Wathelet M G, Clauss I M, Paillard F C, Huez G A
Départment de Biologie Moléculaire, Université Libre de Bruxelles, Rhode-St-Genése, Belgium.
Eur J Biochem. 1989 Oct 1;184(3):503-9. doi: 10.1111/j.1432-1033.1989.tb15043.x.
Interferons, double-stranded RNA and viruses induce the transcription of partly overlapping sets of cellular genes. We have studied the regulation of 11 interferon-inducible genes by these agents and found that four of them were also directly inducible by virus and double-stranded RNA, and two by virus only. We have investigated whether an inhibitor of interferon-beta gene activation, 2-aminopurine, would block this induction process. Induction of these genes by virus and double-stranded RNA was indeed blocked by 2-aminopurine. Since a single cis-acting element can confer inducibility both to interferons, and to virus and double-stranded RNA, we tested the effect of 2-aminopurine on gene activation by interferon-alpha and interferon-gamma. Remarkably, in all the cell lines tested, these induction processes and the establishment of an antiviral state were blocked by the drug. These observations contrast with previous reports. The inhibitory effect of this drug on gene induction was exerted in a selective fashion and at the transcriptional level. This indicate that for the virus-, double-stranded-RNA-, and interferons-mediated gene induction, an early and similar step in signal transduction was affected by 2-aminopurine.
干扰素、双链RNA和病毒可诱导细胞中部分重叠的基因集转录。我们研究了这些因子对11个干扰素诱导基因的调控,发现其中4个基因也可被病毒和双链RNA直接诱导,2个基因仅可被病毒诱导。我们研究了干扰素β基因激活抑制剂2-氨基嘌呤是否会阻断这一诱导过程。2-氨基嘌呤确实阻断了病毒和双链RNA对这些基因的诱导。由于单个顺式作用元件可赋予干扰素、病毒和双链RNA诱导性,我们测试了2-氨基嘌呤对干扰素α和干扰素γ基因激活的影响。值得注意的是,在所有测试的细胞系中,这些诱导过程和抗病毒状态的建立均被该药物阻断。这些观察结果与之前的报道形成对比。该药物对基因诱导的抑制作用以选择性方式在转录水平发挥。这表明对于病毒、双链RNA和干扰素介导的基因诱导,信号转导中一个早期且相似的步骤受到了2-氨基嘌呤的影响。