Ohba R, Matsumoto K, Ishimi Y
Mitsubishi Kasei Institute of Life Sciences, Tokyo, Japan.
Mol Cell Biol. 1996 Oct;16(10):5754-63. doi: 10.1128/MCB.16.10.5754.
An important relationship between transcription and initiation of DNA replication in both eukaryotes and prokaryotes has been suggested. In an attempt to understand the molecular mechanism of this interaction, we examined whether transcription can induce DNA replication in vitro by constructing a system in which both replication and transcription were combined. Relaxed circular DNA possessing a replication initiation zone located upstream of the human c-myc gene and a T7 promoter near the P1 promoter of the gene was replicated in the presence of T7 RNA polymerase. In our model system, replication was carried out with the proteins required for simian virus 40 DNA replication. DNA synthesis, which was dependent on both T7 RNA polymerase and the replication proteins, was detected mainly in the promoter and upstream regions of the c-myc gene. Blocking RNA synthesis at the initial stage of the reaction severely reduced DNA synthesis, suggesting that RNA chain elongation is required to induce DNA synthesis. The results indicated that transcription can induce DNA replication in the upstream region of the transcribed gene, most likely by introducing negative supercoiling into the region, which results in unwinding of the DNA duplex.
有人提出,真核生物和原核生物中DNA复制的起始与转录之间存在重要关系。为了理解这种相互作用的分子机制,我们构建了一个将复制和转录相结合的系统,以研究转录是否能在体外诱导DNA复制。在T7 RNA聚合酶存在的情况下,具有位于人类c-myc基因上游的复制起始区和该基因P1启动子附近的T7启动子的松弛环状DNA得以复制。在我们的模型系统中,复制是用猿猴病毒40 DNA复制所需的蛋白质进行的。主要在c-myc基因的启动子和上游区域检测到了依赖于T7 RNA聚合酶和复制蛋白的DNA合成。在反应初期阻断RNA合成会严重减少DNA合成,这表明诱导DNA合成需要RNA链的延伸。结果表明,转录可以在转录基因的上游区域诱导DNA复制,很可能是通过在该区域引入负超螺旋,从而导致DNA双链解旋。