Milligan Steven G, Veerapraditsin Thanaporn, Ahamet Boolang, Mole Sarah, Graham Sheila V
Rm 2/14 GBRC, IBLS Division of Infection and Immunity, University of Glasgow, 120 University Place, Glasgow, G12 8TA, Scotland, UK.
Virology. 2007 Mar 30;360(1):172-81. doi: 10.1016/j.virol.2006.10.012. Epub 2006 Nov 13.
The life cycle of human papillomavirus type 16 (HPV16) is intimately linked to differentiation of the epithelium it infects, and late events in the life cycle are restricted to the suprabasal layers. Here we have used 5'RACE of polyadenylated RNA isolated from differentiated W12 cells (cervical epithelial cells containing episomal copies of the HPV16 genome) that express virus late proteins to map virus late mRNAs. Thirteen different transcripts were identified. Extensive alternative splicing and use of two late polyadenylation sites were noted. A novel promoter located in the long control region was detected as well as P97 and Plate. Promoters in the E4 and E5 open reading frames were active yielding transcripts where L1 or L2 respectively are the first open reading frames. Finally, mRNAs that could encode novel proteins E6*-- E7, E6-- E4, E1--*E4 and E1-- E2C (putative repressor E2) were identified, indicating that HPV16 may encode more late proteins than previously accepted.
人乳头瘤病毒16型(HPV16)的生命周期与它所感染的上皮细胞的分化密切相关,并且生命周期中的晚期事件局限于基底上层。在这里,我们利用从表达病毒晚期蛋白的分化W12细胞(含有HPV16基因组游离型拷贝的宫颈上皮细胞)中分离出的多聚腺苷酸化RNA进行5'RACE,以绘制病毒晚期mRNA图谱。鉴定出了13种不同的转录本。注意到存在广泛的可变剪接以及两个晚期多聚腺苷酸化位点的使用。检测到一个位于长调控区的新型启动子以及P97和Plate。E4和E5开放阅读框中的启动子是活跃的,产生的转录本中L1或L2分别是第一个开放阅读框。最后,鉴定出了可能编码新型蛋白E6*--E7、E6*--E4、E1--*E4和E1--E2C(假定的阻遏物E2)的mRNA,这表明HPV16可能编码比之前公认的更多的晚期蛋白。