Evidence map›Paper›PMID 39883014›Full record

ArticleNucleic acids research2025

Dual DNA replication modes: varying fork speeds and initiation rates within the spatial replication program in Xenopus.

Diletta Ciardo, Olivier Haccard, Francesco de Carli, Olivier Hyrien, Arach Goldar, Kathrin Marheineke

Abstract read
In one paragraph

Article in Nucleic acids research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Diletta CiardoInstitut de Biologie de l'Ecole Normale Supérieure, Ecole Normale Supérieure, CNRS, INSERM, Université PSL, F-75005 Paris, France.ORCID 0000-0003-0253-4762
Olivier HaccardUniversité Paris-Saclay, CNRS, Institut des Neurosciences Paris-Saclay (NeuroPsi), F-91400 Saclay, France.ORCID 0000-0002-4305-2746
Francesco de CarliInstitut de Biologie de l'Ecole Normale Supérieure, Ecole Normale Supérieure, CNRS, INSERM, Université PSL, F-75005 Paris, France.
Olivier HyrienInstitut de Biologie de l'Ecole Normale Supérieure, Ecole Normale Supérieure, CNRS, INSERM, Université PSL, F-75005 Paris, France.ORCID 0000-0001-8879-675X
Arach GoldarUniversité Paris-Saclay, CEA, CNRS, Institute for Integrative Biology of the Cell, F-91190 Gif-sur-Yvette, France.ORCID 0000-0003-4139-247X
Kathrin MarheinekeUniversité Paris Cité, CNRS, Institut Jacques Monod, F-75013 Paris, France.ORCID 0000-0002-1514-0167

Funding

Agence Nationale de la Recherche ANR-15-CE12-0011-01Centre National de la Recherche ScientifiqueCommissariat à l'Energie AtomiqueFondation pour la Recherche Médicale DEI20151234404Institut National du Cancer PLBIO16-302
6 · The paper itself

Abstract

Large vertebrate genomes duplicate by activating tens of thousands of DNA replication origins, irregularly spaced along the genome. The spatial and temporal regulation of the replication process is not yet fully understood. To investigate the DNA replication dynamics, we developed a methodology called RepliCorr, which uses the spatial correlation between replication patterns observed on stretched single-molecule DNA obtained by either DNA combing or high-throughput optical mapping. The analysis revealed two independent spatiotemporal processes that regulate the replication dynamics in the Xenopus model system. These mechanisms are referred to as a fast and a slow replication mode, differing by their opposite replication fork speed and rate of origin firing. We found that Polo-like kinase 1 (Plk1) depletion abolished the spatial separation of these two replication modes. In contrast, neither replication checkpoint inhibition nor Rap1-interacting factor (Rif1) depletion affected the distribution of these replication patterns. These results suggest that Plk1 plays an essential role in the local coordination of the spatial replication program and the initiation-elongation coupling along the chromosomes in Xenopus, ensuring the timely completion of the S phase.

Indexed as

Cell Cycle ProteinsDNA ReplicationProtein Serine-Threonine KinasesProto-Oncogene ProteinsXenopus laevisAnimalsDNAPolo-Like Kinase 1Replication OriginS PhaseTelomere-Binding ProteinsXenopusXenopus ProteinsCell Cycle ProteinsDNAPolo-Like Kinase 1Protein Serine-Threonine KinasesProto-Oncogene ProteinsTelomere-Binding ProteinsXenopus Proteins

Identifiers

PMID39883014
PMCPMC11781033

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.