Prakash S S, Horwitz B H, Zibello T, Settleman J, DiMaio D
Department of Human Genetics, Yale University School of Medicine, New Haven, Connecticut 06510-8005.
J Virol. 1988 Oct;62(10):3608-13. doi: 10.1128/JVI.62.10.3608-3613.1988.
We have performed transient-expression experiments with CV1 monkey kidney cells to investigate the role of the bovine papillomavirus type 1 (BPV1) E2 gene in the regulation of the E5 transforming gene. Direct analysis of the 7-kilodalton open reading frame (ORF) E5 protein and measurements of the expression of an E5-chloramphenicol acetyltransferase fusion protein indicate that the efficient expression of ORF E5 requires the full-length E2 gene, which can be supplied in trans. The viral long control region is required in cis for this response to ORF E2, and it acts in a position- and orientation-independent fashion characteristic of a transcriptional enhancer. Deletion analysis suggests that the P2443 promoter is required for efficient expression of the E5 gene. The E2 repressor activity encoded in the 3' end of the E2 gene inhibits the expression of ORF E5. These effects define a major BPV1 regulatory circuit and appear to explain the transformation behavior of a variety of BPV1 mutants.
我们用CV1猴肾细胞进行了瞬时表达实验,以研究牛乳头瘤病毒1型(BPV1)E2基因在调控E5转化基因中的作用。对7千道尔顿开放阅读框(ORF)E5蛋白的直接分析以及对E5 - 氯霉素乙酰转移酶融合蛋白表达的测量表明,ORF E5的有效表达需要全长E2基因,该基因可以反式提供。病毒长控制区顺式作用于对ORF E2的这种反应,并且以转录增强子特有的位置和方向独立的方式起作用。缺失分析表明,P2443启动子是E5基因有效表达所必需的。E2基因3'端编码的E2阻遏活性抑制ORF E5的表达。这些效应定义了一个主要的BPV1调控回路,似乎解释了多种BPV1突变体的转化行为。