Evidence map›Paper›PMID 27122604›Full record

ArticleMolecular biology of the cell2016

Quiescent Saccharomyces cerevisiae forms telomere hyperclusters at the nuclear membrane vicinity through a multifaceted mechanism involving Esc1, the Sir complex, and chromatin condensation.

Damien Laporte, Fabien Courtout, Sylvain Tollis, Isabelle Sagot

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 10% 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

32 citing papers in PubMed, 1 synthesis or guideline pooled it, 58 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. A Translocation within thebioRxiv : the preprint server for biology · 2026
    Article
  5. Review
  6. Quiescence Multiverse.Biomolecules · 2025
    Review
  7. Article
  8. Review
  9. Article
  10. Lamins as structural nuclear elements through evolution.Current opinion in cell biology · 2023
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Is There a Histone Code for Cellular Quiescence?Frontiers in cell and developmental biology · 2021
    Review
  19. Review
  20. 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

4 authors at 4 institutions in 2 countries.

Damien LaporteUniversité de Bordeaux-Institut de Biochimie et Génétique Cellulaires, 33000 Bordeaux, France CNRS-UMR5095 Bordeaux, 33077 Bordeaux cedex, France.
Fabien CourtoutUniversité de Bordeaux-Institut de Biochimie et Génétique Cellulaires, 33000 Bordeaux, France CNRS-UMR5095 Bordeaux, 33077 Bordeaux cedex, France.
Sylvain TollisWellcome Trust Centre for Cell Biology, University of Edinburgh, Edinburgh EH93BF, United Kingdom.
Isabelle SagotUniversité de Bordeaux-Institut de Biochimie et Génétique Cellulaires, 33000 Bordeaux, France CNRS-UMR5095 Bordeaux, 33077 Bordeaux cedex, France isabelle.sagot@ibgc.cnrs.fr.
Centre National de la Recherche Scientifique · FRInstitut de Biochimie et Génétique Cellulaires · FRUniversité de Bordeaux · FRUniversity of Edinburgh · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

Like other eukaryotes, Saccharomyces cerevisiae spatially organizes its chromosomes within the nucleus. In G1 phase, the yeast's 32 telomeres are clustered into 6-10 foci that dynamically interact with the nuclear membrane. Here we show that, when cells leave the division cycle and enter quiescence, telomeres gather into two to three hyperclusters at the nuclear membrane vicinity. This localization depends on Esc1 but not on the Ku proteins. Telomere hypercluster formation requires the Sir complex but is independent of the nuclear microtubule bundle that specifically assembles in quiescent cells. Importantly, mutants deleted for the linker histone H1 Hho1 or defective in condensin activity or affected for histone H4 Lys-16 deacetylation are impaired, at least in part, for telomere hypercluster formation in quiescence, suggesting that this process involves chromosome condensation. Finally, we establish that telomere hypercluster formation is not necessary for quiescence establishment, maintenance, and exit, raising the question of the physiological raison d'être of this nuclear reorganization.

Indexed as

Adenosine TriphosphatasesChromatinChromatin Assembly and DisassemblyDNA-Binding ProteinsG1 PhaseHeterochromatinHistonesMultiprotein ComplexesNuclear EnvelopeNuclear ProteinsSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSilent Information Regulator Proteins, Saccharomyces cerevisiaeTelomereAdenosine TriphosphatasesChromatincondensin complexesDNA-Binding ProteinsEsc1 protein, S cerevisiaeHeterochromatinHistonesMultiprotein ComplexesNuclear ProteinsSaccharomyces cerevisiae ProteinsSilent Information Regulator Proteins, Saccharomyces cerevisiae

Identifiers

PMID27122604
PMCPMC4907721
OpenAlexW2342834706

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.