Evidence map›Paper›PMID 39761307›Full record

ArticlePLoS biology2025

PRDM9 drives the location and rapid evolution of recombination hotspots in salmonid fish.

Marie Raynaud, Paola Sanna, Julien Joseph, Julie Clément, Yukiko Imai, Jean-Jacques Lareyre, Audrey Laurent, Nicolas Galtier, Frédéric Baudat, Laurent Duret and 2 more

Abstract read
In one paragraph

Article in PLoS biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Why recombination hotspots?PLoS genetics · 2026
    Review
  5. Article
  6. Meiotic Recombination in Teleosts.Advances in experimental medicine and biology · 2026
    Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Marie RaynaudISEM, Univ Montpellier, CNRS, IRD, Montpellier, France.
Paola SannaInstitut de Génétique Humaine, Univ Montpellier, Centre National de la Recherche Scientifique, Montpellier, France.
Julien JosephLaboratoire de Biométrie et Biologie Évolutive, Universite Claude Bernard Lyon 1, CNRS UMR 5558, Villeurbanne, France.
Julie ClémentIHPE, Univ Montpellier, CNRS, IFREMER, Univ Perpignan Via Domitia, Perpignan, France.
Yukiko ImaiDepartment of Gene Function and Phenomics, National Institute of Genetics, Mishima, Japan.ORCID https://orcid.org/0000-0002-4716-2563
Jean-Jacques LareyreINRAE, UR1037 Fish Physiology and Genomics, F-35000 Rennes, France.
Audrey LaurentINRAE, UR1037 Fish Physiology and Genomics, F-35000 Rennes, France.
Nicolas GaltierISEM, Univ Montpellier, CNRS, IRD, Montpellier, France.
Frédéric BaudatInstitut de Génétique Humaine, Univ Montpellier, Centre National de la Recherche Scientifique, Montpellier, France.ORCID https://orcid.org/0000-0003-2415-8366
Laurent DuretLaboratoire de Biométrie et Biologie Évolutive, Universite Claude Bernard Lyon 1, CNRS UMR 5558, Villeurbanne, France.ORCID https://orcid.org/0000-0003-2836-3463
Pierre-Alexandre GagnaireISEM, Univ Montpellier, CNRS, IRD, Montpellier, France.ORCID https://orcid.org/0000-0002-1908-3235
Bernard de MassyInstitut de Génétique Humaine, Univ Montpellier, Centre National de la Recherche Scientifique, Montpellier, France.ORCID https://orcid.org/0000-0002-0950-2758

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In many eukaryotes, meiotic recombination occurs preferentially at discrete sites, called recombination hotspots. In various lineages, recombination hotspots are located in regions with promoter-like features and are evolutionarily stable. Conversely, in some mammals, hotspots are driven by PRDM9 that targets recombination away from promoters. Paradoxically, PRDM9 induces the self-destruction of its targets and this triggers an ultra-fast evolution of mammalian hotspots. PRDM9 is ancestral to all animals, suggesting a critical importance for the meiotic program, but has been lost in many lineages with surprisingly little effect on meiosis success. However, it is unclear whether the function of PRDM9 described in mammals is shared by other species. To investigate this, we analyzed the recombination landscape of several salmonids, the genome of which harbors one full-length PRDM9 and several truncated paralogs. We identified recombination initiation sites in Oncorhynchus mykiss by mapping meiotic DNA double-strand breaks (DSBs). We found that DSBs clustered at hotspots positioned away from promoters, enriched for the H3K4me3 and H3K36me3 and the location of which depended on the genotype of full-length Prdm9. We observed a high level of polymorphism in the zinc finger domain of full-length Prdm9, indicating diversification driven by positive selection. Moreover, population-scaled recombination maps in O. mykiss, Oncorhynchus kisutch and Salmo salar revealed a rapid turnover of recombination hotspots caused by PRDM9 target motif erosion. Our results imply that PRDM9 function is conserved across vertebrates and that the peculiar evolutionary runaway caused by PRDM9 has been active for several hundred million years.

Indexed as

DNA Breaks, Double-StrandedEvolution, MolecularHistone-Lysine N-MethyltransferaseAnimalsFish ProteinsHistonesMeiosisOncorhynchus mykissPromoter Regions, GeneticRecombination, GeneticSalmonidaeFish ProteinsHistone-Lysine N-MethyltransferaseHistones

Identifiers

PMID39761307
PMCPMC11703093

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.