Hermonat P L, Spalholz B A, Howley P M
Laboratory of Tumor Virus Biology, National Cancer Institute, Bethesda, MD 20892.
EMBO J. 1988 Sep;7(9):2815-22. doi: 10.1002/j.1460-2075.1988.tb03137.x.
The bovine papillomavirus type 1 (BPV-1) P2443 promoter is located just upstream of the E2, E3, E4 and E5 open reading frames (ORFs) and is active in both transformed rodent cells and in productively infected warts. Analysis of viral RNA structures suggests that transcripts from this promoter encode the E2 transactivator as well as the E5 oncoprotein. To study expression of P2443, the chloramphenicol acetyltransferase (CAT) reporter gene was placed downstream of this promoter, deleting the E2 and E5 ORFs, in a plasmid which contained all BPV-1 upstream sequences including the long control region (LCR). By itself, this plasmid demonstrated a low level of activity in transient assays and could be transactivated to a high level by the full-length E2 product. Transactivation of P2443 expression by E2 required the LCR in cis in an orientation- and position-independent manner, suggesting that this transactivation was mediated through the E2 responsive enhancer elements (E2RE) located within the LCR. Primer extension analysis of the 5' ends of the viral transcripts from pooled cells expressing these P2443/CAT plasmids confirmed that E2 transactivation results in an increase in the steady-state levels of RNA initiated from the P2443 promoter. Furthermore, E2 transactivation of the P2443 promoter could be inhibited by the trans-repressor encoded by the 3' portion of the E2 ORF. Thus, expression of the E2 transactivator and the E5 oncoprotein is directly regulated by transcriptional factors encoded by the E2 ORF.
牛乳头瘤病毒1型(BPV-1)的P2443启动子位于E2、E3、E4和E5开放阅读框(ORF)的上游,在转化的啮齿动物细胞和产生性感染的疣中均具有活性。对病毒RNA结构的分析表明,该启动子的转录本编码E2反式激活因子以及E5癌蛋白。为了研究P2443的表达,将氯霉素乙酰转移酶(CAT)报告基因置于该启动子的下游,删除E2和E5 ORF,构建于一个包含所有BPV-1上游序列(包括长控制区,LCR)的质粒中。该质粒本身在瞬时分析中显示出低水平的活性,并且可以被全长E2产物反式激活至高水平。E2对P2443表达的反式激活需要顺式的LCR,且其方向和位置不依赖,这表明这种反式激活是通过位于LCR内的E2反应增强子元件(E2RE)介导的。对表达这些P2443/CAT质粒的混合细胞中病毒转录本5'端的引物延伸分析证实,E2反式激活导致从P2443启动子起始的RNA稳态水平增加。此外,E2 ORF 3'部分编码的反式抑制因子可抑制P2443启动子的E2反式激活。因此,E2反式激活因子和E5癌蛋白的表达直接受E2 ORF编码的转录因子调控。