Evidence map›Paper›PMID 25512564›Full record

ArticleGenes & development2014

Spatial genome organization: contrasting views from chromosome conformation capture and fluorescence in situ hybridization.

Iain Williamson, Soizik Berlivet, Ragnhild Eskeland, Shelagh Boyle, Robert S Illingworth, Denis Paquette, Josée Dostie, Wendy A Bickmore

Open access · diamondAbstract read
In one paragraph

Article in Genes & development, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 142 papers.

0numbers the graph read from it
0cells of the map it votes in
142citing 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

142 citing papers in PubMed, 249 citations in OpenAlex.

  1. Article
  2. Article
  3. Mapping the 3D genome architecture.Computational and structural biotechnology journal · 2025
    Review
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  6. Article
  7. Review
  8. Article
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  12. Review
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  14. Article
  15. The relevance of chromatin architecture to genome rearrangements inPhilosophical transactions of the Royal Society of London. Series B, Biological sciences · 2022
    Article
  16. Article
  17. Article
  18. Nuclear Architecture in the Nervous System.Results and problems in cell differentiation · 2022
    Review
  19. High-Throughput DNA FISH (hiFISH).Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  20. Review

82 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

8 authors at 4 institutions in 3 countries.

Iain WilliamsonMRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh EH4 2XU, United Kingdom;
Soizik BerlivetDepartment of Biochemistry, Goodman Cancer Research Center, McGill University, Montréal, Québec H3G1Y6, Canada.
Ragnhild EskelandMRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh EH4 2XU, United Kingdom;
Shelagh BoyleMRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh EH4 2XU, United Kingdom;
Robert S IllingworthMRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh EH4 2XU, United Kingdom;
Denis PaquetteDepartment of Biochemistry.
Josée DostieDepartment of Biochemistry, wendy.bickmore@igmm.ed.ac.uk josee.dostie@mcgill.ca.
Wendy A BickmoreMRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh EH4 2XU, United Kingdom; wendy.bickmore@igmm.ed.ac.uk josee.dostie@mcgill.ca.
University of Edinburgh · GBLaboratoire de Biochimie · FRMRC Institute of Genetics and Molecular Medicine · GBMcGill University · CA

Funding

CIHR MOP-86716Medical Research Council MC_PC_U127527202
6 · The paper itself

Abstract

Although important for gene regulation, most studies of genome organization use either fluorescence in situ hybridization (FISH) or chromosome conformation capture (3C) methods. FISH directly visualizes the spatial relationship of sequences but is usually applied to a few loci at a time. The frequency at which sequences are ligated together by formaldehyde cross-linking can be measured genome-wide by 3C methods, with higher frequencies thought to reflect shorter distances. FISH and 3C should therefore give the same views of genome organization, but this has not been tested extensively. We investigated the murine HoxD locus with 3C carbon copy (5C) and FISH in different developmental and activity states and in the presence or absence of epigenetic regulators. We identified situations in which the two data sets are concordant but found other conditions under which chromatin topographies extrapolated from 5C or FISH data are not compatible. We suggest that products captured by 3C do not always reflect spatial proximity, with ligation occurring between sequences located hundreds of nanometers apart, influenced by nuclear environment and chromatin composition. We conclude that results obtained at high resolution with either 3C methods or FISH alone must be interpreted with caution and that views about genome organization should be validated by independent methods.

Indexed as

AnimalsCell DifferentiationCells, CulturedChromatinEmbryonic Stem CellsGenetic TechniquesGenomeHomeodomain ProteinsIn Situ Hybridization, FluorescenceMiceMutationPolycomb-Group ProteinsProtein Structure, TertiaryStaining and LabelingChromatinHomeodomain ProteinsHoxd1 protein, mousePolycomb-Group Proteins3CFISHHox genesnuclear organizationpolycomb

Identifiers

PMID25512564
PMCPMC4265680
OpenAlexW2101754326

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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.