Evidence map›Paper›PMID 41233617›Full record

ArticleThe EMBO journal2026

A mammalian-like piRNA pathway in Axolotl reveals the origins of piRNA-directed DNA methylation.

Xinyu Xiang, Anni Gao, Dominik Handler, Francisco Falcon, Diego Rodriguez-Terrones, Sergej Nowoshilow, Wanlu Liu, Elly M Tanaka, Dónal O'Carroll

Abstract read
In one paragraph

Article in The EMBO journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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

9 authors.

Xinyu XiangCentre for Regenerative Medicine, Institute for Regeneration and Repair, Institute for Stem Cell Research, University of Edinburgh, 5 Little France Drive, Edinburgh, EH16 4UU, UK.
Anni GaoZhejiang University-University of Edinburgh Institute (ZJU-UoE Institute), Zhejiang University School of Medicine, International Campus, Zhejiang University, 314400, Haining, China.ORCID http://orcid.org/0009-0007-1733-6554
Dominik HandlerInstitute of Molecular Biotechnology of the Austrian Academy of Sciences (IMBA), Vienna BioCenter (VBC), Campus Vienna Biocenter, Vienna, 1030, Austria.ORCID http://orcid.org/0000-0002-1059-4960
Francisco FalconInstitute of Molecular Pathology (IMP), Vienna Biocenter (VBC), Campus Vienna Biocenter, Vienna, 1030, Austria.
Diego Rodriguez-TerronesInstitute of Molecular Pathology (IMP), Vienna Biocenter (VBC), Campus Vienna Biocenter, Vienna, 1030, Austria.
Sergej NowoshilowInstitute of Molecular Pathology (IMP), Vienna Biocenter (VBC), Campus Vienna Biocenter, Vienna, 1030, Austria.ORCID http://orcid.org/0000-0001-8360-5010
Wanlu LiuZhejiang University-University of Edinburgh Institute (ZJU-UoE Institute), Zhejiang University School of Medicine, International Campus, Zhejiang University, 314400, Haining, China.ORCID http://orcid.org/0000-0001-5963-2908
Elly M TanakaInstitute of Molecular Pathology (IMP), Vienna Biocenter (VBC), Campus Vienna Biocenter, Vienna, 1030, Austria.ORCID http://orcid.org/0000-0003-4240-2158
Dónal O'CarrollCentre for Regenerative Medicine, Institute for Regeneration and Repair, Institute for Stem Cell Research, University of Edinburgh, 5 Little France Drive, Edinburgh, EH16 4UU, UK. donal.ocarroll@ed.ac.uk.ORCID http://orcid.org/0000-0002-8626-2217

Funding

| National Natural Science Foundation of China-Guangdong Joint Fund (-) 32170551Wellcome Trust 092076Wellcome Trust 106144Wellcome Trust 108504Wellcome Trust 203149Wellcome Trust 225237Wellcome Trust 226791
6 · The paper itself

Abstract

The piRNA pathway protects animal germlines from active transposons. Mammals employ a cytoplasmic pathway to destroy transposon transcripts during germline reprogramming. This post-transcriptional mechanism is ancient and found throughout the animal kingdom. A nuclear piRNA pathway mediates transposon DNA re-methylation, which is believed to be bespoke to mammals. However, when exactly piRNA-directed DNA methylation evolved remains unknown. We found that a mammalian-like piRNA pathway evolved early in tetrapod evolution and is found and expressed in its current configuration in the axolotl salamander. Analysis of axolotl testes and oocytes revealed diverse repertoires of piRNAs and pervasive post-transcriptional targeting of young transposons. We identified high levels of genome methylation in axolotl spermatozoa, with full-length transposons being heavily methylated. Our findings reveal that the mammalian nuclear piRNA pathway has ancient vertebrate origins, and it has likely been safeguarding the germline throughout most of tetrapod evolution. Thus, the emergence of piRNA-directed DNA methylation is a pivotal epigenetic evolutionary event that may have laid the foundation for germline reprogramming and genomic imprinting.

Indexed as

Ambystoma mexicanumDNA MethylationRNA, Small InterferingAnimalsDNA Transposable ElementsEvolution, MolecularFemaleGenomic ImprintingMaleOocytesPiwi-Interacting RNASpermatozoaTestisDNA Transposable ElementsPiwi-Interacting RNARNA, Small InterferingDNA MethylationGenomic ImprintingGermlineGermline ReprogrammingpiRNATransposon

Identifiers

PMID41233617
PMCPMC7618676

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.