Kolk D P, Floyd-Smith G
Department of Zoology, Arizona State University, Tempe 85287.
DNA Cell Biol. 1992 Dec;11(10):745-54. doi: 10.1089/dna.1992.11.745.
The murine invariant chain (Ii) gene has been shown to be interferon-gamma (IFN-gamma)-inducible in a number of nonlymphoid cell types. In mouse L cells, steady-state levels of Ii mRNA are barely detectable in untreated cells but increase sharply upon IFN-gamma treatment. In IFN-gamma treated L cells, transcription starts 23, 28, 38, and 40 bases downstream of the TATA box. To identify cis-acting elements regulating expression of the Ii gene, reporter plasmids containing deletions of the Ii promoter have been constructed and transfected into mouse L cells. Deletion of the H box results in a 50-100% increase in basal expression. Deletion of both the H and X boxes increases basal expression by 200-300% above that seen in constructs containing all three elements. A 25% decrease in basal level expression is seen for constructs that lack the Y-box element when compared to constructs containing the Y-box element but not the H- and X-box elements. DNase I footprinting analysis demonstrates protection of the H, X, and Y boxes as well as a nonconserved region between the H and X boxes. Mobility-shift experiments detect a factor specifically interacting with the Y box. Although the H-, X-, and Y-box elements interact with nuclear protein and are regulatory elements in L cells, these elements do not appear to play a role in IFN-gamma induction suggesting that other regulatory mechanisms must account for IFN-gamma's induction of the Ii in L cells.
鼠源恒定链(Ii)基因已被证明在多种非淋巴细胞类型中可被γ干扰素(IFN-γ)诱导。在小鼠L细胞中,未处理细胞中Ii mRNA的稳态水平几乎检测不到,但经IFN-γ处理后会急剧增加。在经IFN-γ处理的L细胞中,转录起始于TATA框下游23、28、38和40个碱基处。为了鉴定调节Ii基因表达的顺式作用元件,构建了含有Ii启动子缺失片段的报告质粒,并将其转染到小鼠L细胞中。缺失H框会导致基础表达增加50 - 100%。同时缺失H框和X框会使基础表达比含有所有三个元件的构建体增加200 - 300%。与含有Y框元件但不含有H框和X框元件的构建体相比,缺乏Y框元件的构建体基础水平表达下降25%。DNA酶I足迹分析表明H框、X框和Y框以及H框和X框之间的一个非保守区域受到保护。凝胶迁移实验检测到一种与Y框特异性相互作用的因子。虽然H框、X框和Y框元件与核蛋白相互作用且是L细胞中的调节元件,但这些元件似乎在IFN-γ诱导过程中不起作用,这表明其他调节机制必定是IFN-γ在L细胞中诱导Ii的原因。