Evidence map›Paper›PMID 30161134›Full record

ReviewPLoS genetics2018

PRDM9, a driver of the genetic map.

Corinne Grey, Frédéric Baudat, Bernard de Massy

Open access · goldAbstract readReview
In one paragraph

Review in PLoS genetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed
4.7field-weighted citation impact, top 4% 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

74 citing papers in PubMed, 120 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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  4. Meiotic Recombination in Teleosts.Advances in experimental medicine and biology · 2026
    Review
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14 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

3 authors at 1 institution in 1 country.

Corinne GreyInstitut de Génétique Humaine, Centre National de la Recherche Scientifique, University of Montpellier, Montpellier, France.
Frédéric BaudatInstitut de Génétique Humaine, Centre National de la Recherche Scientifique, University of Montpellier, Montpellier, France.ORCID 0000-0003-2415-8366
Bernard de MassyInstitut de Génétique Humaine, Centre National de la Recherche Scientifique, University of Montpellier, Montpellier, France.ORCID 0000-0002-0950-2758
Université de Montpellier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During meiosis, maternal and paternal chromosomes undergo exchanges by homologous recombination. This is essential for fertility and contributes to genome evolution. In many eukaryotes, sites of meiotic recombination, also called hotspots, are regions of accessible chromatin, but in many vertebrates, their location follows a distinct pattern and is specified by PR domain-containing protein 9 (PRDM9). The specification of meiotic recombination hotspots is achieved by the different activities of PRDM9: DNA binding, histone methyltransferase, and interaction with other proteins. Remarkably, PRDM9 activity leads to the erosion of its own binding sites and the rapid evolution of its DNA-binding domain. PRDM9 may also contribute to reproductive isolation, as it is involved in hybrid sterility potentially due to a reduction of its activity in specific heterozygous contexts.

Indexed as

Chromosome MappingMeiosisAmino Acid SequenceAnimalsBinding SitesDNA-Binding ProteinsEvolution, MolecularFertilityHeterozygoteHistone-Lysine N-MethyltransferaseHomologous RecombinationHumansInfertilityMaleMiceProtein ConformationDNA-Binding ProteinsHistone-Lysine N-MethyltransferasePRDM9 protein, humanprdm9 protein, mouse

Identifiers

PMID30161134
PMCPMC6116924
OpenAlexW2889542049

What OpenQuestion 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 OpenQuestion graph.