Kamen R, Sedat J, Ziff E
J Virol. 1975 Jan;17(1):212-8. doi: 10.1128/JVI.17.1.212-218.1976.
The chemical polarities of the two strands of polyoma virus DNA with respect to the DNA physical map have been determined by hybridization of restriction endonuclease fragments specifically labeled with [125I]dCMP at their 3' termini to asymmetric polyoma complementary RNA (the product of in vitro transcription of viral DNA by Escherichia coli RNA polymerase). The orientations of the polyoma-specific stable RNA transcripts present in the cytoplasm of productively linfected mouse cells have been deduced from this result: the 5' ends of the early and late viral transcripts map very near the origin of viral DNA replication.
通过用[125I]dCMP在其3'末端特异性标记的限制性内切酶片段与不对称多瘤互补RNA(大肠杆菌RNA聚合酶对病毒DNA进行体外转录的产物)杂交,确定了多瘤病毒DNA两条链相对于DNA物理图谱的化学极性。根据这一结果推断了在高效感染的小鼠细胞胞质中存在的多瘤特异性稳定RNA转录本的方向:早期和晚期病毒转录本的5'末端位于病毒DNA复制起点附近。