Evidence map›Paper›PMID 32461690›Full record

ArticleNature2020

Ensuring meiotic DNA break formation in the mouse pseudoautosomal region.

Laurent Acquaviva, Michiel Boekhout, Mehmet E Karasu, Kevin Brick, Florencia Pratto, Tao Li, Megan van Overbeek, Liisa Kauppi, R Daniel Camerini-Otero, Maria Jasin and 1 more

Abstract read
In one paragraph

Article in Nature, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing 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

68 citing papers in PubMed.

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Laurent AcquavivaMolecular Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA. acquavil@mskcc.org.
Michiel BoekhoutMolecular Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA.ORCID http://orcid.org/0000-0002-9626-438X
Mehmet E KarasuMolecular Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Kevin BrickGenetics and Biochemistry Branch, NIDDK, NIH, Bethesda, MD, USA.
Florencia PrattoGenetics and Biochemistry Branch, NIDDK, NIH, Bethesda, MD, USA.
Tao LiMolecular Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA.ORCID http://orcid.org/0000-0002-5728-3721
Megan van OverbeekMolecular Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Liisa KauppiMolecular Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA.ORCID http://orcid.org/0000-0002-6759-8997
R Daniel Camerini-OteroGenetics and Biochemistry Branch, NIDDK, NIH, Bethesda, MD, USA.
Maria JasinLouis V. Gerstner, Jr. Graduate School of Biomedical Sciences, Memorial Sloan Kettering Cancer Center, New York, NY, USA. m-jasin@ski.mskcc.org.ORCID http://orcid.org/0000-0002-7976-2379
Scott KeeneyMolecular Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA. s-keeney@ski.mskcc.org.ORCID http://orcid.org/0000-0002-1283-6417

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
What determines the location of meiotic crossovers in the mammalian genome?ZIADK052034 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI CAMERINI-OTERO, RAFAEL · 2009 to 2025
$29.8M
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
Acquisition of a DeltaVision OMX SR 3D SIM system for super-resolution imagingS10RR031855 · NCRR · ROCKEFELLER UNIVERSITY · PI NORTH, ALISON JANE · 2011 to 2011
$600k
The Role of Chromatin Architecture in Programmed Double-Strand BreaksF32GM096692 · NIGMS · SLOAN-KETTERING INST CAN RESEARCH · PI VAN OVERBEEK, MEGAN ELIZABETH · 2011 to 2012
$109k
NCI NIH HHS P30 CA008748NCRR NIH HHS S10 RR031855NIGMS NIH HHS F32 GM096692NIGMS NIH HHS R35 GM118092NIGMS NIH HHS R35 GM118175
6 · The paper itself

Abstract

Sex chromosomes in males of most eutherian mammals share only a small homologous segment, the pseudoautosomal region (PAR), in which the formation of double-strand breaks (DSBs), pairing and crossing over must occur for correct meiotic segregation

Indexed as

DNA Breaks, Double-StrandedMeiosisAnimalsCell Cycle ProteinsChromatin Assembly and DisassemblyChromosome PairingDNA-Binding ProteinsFemaleHeterochromatinKineticsMaleMiceMinisatellite RepeatsOocytesPseudoautosomal RegionsRecombination, GeneticAnkrd31 protein, mouseCcnb1ip1 protein, mouseCell Cycle ProteinsDNA-Binding ProteinsHeterochromatinSycp2 protein, mouseUbiquitin-Protein Ligases

Identifiers

PMID32461690
PMCPMC7337327

What OpenQuestion holds

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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.