Daigneault L, Haggarty A, Meng Q H, Skup D
Institut du Cancer de Montreal, Quebec, Canada.
Nucleic Acids Res. 1992 Jun 11;20(11):2749-54. doi: 10.1093/nar/20.11.2749.
Activation and repression of IFN gene expression are controlled primarily at the transcriptional level. In order to elucidate some aspects of the induction mechanism of the IFN genes, we examined the effects of different treatments on IFN production in L929 cells, a well-characterized system, and in primary spleen cells. Our results indicate that 2-Aminopurine (2-AP) inhibits type I IFN (IFN-alpha and IFN-beta) induction in L929 cells but not in spleen cells. In L929 cells, 2-AP inhibited the induction of the MuIFN-beta promoter and of promoters containing tetrahexamer and PRDII sequences linked to a reporter gene. Inhibition of activation of the inducible factors binding to the MuIFN-beta promoter and sub-elements was also observed. In contrast, factors binding to the MuIFN-beta promoter are present constitutively in spleen cell nuclei and their activity is not inhibited by 2-AP. These results suggest that 2-AP inhibits IFN-beta gene induction in L929 cells through blocking of activation of the inducible DNA-binding factors which interact with the IFN-beta promoter.
干扰素基因表达的激活和抑制主要在转录水平上受到控制。为了阐明干扰素基因诱导机制的某些方面,我们研究了不同处理对L929细胞(一个特征明确的系统)和原代脾细胞中干扰素产生的影响。我们的结果表明,2-氨基嘌呤(2-AP)抑制L929细胞中I型干扰素(干扰素-α和干扰素-β)的诱导,但不抑制脾细胞中的诱导。在L929细胞中,2-AP抑制了MuIFN-β启动子以及与报告基因相连的含有四聚体和PRDII序列的启动子的诱导。还观察到与MuIFN-β启动子结合的诱导因子的激活受到抑制以及亚元件也受到抑制。相反,与MuIFN-β启动子结合的因子在脾细胞核中组成性存在,并且它们的活性不受2-AP抑制。这些结果表明,2-AP通过阻断与干扰素-β启动子相互作用的诱导性DNA结合因子的激活来抑制L929细胞中干扰素-β基因的诱导。