Vogel F, Scherneck S
Arch Geschwulstforsch. 1986;56(2):81-7.
Nascent RNA, synthesized by calf thymus RNA polymerase II on restriction endonuclease BamHI linearized hamster papovavirus (HaPV) DNA, was rehybridized to the template strand under conditions allowing transcription R-loop formation. Hybrids, visualized by electron microscopy, were plotted and mapped according to the physical map of HaPV. Two predominant regions of transcription could be localized at 0.10--0.40 and 0.50--0.82 m.u., respectively. For the start sites of transcription at map positions 0.67 and 0.75, respectively, on the HaPV genome a transcription in opposite direction were estimated. This genome region harbours the putative origin of replication of HaPV DNA. These results suggest a distinct relatedness of HaPV to the polyomavirus group.
由小牛胸腺RNA聚合酶II在限制性内切酶BamHI线性化的仓鼠乳头瘤病毒(HaPV)DNA上合成的新生RNA,在允许转录R环形成的条件下与模板链重新杂交。通过电子显微镜观察到的杂交体,根据HaPV的物理图谱进行绘制和定位。两个主要的转录区域分别位于0.10-0.40和0.50-0.82 m.u.处。对于分别位于HaPV基因组图谱位置0.67和0.75处的转录起始位点,估计存在相反方向的转录。该基因组区域包含HaPV DNA的假定复制起点。这些结果表明HaPV与多瘤病毒组有明显的相关性。