Stamps A C, Campo M S
Beatson Institute for Cancer Research, Bearsden, Glasgow, U.K.
J Gen Virol. 1988 Dec;69 ( Pt 12):3033-45. doi: 10.1099/0022-1317-69-12-3033.
A cDNA library was synthesized using RNA from bovine papillomavirus type 4 (BPV-4)-induced papillomas. The major viral transcript was characterized by sequencing of its cDNA, primer extension mapping and S1 nuclease protection studies. The transcript initiates at multiple sites between nucleotide (nt) 777 and nt 902, contains a splice junction between nt 1016 and nt 3376 and terminates at nt 4034, using the early polyadenylation signal at nt 4009. Sequencing of viral cDNAs and mRNA revealed deviations from the reported genomic sequence between nt 3412 and nt 3460. These resulted in a temporary frameshift, abolished the translation termination codon of the E5a open reading frame (ORF), and introduced a new termination codon in the E4 ORF. The new uninterrupted E5 ORF was found to have greater homology to the E4 ORFs of other papillomaviruses than to their E5 ORFs. The E5 ORF of BPV-4 is joined to a five codon ORF in the leader exon of the major transcript, in the same way as the E4 ORF in the major transcripts of BPV-1 and human papillomavirus type 11. On this basis, it has been redesignated E4, and the viral genomic sequence revised. Two novel transcriptional promoters of BPV-4 were defined: a putative controller of the multiple major RNA start sites around nt 870 and a minor TATA box at nt 691. In addition, minor early region transcripts were mapped which initiate between nt 3071 and nt 3152. None of these transcripts utilizes the splice site at nt 3376. These messages may express E2-encoded functions.
使用来自牛乳头瘤病毒4型(BPV-4)诱导的乳头瘤的RNA合成了一个cDNA文库。通过对其cDNA进行测序、引物延伸图谱分析和S1核酸酶保护研究,对主要病毒转录本进行了表征。该转录本在核苷酸(nt)777和nt 902之间的多个位点起始,在nt 1016和nt 3376之间包含一个剪接连接,并在nt 4034处终止,使用nt 4009处的早期多聚腺苷酸化信号。病毒cDNA和mRNA的测序揭示了在nt 3412和nt 3460之间与报道的基因组序列存在偏差。这些偏差导致了一个临时的移码,消除了E5a开放阅读框(ORF)的翻译终止密码子,并在E4 ORF中引入了一个新的终止密码子。发现新的不间断的E5 ORF与其他乳头瘤病毒的E4 ORF比与它们的E5 ORF具有更高的同源性。BPV-4的E5 ORF与主要转录本前导外显子中的一个五密码子ORF相连,方式与BPV-1和人乳头瘤病毒11型主要转录本中的E4 ORF相同。基于此,它被重新命名为E4,并对病毒基因组序列进行了修订。定义了BPV-4的两个新的转录启动子:一个推测的围绕nt 870的多个主要RNA起始位点的调控因子和一个位于nt 691的次要TATA框。此外,还绘制了在nt 3071和nt 3152之间起始的次要早期区域转录本。这些转录本均未利用nt 3376处的剪接位点。这些信息可能表达E2编码的功能。