O'Brien C A, Manolagas S C
Division of Endocrinology, University of Arkansas for Medical Sciences Center of Osteoporosis and Metabolic Bone Diseases, University of Little Rock, Arkansas 72205, USA.
J Biol Chem. 1997 Jun 6;272(23):15003-10. doi: 10.1074/jbc.272.23.15003.
Glycoprotein 130 (gp130), a shared component of all the receptors for the interleukin-6 cytokine family, transduces cytokine signals in part by activating latent cytoplasmic signal transducers and activators of transcription (STATs). STATs subsequently translocate into the nucleus and stimulate gene expression. In the studies reported here, the 5'-flanking region of the human gp130 gene was isolated and the transcription initiation sites were mapped. To demonstrate that the isolated DNA fragment contained a functional promoter, a plasmid construct containing 2433 base pairs of the gp130 5'-flanking region, inserted upstream from the firefly luciferase gene, was transiently transfected into HepG2 hepatoma cells. The construct exhibited constitutive promoter activity. In addition, a 5-h treatment with interleukin-6 or oncostatin M stimulated the activity of this promoter severalfold. Localization of the cytokine response element by 5'-deletion analysis and site-directed mutagenesis revealed a cis-acting binding site for activated STAT complexes. Furthermore, DNA binding analysis demonstrated that this element binds activated STAT1 and STAT3 homo- and heterodimers. This STAT-binding element was sufficient to confer cytokine stimulation to a minimal herpesvirus thymidine kinase promoter. These results establish that the DNA fragment we have isolated contains the human gp130 promoter and that interleukin-6 type cytokines may influence the activity of this promoter via activated STATs.
糖蛋白130(gp130)是白细胞介素-6细胞因子家族所有受体的共同组成部分,它部分地通过激活潜在的细胞质信号转导子和转录激活子(STATs)来转导细胞因子信号。STATs随后转移到细胞核并刺激基因表达。在本文报道的研究中,分离出了人类gp130基因的5'侧翼区域并确定了转录起始位点。为了证明分离出的DNA片段包含一个功能性启动子,将一个含有gp130 5'侧翼区域2433个碱基对的质粒构建体插入萤火虫荧光素酶基因上游,然后瞬时转染到HepG2肝癌细胞中。该构建体表现出组成型启动子活性。此外,用白细胞介素-6或抑瘤素M处理5小时可使该启动子的活性增强数倍。通过5'缺失分析和定点诱变对细胞因子反应元件进行定位,发现了一个激活的STAT复合物的顺式作用结合位点。此外,DNA结合分析表明该元件能结合激活的STAT1和STAT3同二聚体及异二聚体。这个STAT结合元件足以将细胞因子刺激作用赋予最小的单纯疱疹病毒胸苷激酶启动子。这些结果表明,我们分离出的DNA片段包含人类gp130启动子,并且白细胞介素-6型细胞因子可能通过激活的STATs影响该启动子的活性。