Evidence map›Paper›PMID 24002784›Full record

ArticleGenome research2013

Cohesin-based chromatin interactions enable regulated gene expression within preexisting architectural compartments.

Vlad C Seitan, Andre J Faure, Ye Zhan, Rachel Patton McCord, Bryan R Lajoie, Elizabeth Ing-Simmons, Boris Lenhard, Luca Giorgetti, Edith Heard, Amanda G Fisher and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Genome research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 197 papers.

0numbers the graph read from it
0cells of the map it votes in
197citing papers in PubMed
–field-weighted citation impact
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

197 citing papers in PubMed, 334 citations in OpenAlex.

  1. Article
  2. Altered Cohesin Dynamics During Cellular Differentiation.bioRxiv : the preprint server for biology · 2026
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137 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

13 authors at 4 institutions in 3 countries.

Vlad C SeitanLymphocyte Development Group, MRC Clinical Sciences Centre, Imperial College London, London W12 0NN, United Kingdom;
Andre J Faure
Ye Zhan
Rachel Patton McCord
Bryan R Lajoie
Elizabeth Ing-Simmons
Boris Lenhard
Luca Giorgetti
Edith Heard
Amanda G Fisher
Paul Flicek
Job Dekker
Matthias Merkenschlager
Imperial College London · GBUniversity of Massachusetts Chan Medical School · USEuropean Bioinformatics Institute · GBInstitut Curie · FR

Funding

Structural Annotation of the Human GenomeR01HG003143 · NHGRI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI Job Dekker · 2003 to 2026
$15.4M
The Effects of Physical Disruption on Genome Organization and IntegrityF32GM100617 · NIGMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI MCCORD, RACHEL PATTON · 2012 to 2013
$101k
Medical Research Council MC_U120027516Medical Research Council MC_UP_1102/1NHGRI NIH HHS HG003143NHGRI NIH HHS HG003143-06S1NHGRI NIH HHS R01 HG003143NIGMS NIH HHS F32 GM100617Wellcome Trust
6 · The paper itself

Abstract

Chromosome conformation capture approaches have shown that interphase chromatin is partitioned into spatially segregated Mb-sized compartments and sub-Mb-sized topological domains. This compartmentalization is thought to facilitate the matching of genes and regulatory elements, but its precise function and mechanistic basis remain unknown. Cohesin controls chromosome topology to enable DNA repair and chromosome segregation in cycling cells. In addition, cohesin associates with active enhancers and promoters and with CTCF to form long-range interactions important for gene regulation. Although these findings suggest an important role for cohesin in genome organization, this role has not been assessed on a global scale. Unexpectedly, we find that architectural compartments are maintained in noncycling mouse thymocytes after genetic depletion of cohesin in vivo. Cohesin was, however, required for specific long-range interactions within compartments where cohesin-regulated genes reside. Cohesin depletion diminished interactions between cohesin-bound sites, whereas alternative interactions between chromatin features associated with transcriptional activation and repression became more prominent, with corresponding changes in gene expression. Our findings indicate that cohesin-mediated long-range interactions facilitate discrete gene expression states within preexisting chromosomal compartments.

Indexed as

Gene Expression RegulationAnimalsCCCTC-Binding FactorCell CycleCell Cycle ProteinsChromatinChromosomal Proteins, Non-HistoneChromosomes, MammalianCohesinsDNA-Binding ProteinsGene DosageGenomeLinear ModelsMiceNuclear ProteinsPhosphoproteinsCCCTC-Binding FactorCell Cycle ProteinsChromatinChromosomal Proteins, Non-HistoneCohesinsCtcf protein, mouseDNA-Binding ProteinsNipbl protein, mouseNuclear ProteinsPhosphoproteinsRad21 protein, mouseRepressor ProteinsTranscription Factors

Identifiers

PMID24002784
PMCPMC3847776
OpenAlexW2076202384

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.