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Loss of viral genomes from hamster tumor cells and nonrandom alterations in patterns of methylation of integrated adenovirus type 12 DNA.

机译:仓鼠肿瘤细胞的病毒基因组丢失和整合型12型腺病毒DNA甲基化模式的非随机改变。

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摘要

The insertion stability and DNA methylation patterns of integrated adenovirus type 12 (Ad12) genomes were investigated in Ad12-induced tumors and in tumor cell lines established from them as a function of time of passage under culture conditions. Upon subcultivation of cells from some of the tumors, the viral genomes were eliminated, apparently in a stepwise process with segments of the left termini of Ad12 DNAs persisting the longest. Morphological variants of these tumor cells lost all viral DNA and yet retained the oncogenic phenotype. All 13 independently isolated clones from one revertant line were devoid of Ad12 DNA. It could not be ruled out that very short sequence elements of viral DNA, such as promoters or enhancing sequences, could have persisted in these variants. The extent of viral DNA methylation was minimal in Ad12-induced tumors, although the viral genome was not extensively expressed, if at all. Upon passage in culture, the levels of viral DNA methylation increased. It was interesting that establishment of the final methylation pattern of integrated Ad12 DNAs required many cell generations after the fixation of foreign DNA in the host genome. The shift in methylation was nonrandom. The late parts of the inserted viral genomes became methylated more extensively than did the early gene segments.
机译:研究了整合的12型腺病毒(Ad12)基因组在Ad12诱导的肿瘤和由此建立的肿瘤细胞系中作为传代时间在培养条件下的功能的插入稳定性和DNA甲基化模式。在将某些肿瘤细胞传代培养后,病毒基因组被清除,显然是逐步进行的,其中Ad12 DNA左端的片段持续时间最长。这些肿瘤细胞的形态变异丧失了所有病毒DNA,但仍保留了致癌表型。来自一个回复系的所有13个独立分离的克隆均不含Ad12 DNA。不能排除病毒DNA的非常短的序列元素(如启动子或增强序列)可能已经保留在这些变异体中。尽管没有完全表达病毒基因组,但在Ad12诱导的肿瘤中病毒DNA甲基化的程度很小。通过培养后,病毒DNA甲基化水平增加。有趣的是,整合的Ad12 DNA的最终甲基化模式的建立需要在外源DNA固定在宿主基因组中之后需要许多细胞世代。甲基化的变化是非随机的。插入的病毒基因组的晚期部分比早期的基因片段更广泛地被甲基化。

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