Barbosa M S, Wettstein F O
J Virol. 1987 Sep;61(9):2938-42. doi: 10.1128/JVI.61.9.2938-2942.1987.
Cottontail rabbit papillomavirus (CRPV) early proteins are present at very low levels in virus-induced tumors and cannot be detected by immunological methods. Furthermore, cells in culture are not readily transformed by the virus. To overcome these difficulties in identifying and characterizing the putative transforming protein(s) coded by the E6 open reading frame, the early cottontail rabbit papillomavirus region was expressed under the control of the late simian virus 40 promoter. Mapping of the transcripts in transiently transfected COS-7 cells indicated that transcription was initiated in the late region of simian virus 40. Two E6-coded polypeptides were identified, representing translation products initiated at the first and second AUG codons.
棉尾兔乳头瘤病毒(CRPV)早期蛋白在病毒诱导的肿瘤中含量极低,无法通过免疫方法检测到。此外,培养的细胞不易被该病毒转化。为了克服在鉴定和表征由E6开放阅读框编码的假定转化蛋白方面的这些困难,棉尾兔乳头瘤病毒早期区域在猿猴病毒40晚期启动子的控制下表达。对瞬时转染的COS-7细胞中转录本的定位表明,转录起始于猿猴病毒40的晚期区域。鉴定出两种由E6编码的多肽,分别代表在第一个和第二个AUG密码子处起始的翻译产物。