Beischlag Timothy V, Luis Morales J, Hollingshead Brett D, Perdew Gary H
Center for Molecular Toxicology and Carcinogenesis, The Pennsylvania State University, University Park, PA 16802, USA.
Crit Rev Eukaryot Gene Expr. 2008;18(3):207-50. doi: 10.1615/critreveukargeneexpr.v18.i3.20.
The aryl hydrocarbon receptor (AhR) is a ligand-activated transcription factor that controls the expression of a diverse set of genes. The toxicity of the potent AhR ligand 2,3,7,8-tetrachlorodibenzo-p-dioxin is almost exclusively mediated through this receptor. However, the key alterations in gene expression that mediate toxicity are poorly understood. It has been established through characterization of AhR-null mice that the AhR has a required physiological function, yet how endogenous mediators regulate this orphan receptor remains to be established. A picture as to how the AhR/ARNT heterodimer actually mediates gene transcription is starting to emerge. The AhR/ARNT complex can alter transcription both by binding to its cognate response element and through tethering to other transcription factors. In addition, many of the coregulatory proteins necessary for AhR-mediated transcription have been identified. Cross talk between the estrogen receptor and the AhR at the promoter of target genes appears to be an important mode of regulation. Inflammatory signaling pathways and the AhR also appear to be another important site of cross talk at the level of transcription. A major focus of this review is to highlight experimental efforts to characterize nonclassical mechanisms of AhR-mediated modulation of gene transcription.
芳基烃受体(AhR)是一种配体激活的转录因子,可控制多种基因的表达。强效AhR配体2,3,7,8-四氯二苯并对二恶英的毒性几乎完全通过该受体介导。然而,介导毒性的基因表达关键改变却知之甚少。通过对AhR基因敲除小鼠的表征已确定AhR具有必需的生理功能,但内源性介质如何调节这种孤儿受体仍有待确定。关于AhR/ARNT异二聚体实际上如何介导基因转录的情况正开始显现。AhR/ARNT复合物可通过与其同源反应元件结合以及通过与其他转录因子结合来改变转录。此外,已鉴定出许多AhR介导转录所需的共调节蛋白。雌激素受体与AhR在靶基因启动子处的相互作用似乎是一种重要的调节方式。炎症信号通路与AhR在转录水平上似乎也是另一个重要的相互作用位点。本综述的一个主要重点是突出表征AhR介导的基因转录调节非经典机制的实验工作。