Hrisomalos T F, Boggs D L, Fife K H
Department of Medicine, Indiana University School of Medicine, Indianapolis 46202-5124.
J Virol. 1990 Oct;64(10):5188-91. doi: 10.1128/JVI.64.10.5188-5191.1990.
We have identified a region of human papillomavirus type 6 (HPV-6) DNA that hybridizes with human cellular DNA containing no detectable HPV DNA sequences. The region of hybridization has been localized to a segment of the viral long control region between the end of the L1 open reading frame and the late polyadenylation signal and is likely contained within a 94-base-pair insertion at nucleotide 7350 which is present in the cloned HPV-6b DNA used for these studies. Restriction fragments of HPV-6 DNA from seven patients suggested that this insert was present in these naturally occurring viral genomes as well. The presence of this insert was confirmed by direct sequence analysis of polymerase chain reaction-amplified segments from four naturally occurring HPV-6 genomes. By analogy with other systems, this insert and surrounding sequences may function to destabilize the HPV-6 late mRNA.
我们已鉴定出人类乳头瘤病毒6型(HPV - 6)DNA的一个区域,该区域可与不含可检测到的HPV DNA序列的人类细胞DNA杂交。杂交区域已定位到病毒长控制区的一段,位于L1开放阅读框末端和晚期聚腺苷酸化信号之间,并且可能包含在用于这些研究的克隆HPV - 6b DNA中核苷酸7350处的一个94碱基对插入片段内。来自7名患者的HPV - 6 DNA的限制性片段表明,这个插入片段也存在于这些天然存在的病毒基因组中。通过对来自4个天然存在的HPV - 6基因组的聚合酶链反应扩增片段进行直接序列分析,证实了这个插入片段的存在。与其他系统类似,这个插入片段及周围序列可能起到使HPV - 6晚期mRNA不稳定的作用。