression of GAC63 greatly enhanced AHR-regulated reporter gene activity in a ligand-dependent manner in transient transfection assays. Upon ligand treatment, endogenous GAC63 was recruited to the xeno-biotic response element of the mouse CYP1A1 gene, an AHR-responsive gene. Reduction of the endogenous GAC63 level by small interfering RNA inhibited transcriptional activation by AHR. These findings reveal a new function of GAC63 in AHR-mediated gene transcription.
引用
收藏
页码:12242 / 12247
页数:6
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