Evidence map›Paper›PMID 27723721›Full record

ArticleNature cell biology2016

Meiotic DNA break formation requires the unsynapsed chromosome axis-binding protein IHO1 (CCDC36) in mice.

Marcello Stanzione, Marek Baumann, Frantzeskos Papanikos, Ihsan Dereli, Julian Lange, Angelique Ramlal, Daniel Tränkner, Hiroki Shibuya, Bernard de Massy, Yoshinori Watanabe and 3 more

Open access · greenAbstract read
In one paragraph

Article in Nature cell biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 115 papers.

0numbers the graph read from it
0cells of the map it votes in
115citing papers in PubMed
9.4field-weighted citation impact, top 2% 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

115 citing papers in PubMed, 191 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. Review
  4. Article
  5. Article
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  7. Article
  8. Structure and function of the synaptonemal complex.The Journal of cell biology · 2026
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. HEIP1 orchestrates pro-crossover protein activity during mammalian meiosis.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  18. Article
  19. Review
  20. Article

55 more citing papers are in PubMed but not listed here.

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

13 authors at 4 institutions in 4 countries.

Marcello StanzioneInstitute of Physiological Chemistry, Faculty of Medicine at the TU Dresden, Fetscherstraße 74, 01307 Dresden, Germany.
Marek BaumannInstitute of Physiological Chemistry, Faculty of Medicine at the TU Dresden, Fetscherstraße 74, 01307 Dresden, Germany.
Frantzeskos PapanikosInstitute of Physiological Chemistry, Faculty of Medicine at the TU Dresden, Fetscherstraße 74, 01307 Dresden, Germany.
Ihsan DereliInstitute of Physiological Chemistry, Faculty of Medicine at the TU Dresden, Fetscherstraße 74, 01307 Dresden, Germany.
Julian LangeMolecular Biology Program, Memorial Sloan Kettering Cancer Center, New York, New York 10065, USA.
Angelique RamlalInstitute of Physiological Chemistry, Faculty of Medicine at the TU Dresden, Fetscherstraße 74, 01307 Dresden, Germany.
Daniel TränknerInstitute of Physiological Chemistry, Faculty of Medicine at the TU Dresden, Fetscherstraße 74, 01307 Dresden, Germany.
Hiroki ShibuyaInstitute of Molecular and Cellular Biosciences, University of Tokyo, Yayoi 1-1-1, Tokyo 113-0032, Japan.
Bernard de MassyInstitute of Human Genetics, UPR 1142, CNRS, University of Montpellier, 141, rue de la Cardonille, 34396 Montpellier, France.
Yoshinori WatanabeInstitute of Molecular and Cellular Biosciences, University of Tokyo, Yayoi 1-1-1, Tokyo 113-0032, Japan.ORCID http://orcid.org/0000-0002-5488-4812
Maria JasinDevelopmental Biology Program, Memorial Sloan Kettering Cancer Center, New York, New York 10065, USA.
Scott KeeneyMolecular Biology Program, Memorial Sloan Kettering Cancer Center, New York, New York 10065, USA.ORCID http://orcid.org/0000-0002-1283-6417
Attila TóthInstitute of Physiological Chemistry, Faculty of Medicine at the TU Dresden, Fetscherstraße 74, 01307 Dresden, Germany.
Technische Universität Dresden · DEMemorial Sloan Kettering Cancer Center · USThe University of Tokyo · JPCentre National de la Recherche Scientifique · FR

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Mechanism and regulation of meiotic recombinationR35GM118092 · NIGMS · SLOAN-KETTERING INST CAN RESEARCH · PI Scott Keeney · 2016 to 2026
$7.0M
Homologous recombination mechanisms in mammalian cellsR35GM118175 · NIGMS · SLOAN-KETTERING INST CAN RESEARCH · PI JASIN, MARIA · 2016 to 2020
$2.6M
Role of Spo11 and recombination in mouse meiosisR01GM105421 · NIGMS · SLOAN-KETTERING INST CAN RESEARCH · PI JASIN, MARIA, KEENEY, SCOTT · 2013 to 2016
$2.4M
NCI NIH HHS P30 CA008748NIGMS NIH HHS R01 GM105421NIGMS NIH HHS R35 GM118092NIGMS NIH HHS R35 GM118175
6 · The paper itself

Abstract

DNA double-strand breaks (DSBs) are induced by SPO11 during meiosis to initiate recombination-mediated pairing and synapsis of homologous chromosomes. Germline genome integrity requires spatiotemporal control of DSB formation, which involves the proteinaceous chromosome axis along the core of each meiotic chromosome. In particular, a component of unsynapsed axes, HORMAD1, promotes DSB formation in unsynapsed regions where DSB formation must occur to ensure completion of synapsis. Despite its importance, the underlying mechanism has remained elusive. We identify CCDC36 as a direct interactor of HORMAD1 (IHO1) that is essential for DSB formation. Underpinning this function, IHO1 and conserved SPO11-auxiliary proteins MEI4 and REC114 assemble chromatin-bound recombinosomes that are predicted activators of DSB formation. HORMAD1 is needed for robust recruitment of IHO1 to unsynapsed axes and efficient formation and/or stabilization of these recombinosomes. Thus, we propose that HORMAD1-IHO1 interaction provides a mechanism for the selective promotion of DSB formation along unsynapsed chromosome axes.

Indexed as

DNA Breaks, Double-StrandedAnimalsCell Cycle ProteinsChromatinDNA ReplicationEndodeoxyribonucleasesMeiosisMeiotic Recombination Protein SPO11Mice, KnockoutNuclear ProteinsRecombination, GeneticSynaptonemal ComplexCell Cycle ProteinsChromatinEndodeoxyribonucleasesMeiotic Recombination Protein SPO11Nohma protein, mouseNuclear Proteins

Identifiers

PMID27723721
PMCPMC5089853
OpenAlexW2529866986

What OpenQuestion holds

Textmetadata
LicenceTDM
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.