Evidence map›Paper›PMID 32513739›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2020

Sir2 mitigates an intrinsic imbalance in origin licensing efficiency between early- and late-replicating euchromatin.

Timothy Hoggard, Carolin A Müller, Conrad A Nieduszynski, Michael Weinreich, Catherine A Fox

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Contributions of a Histone Deacetylase (SirT2/Hst2) toJournal of fungi (Basel, Switzerland) · 2022
    Article
  10. Review
  11. Review
  12. Review
  13. Sir2 takes affirmative action to ensure equal opportunity in replication origin licensing.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 2 countries.

Timothy HoggardDepartment of Biomolecular Chemistry, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI 53706.ORCID 0000-0003-0589-1271
Carolin A MüllerSir William Dunn School of Pathology, University of Oxford, OX1 3RE Oxford, United Kingdom.ORCID 0000-0002-7422-5582
Conrad A NieduszynskiSir William Dunn School of Pathology, University of Oxford, OX1 3RE Oxford, United Kingdom.ORCID 0000-0003-2001-076X
Michael WeinreichDivision of Molecular and Cellular Biosciences, National Science Foundation, Alexandria, VA 22314.
Catherine A FoxDepartment of Biomolecular Chemistry, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI 53706; cfox@wisc.edu.ORCID 0000-0002-6190-6207
University of Oxford · GBUniversity of Wisconsin–Madison · USU.S. National Science Foundation · US

Funding

Origin Recognition Complex at Transcriptional SilencersR01GM056890 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI FOX, CATHERINE A · 1998 to 2020
$6.4M
Biotechnology and Biological Sciences Research Council BB/N016858Biotechnology and Biological Sciences Research Council BB/N016858/1NIGMS NIH HHS R01 GM056890Wellcome TrustWellcome Trust 110064/Z/15/Z
6 · The paper itself

Abstract

A eukaryotic chromosome relies on the function of multiple spatially distributed DNA replication origins for its stable inheritance. The spatial location of an origin is determined by the chromosomal position of an MCM complex, the inactive form of the DNA replicative helicase that is assembled onto DNA in G1-phase (also known as origin licensing). While the biochemistry of origin licensing is understood, the mechanisms that promote an adequate spatial distribution of MCM complexes across chromosomes are not. We have elucidated a role for the Sir2 histone deacetylase in establishing the normal distribution of MCM complexes across

Indexed as

Cell Cycle ProteinsChromosomal Proteins, Non-HistoneChromosomesDNA HelicasesDNA ReplicationEuchromatinHeterochromatinReplication OriginSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSilent Information Regulator Proteins, Saccharomyces cerevisiaeSirtuin 2Cell Cycle ProteinsChromosomal Proteins, Non-HistoneDNA HelicasesEuchromatinHeterochromatinSaccharomyces cerevisiae ProteinsSilent Information Regulator Proteins, Saccharomyces cerevisiaeSIR2 protein, S cerevisiaeSirtuin 2chromatinchromosomesorigin licensingSiryeast

Identifiers

PMID32513739
PMCPMC7322022
OpenAlexW3033757850

What OpenQuestion holds

Textmetadata
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.