Evidence map›Paper›PMID 41992225›Full record

ArticleBMC biology2026

The tiny germline chromosomes of Paramecium aurelia have an exceptionally high recombination rate and are capped by a new class of Helitrons.

Olivier Arnaiz, Frédéric Guérin, Arnaud Couloux, Caridad Miró-Pina, Guillaume Pellerin, Irina Nekrasova, Joëlle Amselem, Jean-Marc Aury, Simran Bhullar, Andrea Frapporti and 17 more

Abstract read
In one paragraph

Article in BMC biology, 2026. 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

27 authors.

Olivier ArnaizUniversité Paris-Saclay, CEA, CNRS - Institute for Integrative Biology of the Cell (I2BC), Gif-Sur-Yvette, France.
Frédéric GuérinUniversité Paris Cité, CNRS, Institut Jacques Monod, Paris, F-75013, France.
Arnaud CoulouxGénomique Métabolique, Genoscope, Institut François Jacob, CEA, CNRS, Université Evry, Université Paris-Saclay, Evry, 91057, France.
Caridad Miró-PinaUniversité Paris Cité, CNRS, Institut Jacques Monod, Paris, F-75013, France.
Guillaume PellerinInstitut de Biologie de l'ENS (IBENS), Département de Biologie, École Normale Supérieure, CNRS, INSERM, Université PSL, Paris, 75005, France.
Irina NekrasovaInstitut de Biologie de l'ENS (IBENS), Département de Biologie, École Normale Supérieure, CNRS, INSERM, Université PSL, Paris, 75005, France.
Joëlle AmselemUniversité Paris-Saclay, INRAE, URGI, Versailles, 78026, France.
Jean-Marc AuryGénomique Métabolique, Genoscope, Institut François Jacob, CEA, CNRS, Université Evry, Université Paris-Saclay, Evry, 91057, France.
Simran BhullarInstitut de Biologie de l'ENS (IBENS), Département de Biologie, École Normale Supérieure, CNRS, INSERM, Université PSL, Paris, 75005, France.
Andrea FrapportiUniversité Paris Cité, CNRS, Institut Jacques Monod, Paris, F-75013, France.
Emmanuelle LeratUniversite Claude Bernard Lyon 1, LBBE, UMR 5558, CNRS, VAS, Villeurbanne, France.
Isabelle LuytenUniversité Paris-Saclay, INRAE, URGI, Versailles, 78026, France.
Sophie MalinskyInstitut de Biologie de l'ENS (IBENS), Département de Biologie, École Normale Supérieure, CNRS, INSERM, Université PSL, Paris, 75005, France.
Nathalie MathyUniversité Paris-Saclay, CEA, CNRS - Institute for Integrative Biology of the Cell (I2BC), Gif-Sur-Yvette, France.
Alexey PotekhinInstitut de Biologie de l'ENS (IBENS), Département de Biologie, École Normale Supérieure, CNRS, INSERM, Université PSL, Paris, 75005, France.
Vinciane RégnierUniversité Paris-Saclay, CEA, CNRS - Institute for Integrative Biology of the Cell (I2BC), Gif-Sur-Yvette, France.
Natalia Sawka-GądekInstitut de Biologie de l'ENS (IBENS), Département de Biologie, École Normale Supérieure, CNRS, INSERM, Université PSL, Paris, 75005, France.
Amandine TouzeauUniversité Paris Cité, CNRS, Institut Jacques Monod, Paris, F-75013, France.
Augustin de VanssayUniversité Paris Cité, CNRS, Institut Jacques Monod, Paris, F-75013, France.
Coralie ZangarelliUniversité Paris-Saclay, CEA, CNRS - Institute for Integrative Biology of the Cell (I2BC), Gif-Sur-Yvette, France.
Hadi QuesnevilleUniversité Paris-Saclay, INRAE, URGI, Versailles, 78026, France.
Mireille BétermierUniversité Paris-Saclay, CEA, CNRS - Institute for Integrative Biology of the Cell (I2BC), Gif-Sur-Yvette, France.
Karine LabadieGénomique Métabolique, Genoscope, Institut François Jacob, CEA, CNRS, Université Evry, Université Paris-Saclay, Evry, 91057, France.
Laurent DuretUniversite Claude Bernard Lyon 1, LBBE, UMR 5558, CNRS, VAS, Villeurbanne, France.
Eric MeyerInstitut de Biologie de l'ENS (IBENS), Département de Biologie, École Normale Supérieure, CNRS, INSERM, Université PSL, Paris, 75005, France. emeyer@biologie.ens.fr.
Sandra DuharcourtUniversité Paris Cité, CNRS, Institut Jacques Monod, Paris, F-75013, France. sandra.duharcourt@ijm.fr.
Linda SperlingUniversité Paris-Saclay, CEA, CNRS - Institute for Integrative Biology of the Cell (I2BC), Gif-Sur-Yvette, France. linda.sperling@i2bc.paris-saclay.fr.

Funding

Agence Nationale de la Recherche ANR-11-INBS-0012Agence Nationale de la Recherche ANR-18-CE12-0005Agence Nationale de la Recherche ANR-18-CE12-0005, ANR-19-CE12-0015, ANR-23-CE12-0027, ANR-25-CE12-7757Agence Nationale de la Recherche ANR-19-CE12-0015Fondation pour la Recherche Médicale Equipe FRM EQU202103012766Fondation pour la Recherche Médicale Equipe FRM EQU202203014643
6 · The paper itself

Abstract

backgroundParamecia belong to the ciliate phylum of unicellular eukaryotes characterized by nuclear dimorphism. A diploid germline micronucleus (MIC) transmits genetic information across sexual generations. A polyploid transcriptionally active somatic macronucleus (MAC) develops at each sexual generation from a copy of the MIC through programmed DNA elimination (PDE) of > 30% of germline DNA. PDE requires the domesticated PiggyMac (Pgm) transposase. Assembly of Paramecium germline genomes has presented an enormous challenge owing to the difficulty of MIC isolation.

resultsWe report chromosome-scale short-read MIC assemblies for 7 species from the P. aurelia species complex. We discovered a novel clade of Helitrons, with 9-10-kb transposase ORFs under purifying selection, that have remained active in all P. aurelia lineages. A long-read assembly for P. tetraurelia together with a genetic linkage map provided a nearly telomere-to-telomere assembly.

conclusionsThe ~ 100-Mb genome consists of tiny (300 kb-1.2 Mb) and numerous (~ 160) germline chromosomes with the highest recombination rate ever reported for a eukaryote (420 cM/Mb). The ends of the chromosomes consist of Helitrons inserted in telomeric C

Indexed as

ChromosomesGenome, ProtozoanParamecium aureliaRecombination, GeneticMicronucleus, GermlineAneuploidyCiliateComparative genomicsGenetic linkage mapG-quadruplexHelitronHorizontal transferNuclear dimorphismRecombination rateTelomere

Identifiers

PMID41992225
PMCPMC13085455

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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 OpenQuestion graph.