Hiasa H, DiGate R J, Marians K J
Molecular Biology Program, Memorial Sloan-Kettering Cancer Center, New York, New York 10021.
J Biol Chem. 1994 Jan 21;269(3):2093-9.
oriC and pBR322 DNA replication, reconstituted with purified replication proteins, has been used to study the functional activities of Escherichia coli topoisomerase I, DNA gyrase, and topoisomerase III during the final stages of DNA replication. In the oriC system, DNA gyrase-catalyzed decatenation of daughter DNA molecules was very inefficient, whereas topoisomerase III could catalyze complete decatenation. In the pBR322 DNA replication system, almost all the daughter DNA molecules could be decatenated by DNA gyrase alone in the absence of salt. Decatenation by DNA gyrase in the pBR322 system was completely inhibited, without a concomitant inhibition of DNA synthesis, by the addition of physiological concentrations of salt. Topoisomerase III, however, could decatenate all of the daughter DNA molecules in the pBR322 system, even in the presence of high concentrations of salt. A similar effect could not be observed in the oriC system, because the addition of salt inhibited DNA synthesis. Topoisomerase I was incapable of catalyzing decatenation under any conditions examined in either the oriC or pBR322 replication system. The addition of topoisomerase I to the replication systems resulted only in an inhibition of DNA synthesis.
用纯化的复制蛋白重建的oriC和pBR322 DNA复制体系,已被用于研究大肠杆菌拓扑异构酶I、DNA促旋酶和拓扑异构酶III在DNA复制最后阶段的功能活性。在oriC体系中,DNA促旋酶催化子代DNA分子的解连环作用效率很低,而拓扑异构酶III能催化完全解连环。在pBR322 DNA复制体系中,在无盐的情况下,几乎所有子代DNA分子仅靠DNA促旋酶就能解连环。在pBR322体系中,加入生理浓度的盐会完全抑制DNA促旋酶的解连环作用,而不伴随DNA合成的抑制。然而,即使在高盐浓度下,拓扑异构酶III仍能使pBR322体系中的所有子代DNA分子解连环。在oriC体系中未观察到类似效应,因为加盐会抑制DNA合成。在oriC或pBR322复制体系中所检测的任何条件下,拓扑异构酶I都不能催化解连环。向复制体系中加入拓扑异构酶I只会导致DNA合成受到抑制。