Evidence map›Paper›PMID 30104203›Full record

ArticleEMBO reports2018

Budding yeast Rif1 binds to replication origins and protects DNA at blocked replication forks.

Shin-Ichiro Hiraga, Chandre Monerawela, Yuki Katou, Sophie Shaw, Kate Rm Clark, Katsuhiko Shirahige, Anne D Donaldson

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in EMBO reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

18 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Temporal control of late replication and coordination of origin firing by self-stabilizing Rif1-PP1 hubs inProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  7. Review
  8. Review
  9. Mammalian DNA Replication Timing.Cold Spring Harbor perspectives in biology · 2021
    Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Control of DNA replication timing in the 3D genome.Nature reviews. Molecular cell biology · 2019
    Review
  16. Article
  17. Review
  18. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 2 countries.

Shin-Ichiro HiragaInstitute of Medical Sciences, University of Aberdeen, Aberdeen, UK s.hiraga@abdn.ac.uk a.d.donaldson@abdn.ac.uk.ORCID 0000-0002-8722-3869
Chandre MonerawelaInstitute of Medical Sciences, University of Aberdeen, Aberdeen, UK.
Yuki KatouInstitute for Quantitative Biosciences, University of Tokyo, Tokyo, Japan.
Sophie ShawCentre for Genome-Enabled Biology and Medicine, University of Aberdeen, Aberdeen, UK.ORCID 0000-0003-2367-2670
Kate Rm ClarkInstitute of Medical Sciences, University of Aberdeen, Aberdeen, UK.
Katsuhiko ShirahigeInstitute for Quantitative Biosciences, University of Tokyo, Tokyo, Japan.
Anne D DonaldsonInstitute of Medical Sciences, University of Aberdeen, Aberdeen, UK s.hiraga@abdn.ac.uk a.d.donaldson@abdn.ac.uk.ORCID 0000-0001-7842-8136
University of Aberdeen · GBThe University of Tokyo · JP

Funding

Cancer Research UK 19059Cancer Research UK A19059
6 · The paper itself

Abstract

Despite its evolutionarily conserved function in controlling DNA replication, the chromosomal binding sites of the budding yeast Rif1 protein are not well understood. Here, we analyse genome-wide binding of budding yeast Rif1 by chromatin immunoprecipitation, during G1 phase and in S phase with replication progressing normally or blocked by hydroxyurea. Rif1 associates strongly with telomeres through interaction with Rap1. By comparing genomic binding of wild-type Rif1 and truncated Rif1 lacking the Rap1-interaction domain, we identify hundreds of Rap1-dependent and Rap1-independent chromosome interaction sites. Rif1 binds to centromeres, highly transcribed genes and replication origins in a Rap1-independent manner, associating with both early and late-initiating origins. Interestingly, Rif1 also binds around activated origins when replication progression is blocked by hydroxyurea, suggesting association with blocked forks. Using nascent DNA labelling and DNA combing techniques, we find that in cells treated with hydroxyurea, yeast Rif1 stabilises recently synthesised DNA Our results indicate that, in addition to controlling DNA replication initiation, budding yeast Rif1 plays an ongoing role after initiation and controls events at blocked replication forks.

Indexed as

Binding SitesCell CycleCell Cycle ProteinsCentromereChromosomes, PlantDNADNA ReplicationDNA Replication TimingMinichromosome Maintenance ProteinsMutationProtein Phosphatase 1Protein Serine-Threonine KinasesReplication OriginRepressor ProteinsSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsCDC7 protein, S cerevisiaeCell Cycle ProteinsDNAMinichromosome Maintenance ProteinsProtein Phosphatase 1Protein Serine-Threonine KinasesRAP1 protein, S cerevisiaeRepressor ProteinsRIF1 protein, S cerevisiaeSaccharomyces cerevisiae ProteinsShelterin ComplexTelomere-Binding ProteinsTranscription FactorscentromereChIP‐SeqDNA replication originnascent DNARif1

Identifiers

PMID30104203
PMCPMC6123642
OpenAlexW2885440056

What Socratic 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 Socratic graph.