Evidence map›Paper›PMID 40016420›Full record

ArticleThe EMBO journal2025

Parasitic plasmids are anchored to inactive regions of eukaryotic chromosomes through a nucleosome signal.

Fabien Girard, Antoine Even, Agnès Thierry, Myriam Ruault, Léa Meneu, Pauline Larrous, Mickaël Garnier, Sandrine Adiba, Angela Taddei, Romain Koszul and 1 more

Abstract read
In one paragraph

Article in The EMBO journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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

11 authors.

Fabien GirardInstitut Pasteur, CNRS UMR 3525, Université Paris Cité, Unité Régulation Spatiale des Génomes, 75015, Paris, France.
Antoine EvenInstitut Curie, PSL University, Sorbonne Université, CNRS UMR 3664, Nuclear Dynamics, Paris, France.
Agnès ThierryInstitut Pasteur, CNRS UMR 3525, Université Paris Cité, Unité Régulation Spatiale des Génomes, 75015, Paris, France.ORCID http://orcid.org/0000-0002-1566-0664
Myriam RuaultInstitut Curie, PSL University, Sorbonne Université, CNRS UMR 3664, Nuclear Dynamics, Paris, France.
Léa MeneuInstitut Pasteur, CNRS UMR 3525, Université Paris Cité, Unité Régulation Spatiale des Génomes, 75015, Paris, France.ORCID http://orcid.org/0000-0003-4245-6762
Pauline LarrousInstitut Pasteur, CNRS UMR 3525, Université Paris Cité, Unité Régulation Spatiale des Génomes, 75015, Paris, France.ORCID http://orcid.org/0000-0002-8410-0513
Mickaël GarnierInstitut Curie, PSL University, Sorbonne Université, CNRS UMR 3664, Nuclear Dynamics, Paris, France.ORCID http://orcid.org/0000-0002-3999-0879
Sandrine AdibaInstitut de Biologie de l'Ecole Normale Supérieure, Département de Biologie, Ecole Normale Supérieure, CNRS, INSERM, PSL Research University, Paris, France.
Angela TaddeiInstitut Curie, PSL University, Sorbonne Université, CNRS UMR 3664, Nuclear Dynamics, Paris, France.
Romain KoszulInstitut Pasteur, CNRS UMR 3525, Université Paris Cité, Unité Régulation Spatiale des Génomes, 75015, Paris, France. romain.koszul@pasteur.fr.ORCID http://orcid.org/0000-0002-3086-1173
Axel CournacInstitut Pasteur, CNRS UMR 3525, Université Paris Cité, Unité Régulation Spatiale des Génomes, 75015, Paris, France. axel.cournac@pasteur.fr.ORCID http://orcid.org/0000-0003-3523-2453

Funding

Agence Nationale de la Recherche (ANR) ANR-10-IDEX-0001-02Agence Nationale de la Recherche (ANR) ANR-10-INBS-04Agence Nationale de la Recherche (ANR) ANR-10-LABX-54Agence Nationale de la Recherche (ANR) ANR-17-CONV-6150005Agence Nationale de la Recherche (ANR) ANR-19-CE45-0003-01Agence Nationale de la Recherche (ANR) ANR-22-CE12-0013-01EC | European Research Council (ERC) 771813
6 · The paper itself

Abstract

Natural plasmids are common in prokaryotes, but few have been documented in eukaryotes. The natural 2µ plasmid present in the yeast Saccharomyces cerevisiae is one of these best-characterized exceptions. This highly stable genetic element has coexisted with its host for millions of years, faithfully segregating at each cell division through a mechanism that remains unclear. Using proximity ligation methods (such as Hi-C, Micro-C) to map the contacts between 2µ plasmid and yeast chromosomes under dozens of different biological conditions, we found that the plasmid is tethered preferentially to regions with low transcriptional activity, often corresponding to long, inactive genes. These contacts do not depend on common chromosome-structuring factors, such as members of the structural maintenance of chromosome complexes (SMC) but depend on a nucleosome-encoded signal associated with RNA Pol II depletion. They appear stable throughout the cell cycle and can be established within minutes. This chromosome hitchhiking strategy may extend beyond the 2µ plasmid/S. cerevisiae pair, as suggested by the binding pattern of the natural eukaryotic plasmid Ddp5 along silent chromosome regions of the amoeba Dictyostelium discoideum.

Indexed as

Chromosomes, FungalDictyosteliumNucleosomesPlasmidsSaccharomyces cerevisiaeNucleosomesDictyostelium discoideumEukaryotic PlasmidNuclear organizationSaccharomyces cerevisiaeTwo micron plasmid

Identifiers

PMID40016420
PMCPMC11962162

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 Socratic graph.