Daigneault L, Coulombe B, Skup D
Institut du Cancer de Montréal, Centre Hospitalier Notre-Dame, Quebec, Canada.
J Virol. 1988 Apr;62(4):1125-31. doi: 10.1128/JVI.62.4.1125-1131.1988.
We have examined the mechanism of action of the If-1 interferon (IFN) regulatory locus. This locus controls the level of circulating IFN produced in inbred mice in response to intravenous injection of Newcastle disease virus. Mice carrying the If-1h (high) allele show circulating IFN levels 10- to 15-fold higher than those carrying the If-1l (low) allele. In this report we show that induced splenocytes from If-1h and If-1l mice produce IFN at levels which are in the same proportions as those found in the circulation. Higher levels of IFN-specific mRNA were observed in splenocyte populations from If-1h animals. This was due to increased transcription of IFN genes. At the same time, the high- and low-producing populations showed no significant difference in the number of IFN mRNA-containing cells. We conclude that the effect of If-1 in the spleen is to control the levels of transcription of the IFN genes in individual induced splenocytes.
我们研究了If-1干扰素(IFN)调控基因座的作用机制。该基因座控制近交系小鼠静脉注射新城疫病毒后产生的循环IFN水平。携带If-1h(高)等位基因的小鼠循环IFN水平比携带If-1l(低)等位基因的小鼠高10至15倍。在本报告中,我们表明,来自If-1h和If-1l小鼠的诱导脾细胞产生IFN的水平与循环中发现的水平比例相同。在If-1h动物的脾细胞群体中观察到更高水平的IFN特异性mRNA。这是由于IFN基因转录增加所致。同时,高产量和低产量群体中含IFN mRNA的细胞数量没有显著差异。我们得出结论,If-1在脾脏中的作用是控制单个诱导脾细胞中IFN基因的转录水平。