Schindler U, Baichwal V R
Tularik Inc., South San Francisco, California 94080.
Mol Cell Biol. 1994 Sep;14(9):5820-31. doi: 10.1128/mcb.14.9.5820-5831.1994.
Transcription of the gene encoding the endothelial cell-leukocyte adhesion molecule (ELAM-1; E-selectin) is induced in response to various cytokines, including tumor necrosis factor-alpha (TNF-alpha) and interleukin-1. A DNase I-hypersensitive site in the 5' proximal promoter region of the E-selectin gene is observed in human umbilical vein endothelial cells only following TNF-alpha treatment, suggesting the presence of a TNF-alpha-inducible element close to the transcriptional start site. Transient transfection studies in endothelial cells demonstrated that 170 bp of upstream sequences is sufficient to confer TNF-alpha inducibility. Systematic site-directed mutagenesis of this region revealed two regulatory elements (-129 to -110 and -99 to -80) that are essential for maximal promoter activity following cytokine treatment. Protein binding studies with crude nuclear extracts and recombinant proteins revealed that the two elements correspond to three NF-kappa B binding sites (site 1, -126; site 2, 116; and site 3, -94). All three sites can be bound by NF-kappa B when used as independent oligonucleotides in mobility shift assays. However, within the context of a larger promoter fragment, sites 2 and 3 are preferentially occupied over site 1. These data are consistent with results obtained in transfection studies demonstrating that mutations in sites 2 and 3 are more detrimental than mutations within site 1. Hence, inducibility of the E-selectin gene requires the interaction of NF-kappa B proteins bound to multiple regulatory elements.
编码内皮细胞-白细胞黏附分子(ELAM-1;E-选择素)的基因转录是在对包括肿瘤坏死因子-α(TNF-α)和白细胞介素-1在内的多种细胞因子作出反应时被诱导的。仅在TNF-α处理后人脐静脉内皮细胞中观察到E-选择素基因5'近端启动子区域存在一个对DNA酶I敏感的位点,这表明在转录起始位点附近存在一个TNF-α诱导元件。在内皮细胞中的瞬时转染研究表明,170 bp的上游序列足以赋予TNF-α诱导性。对该区域进行系统性的定点诱变揭示了两个调控元件(-129至-110和-99至-80),它们对于细胞因子处理后最大启动子活性至关重要。用粗核提取物和重组蛋白进行的蛋白质结合研究表明,这两个元件对应于三个核因子-κB结合位点(位点1,-126;位点2,-116;位点3,-94)。在迁移率变动分析中,当用作独立的寡核苷酸时,所有三个位点都能被核因子-κB结合。然而,在更大的启动子片段背景下,位点2和位点3比位点1更优先被占据。这些数据与转染研究中获得的结果一致,表明位点2和位点3中的突变比位点1中的突变更具危害性。因此,E-选择素基因的诱导性需要与多个调控元件结合的核因子-κB蛋白之间的相互作用。