Simmons D T, Roy R, Chen L, Gai D, Trowbridge P W
Department of Biological Sciences, University of Delaware, Newark, Delaware 19716-2590, USA.
J Biol Chem. 1998 Aug 7;273(32):20390-6. doi: 10.1074/jbc.273.32.20390.
When simian virus 40 (SV40) large T antigen binds to the virus origin of replication, it forms a double hexamer that functions as a helicase to unwind the DNA bidirectionally. We demonstrate in this report that T antigen can unwind and release an origin DNA single strand of less than full length in the presence of purified human topoisomerase I. The sites nicked by topoisomerase I in the strands released by T antigen during DNA unwinding were localized primarily to the "late" side of the origin, and the template for lagging strand synthesis was preferred significantly over the one for leading strand synthesis. Importantly, these sites were, for the most part, different from the sites nicked by topoisomerase I in the absence of T antigen. These data indicate that T antigen activates topoisomerase I nicking at discrete sites and releases these nicked strands during unwinding. We hypothesize that a single molecule of topoisomerase I can form a functional complex with a double hexamer of T antigen to simultaneously relax and unwind double-stranded origin-containing DNA.
当猴病毒40(SV40)大T抗原与病毒复制起点结合时,它会形成一个双六聚体,作为解旋酶双向解开DNA。我们在本报告中证明,在纯化的人拓扑异构酶I存在的情况下,T抗原可以解开并释放一条长度小于全长的起点DNA单链。在DNA解旋过程中,T抗原释放的链中被拓扑异构酶I切割的位点主要位于起点的“晚期”一侧,并且滞后链合成的模板比前导链合成的模板更受青睐。重要的是,这些位点在很大程度上与没有T抗原时被拓扑异构酶I切割的位点不同。这些数据表明,T抗原在离散位点激活拓扑异构酶I的切割,并在解旋过程中释放这些被切割的链。我们假设,单个拓扑异构酶I分子可以与T抗原的双六聚体形成功能复合物,以同时松弛和解开含双链起点的DNA。