Inagaki Y, Tsunokawa Y, Takebe N, Nawa H, Nakanishi S, Terada M, Sugimura T
National Cancer Center Research Institute, Tokyo, Japan.
J Virol. 1988 May;62(5):1640-6. doi: 10.1128/JVI.62.5.1640-1646.1988.
HeLa cells expressed 3.4- and 1.6-kilobase (kb) transcripts of the integrated human papillomavirus (HPV) type 18 genome. Two types of cDNA clones representing each size of HPV type 18 transcript were isolated. Sequence analysis of these two types of cDNA clones revealed that the 3.4-kb transcript contained E6, E7, the 5' portion of E1, and human sequence and that the 1.6-kb transcript contained spliced and frameshifted E6 (E6*), E7, and human sequence. There was a common human sequence containing a poly(A) addition signal in the 3' end portions of both transcripts, indicating that they were transcribed from the HPV genome at the same integration site with different splicing. Furthermore, the 1.6-kb transcript contained both of the two viral TATA boxes upstream of E6, strongly indicating that a cellular promoter was used for its transcription.
HeLa细胞表达整合的人乳头瘤病毒18型(HPV-18)基因组的3.4千碱基(kb)和1.6 kb转录本。分离出了代表HPV-18转录本每种大小的两种cDNA克隆。对这两种cDNA克隆的序列分析表明,3.4 kb转录本包含E6、E7、E1的5′部分和人源序列,而1.6 kb转录本包含剪接和移码的E6(E6*)、E7和人源序列。在两种转录本的3′末端部分存在一个含有多聚腺苷酸化信号的共同人源序列,表明它们是从HPV基因组的同一整合位点转录而来,但剪接方式不同。此外,1.6 kb转录本在E6上游含有两个病毒TATA框,强烈表明其转录使用了细胞启动子。