Lichy J H, Field J, Horwitz M S, Hurwitz J
Proc Natl Acad Sci U S A. 1982 Sep;79(17):5225-9. doi: 10.1073/pnas.79.17.5225.
A complex containing the 80,000-dalton precursor to the adenovirus (Ad)-encoded terminal protein (pTP) and a 140,000-dalton protein is required for Ad DNA replication in vitro. This complex has been separated into subunits by glycerol gradient centrifugation in the presence of urea. The isolated 140,000-dalton subunit contains a DNA polymerase activity which can be differentiated from all host DNA polymerases. No enzyme activity was detected with the isolated pTP. The requirements for reactions involved in the initiation of Ad DNA replication were determined by using the isolated subunits. The covalent addition of dCMP, the first nucleotide in the DNA chain, to the pTP, which serves as the primer for replication, required the DNA polymerase subunit as well as the pTP. Synthesis of viral DNA in vitro also required both subunits. The properties of the DNA polymerase suggest that it may be a viral gene product.
腺病毒(Ad)编码的末端蛋白(pTP)的80,000道尔顿前体与一种140,000道尔顿蛋白质组成的复合物是Ad DNA体外复制所必需的。在尿素存在的情况下,通过甘油梯度离心已将该复合物分离成亚基。分离出的140,000道尔顿亚基含有一种DNA聚合酶活性,该活性可与所有宿主DNA聚合酶区分开来。分离出的pTP未检测到酶活性。通过使用分离出的亚基确定了Ad DNA复制起始所涉及反应的要求。作为复制引物的pTP上共价添加DNA链中的第一个核苷酸dCMP,需要DNA聚合酶亚基以及pTP。体外病毒DNA的合成也需要这两个亚基。DNA聚合酶的特性表明它可能是一种病毒基因产物。