Evidence map›Paper›PMID 41203935›Full record

ArticleNature plants2025

Major alleles of CDCA7 shape CG methylation in Arabidopsis thaliana.

Pierre Bourguet, Zdravko J Lorković, Darya Kripkiy Casado, Valentin Bapteste, Chung Hyun Cho, Anna A Igolkina, Cheng-Ruei Lee, Magnus Nordborg, Frédéric Berger, Eriko Sasaki

Abstract read
In one paragraph

Article in Nature plants, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. CDCA7 facilitates MET1-mediated CG DNA methylation maintenance in centromeric heterochromatin via linker histone H1.Proceedings of the National Academy of Sciences of the United States of America · 2025
    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

10 authors.

Pierre BourguetGregor Mendel Institute of Molecular Plant Biology, Austrian Academy of Sciences, Vienna BioCenter, Vienna, Austria. pierre.bourguet@gmi.oeaw.ac.at.ORCID 0000-0002-5019-4179
Zdravko J LorkovićGregor Mendel Institute of Molecular Plant Biology, Austrian Academy of Sciences, Vienna BioCenter, Vienna, Austria.ORCID 0000-0002-3074-7258
Darya Kripkiy CasadoGregor Mendel Institute of Molecular Plant Biology, Austrian Academy of Sciences, Vienna BioCenter, Vienna, Austria.
Valentin BaptesteGregor Mendel Institute of Molecular Plant Biology, Austrian Academy of Sciences, Vienna BioCenter, Vienna, Austria.
Chung Hyun ChoGregor Mendel Institute of Molecular Plant Biology, Austrian Academy of Sciences, Vienna BioCenter, Vienna, Austria.ORCID 0000-0003-3105-8750
Anna A IgolkinaGregor Mendel Institute of Molecular Plant Biology, Austrian Academy of Sciences, Vienna BioCenter, Vienna, Austria.
Cheng-Ruei LeeInstitute of Ecology and Evolutionary Biology, National Taiwan University, Taipei, Taiwan.ORCID 0000-0002-1913-9964
Magnus NordborgGregor Mendel Institute of Molecular Plant Biology, Austrian Academy of Sciences, Vienna BioCenter, Vienna, Austria.ORCID 0000-0001-7178-9748
Frédéric BergerGregor Mendel Institute of Molecular Plant Biology, Austrian Academy of Sciences, Vienna BioCenter, Vienna, Austria. frederic.berger@gmi.oeaw.ac.at.ORCID 0000-0002-3609-8260
Eriko SasakiFaculty of Science, Kyushu University, Fukuoka, Japan. sasaki.eriko.997@m.kyushu-u.ac.jp.ORCID 0000-0002-0878-364X

Funding

Austrian Science Fund (Fonds zur Förderung der Wissenschaftlichen Forschung) P32054Austrian Science Fund (Fonds zur Förderung der Wissenschaftlichen Forschung) P33380Austrian Science Fund (Fonds zur Förderung der Wissenschaftlichen Forschung) PAT6138924EC | EU Framework Programme for Research and Innovation H2020 | H2020 Priority Excellent Science | H2020 Marie Sklodowska-Curie Actions (H2020 Excellent Science - Marie Sklodowska-Curie Actions) 847548MEXT | Japan Society for the Promotion of Science (JSPS) 20 K22671MEXT | Japan Society for the Promotion of Science (JSPS) 21 H02538
6 · The paper itself

Abstract

DNA methylation is a key epigenetic mark that impacts gene expression and represses transposable elements in eukaryotes. Numerous examples of cis elements targeted by DNA methylation, particularly at CG sites (mCG), have been reported to be under selective pressure in animals and plants. By contrast, there is limited knowledge of trans regulators of mCG leading to adaptation. Here, a genome-wide association study identifies CELL DIVISION CYCLE-ASSOCIATED PROTEIN 7 (CDCA7) as a major trans determinant of mCG in natural populations of Arabidopsis thaliana. CDCA7 or its paralogue physically binds the chromatin remodeller DECREASE IN DNA METHYLATION 1 (DDM1), which facilitates access of methyltransferases to DNA. Epigenomic analysis shows that while CDCA7 proteins control all DDM1-dependent processes, their predominant function is the maintenance of mCG. We identify a 26-bp promoter indel modulating CDCA7 expression in natural populations and determining the degree of mCG and transposable element silencing. The geographic distribution of CDCA7 alleles suggests that new alleles have repeatedly expanded to novel ecological niches, indicating a potential role in local adaptation. Our findings establish CDCA7 proteins as dedicated regulators of mCG and imply that DDM1 relies on alternative partners to regulate other chromatin features. Broadly, they illustrate how changes in global DNA methylation levels through transcriptional regulation of the epigenetic machinery have the capacity to facilitate local adaptation.

Indexed as

ArabidopsisArabidopsis ProteinsCell Cycle ProteinsDNA MethylationAllelesEpigenesis, GeneticGene Expression Regulation, PlantGenome-Wide Association StudyArabidopsis ProteinsCell Cycle Proteins

Identifiers

PMID41203935
PMCPMC12711577

What OpenQuestion holds

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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.