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Series GSE231492 Query DataSets for GSE231492
Status Public on Jul 19, 2023
Title Dimeric G-quadruplex motifs-induced NFRs determine strong replication origins in vertebrates
Platform organism Gallus gallus
Sample organisms Gallus gallus; Homo sapiens; Mus musculus
Experiment type Third-party reanalysis
Expression profiling by high throughput sequencing
Genome binding/occupancy profiling by high throughput sequencing
Other
Summary Replication of vertebrate genomes is tightly regulated to ensure accurate duplication, but our understanding of the interplay between genetic and epigenetic factors in this regulation remains incomplete. Here, we investigated the involvement of three elements enriched at gene promoters and replication origins: guanine-rich motifs potentially forming G-quadruplexes (pG4s), nucleosome-free regions (NFRs), and the histone variant H2A.Z, in the firing of origins of replication in vertebrates. We show that two pG4s on the same DNA strand (dimeric pG4s) are sufficient to induce assembly of an efficient minimal replication origin without inducing transcription. Dimeric pG4s in replication origins trigger formation of an NFR next to precisely positioned nucleosomes enriched in H2A.Z on this minimal origin and genome-wide. Thus, our data suggest a crucial role for dimeric pG4s in the organization and duplication of vertebrate genomes. It supports the hypothesis that a nucleosome close to an NFR is a shared signal for the formation of replication origins in eukaryotes.
 
Overall design A Wt DT40 chicken cell line and clonal heterozygous or homozygous cell lines containing mutated version of the βA-globin fused to the IL2R gene and SV40 PolyA sequence, flanked with two USF binding sites inserted into a mid-late replicating region of chromosome one (chr1:71,981,290-73,532,377 bp, galGal5) were analyzed. Profiles of the histone variant H2AZ enrichments were obtained by chromatin immunoprecipitation DNA-sequencing (ChIP-seq). NFR and Nucleosome coverage profiles were obtained from MNAse-Seq and ATAC-seq experiments respectively. Isolated and clustered pG4 profiles were obtained from datas published in Zheng et al. 2020 under the accession number GSE133379 (supplementary files). We also considered G4s detected by ChIPSeq with a G4P protein (Zheng et al. 2020, GSE133379) for human 293T cells (GSM3907020,GSM3907021, GSM3907022, GSM3907023); human A549 cells (GSM3907012, GSM3907013, GSM3907014, GSM3907015); human H1975 cells (GSM3907016, GSM3907017, GSM3907018, GSM3907019); human HeLa-S3 cells (GSM3907024, GSM3907025), chicken DF-1 cells (GSM3907028, GSM3907029) and mouse 3T3 cells (GSM3907026, GSM3907027). Human ChIP-G4s were combined. Coverage plots represent the average number of genomic features in sliding windows of 20 bp, overlapping by 10 bp. Bed Graph files were generated.
 
Contributor(s) Poulet-Benedetti J, Tonnerre-Doncarli C, Valton A, Laurent M, Gérard M, Barinova N, Parisis N, Massip F, Picard F, Prioleau M
Citation(s) 37563125
Submission date May 02, 2023
Last update date Oct 18, 2023
Contact name Caroline Tonnerre-Doncarli
E-mail(s) caroline.doncarli@ijm.fr
Phone +33157248124
Organization name Institut Jacques Monod, CNRS UMR7592, Université Paris cité
Lab Domaines chromatiniens et réplication
Street address 15 rue Hélène Brion
City Paris
ZIP/Postal code 75013
Country France
 
Platforms (1)
GPL19787 Illumina NextSeq 500 (Gallus gallus)
Samples (14)
GSM7286713 ChIp_H2AZ_2xMinikirikou_12-7
GSM7286714 Input_2xMinikirikou_12-7
GSM7286715 F2-ATAC
Relations
Reanalysis of GSM3907012
Reanalysis of GSM3907013
Reanalysis of GSM3907014
Reanalysis of GSM3907015
Reanalysis of GSM3907016
Reanalysis of GSM3907017
Reanalysis of GSM3907018
Reanalysis of GSM3907019
Reanalysis of GSM3907020
Reanalysis of GSM3907021
Reanalysis of GSM3907022
Reanalysis of GSM3907023
Reanalysis of GSM3907024
Reanalysis of GSM3907025
Reanalysis of GSM3907026
Reanalysis of GSM3907027
Reanalysis of GSM3907028
Reanalysis of GSM3907029
BioProject PRJNA966151

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Supplementary file Size Download File type/resource
GSE231492_RAW.tar 3.9 Gb (http)(custom) TAR (of BED, BIGWIG, NARROWPEAK)
GSE231492_cluster.G4minus-merged-100bp-gal5.bed.gz 224.2 Kb (ftp)(http) BED
GSE231492_cluster.G4minus-merged-100bp-hg19.bed.gz 647.4 Kb (ftp)(http) BED
GSE231492_cluster.G4minus-merged-100bp-mm10.bed.gz 648.7 Kb (ftp)(http) BED
GSE231492_cluster.G4plus-merged-100bp-gal5.bed.gz 198.2 Kb (ftp)(http) BED
GSE231492_cluster.G4plus-merged-100bp-hg19.bed.gz 589.2 Kb (ftp)(http) BED
GSE231492_cluster.G4plus-merged-100bp-mm10.bed.gz 594.3 Kb (ftp)(http) BED
GSE231492_isolated.G4minus-merged-100bp-gal5.bed.gz 1.0 Mb (ftp)(http) BED
GSE231492_isolated.G4minus-merged-100bp-hg19.bed.gz 3.6 Mb (ftp)(http) BED
GSE231492_isolated.G4minus-merged-100bp-mm10.bed.gz 3.5 Mb (ftp)(http) BED
GSE231492_isolated.G4plus-merged-100bp-hg19.bed.gz 3.5 Mb (ftp)(http) BED
GSE231492_isolated.G4plus-merged-100bp-mm10.bed.gz 3.4 Mb (ftp)(http) BED
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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