Hiasa H, Marians K J
Molecular Biology Program, Memorial Sloan-Kettering Cancer Center, New York, New York 10021.
J Biol Chem. 1994 Jun 10;269(23):16371-5.
Escherichia coli has two type II topoisomerases, DNA gyrase and topoisomerase IV (Topo IV). Topo IV is required for the decatenation of the linked daughter chromosomes at the terminal stages of DNA replication, whereas gyrase, because of its ability to convert to negative supercoils the positive supercoils generated by replication fork progression in a circular chromosome, is required to support nascent chain elongation. Using an oriC DNA replication system in vitro, we show that Topo IV, which can relax positive supercoils, can also support replication fork progression. This activity is only observed at substoichiometric ratios of Topo IV to template, at higher ratios, the template becomes relaxed and initiation of DNA replication cannot occur. Topo IV was capable of supporting bidirectional DNA replication from oriC, although, unlike the case with gyrase, some templates apparently replicated unidirectionally. This suggests that either gyrase itself or a certain minimum superhelical density is required for proper initiation of DNA replication from oriC.
大肠杆菌有两种II型拓扑异构酶,即DNA促旋酶和拓扑异构酶IV(Topo IV)。在DNA复制的终末阶段,子代染色体的解连环需要Topo IV,而促旋酶由于能够将环状染色体中复制叉前进产生的正超螺旋转化为负超螺旋,因而对支持新生链的延伸是必需的。利用体外oriC DNA复制系统,我们发现能够松弛正超螺旋的Topo IV也能支持复制叉前进。这种活性仅在Topo IV与模板的亚化学计量比时观察到,比例更高时,模板会松弛,DNA复制无法起始。Topo IV能够支持从oriC开始的双向DNA复制,不过,与促旋酶的情况不同,一些模板显然是单向复制的。这表明从oriC正确起始DNA复制,要么需要促旋酶本身,要么需要一定的最小超螺旋密度。