<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>26(4)</volume><submitter>Abdurashidova G</submitter><pubmed_abstract>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 topoisomerase</pubmed_abstract><journal>The EMBO journal</journal><pagination>998-1009</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC1852844</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Functional interactions of DNA topoisomerases with a human replication origin.</pubmed_title><pmcid>PMC1852844</pmcid><pubmed_authors>Sandoval O</pubmed_authors><pubmed_authors>Danailov MB</pubmed_authors><pubmed_authors>Abdurashidova G</pubmed_authors><pubmed_authors>Biamonti G</pubmed_authors><pubmed_authors>Radulescu S</pubmed_authors><pubmed_authors>Riva S</pubmed_authors><pubmed_authors>Zahariev S</pubmed_authors><pubmed_authors>Demidovich A</pubmed_authors><pubmed_authors>Santamaria L</pubmed_authors><pubmed_authors>Falaschi A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Functional interactions of DNA topoisomerases with a human replication origin.</name><description>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 topoisomerase</description><dates><release>2007-01-01T00:00:00Z</release><publication>2007 Feb</publication><modification>2026-07-09T11:00:50.96Z</modification><creation>2026-07-09T10:31:49.835Z</creation></dates><accession>S-EPMC1852844</accession><cross_references><pubmed>17290216</pubmed><doi>10.1038/sj.emboj.7601578</doi></cross_references></HashMap>