Yasue H, Ishibashi M
Gan To Kagaku Ryoho. 1984 Mar;11(3 Pt 2):579-86.
Adenovirus-induced tumor cells (including transformed cells) examined contain a part of the viral genome. However, number of molecules of the virus DNA persisting in a cell varies in the tumor cell lines. Tumor cell lines which were induced by CELO virus, an avian adenovirus, carried the virus DNA in the range from 1 to 920 molecules Per cell. Of the tumor cell line which carried large numbers of molecules of the virus DNR, one tumor cell line, RT 13 (160 molecules/cell), was studied both at the molecular level using DNA cloning and southern blot hybridization and at the cytological level using in situ hybridization, in order to elucidate the mode of existence of virus DNA and to reveal how such mode of existence emerged. This study indicated the followings: During the course of tumorigenesis, the virus DNA sequence (14.1 kilo base pairs) together with flanking cellular sequences formed "amplification" unit, and the unit was amplified about 160 times. The amplified cellular DNA sequences flanking to the left and right termini of the virus DNA sequence were longer than 6.8 and 16.3 kilo base pairs, respectively. Most of these amplified DNA sequences were localized in the limited region of specific chromosome (s). Possible effect of the amplification of virus DNA sequence on malignant cell transformation is discussed in the text, being referred to the amplification of cellular onc-genes reported recently.
所检测的腺病毒诱导的肿瘤细胞(包括转化细胞)含有部分病毒基因组。然而,肿瘤细胞系中持续存在的病毒DNA分子数量各不相同。由禽腺病毒CELO病毒诱导产生的肿瘤细胞系,每个细胞携带的病毒DNA分子数量在1至920个之间。在携带大量病毒DNA分子的肿瘤细胞系中,选取了一个肿瘤细胞系RT 13(160个分子/细胞),从分子水平上运用DNA克隆和Southern印迹杂交技术进行研究,并从细胞学水平上运用原位杂交技术进行研究,以阐明病毒DNA的存在方式,并揭示这种存在方式是如何出现的。这项研究表明:在肿瘤发生过程中,病毒DNA序列(14.1千碱基对)与侧翼细胞序列形成了“扩增”单元,该单元被扩增了约160倍。病毒DNA序列左右两端侧翼的扩增细胞DNA序列分别长于6.8千碱基对和16.3千碱基对。这些扩增的DNA序列大多定位于特定染色体的有限区域。文中讨论了病毒DNA序列扩增对恶性细胞转化的可能影响,并提及了最近报道的细胞癌基因的扩增。