[Serum stimulates the transcriptional activity of the enhancer of the immediate-early genes of the murine cytomegalovirus through p21 ras].

A Angeretti, D Lembo, R Cavallo, M Gariglio, G Gribaudo, S Landolfo
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Abstract

The analysis of the MCMV IE enhancer revealed the presence of many putative binding sites for the transcription factors AP-1 and NFkB. Previous studies suggested that such factors represent a final target for the metabolic cascade triggered by serum and growth factors. On these basis we wanted to verify if serum stimulates the transcriptional activity of the MCMV IE enhancer through p21ras and AP-1 and NFkB according to the actual model of transduction of the mitogenic signal. Our data demonstrate that serum stimulates the MCMV IE enhancer through a pathway in which the p21ras is involded, as demonstrated by using the dominant inhibitory mutant ras(Asn 17). Moreover deletion mutant analysis of the enhancer showed that the serum responsive region lies between nucleotides -1280 and -285 and contains a high concentration of putative AP-1 and NFkB binding sites.

[血清通过p21 ras刺激小鼠巨细胞病毒立即早期基因增强子的转录活性]。
对MCMV IE增强子的分析揭示了转录因子AP-1和NFkB的许多假定结合位点的存在。以往的研究表明,这些因子代表了血清和生长因子引发的代谢级联反应的最终目标。在此基础上,我们想根据有丝分裂信号的实际转导模型,验证血清是否通过p21ras、AP-1和NFkB来刺激MCMV IE增强子的转录活性。我们的数据表明,血清通过p21ras参与的途径刺激MCMV IE增强子,正如使用显性抑制突变体ras(Asn 17)所证明的那样。此外,对增强子的缺失突变分析表明,血清应答区位于核苷酸-1280和-285之间,含有高浓度的AP-1和NFkB结合位点。
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