Evidence map›Paper›PMID 39152239›Full record

ArticleNature structural & molecular biology2024

A PRE loop at the dac locus acts as a topological chromatin structure that restricts and specifies enhancer-promoter communication.

Sandrine Denaud, Marion Bardou, Giorgio-Lucio Papadopoulos, Stefan Grob, Marco Di Stefano, Gonzalo Sabarís, Marcelo Nollmann, Bernd Schuettengruber, Giacomo Cavalli

Abstract read
In one paragraph

Article in Nature structural & molecular biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
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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.

Sandrine DenaudInstitute of Human Genetics, UMR9002 CNRS, University of Montpellier, Montpellier, France.
Marion Bardou *Centre de Biologie Structurale, IUMR5048 CNRS, INSERM U1054, University of Montpellier, Montpellier, France.ORCID http://orcid.org/0000-0003-1882-6065
Giorgio-Lucio Papadopoulos *Institute of Human Genetics, UMR9002 CNRS, University of Montpellier, Montpellier, France.
Stefan GrobDepartment of Plant and Microbial Biology and Zurich-Basel Plant Science Center, University of Zurich, Zurich, Switzerland.
Marco Di StefanoInstitute of Human Genetics, UMR9002 CNRS, University of Montpellier, Montpellier, France.ORCID http://orcid.org/0000-0001-6195-4754
Gonzalo SabarísInstitute of Human Genetics, UMR9002 CNRS, University of Montpellier, Montpellier, France.ORCID http://orcid.org/0000-0002-7797-6824
Marcelo NollmannCentre de Biologie Structurale, IUMR5048 CNRS, INSERM U1054, University of Montpellier, Montpellier, France.ORCID http://orcid.org/0000-0003-3339-2349
Bernd SchuettengruberInstitute of Human Genetics, UMR9002 CNRS, University of Montpellier, Montpellier, France. bernd.schuttengruber@igh.cnrs.fr.ORCID http://orcid.org/0000-0001-7338-4648
Giacomo CavalliInstitute of Human Genetics, UMR9002 CNRS, University of Montpellier, Montpellier, France. giacomo.cavalli@igh.cnrs.fr.ORCID http://orcid.org/0000-0003-3709-3469

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Three-dimensional (3D) genome folding has a fundamental role in the regulation of developmental genes by facilitating or constraining chromatin interactions between cis-regulatory elements (CREs). Polycomb response elements (PREs) are a specific kind of CRE involved in the memory of transcriptional states in Drosophila melanogaster. PREs act as nucleation sites for Polycomb group (PcG) proteins, which deposit the repressive histone mark H3K27me3, leading to the formation of a class of topologically associating domain (TAD) called a Polycomb domain. PREs can establish looping contacts that stabilize the gene repression of key developmental genes during development. However, the mechanism by which PRE loops fine-tune gene expression is unknown. Using clustered regularly interspaced short palindromic repeats and Cas9 genome engineering, we specifically perturbed PRE contacts or enhancer function and used complementary approaches including 4C-seq, Hi-C and Hi-M to analyze how chromatin architecture perturbation affects gene expression. Our results suggest that the PRE loop at the dac gene locus acts as a constitutive 3D chromatin scaffold during Drosophila development that forms independently of gene expression states and has a versatile function; it restricts enhancer-promoter communication and contributes to enhancer specificity.

Indexed as

ChromatinDrosophila melanogasterDrosophila ProteinsEnhancer Elements, GeneticPromoter Regions, GeneticAnimalsGene Expression Regulation, DevelopmentalPolycomb-Group ProteinsResponse ElementsChromatinDrosophila ProteinsPolycomb-Group Proteins

Identifiers

PMID39152239
PMCPMC11638067

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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.