Evidence map›Paper›PMID 36335096›Full record

ArticleNature communications2022

FRET-FISH probes chromatin compaction at individual genomic loci in single cells.

Ana Mota, Szymon Berezicki, Erik Wernersson, Luuk Harbers, Xiaoze Li-Wang, Katarina Gradin, Christiane Peuckert, Nicola Crosetto, Magda Bienko

Abstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
  2. Article
  3. Chromatin enables precise and scalable gene regulation with factors of limited specificity.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Article
  5. Review
  6. Introduction to bioimaging-based spatial multi-omic novel methods.Quantitative biology (Beijing, China) · 2023
    Review
  7. 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

9 authors.

Ana MotaDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, SE-17165, Sweden.ORCID 0000-0001-8592-9764
Szymon BerezickiDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, SE-17165, Sweden.ORCID 0000-0003-3980-6290
Erik WernerssonDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, SE-17165, Sweden.ORCID 0000-0003-4778-1660
Luuk HarbersDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, SE-17165, Sweden.ORCID 0000-0003-3910-6497
Xiaoze Li-WangDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, SE-17165, Sweden.
Katarina GradinDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, SE-17165, Sweden.
Christiane PeuckertStockholm University, The Department of Molecular Biosciences, The Wenner-Gren Institute, Stockholm, Sweden.
Nicola CrosettoDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, SE-17165, Sweden.ORCID 0000-0002-3019-6978
Magda BienkoDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, SE-17165, Sweden. magda.bienko@ki.se.ORCID 0000-0002-6499-9082

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chromatin compaction is a key biophysical property that influences multiple DNA transactions. Lack of chromatin accessibility is frequently used as proxy for chromatin compaction. However, we currently lack tools for directly probing chromatin compaction at individual genomic loci. To fill this gap, here we present FRET-FISH, a method combining fluorescence resonance energy transfer (FRET) with DNA fluorescence in situ hybridization (FISH) to probe chromatin compaction at select loci in single cells. We first validate FRET-FISH by comparing it with ATAC-seq, demonstrating that local compaction and accessibility are strongly correlated. FRET-FISH also detects expected differences in compaction upon treatment with drugs perturbing global chromatin condensation. We then leverage FRET-FISH to study local chromatin compaction on the active and inactive X chromosome, along the nuclear radius, in different cell cycle phases, and during increasing passage number. FRET-FISH is a robust tool for probing local chromatin compaction in single cells.

Indexed as

ChromatinFluorescence Resonance Energy TransferDNAGenomicsIn Situ Hybridization, FluorescenceChromatinDNA

Identifiers

PMID36335096
PMCPMC9637210

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.