Evidence map›Paper›PMID 38886577›Full record

ArticleNature methods2024

Quantifying DNA replication speeds in single cells by scEdU-seq.

Jeroen van den Berg, Vincent van Batenburg, Christoph Geisenberger, Rinskje B Tjeerdsma, Anchel de Jaime-Soguero, Sergio P Acebrón, Marcel A T M van Vugt, Alexander van Oudenaarden

Abstract read
In one paragraph

Article in Nature methods, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing 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

33 citing papers in PubMed.

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  13. Morphogen Gradients as Drivers of Mosaicism During Early Human Development.BioEssays : news and reviews in molecular, cellular and developmental biology · 2026
    Review
  14. Article
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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

8 authors.

Jeroen van den Berg *Oncode Institute, Hubrecht Institute-KNAW (Royal Netherlands Academy of Arts and Sciences) and University Medical Center Utrecht, Utrecht, The Netherlands. j.berg@hubrecht.eu.ORCID http://orcid.org/0000-0002-9430-7155
Vincent van Batenburg *Oncode Institute, Hubrecht Institute-KNAW (Royal Netherlands Academy of Arts and Sciences) and University Medical Center Utrecht, Utrecht, The Netherlands.ORCID http://orcid.org/0000-0003-4203-9571
Christoph GeisenbergerOncode Institute, Hubrecht Institute-KNAW (Royal Netherlands Academy of Arts and Sciences) and University Medical Center Utrecht, Utrecht, The Netherlands.ORCID http://orcid.org/0000-0002-5846-7127
Rinskje B TjeerdsmaDepartment of Medical Oncology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.ORCID http://orcid.org/0009-0000-1175-8333
Anchel de Jaime-SogueroCentre for Organismal Studies (COS), Heidelberg University, Heidelberg, Germany.ORCID http://orcid.org/0000-0002-9358-3676
Sergio P AcebrónCentre for Organismal Studies (COS), Heidelberg University, Heidelberg, Germany.ORCID http://orcid.org/0000-0002-7694-2497
Marcel A T M van VugtDepartment of Medical Oncology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
Alexander van OudenaardenOncode Institute, Hubrecht Institute-KNAW (Royal Netherlands Academy of Arts and Sciences) and University Medical Center Utrecht, Utrecht, The Netherlands. a.vanoudenaarden@hubrecht.eu.ORCID http://orcid.org/0000-0002-9442-3551

Funding

EC | EU Framework Programme for Research and Innovation H2020 | H2020 Priority Excellent Science | H2020 European Research Council (H2020 Excellent Science - European Research Council) ERC-AdG 101053581-scTranslatomicsNederlandse Organisatie voor Wetenschappelijk Onderzoek (Netherlands Organisation for Scientific Research) 09150182110019Nederlandse Organisatie voor Wetenschappelijk Onderzoek (Netherlands Organisation for Scientific Research) NWO-CW 714.016.001
6 · The paper itself

Abstract

In a human cell, thousands of replication forks simultaneously coordinate duplication of the entire genome. The rate at which this process occurs might depend on the epigenetic state of the genome and vary between, or even within, cell types. To accurately measure DNA replication speeds, we developed single-cell 5-ethynyl-2'-deoxyuridine sequencing to detect nascent replicated DNA. We observed that the DNA replication speed is not constant but increases during S phase of the cell cycle. Using genetic and pharmacological perturbations we were able to alter this acceleration of replication and conclude that DNA damage inflicted by the process of transcription limits the speed of replication during early S phase. In late S phase, during which less-transcribed regions replicate, replication accelerates and approaches its maximum speed.

Indexed as

DNA ReplicationSingle-Cell AnalysisDeoxyuridineDNADNA DamageHumansSequence Analysis, DNAS Phase5-ethynyl-2'-deoxyuridineDeoxyuridineDNA

Identifiers

PMID38886577
PMCPMC11239516

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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.