Akira S, Isshiki H, Sugita T, Tanabe O, Kinoshita S, Nishio Y, Nakajima T, Hirano T, Kishimoto T
Institute for Molecular and Cellular Biology, Osaka University, Japan.
EMBO J. 1990 Jun;9(6):1897-906. doi: 10.1002/j.1460-2075.1990.tb08316.x.
NF-IL6 is a nuclear factor that specifically binds to an IL1-responsive element in the IL-6 gene. In this study the gene encoding NF-IL6 has been cloned by direct screening of a lambda gt11 library using NF-IL6 binding sequence as a ligand. The full-length cDNA encoded a 345 amino acid protein with a potential leucine zipper structure and revealed a high degree of homology to a liver-specific transcriptional factor, C/EBP, at the C-terminal portion. The bacterial fusion protein bound to the CCAAT homology as well as the viral enhancer core sequences as in the case of C/EBP. Recombinant NF-IL6 activated the human IL-6 promoter in a sequence-specific manner. Southern blot analysis demonstrated the high-degree conservation of the NF-IL6 gene through evolution and the existence of several other related genes sharing the DNA-binding domain. NF-IL6 mRNA was normally not expressed, but induced by the stimulation with either LPS, IL-1 or IL-6. Interestingly, NF-IL6 was shown to bind to the regulatory regions for various acute-phase protein genes and several other cytokine genes such as TNF, IL-8 and G-CSF, implying that NF-IL6 has a role in regulation not only for the IL-6 gene but also for several other genes involved in acute-phase reaction, inflammation and hemopoiesis.
NF-IL6是一种核因子,它能特异性地与白细胞介素6(IL-6)基因中的IL1反应元件结合。在本研究中,通过使用NF-IL6结合序列作为配体直接筛选λgt11文库,克隆了编码NF-IL6的基因。全长cDNA编码一个含有潜在亮氨酸拉链结构的345个氨基酸的蛋白质,并在C末端部分显示出与肝脏特异性转录因子C/EBP高度同源。细菌融合蛋白与CCAAT同源序列以及病毒增强子核心序列结合,就像C/EBP一样。重组NF-IL6以序列特异性方式激活人IL-6启动子。Southern印迹分析表明,NF-IL6基因在进化过程中高度保守,并且存在其他几个共享DNA结合结构域的相关基因。NF-IL6 mRNA通常不表达,但可由脂多糖(LPS)、IL-1或IL-6刺激诱导表达。有趣的是,NF-IL6被证明能与各种急性期蛋白基因以及其他几种细胞因子基因(如肿瘤坏死因子(TNF)、IL-8和粒细胞集落刺激因子(G-CSF))的调控区域结合,这意味着NF-IL6不仅在IL-6基因的调控中起作用,而且在参与急性期反应、炎症和造血的其他几个基因的调控中也起作用。