Falkner K Cameron, Prough Russell A
Department of Biochemistry and Molecular Biology, University of Louisville School of Medicine, Louisville, Kentucky 40292, USA.
Drug Metab Rev. 2007;39(2-3):401-18. doi: 10.1080/03602530701511216.
Regulation of the rat glutathione S-transferase A2 (GSTA2) gene by glucocorticoids is biphasic in its concentration dependence to glucocorticoids, with concentrations of 10-100 nM repressing gene activity (GR-dependent), and concentrations above 1 microM increasing transactivation (PXR-dependent) in adult rat hepatocytes or transient transfection assays. Over-expression of either C/EBP alpha or beta negatively regulates basal and inducible expression of a 1.65 Kb GSTA2 luciferase reporter, and synergizes the response to glucocorticoids (GC). C/EBP responsive elements have been identified in the GSTA2 5'-flanking sequence, associated with the palindrominic Glucocorticoid Responsive Element (GRE), the Ah receptor response elements, and the antioxidant response element. In reporters lacking the palindromic GRE, negative regulation by GC is observed only when C/EBP alpha is co-expressed. Co-transfection of C/EBP alpha/beta induced gene expression of the GSTA2 XRE reporter, but negatively regulated the GSTA2 ARE-reporter. In contrast, the ARE from the rat NAD(P)H quinone oxidoreductase gene was induced by co-transfection of C/EBPs, but was still negatively regulated by GC. PXR-induction of the GSTA2 reporter was partially ablated by co-transfection of C/EBP alpha and enhanced by co-transfection of C/EBPbeta. We conclude that C/EBP alpha and beta are involved in GC-dependent repression of GSTA2 gene expression and ARE sequences that bind C/EBPs appears to be critical for these responses.
糖皮质激素对大鼠谷胱甘肽S-转移酶A2(GSTA2)基因的调控在其对糖皮质激素的浓度依赖性上呈双相性,在成年大鼠肝细胞或瞬时转染实验中,10 - 100 nM的浓度会抑制基因活性(糖皮质激素受体依赖性),而高于1 μM的浓度会增加反式激活(孕烷X受体依赖性)。C/EBPα或β的过表达会负向调节1.65 Kb GSTA2荧光素酶报告基因的基础表达和诱导表达,并协同对糖皮质激素(GC)的反应。在GSTA2 5'侧翼序列中已鉴定出C/EBP反应元件,其与回文糖皮质激素反应元件(GRE)、芳烃受体反应元件和抗氧化反应元件相关。在缺乏回文GRE的报告基因中,仅当C/EBPα共表达时才观察到GC的负向调节。C/EBPα/β的共转染诱导了GSTA2 XRE报告基因的表达,但负向调节了GSTA2 ARE报告基因。相反,大鼠NAD(P)H醌氧化还原酶基因的ARE在C/EBPs共转染时被诱导,但仍受GC负向调节。C/EBPα的共转染部分消除了GSTA2报告基因的孕烷X受体诱导作用,而C/EBPβ的共转染增强了该诱导作用。我们得出结论,C/EBPα和β参与了GC依赖性的GSTA2基因表达抑制,并且与C/EBPs结合的ARE序列似乎对这些反应至关重要。