Evidence map›Paper›PMID 25835602›Full record

ArticleNucleus (Austin, Tex.)2015

Termination of DNA replication forks: "Breaking up is hard to do".

Rachael Bailey, Sara Priego Moreno, Agnieszka Gambus

Abstract read
In one paragraph

Article in Nucleus (Austin, Tex.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. RANBP9 and RANBP10 cooperate in regulating non-small cell lung cancer proliferation.Journal of experimental & clinical cancer research : CR · 2025
    Article
  2. Yeast Tools for Studying Type II Topoisomerases in Budding Yeast.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  3. Review
  4. Review
  5. Review
  6. Open biology · 2020
    Review
  7. Mechanisms of eukaryotic replisome disassembly.Biochemical Society transactions · 2020
    Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Progerin sequestration of PCNA promotes replication fork collapse and mislocalization of XPA in laminopathy-related progeroid syndromes.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2017
    Article
  13. Review
  14. Review
  15. Review
  16. Article
  17. Article
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

3 authors.

Rachael Baileya School of Cancer Sciences; University of Birmingham ; Birmingham , UK.
Sara Priego Moreno
Agnieszka Gambus

Funding

Medical Research Council MR/K007106/1
6 · The paper itself

Abstract

To ensure duplication of the entire genome, eukaryotic DNA replication initiates from thousands of replication origins. The replication forks move through the chromatin until they encounter forks from neighboring origins. During replication fork termination forks converge, the replisomes disassemble and topoisomerase II resolves the daughter DNA molecules. If not resolved efficiently, terminating forks result in genomic instability through the formation of pathogenic structures. Our recent findings shed light onto the mechanism of replisome disassembly upon replication fork termination. We have shown that termination-specific polyubiquitylation of the replicative helicase component - Mcm7, leads to dissolution of the active helicase in a process dependent on the p97/VCP/Cdc48 segregase. The inhibition of terminating helicase disassembly resulted in a replication termination defect. In this extended view we present hypothetical models of replication fork termination and discuss remaining and emerging questions in the DNA replication termination field.

Indexed as

DNA ReplicationAdenosine TriphosphatasesAnimalsCell Cycle ProteinsChromatinDNADNA Polymerase IDNA Polymerase IIDNA Polymerase IIIDNA Topoisomerases, Type IIGene Expression RegulationGenomic InstabilityHumansMinichromosome Maintenance ProteinsPolyubiquitinSaccharomyces cerevisiaeAdenosine TriphosphatasesCDC48 protein, S cerevisiaeCell Cycle ProteinsChromatinDNADNA Polymerase IDNA Polymerase IIDNA Polymerase IIIDNA Topoisomerases, Type IIMinichromosome Maintenance ProteinsPolyubiquitinSaccharomyces cerevisiae ProteinsValosin Containing ProteinVCP protein, humanCMG, Cdc45, Mcm2–7, GINS complexCRL, cullin-RING ligaseDDR, DNA damage responseD loop, displacement loopDNA replicationDSB, double strand breakDUB, deubiquitylating enzymeERAD, endoplasmic reticulum associated protein degradationER, endoplasmic reticulumGINS, Go-Ichi-Ni-San, complex made of Sld5, Psf1, Psf2, Psf3ICL, intra-strand crosslinkMcm2–7MCM, Minichromosome maintenanceOriC, chromosomal replication originp97 segregasereplication terminationreplicative helicasereplisomeRING, really interesting geneR loop, RNA:DNA hybridRPC, Replisome Progression ComplexTer, termination siteTus-Ter, terminus utilisation substance - terminationubiquitinXenopus

Identifiers

PMID25835602
PMCPMC4615769

What OpenQuestion holds

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LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.