Evidence map›Paper›PMID 28481910›Full record

ArticlePLoS genetics2017

PCNA ubiquitylation ensures timely completion of unperturbed DNA replication in fission yeast.

Yasukazu Daigaku, Thomas J Etheridge, Yuka Nakazawa, Mayumi Nakayama, Adam T Watson, Izumi Miyabe, Tomoo Ogi, Mark A Osborne, Antony M Carr

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

16 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Generation and Repair of Postreplication Gaps in Escherichia coli.Microbiology and molecular biology reviews : MMBR · 2023
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Ubiquitin and SUMO pathways in DNA replication and replication-coupled repair.Critical reviews in biochemistry and molecular biology
    Review
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 4 institutions in 2 countries.

Yasukazu DaigakuGenome Damage and Stability Centre, School of Life Sciences, University of Sussex, Falmer, United Kingdom.
Thomas J EtheridgeGenome Damage and Stability Centre, School of Life Sciences, University of Sussex, Falmer, United Kingdom.ORCID http://orcid.org/0000-0001-8144-6917
Yuka NakazawaResearch Institute of Environmental Medicine, Nagoya University, Nagoya, Japan.
Mayumi NakayamaFrontier Research Institute for Interdisciplinary Sciences, Tohoku University, Sendai, Japan.
Adam T WatsonGenome Damage and Stability Centre, School of Life Sciences, University of Sussex, Falmer, United Kingdom.
Izumi MiyabeGenome Damage and Stability Centre, School of Life Sciences, University of Sussex, Falmer, United Kingdom.
Tomoo OgiResearch Institute of Environmental Medicine, Nagoya University, Nagoya, Japan.
Mark A OsborneDepartment of Chemistry, School of Life Sciences, University of Sussex, Falmer, United Kingdom.ORCID http://orcid.org/0000-0001-6660-2985
Antony M CarrGenome Damage and Stability Centre, School of Life Sciences, University of Sussex, Falmer, United Kingdom.ORCID http://orcid.org/0000-0002-2028-2389
University of Sussex · GBNagasaki University · JPNagoya University · JPTohoku University · JP

Funding

Medical Research Council G1100074
6 · The paper itself

Abstract

PCNA ubiquitylation on lysine 164 is required for DNA damage tolerance. In many organisms PCNA is also ubiquitylated in unchallenged S phase but the significance of this has not been established. Using Schizosaccharomyces pombe, we demonstrate that lysine 164 ubiquitylation of PCNA contributes to efficient DNA replication in the absence of DNA damage. Loss of PCNA ubiquitylation manifests most strongly at late replicating regions and increases the frequency of replication gaps. We show that PCNA ubiquitylation increases the proportion of chromatin associated PCNA and the co-immunoprecipitation of Polymerase δ with PCNA during unperturbed replication and propose that ubiquitylation acts to prolong the chromatin association of these replication proteins to allow the efficient completion of Okazaki fragment synthesis by mediating gap filling.

Indexed as

DNA ReplicationUbiquitinationCell Line, TumorChromatinDNA-Directed DNA PolymeraseHumansProliferating Cell Nuclear AntigenSchizosaccharomycesChromatinDNA-Directed DNA PolymeraseProliferating Cell Nuclear Antigen

Identifiers

PMID28481910
PMCPMC5440044
OpenAlexW2612055329

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.