Evidence map›Paper›PMID 30595435›Full record

ArticleMolecular cell2019

Condensin-Dependent Chromatin Compaction Represses Transcription Globally during Quiescence.

Sarah G Swygert, Seungsoo Kim, Xiaoying Wu, Tianhong Fu, Tsung-Han Hsieh, Oliver J Rando, Robert N Eisenman, Jay Shendure, Jeffrey N McKnight, Toshio Tsukiyama

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cell, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed, 1 pooled it
4.7field-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

70 citing papers in PubMed, 1 synthesis or guideline pooled it, 115 citations in OpenAlex.

  1. Pooled it
  2. An atlas of thebioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Stage-specific MCM protein expression inFrontiers in cellular and infection microbiology · 2025
    Article
  20. Article

10 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

10 authors at 5 institutions in 2 countries.

Sarah G SwygertBasic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
Seungsoo KimGenome Sciences, University of Washington, Seattle, WA 98195, USA.
Xiaoying WuBasic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
Tianhong FuBasic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
Tsung-Han HsiehBiochemistry and Molecular Pharmacology, University of Massachusetts, Worcester, MA 01605, USA.
Oliver J RandoBiochemistry and Molecular Pharmacology, University of Massachusetts, Worcester, MA 01605, USA.
Robert N EisenmanBasic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
Jay ShendureGenome Sciences, University of Washington, Seattle, WA 98195, USA; Howard Hughes Medical Institute, Seattle, WA 98195, USA.
Jeffrey N McKnightBasic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
Toshio TsukiyamaBasic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA. Electronic address: ttsukiya@fredhutch.org.
Fred Hutch Cancer Center · USUniversity of Massachusetts Chan Medical School · USCape Town HVTN Immunology Laboratory / Hutchinson Centre Research Institute of South Africa · ZAHoward Hughes Medical Institute · USUniversity of Washington · US

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Eric Collisson · 1985 to 2026
$296.4M
Chromosome Metabolism and Cancer Training GrantT32CA009657 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI EISENMAN, ROBERT NEIL · 1991 to 2020
$7.6M
The MYC Transcription Factor Network and the Path to CancerR35CA231989 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI EISENMAN, ROBERT NEIL · 2018 to 2024
$6.3M
MYC ONCOPROTEIN FUNCTIONR01CA057138 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI EISENMAN, ROBERT NEIL · 1991 to 2018
$4.9M
Genomic analysis of histone replacement dynamics in yeastR01GM079205 · NIGMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI RANDO, OLIVER J · 2008 to 2016
$3.3M
Mechanisms and functions of chromatin regulation for cell-cycle controlR01GM111428 · NIGMS · FRED HUTCHINSON CANCER RESEARCH CENTER · PI TSUKIYAMA, TOSHIO · 2015 to 2020
$2.4M
FHCRC High-Performance Computing ClusterS10OD020069 · OD · FRED HUTCHINSON CANCER RESEARCH CENTER · PI KOOPERBERG, CHARLES L · 2015 to 2015
$600k
The effect of local inter-nucleosomal interactions and chromatin remodeling on in vivo chromatin fiber foldingF32GM120962 · NIGMS · FRED HUTCHINSON CANCER RESEARCH CENTER · PI SWYGERT, SARAH GRACE · 2017 to 2018
$116k
NCI NIH HHS P30 CA015704NCI NIH HHS R01 CA057138NCI NIH HHS R35 CA231989NCI NIH HHS T32 CA009657NIGMS NIH HHS F32 GM120962NIGMS NIH HHS R01 GM079205NIGMS NIH HHS R01 GM111428NIH HHS S10 OD020069
6 · The paper itself

Abstract

Quiescence is a stress-resistant state in which cells reversibly exit the cell cycle and suspend most processes. Quiescence is essential for stem cell maintenance, and its misregulation is implicated in tumor formation. One of the hallmarks of quiescent cells is highly condensed chromatin. Because condensed chromatin often correlates with transcriptional silencing, it has been hypothesized that chromatin compaction represses transcription during quiescence. However, the technology to test this model by determining chromatin structure within cells at gene resolution has not previously been available. Here, we use Micro-C XL to map chromatin contacts at single-nucleosome resolution genome-wide in quiescent Saccharomyces cerevisiae cells. We describe chromatin domains on the order of 10-60 kilobases that, only in quiescent cells, are formed by condensin-mediated loops. Condensin depletion prevents the compaction of chromatin within domains and leads to widespread transcriptional de-repression. Finally, we demonstrate that condensin-dependent chromatin compaction is conserved in quiescent human fibroblasts.

Indexed as

Cellular SenescenceChromatin Assembly and DisassemblyTranscription, GeneticAdenosine TriphosphatasesBinding SitesCell ProliferationCells, CulturedChromatinDNA-Binding ProteinsFibroblastsGene Expression Regulation, FungalHumansMultiprotein ComplexesProtein BindingSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsAdenosine TriphosphatasesChromatincondensin complexesDNA-Binding ProteinsMultiprotein ComplexesSaccharomyces cerevisiae Proteinschromatin boundarychromatin condensationchromatin domainscondensinMicro-Cquiescencetranscriptional repression

Identifiers

PMID30595435
PMCPMC6368455
OpenAlexW2951447445

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.