| Literature DB >> 31332171 |
Paulina Prorok1, Marie Artufel2, Antoine Aze1, Philippe Coulombe1, Isabelle Peiffer1, Laurent Lacroix3, Aurore Guédin4, Jean-Louis Mergny4,5, Julia Damaschke6, Aloys Schepers6,7, Christelle Cayrou1,8, Marie-Paule Teulade-Fichou9, Benoit Ballester10, Marcel Méchali11.
Abstract
Genome-wide studies of DNA replication origins revealed that origins preferentially associate with an Origin G-rich Repeated Element (OGRE), potentially forming G-quadruplexes (G4). Here, we functionally address their requirements for DNA replication initiation in a series of independent approaches. Deletion of the OGRE/G4 sequence strongly decreased the corresponding origin activity. Conversely, the insertion of an OGRE/G4 element created a new replication origin. This element also promoted replication of episomal EBV vectors lacking the viral origin, but not if the OGRE/G4 sequence was deleted. A potent G4 ligand, PhenDC3, stabilized G4s but did not alter the global origin activity. However, a set of new, G4-associated origins was created, whereas suppressed origins were largely G4-free. In vitro Xenopus laevis replication systems showed that OGRE/G4 sequences are involved in the activation of DNA replication, but not in the pre-replication complex formation. Altogether, these results converge to the functional importance of OGRE/G4 elements in DNA replication initiation.Entities:
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Year: 2019 PMID: 31332171 PMCID: PMC6646384 DOI: 10.1038/s41467-019-11104-0
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919