Sadat M A, Kumatori A, Suzuki S, Yamaguchi Y, Tsuji Y, Nakamura M
Department of Pediatrics, Nagasaki University School of Medicine, Sakamoto, Japan.
FEBS Lett. 1998 Oct 9;436(3):390-4. doi: 10.1016/s0014-5793(98)01182-x.
To study the regulatory mechanism of gp91phox gene expression in eosinophils, we transiently transfected eosinophil-committed HL-60-C15 cells with gp91phox promoter constructs, and identified a negative element from bp -267 to -246 of the gp91phox gene, the deletion of which caused an 83% increase in promoter activity. Electrophoresis mobility shift assays demonstrated GATA-3 binds to the GATA consensus site from bp -256 to -250. An 81% increment in promoter activity was obtained when a mutation was introduced in the GATA-3 binding site of the bp -267 to +12 construct, which is comparable to that of the bp -245 to +12 construct. We therefore conclude that GATA-3 specifically binding to the GATA site negatively regulates the expression of the gene in HL-60-C15 cells.
为研究嗜酸性粒细胞中gp91phox基因表达的调控机制,我们用gp91phox启动子构建体瞬时转染嗜酸性粒细胞定向分化的HL-60-C15细胞,并在gp91phox基因的-267至-246碱基对处鉴定出一个负性元件,该元件缺失导致启动子活性增加83%。电泳迁移率变动分析表明,GATA-3与-256至-250碱基对处的GATA共有序列结合。当在-267至+12构建体的GATA-3结合位点引入突变时,启动子活性增加81%,这与-245至+12构建体相当。因此,我们得出结论,GATA-3特异性结合GATA位点可负向调节HL-60-C15细胞中该基因的表达。