Evidence map›Paper›PMID 40640210›Full record

ArticleNature communications2025

HP1 loses its chromatin clustering and phase separation function across evolution.

Sanâa Bensaha, Dominika Lewandowska, Fernando Muzzopappa, Stephanie Hutin, Mark D Tully, Michela Anfossi, Florence M Cammas, Christophe Normand, Fabian Erdel

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

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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.

Sanâa Bensaha *MCD, Center for Integrative Biology (CBI), University of Toulouse, CNRS, Toulouse, France.ORCID http://orcid.org/0009-0005-0614-5256
Dominika Lewandowska *MCD, Center for Integrative Biology (CBI), University of Toulouse, CNRS, Toulouse, France.
Fernando MuzzopappaMCD, Center for Integrative Biology (CBI), University of Toulouse, CNRS, Toulouse, France.ORCID http://orcid.org/0000-0001-6420-828X
Stephanie HutinCell & Plant Physiology Laboratory, University Grenoble Alpes, CNRS, CEA, INRAE, IRIG, Grenoble, France.ORCID http://orcid.org/0000-0002-2168-5841
Mark D TullyEuropean Synchrotron Radiation Facility, Structural Biology Group, Grenoble, France.ORCID http://orcid.org/0000-0001-5450-9900
Michela AnfossiMCD, Center for Integrative Biology (CBI), University of Toulouse, CNRS, Toulouse, France.ORCID http://orcid.org/0000-0002-1329-9801
Florence M CammasMontpellier Cancer Research Institute (IRCM), University of Montpellier, INSERM, ICM, CNRS, Montpellier, France.
Christophe NormandMCD, Center for Integrative Biology (CBI), University of Toulouse, CNRS, Toulouse, France.
Fabian ErdelMCD, Center for Integrative Biology (CBI), University of Toulouse, CNRS, Toulouse, France. fabian.erdel@cnrs.fr.ORCID http://orcid.org/0000-0003-2888-7777

Funding

EC | EU Framework Programme for Research and Innovation H2020 | H2020 Priority Excellent Science | H2020 European Research Council (H2020 Excellent Science - European Research Council) 101170239EC | EU Framework Programme for Research and Innovation H2020 | H2020 Priority Excellent Science | H2020 European Research Council (H2020 Excellent Science - European Research Council) 804023
6 · The paper itself

Abstract

Heterochromatin protein 1 (HP1) is a multifunctional chromatin-associated protein conserved from fission yeast to mammals. HP1 has been suggested to drive heterochromatin formation via phase separation. However, there is seemingly conflicting evidence about HP1 phase-separating in different systems or not. Here, we assess the phase separation behavior of HP1 from fission yeast, fruit fly and mouse in vitro and in mammalian cells side-by-side. We find that HP1 from fission yeast and fly can undergo liquid-liquid phase separation and induce heterochromatin coalescence in mouse cells, in stark contrast to HP1 from mouse. Induced heterochromatin coalescence has only mild effects on gene expression. We link the decreasing phase separation propensity of HP1 homologs to their decreasing intrinsic disorder and their increasing sensitivity to HP1 paralogs antagonizing phase separation. Our work elucidates the relationship between phase separation, nuclear organization and gene expression, and highlights the evolutionary dimension of protein phase separation control.

Indexed as

ChromatinChromosomal Proteins, Non-HistoneHeterochromatinAnimalsChromobox Protein Homolog 5Drosophila melanogasterEvolution, MolecularHumansMicePhase SeparationSchizosaccharomycesSchizosaccharomyces pombe ProteinsChromatinChromobox Protein Homolog 5Chromosomal Proteins, Non-HistoneHeterochromatinSchizosaccharomyces pombe Proteins

Identifiers

PMID40640210
PMCPMC12246093

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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.