Ahola H, Stenlund A, Moreno-López J, Pettersson U
J Virol. 1987 Jul;61(7):2240-4. doi: 10.1128/JVI.61.7.2240-2244.1987.
The mRNAs present in bovine papillomavirus type 1 (BPV-1)-transformed C127 cells were studied by primer extension. The results show that two internal promoters are present in the E region of BPV-1 in addition to the previously identified promoter at coordinate 1 (H. Ahola, A. Stenlund, J. Moreno-López, and U. Pettersson, Nucleic Acids Res. 11:2639-2650, 1983). One, located at coordinate 31, generated a set of mRNAs with heterogeneous 5' ends, which may encode the major transforming protein of BPV-1, the E5 protein. The second promoter, which is located at coordinate 39, generates colinear mRNAs which encode either the E4 protein or a truncated form of the E2 protein. Unlike the cottontail rabbit papillomavirus (O. Danos, E. Georges, G. Orth, and M. Yaniv, J. Virol. 53:735-741, 1985), BPV-1 appears to lack a separate promoter for expression of the E7 protein. The major splice sites in the transforming region (E region) of the BPV-1 genome were also identified by nucleotide sequence analysis.
通过引物延伸法研究了1型牛乳头瘤病毒(BPV-1)转化的C127细胞中存在的mRNA。结果表明,除了先前在坐标1处鉴定出的启动子外,BPV-1的E区域还存在两个内部启动子(H. Ahola、A. Stenlund、J. Moreno-López和U. Pettersson,《核酸研究》11:2639 - 2650,1983年)。一个位于坐标31处,产生了一组5'端异质的mRNA,这些mRNA可能编码BPV-1的主要转化蛋白E5蛋白。第二个启动子位于坐标39处,产生共线性mRNA,其编码E4蛋白或E2蛋白的截短形式。与棉尾兔乳头瘤病毒不同(O. Danos、E. Georges、G. Orth和M. Yaniv,《病毒学杂志》53:735 - 741,1985年),BPV-1似乎缺乏用于表达E7蛋白的单独启动子。还通过核苷酸序列分析确定了BPV-1基因组转化区域(E区域)中的主要剪接位点。