FEBS Lett. 2013 Nov 29;587(23):3883-90.
Nur77 is a stress sensor in pancreatic β-cells, which negatively regulates glucose-stimulated insulin secretion. We recently showed that a lipotoxic shock caused by exposure of β-cells to the saturated fatty acid palmitate strongly increases Nur77 expression. Here, using dual luciferase reporter assays and Nur77 promoter deletion constructs, we identified a regulatory cassette between -1534 and -1512 bp upstream from the translational start site mediating Nur77 promoter activation in response to palmitate exposure. Chromatin immunoprecipitation, transient transfection and siRNA-mediated knockdown assays revealed that palmitate induced Nur77 promoter activation involves Sp1 recruitment and ZBP89 release from the gene promoter.
Nur77 是胰腺β细胞中的应激传感器,可负向调节葡萄糖刺激的胰岛素分泌。我们最近发现,β细胞暴露于饱和脂肪酸棕榈酸酯引起的脂毒性冲击会强烈增加 Nur77 的表达。在这里,我们使用双荧光素酶报告基因检测和 Nur77 启动子缺失构建体,鉴定出一个位于翻译起始位点上游-1534 至-1512bp 之间的调节盒,介导 Nur77 启动子在受到棕榈酸酯暴露时的激活。染色质免疫沉淀、瞬时转染和 siRNA 介导的敲低实验表明,棕榈酸酯诱导 Nur77 启动子激活涉及 Sp1 的募集和 ZBP89 从基因启动子上的释放。