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      Involvement of G-quadruplex regions in mammalian replication origin activity

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          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.

          Abstract

          Origins of replications are associated with potential G quadruplexes forming structures (G4s). Here the authors reveal the functional role of G4 elements in DNA replication initiation.

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          Most cited references57

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          Conserved nucleosome positioning defines replication origins.

          The origin recognition complex (ORC) specifies replication origin location. The Saccharomyces cerevisiae ORC recognizes the ARS (autonomously replicating sequence) consensus sequence (ACS), but only a subset of potential genomic sites are bound, suggesting other chromosomal features influence ORC binding. Using high-throughput sequencing to map ORC binding and nucleosome positioning, we show that yeast origins are characterized by an asymmetric pattern of positioned nucleosomes flanking the ACS. The origin sequences are sufficient to maintain a nucleosome-free origin; however, ORC is required for the precise positioning of nucleosomes flanking the origin. These findings identify local nucleosomes as an important determinant for origin selection and function.
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            RSAT 2015: Regulatory Sequence Analysis Tools

            RSAT (Regulatory Sequence Analysis Tools) is a modular software suite for the analysis of cis-regulatory elements in genome sequences. Its main applications are (i) motif discovery, appropriate to genome-wide data sets like ChIP-seq, (ii) transcription factor binding motif analysis (quality assessment, comparisons and clustering), (iii) comparative genomics and (iv) analysis of regulatory variations. Nine new programs have been added to the 43 described in the 2011 NAR Web Software Issue, including a tool to extract sequences from a list of coordinates (fetch-sequences from UCSC), novel programs dedicated to the analysis of regulatory variants from GWAS or population genomics (retrieve-variation-seq and variation-scan), a program to cluster motifs and visualize the similarities as trees (matrix-clustering). To deal with the drastic increase of sequenced genomes, RSAT public sites have been reorganized into taxon-specific servers. The suite is well-documented with tutorials and published protocols. The software suite is available through Web sites, SOAP/WSDL Web services, virtual machines and stand-alone programs at http://www.rsat.eu/.
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              Genome-scale analysis of metazoan replication origins reveals their organization in specific but flexible sites defined by conserved features.

              In metazoans, thousands of DNA replication origins (Oris) are activated at each cell cycle. Their genomic organization and their genetic nature remain elusive. Here, we characterized Oris by nascent strand (NS) purification and a genome-wide analysis in Drosophila and mouse cells. We show that in both species most CpG islands (CGI) contain Oris, although methylation is nearly absent in Drosophila, indicating that this epigenetic mark is not crucial for defining the activated origin. Initiation of DNA synthesis starts at the borders of CGI, resulting in a striking bimodal distribution of NS, suggestive of a dual initiation event. Oris contain a unique nucleotide skew around NS peaks, characterized by G/T and C/A overrepresentation at the 5' and 3' of Ori sites, respectively. Repeated GC-rich elements were detected, which are good predictors of Oris, suggesting that common sequence features are part of metazoan Oris. In the heterochromatic chromosome 4 of Drosophila, Oris correlated with HP1 binding sites. At the chromosome level, regions rich in Oris are early replicating, whereas Ori-poor regions are late replicating. The genome-wide analysis was coupled with a DNA combing analysis to unravel the organization of Oris. The results indicate that Oris are in a large excess, but their activation does not occur at random. They are organized in groups of site-specific but flexible origins that define replicons, where a single origin is activated in each replicon. This organization provides both site specificity and Ori firing flexibility in each replicon, allowing possible adaptation to environmental cues and cell fates.
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                Author and article information

                Contributors
                benoit.ballester@inserm.fr
                marcel.mechali@igh.cnrs.fr
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                22 July 2019
                22 July 2019
                2019
                : 10
                : 3274
                Affiliations
                [1 ]ISNI 0000 0001 2097 0141, GRID grid.121334.6, Institute of Human Genetics, , CNRS-University of Montpellier, ; 141 rue de la Cardonille, 34396 Montpellier, France
                [2 ]ISNI 0000 0001 2176 4817, GRID grid.5399.6, Aix Marseille Univ, INSERM, TAGC, ; Marseille, France
                [3 ]ISNI 0000000121885934, GRID grid.5335.0, Balasubramanian group, Department of Chemistry, , University of Cambridge, ; Lensfield Road, Cambridge, CB2 1EW UK
                [4 ]ISNI 0000 0004 0386 2845, GRID grid.503246.6, ARNA Laboratory, Université de Bordeaux, Inserm U1212, CNRS UMR5320, Institut Européen de Chimie Biologie (IECB), ; Pessac, 33607 France
                [5 ]ISNI 0000 0004 0639 6384, GRID grid.418596.7, Institut Curie, CNRS UMR9187, Inserm U1196, Universite Paris Saclay, ; Orsay, France
                [6 ]ISNI 0000 0004 0483 2525, GRID grid.4567.0, Research Unit Gene Vectors, Helmholtz Zentrum München (GmbH), , German Research Center for Environmental Health, ; Marchioninistraße 25, 81377 Munich, Germany
                [7 ]ISNI 0000 0004 0483 2525, GRID grid.4567.0, Monoclonal Antibody Core Facility & Research Group, , Institute for Diabetes and Obesity, Helmholtz Zentrum München, Ingolstädter Landstrasse, ; 85764 Neuherberg, Germany
                Author information
                http://orcid.org/0000-0003-3043-8401
                http://orcid.org/0000-0002-0834-7135
                Article
                11104
                10.1038/s41467-019-11104-0
                6646384
                31332171
                03ded20b-158d-416e-97e3-9d5198a8be5c
                © The Author(s) 2019

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 13 November 2018
                : 8 May 2019
                Categories
                Article
                Custom metadata
                © The Author(s) 2019

                Uncategorized
                molecular biology,origin selection,chromatin
                Uncategorized
                molecular biology, origin selection, chromatin

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