Patel K R, Smith K T, Campo M S
J Gen Virol. 1987 Aug;68 ( Pt 8):2117-28. doi: 10.1099/0022-1317-68-8-2117.
The nucleotide sequence of bovine papillomavirus type 4 (BPV-4) was determined. The viral genome is 7261 base pairs long. Several overlapping open reading frames (ORFs) have been identified both on the basis of amino acid comparison with other papillomaviruses and on their transcriptional pattern. Eight early ORFs (E1 to 8) were recognized, coding for DNA replication and cell transformation functions, and three late ORFs (L1 to 3), coding for structural proteins. Like the E5 ORF of human papillomavirus type 6 the E5 ORF of BPV-4 is discontinuous. Unlike other papillomaviruses, the non-coding region upstream of the early ORFs (ncr-1) is short (385 base pairs), but there is another non-coding region (ncr-2) of nearly 500 base pairs between the L2 and L1 ORFs. Most of the putative regulatory sites are located in the ncr-1, although potential controlling elements are also found in other parts of the genome. Polyadenylation sites are present at the 3' end of both the early and the late transcription units. Comparison between the polypeptides of BPV-4 and other papillomaviruses showed that BPV-4 is evolutionarily closer to the epitheliotropic human and rabbit viruses than to BPV-1.
测定了牛乳头瘤病毒4型(BPV - 4)的核苷酸序列。病毒基因组长度为7261个碱基对。基于与其他乳头瘤病毒的氨基酸比较及其转录模式,已鉴定出几个重叠的开放阅读框(ORF)。识别出八个早期ORF(E1至E8),编码DNA复制和细胞转化功能,以及三个晚期ORF(L1至L3),编码结构蛋白。与人类乳头瘤病毒6型的E5 ORF一样,BPV - 4的E5 ORF是不连续的。与其他乳头瘤病毒不同,早期ORF上游的非编码区(ncr - 1)较短(385个碱基对),但在L2和L1 ORF之间还有一个近500个碱基对的非编码区(ncr - 2)。大多数推定的调控位点位于ncr - 1中,尽管在基因组的其他部分也发现了潜在的控制元件。早期和晚期转录单位的3'端均存在多聚腺苷酸化位点。BPV - 4与其他乳头瘤病毒多肽的比较表明,BPV - 4在进化上更接近嗜上皮性人类和兔病毒,而不是BPV - 1。