Wright T M, Farber J M
Division of Molecular and Clinical Rheumatology, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.
J Exp Med. 1991 Feb 1;173(2):417-22. doi: 10.1084/jem.173.2.417.
A newly described member of the platelet factor 4 family of cytokine genes, mig, is selectively induced by interferon gamma (IFN-gamma), and not IFN-alpha, in the mouse macrophage-like cell line RAW 264.7. Treatment of RAW 264.7 cells with IFN-gamma activated mig gene transcription as determined by nuclear run-on assays. mig genomic clones were isolated, and constructs containing genomic fragments that included the mig promoter region and the CAT reporter gene were prepared. In RAW 264.7 cells transfected with these constructs, CAT activity was found to be selectively induced by IFN-gamma. A 278-bp genomic fragment containing 235 nucleotides 5' of the transcription start site was sufficient for IFN-gamma-selective induction of CAT activity. Analysis of 5' deletion mutants localized a region essential for activation by IFN-gamma to within 64 nucleotides extending from -235 to -172. A genomic fragment containing this sequence was capable of conferring IFN-gamma inducibility to constructs with a heterologous promoter.
细胞因子基因血小板因子4家族中一个新描述的成员mig,在小鼠巨噬细胞样细胞系RAW 264.7中,由γ干扰素(IFN-γ)而非α干扰素选择性诱导。通过核转录分析确定,用IFN-γ处理RAW 264.7细胞可激活mig基因转录。分离出mig基因组克隆,并制备了包含mig启动子区域和CAT报告基因的基因组片段的构建体。在用这些构建体转染的RAW 264.7细胞中,发现CAT活性由IFN-γ选择性诱导。一个包含转录起始位点上游235个核苷酸的278碱基对基因组片段足以实现IFN-γ对CAT活性的选择性诱导。对5'缺失突变体的分析将IFN-γ激活所必需的区域定位在从-235延伸至-172的64个核苷酸范围内。包含该序列的基因组片段能够赋予异源启动子构建体IFN-γ诱导性。