Taneja Poonam, Nasheuer Heinz-Peter, Hartmann Hella, Grosse Frank, Fanning Ellen, Weisshart Klaus
Department of Biological Sciences, Vanderbilt University, 465 21st Avenue South, Nashville, TN 37235, USA.
Biochem J. 2007 Oct 15;407(2):313-20. doi: 10.1042/BJ20070794.
The initiation of SV40 (simian virus 40) DNA replication requires the co-operative interactions between the viral Tag (large T-antigen), RPA (replication protein A) and Pol (DNA polymerase alpha-primase) on the template DNA. Binding interfaces mapped on these enzymes and expressed as peptides competed with the mutual interactions of the native proteins. Prevention of the genuine interactions was accomplished only prior to the primer synthesis step and blocked the assembly of a productive initiation complex. Once the complex was engaged in the synthesis of an RNA primer and its extension, the interfering effects of the peptides ceased, suggesting a stable association of the replication factors during the initiation phase. Specific antibodies were still able to disrupt preformed interactions and inhibited primer synthesis and extension activities, underlining the crucial role of specific protein-protein contacts during the entire initiation process.
SV40(猴病毒40)DNA复制的起始需要病毒Tag(大T抗原)、RPA(复制蛋白A)和Pol(DNA聚合酶α-引发酶)在模板DNA上的协同相互作用。映射在这些酶上并以肽形式表达的结合界面与天然蛋白质的相互作用相互竞争。只有在引物合成步骤之前才能阻止真正的相互作用,并阻断有生产性的起始复合物的组装。一旦复合物参与RNA引物的合成及其延伸,肽的干扰作用就会停止,这表明复制因子在起始阶段存在稳定的结合。特异性抗体仍然能够破坏预先形成的相互作用,并抑制引物合成和延伸活性,突显了特定蛋白质-蛋白质接触在整个起始过程中的关键作用。