Wettstein F O, Barbosa M S, Nasseri M
Virology. 1987 Aug;159(2):321-8. doi: 10.1016/0042-6822(87)90470-3.
The capsite of the 2.6- and 4.8-kb major late transcripts of cottontail rabbit papillomavirus (CRPV) has been mapped by primer extension. A leader exon of about 300 nucleotides common to both RNAs is located in the untranslated region of the genome upstream of the capsites for early transcripts. In contrast to the early capsites which are all preceded by TATA boxes, no such sequence is present 30 nucleotides upstream of the late capsite. These data indicate that the switch from early to late transcription involves recognition of a new promoter and suppression of transcription termination at the early polyadenylation site. We have also identified a minor exon with a coding potential for a putative E2 transactivating protein. Quantitation by S1 mapping of the E2 coding exon and a minor exon coding for a full-sized E6 protein unique in size to the highly oncogenic CRPV did not reveal differences in the level of transcription between papillomas and carcinomas.
通过引物延伸法已确定了棉尾兔乳头瘤病毒(CRPV)2.6kb和4.8kb主要晚期转录本的帽位点。两种RNA共有的约300个核苷酸的前导外显子位于基因组的非翻译区,在早期转录本帽位点的上游。与所有早期帽位点之前都有TATA框不同,晚期帽位点上游30个核苷酸处不存在这样的序列。这些数据表明,从早期转录到晚期转录的转换涉及识别一个新的启动子,并抑制早期聚腺苷酸化位点处的转录终止。我们还鉴定出一个小外显子,它具有编码假定的E2反式激活蛋白的潜力。通过S1作图对E2编码外显子和一个编码全长E6蛋白的小外显子进行定量分析,该E6蛋白在大小上是高度致癌的CRPV所特有的,结果显示乳头状瘤和癌之间转录水平没有差异。