Evidence map›Paper›PMID 34951404›Full record

ArticleeLife2021

Novel mechanistic insights into the role of Mer2 as the keystone of meiotic DNA break formation.

Dorota Rousová, Vaishnavi Nivsarkar, Veronika Altmannova, Vivek B Raina, Saskia K Funk, David Liedtke, Petra Janning, Franziska Müller, Heidi Reichle, Gerben Vader and 1 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.2field-weighted citation impact, top 11% 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

22 citing papers in PubMed, 35 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
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  5. Structure and function of the synaptonemal complex.The Journal of cell biology · 2026
    Review
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  7. Article
  8. Review
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  11. Article
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  14. The molecular machinery of meiotic recombination.Biochemical Society transactions · 2024
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. 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 at 3 institutions in 2 countries.

Dorota RousováFriedrich Miescher Laboratory of the Max Planck Society, Tübingen, Germany.ORCID 0000-0001-7395-2596
Vaishnavi Nivsarkar *Department of Mechanistic Cell Biology, Max Planck Institute of Molecular Physiology, Dortmund, Germany.
Veronika Altmannova *Friedrich Miescher Laboratory of the Max Planck Society, Tübingen, Germany.
Vivek B Raina *Department of Mechanistic Cell Biology, Max Planck Institute of Molecular Physiology, Dortmund, Germany.ORCID 0000-0003-0507-9208
Saskia K FunkFriedrich Miescher Laboratory of the Max Planck Society, Tübingen, Germany.
David LiedtkeFriedrich Miescher Laboratory of the Max Planck Society, Tübingen, Germany.
Petra JanningDepartment of Chemical Biology, Max Planck Institute of Molecular Physiology, Dortmund, Germany.
Franziska MüllerDepartment of Mechanistic Cell Biology, Max Planck Institute of Molecular Physiology, Dortmund, Germany.
Heidi ReichleFriedrich Miescher Laboratory of the Max Planck Society, Tübingen, Germany.
Gerben VaderDepartment of Mechanistic Cell Biology, Max Planck Institute of Molecular Physiology, Dortmund, Germany.ORCID 0000-0001-5729-0991
John R WeirFriedrich Miescher Laboratory of the Max Planck Society, Tübingen, Germany.ORCID 0000-0002-6904-0284
Max Planck Society · DEMax Planck Institute of Molecular Physiology · DEColumbia University Irving Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In meiosis, DNA double-strand break (DSB) formation by Spo11 initiates recombination and enables chromosome segregation. Numerous factors are required for Spo11 activity, and couple the DSB machinery to the development of a meiosis-specific 'axis-tethered loop' chromosome organisation. Through in vitro reconstitution and budding yeast genetics, we here provide architectural insight into the DSB machinery by focussing on a foundational DSB factor, Mer2. We characterise the interaction of Mer2 with the histone reader Spp1, and show that Mer2 directly associates with nucleosomes, likely highlighting a contribution of Mer2 to tethering DSB factors to chromatin. We reveal the biochemical basis of Mer2 association with Hop1, a HORMA domain-containing chromosomal axis factor. Finally, we identify a conserved region within Mer2 crucial for DSB activity, and show that this region of Mer2 interacts with the DSB factor Mre11. In combination with previous work, we establish Mer2 as a keystone of the DSB machinery by bridging key protein complexes involved in the initiation of meiotic recombination.

Indexed as

DNA Breaks, Double-StrandedMeiosisChromatinSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsChromatinREC107 protein, S cerevisiaeSaccharomyces cerevisiae Proteinsbiochemistrychemical biologychromosomesgene expressionmeiosisnucleosomesprotein-protein interactionsS. cerevisiae

Identifiers

PMID34951404
PMCPMC8848140
OpenAlexW4225808281

What OpenQuestion holds

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Registered trials

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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.