Tanaka Hiromasa, Kamita Shizuo G, Wolf Nicola M, Harris Todd R, Wu Zhaoju, Morisseau Christophe, Hammock Bruce D
Department of Entomology and the Cancer Research Center, University of California, Davis, CA 95616, USA.
Biochim Biophys Acta. 2008 Jan;1779(1):17-27. doi: 10.1016/j.bbagrm.2007.11.005. Epub 2007 Dec 3.
Soluble epoxide hydrolase (sEH) is a multifunctional protein encoded by the EPHX2 gene. The biological functions and enzyme kinetics of sEH have been extensively investigated, however, little is known about its transcriptional regulation and mechanisms of tissue specific expression. Here, a luciferase gene based reporter assay was used to identify the minimal promoter and cis regulatory elements of EPHX2. The minimal promoter was identified as a GC-rich region between nts -374 and +28 with respect to the putative transcriptional start site. A reporter plasmid carrying this minimal promoter showed higher or similar activities in comparison to a reporter plasmid carrying nts -5,974 to +28 of EPHX2 in 9 human cell lines that were tested. Sp1 binding sites that are involved in augmenting the minimal promoter activity of EPHX2 were identified by nested deletion analysis, site-specific mutation, electrophoretic mobility shift assay, and chromatin immunoprecipitation assay.
可溶性环氧化物水解酶(sEH)是一种由EPHX2基因编码的多功能蛋白质。sEH的生物学功能和酶动力学已得到广泛研究,然而,关于其转录调控和组织特异性表达机制却知之甚少。在此,基于荧光素酶基因的报告基因检测被用于鉴定EPHX2的最小启动子和顺式调控元件。最小启动子被确定为相对于假定转录起始位点在nts -374至+28之间的富含GC的区域。在9种测试的人类细胞系中,携带该最小启动子的报告质粒与携带EPHX2的nts -5,974至+28的报告质粒相比,表现出更高或相似的活性。通过巢式缺失分析、位点特异性突变、电泳迁移率变动分析和染色质免疫沉淀分析,鉴定出了参与增强EPHX2最小启动子活性的Sp1结合位点。