Evidence map›Paper›PMID 37431931›Full record

ArticleThe EMBO journal2023

Characterization of the REC114-MEI4-IHO1 complex regulating meiotic DNA double-strand break formation.

Hamida Laroussi, Ariadna B Juarez-Martinez, Aline Le Roy, Elisabetta Boeri Erba, Frank Gabel, Bernard de Massy, Jan Kadlec

Open access · hybridAbstract read
In one paragraph

Article in The EMBO journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.1field-weighted citation impact, top 8% of its field
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

18 citing papers in PubMed, 20 citations in OpenAlex.

  1. Controlling Meiotic Double-Strand Break Formation in Mice: A Web of Multivalent Protein-Protein Interactions.BioEssays : news and reviews in molecular, cellular and developmental biology · 2026
    Review
  2. Article
  3. Multifaceted and evolutionarily dynamic interactions betweenbioRxiv : the preprint server for biology · 2026
    Article
  4. Structure and function of the synaptonemal complex.The Journal of cell biology · 2026
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Exome sequencing identifies genes for socioeconomic status in 350,770 individuals.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  10. Article
  11. Cryo-EM structures of the Spo11 core complex bound to DNA.Nature structural & molecular biology · 2025
    Article
  12. Article
  13. Article
  14. The molecular machinery of meiotic recombination.Biochemical Society transactions · 2024
    Review
  15. Cryo-EM structure of the Spo11 core complex bound to DNA.bioRxiv : the preprint server for biology · 2023
    Article
  16. Article
  17. Article
  18. 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

7 authors at 2 institutions in 1 country.

Hamida LaroussiUniversité Grenoble Alpes, CNRS, CEA, IBS, Grenoble, France.
Ariadna B Juarez-MartinezUniversité Grenoble Alpes, CNRS, CEA, IBS, Grenoble, France.ORCID 0000-0003-1257-6018
Aline Le RoyUniversité Grenoble Alpes, CNRS, CEA, IBS, Grenoble, France.
Elisabetta Boeri ErbaUniversité Grenoble Alpes, CNRS, CEA, IBS, Grenoble, France.ORCID 0000-0002-5910-4707
Frank GabelUniversité Grenoble Alpes, CNRS, CEA, IBS, Grenoble, France.ORCID 0000-0003-3446-2601
Bernard de MassyInstitut de Génétique Humaine (IGH), Centre National de la Recherche Scientifique, University of Montpellier, Montpellier, France.ORCID 0000-0002-0950-2758
Jan KadlecUniversité Grenoble Alpes, CNRS, CEA, IBS, Grenoble, France.ORCID 0000-0002-4853-6918
Centre National de la Recherche Scientifique · FRUniversité de Montpellier · FR

Funding

European Research Council 883605
6 · The paper itself

Abstract

Meiotic recombination is initiated by the formation of DNA double-strand breaks (DSBs), essential for fertility and genetic diversity. In the mouse, DSBs are formed by the catalytic TOPOVIL complex consisting of SPO11 and TOPOVIBL. To preserve genome integrity, the activity of the TOPOVIL complex is finely controlled by several meiotic factors including REC114, MEI4, and IHO1, but the underlying mechanism is poorly understood. Here, we report that mouse REC114 forms homodimers, that it associates with MEI4 as a 2:1 heterotrimer that further dimerizes, and that IHO1 forms coiled-coil-based tetramers. Using AlphaFold2 modeling combined with biochemical characterization, we uncovered the molecular details of these assemblies. Finally, we show that IHO1 directly interacts with the PH domain of REC114 by recognizing the same surface as TOPOVIBL and another meiotic factor ANKRD31. These results provide strong evidence for the existence of a ternary IHO1-REC114-MEI4 complex and suggest that REC114 could act as a potential regulatory platform mediating mutually exclusive interactions with several partners.

Indexed as

Cell Cycle ProteinsHomologous RecombinationAnimalsDNAMeiosisMiceUbiquitin-Protein LigasesCcnb1ip1 protein, mouseCell Cycle ProteinsDNAIho1 protein, mouseRec114 protein, mouseUbiquitin-Protein LigasesDNA double-strand breaksmeiosisprotein complexesproteins structurerecombination

Identifiers

PMID37431931
PMCPMC10425845
OpenAlexW4383873224

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.