Horwitz M S
J Virol. 1976 Apr;18(1):307-15. doi: 10.1128/JVI.18.1.307-315.1976.
After short periods of labeling with [3H]thymidine, recently completed adenovirus DNA molecules were isolated and cleaved with restriction endonucleases. The strands (heavy and light) of most of the restriction endonuclease fragments were separated. The pattern of labeling clearly shows an asymmetry of radioactivity on the isolated strands of each restriction endonuclease piece. The data is consistent with replication proceeding in the 5' to 3' direction on each strand. Thus, there is an initiation point placed at or near each end of the molecule.
用[3H]胸苷进行短时间标记后,分离出最近完成的腺病毒DNA分子,并用限制性内切酶进行切割。大多数限制性内切酶片段的链(重链和轻链)被分开。标记模式清楚地显示出每个限制性内切酶片段的分离链上放射性的不对称性。数据与每条链上5'至3'方向的复制过程一致。因此,在分子的每个末端或其附近都有一个起始点。