Watabe K, Shih M F, Sugino A, Ito J
Proc Natl Acad Sci U S A. 1982 Sep;79(17):5245-8. doi: 10.1073/pnas.79.17.5245.
We have been studying the mechanisms of linear DNA replication by using Bacillus bacteriophage phi 29 as a model system. To isolate and characterize the proteins required for phi 29 DNA replication, we have developed a cell-free replication system. A cell-free extract prepared from phi 29-infected Bacillus subtilis catalyzes the semiconservative replication of phi 29 DNA, but only if exogenous phi 29 DNA-protein complex is used as the template. This template consists of linear duplex DNA with a 30,000-dalton terminal protein attached covalently to both 5' ends. Replication starts nonsimultaneously at or near both ends of the template. The extract also catalyzes the specific binding between dATP and the phi 29 terminal protein. Thus, the in vitro system closely mimics the in vivo replication of phi 29 DNA. This system should allow characterization of the phi 29 DNA replication machinery.
我们一直在利用芽孢杆菌噬菌体 phi 29 作为模型系统来研究线性 DNA 复制的机制。为了分离和鉴定 phi 29 DNA 复制所需的蛋白质,我们开发了一种无细胞复制系统。从感染 phi 29 的枯草芽孢杆菌制备的无细胞提取物催化 phi 29 DNA 的半保留复制,但前提是使用外源 phi 29 DNA-蛋白质复合物作为模板。该模板由线性双链 DNA 组成,其 5' 末端共价连接有一个 30,000 道尔顿的末端蛋白。复制在模板的两端或其附近非同时开始。该提取物还催化 dATP 与 phi 29 末端蛋白之间的特异性结合。因此,体外系统紧密模拟了 phi 29 DNA 的体内复制。该系统应该能够对 phi 29 DNA 复制机制进行表征。