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Emergence of infectious simian virus 40 whose AT tract in the replication origin/early promoter region is substituted by cellular or viral DNAs

机译:猿猴病毒40的复制出现,其复制起点/早期启动子区域的AT通道被细胞或病毒DNA取代

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In simian virus 40 (SV40) and several other polyomaviruses, the TATA box of the early promoter is embedded in an AT tract that is also an essential part of the replication origin. We generated an ‘AT trap’, an SV40 genome lacking the AT tract and unable to grow in CV-1 monkey cells. Co-transfection of the AT trap with oligonucleotides containing AT tracts of human polyomaviruses, a poly(A?:?T) tract or variants of the SV40 WT sequence all restored infectious virus. In a transfection of the AT trap without a suitable oligonucleotide, an AT-rich segment was incorporated, stemming either from bovine (calf serum) or monkey (host cell) DNA. Similarly, when cells were grown with human serum, a human DNA segment was captured by SV40 to substitute for the missing AT stretch. We conclude that the virus is quite opportunistic in accepting heterologous substitutes, and that even low-abundance DNA from serum can be incorporated into the viral genome.
机译:在猿猴病毒40(SV40)和其他几种多瘤病毒中,早期启动子的TATA盒嵌入AT管道中,该管道也是复制起点的重要组成部分。我们生成了一个“ AT陷阱”,即一个缺少AT道且无法在CV-1猴细胞中生长的SV40基因组。用含有人多瘤病毒的AT片段,聚(Aβ:ΔT)片段或SV40WT序列变体的寡核苷酸共转染AT捕集器,它们全部恢复了感染性病毒。在不使用合适的寡核苷酸的AT捕集器转染中,掺入了富含AT的片段,该片段源自牛(小牛血清)或猴(宿主细胞)DNA。同样,当细胞与人血清一起生长时,SV40会捕获人DNA片段,以替代缺失的AT片段。我们得出的结论是,该病毒在接受异源替代物方面的机会很大,甚至血清中的低丰度DNA都可以整合到病毒基因组中。

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