Klemsz M J, Maki R A, Papayannopoulou T, Moore J, Hromas R
Department of Microbiology and Immunology, Indiana University Medical Center, Indianapolis 46202.
J Biol Chem. 1993 Mar 15;268(8):5769-73.
The recently cloned fli-1 gene is a member of the ets oncogene family that is preferentially expressed in hematopoietic cells. It is a target of dysregulation by Friend leukemia virus insertion and translocation in Ewing's sarcoma and neuroepithelioma. In this report, we have studied the function and regulation of both murine and human fli-1. Analysis of the human and mouse fli-1 proteins showed that fli-1 binds to specific DNA sequences highly related to m-ets-2 binding sites. Methylation protection experiments showed that fli-1 and m-ets-2 contacted the same nucleotides in two different binding sites. The fli-1 protein was shown to be a transcriptional activator in co-transfection studies. Stimulation of murine bone marrow macrophages by mediators of inflammation, such as lipopolysaccharide, phorbol 12-myristate 13-acetate, interleukin-1, and interferon-gamma resulted in the reduced expression of fli-1 mRNA. fli-1 was only expressed in a defined subset of human erythroleukemia cell lines.
最近克隆的fli-1基因是ets癌基因家族的成员,在造血细胞中优先表达。它是弗瑞德白血病病毒插入以及在尤因肉瘤和神经上皮瘤中发生易位导致失调的靶点。在本报告中,我们研究了小鼠和人类fli-1的功能及调控。对人类和小鼠fli-1蛋白的分析表明,fli-1与和m-ets-2结合位点高度相关的特定DNA序列结合。甲基化保护实验表明,fli-1和m-ets-2在两个不同的结合位点接触相同的核苷酸。在共转染研究中,fli-1蛋白被证明是一种转录激活因子。用炎症介质如脂多糖、佛波醇12-肉豆蔻酸酯13-乙酸酯、白细胞介素-1和γ-干扰素刺激小鼠骨髓巨噬细胞,导致fli-1 mRNA表达降低。fli-1仅在特定的人类红白血病细胞系亚群中表达。