Evidence map›Paper›PMID 28854222›Full record

ArticlePLoS genetics2017

rahu is a mutant allele of Dnmt3c, encoding a DNA methyltransferase homolog required for meiosis and transposon repression in the mouse male germline.

Devanshi Jain, Cem Meydan, Julian Lange, Corentin Claeys Bouuaert, Nathalie Lailler, Christopher E Mason, Kathryn V Anderson, Scott Keeney

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

53 citing papers in PubMed, 84 citations in OpenAlex.

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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

8 authors at 2 institutions in 1 country.

Devanshi JainMolecular Biology Program, Memorial Sloan Kettering Cancer Center, New York, United States of America.ORCID http://orcid.org/0000-0002-5027-0549
Cem MeydanDepartment of Physiology and Biophysics, Weill Cornell Medical College, New York, United States of America.ORCID http://orcid.org/0000-0002-0663-6216
Julian LangeMolecular Biology Program, Memorial Sloan Kettering Cancer Center, New York, United States of America.
Corentin Claeys BouuaertMolecular Biology Program, Memorial Sloan Kettering Cancer Center, New York, United States of America.ORCID http://orcid.org/0000-0001-5801-7313
Nathalie LaillerIntegrated Genomics Operation, Memorial Sloan Kettering Cancer Center, New York, United States of America.
Christopher E MasonDepartment of Physiology and Biophysics, Weill Cornell Medical College, New York, United States of America.ORCID http://orcid.org/0000-0002-1850-1642
Kathryn V AndersonDevelopmental Biology Program, Memorial Sloan Kettering Cancer Center, New York, United States of America.ORCID http://orcid.org/0000-0003-1657-2161
Scott KeeneyMolecular Biology Program, Memorial Sloan Kettering Cancer Center, New York, United States of America.ORCID http://orcid.org/0000-0002-1283-6417
Memorial Sloan Kettering Cancer Center · USCornell University · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Isolation of Novel Mutations Affecting the Mouse EmbryoR37HD035455 · NICHD · SLOAN-KETTERING INST CAN RESEARCH · PI ANDERSON, KATHRYN V · 2008 to 2017
$6.9M
NCI NIH HHS P30 CA008748NICHD NIH HHS R37 HD035455
6 · The paper itself

Abstract

Transcriptional silencing by heritable cytosine-5 methylation is an ancient strategy to repress transposable elements. It was previously thought that mammals possess four DNA methyltransferase paralogs-Dnmt1, Dnmt3a, Dnmt3b and Dnmt3l-that establish and maintain cytosine-5 methylation. Here we identify a fifth paralog, Dnmt3c, that is essential for retrotransposon methylation and repression in the mouse male germline. From a phenotype-based forward genetics screen, we isolated a mutant mouse called 'rahu', which displays severe defects in double-strand-break repair and homologous chromosome synapsis during male meiosis, resulting in sterility. rahu is an allele of a transcription unit (Gm14490, renamed Dnmt3c) that was previously mis-annotated as a Dnmt3-family pseudogene. Dnmt3c encodes a cytosine methyltransferase homolog, and Dnmt3crahu mutants harbor a non-synonymous mutation of a conserved residue within one of its cytosine methyltransferase motifs, similar to a mutation in human DNMT3B observed in patients with immunodeficiency, centromeric instability and facial anomalies syndrome. The rahu mutation lies at a potential dimerization interface and near the potential DNA binding interface, suggesting that it compromises protein-protein and/or protein-DNA interactions required for normal DNMT3C function. Dnmt3crahu mutant males fail to establish normal methylation within LINE and LTR retrotransposon sequences in the germline and accumulate higher levels of transposon-derived transcripts and proteins, particularly from distinct L1 and ERVK retrotransposon families. Phylogenetic analysis indicates that Dnmt3c arose during rodent evolution by tandem duplication of Dnmt3b, after the divergence of the Dipodoidea and Muroidea superfamilies. These findings provide insight into the evolutionary dynamics and functional specialization of the transposon suppression machinery critical for mammalian sexual reproduction and epigenetic regulation.

Indexed as

Epigenetic RepressionAllelesAmino Acid SequenceAnimalsChromosome MappingDNA Breaks, Double-StrandedDNA (Cytosine-5-)-MethyltransferasesDNA MethylationDNA RepairGerm CellsInfertility, MaleMaleMeiosisMiceMice, Inbred C57BLMutationDNA (Cytosine-5-)-MethyltransferasesRetroelements

Identifiers

PMID28854222
PMCPMC5607212
OpenAlexW2950392128

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.