Lv Ben, Tang Yiting, Li Xiayu, Wang Guiliang, Yuan Can, Liu Ying, Jiang Lei, Xiao Xianzhong
Department of Pathophysiology, Xiangya School of Medicine, Central South University, Changsha 410078, China.
Acta Biochim Biophys Sin (Shanghai). 2009 Apr;41(4):309-15. doi: 10.1093/abbs/gmp019.
Mipu1, a novel gene encoding a KRAB/C2H2 zinc finger protein, was first reported to be up-regulated in myocardial ischemia-reperfusion injury, functioning to protect cells against oxidative stress. To map the promoter region of the gene and to understand its regulation, we identified the transcription start site and revealed that the 1366-bp fragment upstream of the transcription start site possesses promoter activity. Deletion constructs of the 5'-flanking region of Mipu1 lead to the identification of a minimal promoter, in which neither a TATA box nor a CAAT box was detected. Two GC boxes were found; however, they are the specific binding sites for Sp1-family transcription factors. Mutations in these GC boxes resulted in the total loss of Mipu1 minimal promoter activity. Finally, WP631, an Sp1-family-specific inhibitor, was found to decrease the promoter activity in a dose-dependent manner, indicating that the GC boxes are essential for the activity of the Mipu1 minimal promoter activity.
Mipu1是一种编码KRAB/C2H2锌指蛋白的新基因,首次报道其在心肌缺血再灌注损伤中上调,具有保护细胞免受氧化应激的作用。为了定位该基因的启动子区域并了解其调控机制,我们确定了转录起始位点,并发现转录起始位点上游1366 bp的片段具有启动子活性。Mipu1 5'侧翼区域的缺失构建体导致鉴定出一个最小启动子,在该启动子中未检测到TATA盒和CAAT盒。发现了两个GC盒;然而,它们是Sp1家族转录因子的特异性结合位点。这些GC盒中的突变导致Mipu1最小启动子活性完全丧失。最后,发现Sp1家族特异性抑制剂WP631以剂量依赖性方式降低启动子活性,表明GC盒对于Mipu1最小启动子活性至关重要。