Nabel G J, Gorka C, Baltimore D
Whitehead Institute for Biomedical Research, Cambridge, MA 02142.
Proc Natl Acad Sci U S A. 1988 May;85(9):2934-8. doi: 10.1073/pnas.85.9.2934.
To understand the basis for T-cell-specific induction of interleukin 2 (IL-2), we have analyzed nuclear factors from the Jurkat T-lymphoid leukemia cell, which can be induced to secrete IL-2. We have used an electrophoretic mobility shift assay to examine binding of proteins to the upstream regulatory region, before and after activation with mitogens. We find two types of binding sites. One resembles an inducible enhancer element, but the protein that recognizes it is found in non-T cells and is unlikely to determine T-cell-specific expression of IL-2. A second site negatively regulates expression in resting T cells. A complex that binds to a DNA fragment containing this site is modified only when IL-2 is expressed, and it lies near a specific inducible DNase hypersensitive region. We suggest that negative regulation at this site, mediated by its associated protein(s), may contribute to the cell-specific expression of IL-2.
为了解白细胞介素2(IL-2)在T细胞中特异性诱导的基础,我们分析了来自Jurkat T淋巴细胞白血病细胞的核因子,该细胞可被诱导分泌IL-2。我们使用电泳迁移率变动分析来检测有丝分裂原激活前后蛋白质与上游调控区域的结合情况。我们发现了两种结合位点。一种类似于可诱导的增强子元件,但识别它的蛋白质在非T细胞中也有,不太可能决定IL-2的T细胞特异性表达。第二个位点对静息T细胞中的表达起负调控作用。与包含该位点的DNA片段结合的复合物仅在IL-2表达时发生改变,并且它位于一个特定的可诱导的DNA酶超敏感区域附近。我们认为,由其相关蛋白质介导的该位点的负调控可能有助于IL-2的细胞特异性表达。