Evidence map›Paper›PMID 41840057›Full record

ArticleThe EMBO journal2026

A functional overlap between actively transcribed genes and chromatin insulator elements.

Lucy J Cornell, Caroline L Harrold, Susannah Holliman, Felice Tsang, Matthew E Gosden, Lars L P Hanssen, Rosa Stolper, Damien J Downes, Daniel Biggs, Chris Preece and 7 more

Abstract read
In one paragraph

Article in The EMBO journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
  2. Article
  3. Facilitators may represent a new class of regulatory elements.Current opinion in genetics & development · 2026
    Review
  4. Review
  5. Mechanisms of Globin Gene Regulation in Mammals.Annual review of genetics · 2025
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
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

17 authors.

Lucy J Cornell *MRC Weatherall Institute of Molecular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
Caroline L Harrold *MRC Weatherall Institute of Molecular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
Susannah HollimanMRC Weatherall Institute of Molecular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
Felice TsangMRC Weatherall Institute of Molecular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
Matthew E GosdenMRC Weatherall Institute of Molecular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
Lars L P HanssenMRC Weatherall Institute of Molecular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0002-2551-2278
Rosa StolperMRC Weatherall Institute of Molecular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
Damien J DownesMRC Weatherall Institute of Molecular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0002-5034-0869
Daniel BiggsBiomedical Services, Medical Sciences Division, University of Oxford, Oxford, UK.
Chris PreeceBiomedical Services, Medical Sciences Division, University of Oxford, Oxford, UK.
Samy AlghadbanBiomedical Services, Medical Sciences Division, University of Oxford, Oxford, UK.
Jacqueline A SharpeMRC Weatherall Institute of Molecular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
Benjamin DaviesThe Francis Crick Institute, London, UK.ORCID http://orcid.org/0000-0003-3623-600X
Jacqueline A Sloane-StanleyMRC Weatherall Institute of Molecular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
Jim R HughesMRC Weatherall Institute of Molecular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, UK. jim.hughes@imm.ox.ac.uk.ORCID http://orcid.org/0000-0002-8955-7256
Douglas R HiggsMRC Weatherall Institute of Molecular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, UK. doug.higgs@imm.ox.ac.uk.ORCID http://orcid.org/0000-0003-3579-8705
Mira T KassoufMRC Weatherall Institute of Molecular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, UK. mira.kassouf@imm.ox.ac.uk.ORCID http://orcid.org/0000-0002-9781-921X

Funding

CAMS | Chinese Academy of Medical Sciences Initiative for Innovative Medicine () 2018-I2M-2-002UKRI | Biotechnology and Biological Sciences Research Council (BBSRC) BB/Y008898/1UKRI | Medical Research Council (MRC) MR/N00969X/1UKRI | Medical Research Council (MRC) MR/T014067/1Wellcome TrustWellcome Trust (WT) 099684/Z/12/ZWellcome Trust (WT) 106130/Z/14/ZWellcome Trust (WT) 109110/Z/15/ZWellcome Trust (WT) 203141/Z/16/ZWellcome Trust (WT) 215111/Z/18/ZWellcome Trust (WT) 222843/Z/21/Z
6 · The paper itself

Abstract

The mammalian genome is organised into large topologically associating domains (TADs) and smaller sub-TADs or enhancer-promoter loops, which may contribute to the regulation of gene expression. These dynamic structures arise, at least partly, via cohesin-mediated loop extrusion delimited by insulator elements. By studying the structure and function of the alpha-globin locus during erythroid differentiation, we have previously shown that the juxtaposition of the enhancers and promoters during this process partly depends on cohesin-mediated loop extrusion, which appears to be delimited by 12 largely convergently orientated CTCF boundary elements. To define the downstream boundary of the sub-TAD, we removed four CTCF sites in informative combinations. This showed that rather than CTCF insulators, it is the transcriptionally active alpha-globin gene that defines the downstream boundary of the sub-TAD. Further, insertion of actively transcribed fragments of the α-globin gene between the enhancers and native genes leads to a reduction in native α-globin expression and accumulation of cohesin at the insertion site. This highlights an overlap in the functional role of the fundamental elements of the genome.

Indexed as

alpha-GlobinsChromatinInsulator ElementsTranscription, GeneticAnimalsCCCTC-Binding FactorCell Cycle ProteinsChromosomal Proteins, Non-HistoneCohesinsEnhancer Elements, GeneticGene Expression RegulationMicePromoter Regions, Geneticalpha-GlobinsCCCTC-Binding FactorCell Cycle ProteinsChromatinChromosomal Proteins, Non-HistoneCohesinsCtcf protein, mouseCTCFDomainsInsulatorsRegulationTranscription

Identifiers

PMID41840057
PMCPMC13083895

What OpenQuestion holds

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Registered trials

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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.