Levac P, Moss T
Centre de Recherche en Cancérologie et Département de Biochimie, Université Laval, Hôtel Dieu de Québec, 11 Côte du Palais, G1R 2J6 Québec, Canada.
Chromosoma. 1996 Oct;105(4):250-60. doi: 10.1007/BF02528774.
Topoisomerase I is believed to be sufficient for early replication of circular viral genomes such as those of SV40 and of yeast plasmids. Topoisomerase II is required for the decatenation of the daughter genomes and probably also for fork elongation during the later stages of SV40 replication. Using the neutral-neutral two-dimensional gel system, we have followed the progression of replication of both SV40 and the yeast 2 micron plasmid under various conditions of topoisomerase inhibition. During SV40 replication, inhibition of topoisomerase II by VP16, VM26 or hypertonic shock (but not by merbarone), and inhibition of topoisomerase I by camptothecin all led to the accumulation of aberrant DNA structures containing two almost completely replicated genomes. These aberrant structures resembled either recombination intermediates or late Cairns structures in which the site of replication termination had shifted and now mapped to a continuum of sites throughout the genome. Replication of the 2 micron plasmid in a topoisomerase II- but not a topoisomerase I-deficient yeast gave rise to very similar structures. The data suggest that inactivation of topoisomerase I or II either stimulates recombination or, by differentially affecting replication fork progression, leads to aberrant replication termination.
拓扑异构酶I被认为足以用于环状病毒基因组(如SV40和酵母质粒的基因组)的早期复制。拓扑异构酶II对于子代基因组的解连环是必需的,并且可能在SV40复制后期的叉状延伸过程中也是必需的。使用中性-中性二维凝胶系统,我们在拓扑异构酶抑制的各种条件下跟踪了SV40和酵母2微米质粒的复制进程。在SV40复制期间,VP16、VM26或高渗休克(但不是美巴龙)对拓扑异构酶II的抑制,以及喜树碱对拓扑异构酶I的抑制,均导致含有两个几乎完全复制基因组的异常DNA结构的积累。这些异常结构类似于重组中间体或晚期凯恩斯结构,其中复制终止位点发生了移动,现在映射到整个基因组的一系列位点。在拓扑异构酶II缺陷但拓扑异构酶I不缺陷的酵母中2微米质粒的复制产生了非常相似的结构。数据表明,拓扑异构酶I或II的失活要么刺激重组,要么通过差异影响复制叉的进展,导致异常的复制终止。