Evidence map›Paper›PMID 41484367›Full record

ArticleThe EMBO journal2026

Pre-meiotic H1.1 degradation is essential for Arabidopsis gametogenesis.

Yanru Li, Danli Fei, Jasmin Schubert, Kinga Rutowicz, Zuzanna Kaczmarska, Alberto Linares, Alejandro Giraldo Fonseca, Sylvain Bischof, Ueli Grossniklaus, Célia Baroux

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 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

10 authors.

Yanru Li *Department of Plant and Microbial Biology & Zurich-Basel Plant Science Center, University of Zurich, Zurich, Switzerland.
Danli Fei *Department of Plant and Microbial Biology & Zurich-Basel Plant Science Center, University of Zurich, Zurich, Switzerland.
Jasmin Schubert *Department of Plant and Microbial Biology & Zurich-Basel Plant Science Center, University of Zurich, Zurich, Switzerland.
Kinga RutowiczDepartment of Plant and Microbial Biology & Zurich-Basel Plant Science Center, University of Zurich, Zurich, Switzerland.
Zuzanna KaczmarskaEuropean Molecular Biology Laboratory (EMBL) Grenoble, Grenoble, France.
Alberto LinaresDepartment of Plant and Microbial Biology & Zurich-Basel Plant Science Center, University of Zurich, Zurich, Switzerland.
Alejandro Giraldo FonsecaDepartment of Plant and Microbial Biology & Zurich-Basel Plant Science Center, University of Zurich, Zurich, Switzerland.
Sylvain BischofDepartment of Plant and Microbial Biology & Zurich-Basel Plant Science Center, University of Zurich, Zurich, Switzerland.
Ueli GrossniklausDepartment of Plant and Microbial Biology & Zurich-Basel Plant Science Center, University of Zurich, Zurich, Switzerland.ORCID http://orcid.org/0000-0002-0522-8974
Célia BarouxDepartment of Plant and Microbial Biology & Zurich-Basel Plant Science Center, University of Zurich, Zurich, Switzerland. cbaroux@botinst.uzh.ch.ORCID http://orcid.org/0000-0001-6307-2229

Funding

EC | Horizon Europe | Excellent Science | HORIZON EUROPE Marie Sklodowska-Curie Actions (MSCA) Grant agreement No. 847585EC | HORIZON EUROPE Framework Programme (Horizon Europe) COST Action CA16212Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (SNF) #310030_185186Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (SNF) 31003A_149974Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (SNF) 31003A_179553Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (SNF) Project Nr 176957
6 · The paper itself

Abstract

Despite being evolutionary distant, plants and animals exhibit a shared phenomenon during the transition from somatic-to-reproductive cell fate marked by extensive structural and compositional changes in chromatin. This chromatin reprogramming occurs in the plant SMCs (Spore Mother Cells) and animal PGCs (primordial germ cells) and is initiated by the loss of linker histones (H1). H1 loss is essential to establish pluripotency in animal PGCs but its role is not known in plants. Here, we identified two regulatory pathways involving a citrullinase and an E3-ubiquitin ligase that contribute H1.1 loss in female SMCs in Arabidopsis. We also identified roles for two specific residues: an arginine, whose positive charge contributes to H1.1 destabilization from chromatin, and a lysine in the globular domain that is essential for H1.1 degradation. Ovules with impaired H1.1 loss in the SMC proceed through sporogenesis but fail to complete gametogenesis. We propose that a citrullination-ubiquitination pathway governs pre-meiotic H1 depletion as a critical mechanism for establishing post-meiotic competence in the Arabidopsis germline.

Indexed as

ArabidopsisArabidopsis ProteinsGametogenesisGametogenesis, PlantHistonesChromatinMeiosisProteolysisUbiquitinationUbiquitin-Protein LigasesArabidopsis ProteinsChromatinHistonesUbiquitin-Protein LigasesArabidopsisCitrullinationGametogenesisLinker HistoneUbiquitination

Identifiers

PMID41484367
PMCPMC12864861

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.