Wagatsuma M, Hashimoto K, Matsukura T
Department of Virology and Rickettsiology, National Institute of Health, Tokyo, Japan.
J Virol. 1990 Feb;64(2):813-21. doi: 10.1128/JVI.64.2.813-821.1990.
We have isolated four clones of integrated human papillomavirus type 16 (HPV-16) DNA from four different primary cervical cancer specimens. All clones were found to be monomeric or dimeric forms of HPV-16 DNA with cellular flanking sequences at both ends. Analysis of the viral sequences in these clones showed that E6/E7 open reading frames and the long control region were conserved and that no region specific for the integration was detected. Analysis of the cellular flanking sequences revealed no significant homology with any known human DNA sequences, except Alu sequences, and no homology among the clones, indicating no cellular sequence specific for the integration. By probing with single-copy cellular flanking sequences from the clones, it was demonstrated that the integrated HPV-16 DNAs, with different sizes in the same specimens, shared the same cellular flanking sequences at the ends. Furthermore, it was shown that the viral sequences together with cellular flanking sequences were amplified. The possible process of viral integration into cell chromosomes in cervical cancer is discussed.
我们从四个不同的原发性宫颈癌标本中分离出了四个整合型人乳头瘤病毒16型(HPV-16)DNA克隆。所有克隆均被发现为HPV-16 DNA的单体或二聚体形式,两端带有细胞侧翼序列。对这些克隆中病毒序列的分析表明,E6/E7开放阅读框和长控制区是保守的,未检测到整合特异性区域。对细胞侧翼序列的分析显示,除了Alu序列外,与任何已知人类DNA序列均无明显同源性,且各克隆之间也无同源性,这表明不存在整合特异性的细胞序列。通过用来自克隆的单拷贝细胞侧翼序列进行探针杂交,证明在同一标本中大小不同的整合型HPV-16 DNA在末端共享相同的细胞侧翼序列。此外,还表明病毒序列与细胞侧翼序列一起被扩增。本文讨论了宫颈癌中病毒整合到细胞染色体的可能过程。