Evidence map›Paper›PMID 26436826›Full record

ArticleNature structural & molecular biology2015

Polymerase δ replicates both strands after homologous recombination-dependent fork restart.

Izumi Miyabe, Ken'Ichi Mizuno, Andrea Keszthelyi, Yasukazu Daigaku, Meliti Skouteri, Saed Mohebi, Thomas A Kunkel, Johanne M Murray, Antony M Carr

Open access · greenAbstract read
In one paragraph

Article in Nature structural & molecular biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed
4.8field-weighted citation impact, top 4% of its field
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

69 citing papers in PubMed, 98 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. eLife · 2023
    Article
  15. Article
  16. Creation and resolution of non-B-DNA structural impediments during replication.Critical reviews in biochemistry and molecular biology · 2022
    Article
  17. Article
  18. Review
  19. Recombination and restart at blocked replication forks.Current opinion in genetics & development · 2021
    Review
  20. How asymmetric DNA replication achieves symmetrical fidelity.Nature structural & molecular biology · 2021
    Article

9 more citing papers are in PubMed but not listed here.

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

9 authors at 3 institutions in 3 countries.

Izumi MiyabeGenome Damage and Stability Centre, University of Sussex, Brighton, UK.
Ken'Ichi MizunoGenome Damage and Stability Centre, University of Sussex, Brighton, UK.ORCID http://orcid.org/0000-0001-8115-7808
Andrea KeszthelyiGenome Damage and Stability Centre, University of Sussex, Brighton, UK.
Yasukazu DaigakuFrontier Research Institute for Interdisciplinary Sciences, Tohoku University, Sendai, Japan.
Meliti SkouteriGenome Damage and Stability Centre, University of Sussex, Brighton, UK.
Saed MohebiGenome Damage and Stability Centre, University of Sussex, Brighton, UK.
Thomas A KunkelGenome Integrity and Structural Biology Laboratory, National Institute of Environmental Health Sciences, National Institutes of Health, Department of Health and Human Services, Research Triangle Park, North Carolina, USA.
Johanne M MurrayGenome Damage and Stability Centre, University of Sussex, Brighton, UK.
Antony M CarrGenome Damage and Stability Centre, University of Sussex, Brighton, UK.
University of Sussex · GBNational Institutes of Health · USTohoku University · JP

Funding

Structure-Function Studies Of DNA Replication FidelityZIAES065070 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI KUNKEL, THOMAS A · 2009 to 2025
$30.6M
Structure-Function Studies Of DNA Replication FidelityZ01ES065070 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI KUNKEL, THOMAS A · 1991 to 2008
$4.3M
European Research Council 268788Intramural NIH HHS Z01 ES065070Medical Research Council G0801078Medical Research Council G1100074Worldwide Cancer Research 10-0273
6 · The paper itself

Abstract

To maintain genetic stability, DNA must be replicated only once per cell cycle, and replication must be completed even when individual replication forks are inactivated. Because fork inactivation is common, passive convergence of an adjacent fork is insufficient to rescue all inactive forks. Thus, eukaryotic cells have evolved homologous recombination-dependent mechanisms to restart persistent inactive forks. Completing DNA synthesis via homologous recombination-restarted replication (HoRReR) ensures cell survival, but at a cost. One such cost is increased mutagenesis because HoRReR is more error prone than canonical replication. This increased error rate implies the HoRReR mechanism is distinct from that of a canonical fork. Here we demonstrate, in Schizosaccharomyces pombe, that a DNA sequence duplicated by HoRReR during S phase is replicated semiconservatively, but both the leading and lagging strands are synthesized by DNA polymerase δ.

Indexed as

DNA ReplicationHomologous RecombinationCell DivisionDNA Polymerase IIISchizosaccharomycesDNA Polymerase III

Identifiers

PMID26436826
PMCPMC4655445
OpenAlexW2136341398

What OpenQuestion holds

Textmetadata
LicenceTDM
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.