Abdurashidova Gulnara, Radulescu Sorina, Sandoval Oscar, Zahariev Sotir, Danailov Miltcho B, Demidovich Alexander, Santamaria Laura, Biamonti Giuseppe, Riva Silvano, Falaschi Arturo
Molecular Biology Group, International Centre for Genetic Engineering and Biotechnology, Trieste, Italy.
EMBO J. 2007 Feb 21;26(4):998-1009. doi: 10.1038/sj.emboj.7601578. Epub 2007 Feb 8.
The human DNA replication origin, located in the lamin B2 gene, interacts with the DNA topoisomerases I and II in a cell cycle-modulated manner. The topoisomerases interact in vivo and in vitro with precise bonds ahead of the start sites of bidirectional replication, within the pre-replicative complex region; topoisomerase I is bound in M, early G1 and G1/S border and topoisomerase II in M and the middle of G1. The Orc2 protein competes for the same sites of the origin bound by either topoisomerase in different moments of the cell cycle; furthermore, it interacts on the DNA with topoisomerase II during the assembly of the pre-replicative complex and with DNA-bound topoisomerase I at the G1/S border. Inhibition of topoisomerase I activity abolishes origin firing. Thus, the two topoisomerases are closely associated with the replicative complexes, and DNA topology plays an essential functional role in origin activation.
位于层粘连蛋白B2基因中的人类DNA复制起点,以细胞周期调节的方式与DNA拓扑异构酶I和II相互作用。拓扑异构酶在体内和体外与双向复制起始位点之前、复制前复合体区域内的精确位点相互作用;拓扑异构酶I在M期、G1早期和G1/S边界结合,拓扑异构酶II在M期和G1中期结合。Orc2蛋白在细胞周期的不同时刻竞争与两种拓扑异构酶结合的复制起点相同位点;此外,在复制前复合体组装过程中,它与拓扑异构酶II在DNA上相互作用,并在G1/S边界与结合DNA的拓扑异构酶I相互作用。抑制拓扑异构酶I的活性会消除复制起点的激活。因此,这两种拓扑异构酶与复制复合体密切相关,并且DNA拓扑结构在复制起点激活中发挥着重要的功能作用。