Evidence map›Paper›PMID 38676941›Full record

ArticleNucleic acids research2024

Simultaneous profiling of chromatin accessibility and DNA methylation in complete plant genomes using long-read sequencing.

Basile Leduque, Alejandro Edera, Clémentine Vitte, Leandro Quadrana

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
5.1field-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

13 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
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  3. Single-molecule views of chromatin accessibility and structure during photomorphogenesis.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
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  6. Targeting NHypertension (Dallas, Tex. : 1979) · 2025
    Article
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  12. DNA methylation in wheat: current understanding and future potential for enhancing biotic and abiotic stress tolerance.Physiology and molecular biology of plants : an international journal of functional plant biology · 2024
    Review
  13. 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

4 authors at 2 institutions in 1 country.

Basile LeduqueInstitute of Plant Sciences Paris-Saclay, Centre Nationale de la Recherche Scientifique, Institute National de la Recherche Agronomique, Université Evry, Université Paris-Saclay, Orsay, France.
Alejandro EderaInstitute of Plant Sciences Paris-Saclay, Centre Nationale de la Recherche Scientifique, Institute National de la Recherche Agronomique, Université Evry, Université Paris-Saclay, Orsay, France.
Clémentine VitteUniversité Paris-Saclay, INRAE, CNRS, AgroParisTech, GQE - Le Moulon, Gif-sur-Yvette, France.
Leandro QuadranaInstitute of Plant Sciences Paris-Saclay, Centre Nationale de la Recherche Scientifique, Institute National de la Recherche Agronomique, Université Evry, Université Paris-Saclay, Orsay, France.ORCID 0000-0001-6279-211X
Université Paris-Saclay · FRCentre National de la Recherche Scientifique · FR

Funding

Agence Nationale de la Recherche ANR-22-CE20-0001European Research CouncilEuropean Union's Horizon 2020 948674LabEx Saclay Plant Sciences-SPS ANR-10-LABX-0040-SPS
6 · The paper itself

Abstract

Epigenetic regulations, including chromatin accessibility, nucleosome positioning and DNA methylation intricately shape genome function. However, current chromatin profiling techniques relying on short-read sequencing technologies fail to characterise highly repetitive genomic regions and cannot detect multiple chromatin features simultaneously. Here, we performed Simultaneous Accessibility and DNA Methylation Sequencing (SAM-seq) of purified plant nuclei. Thanks to the use of long-read nanopore sequencing, SAM-seq enables high-resolution profiling of m6A-tagged chromatin accessibility together with endogenous cytosine methylation in plants. Analysis of naked genomic DNA revealed significant sequence preference biases of m6A-MTases, controllable through a normalisation step. By applying SAM-seq to Arabidopsis and maize nuclei we obtained fine-grained accessibility and DNA methylation landscapes genome-wide. We uncovered crosstalk between chromatin accessibility and DNA methylation within nucleosomes of genes, TEs, and centromeric repeats. SAM-seq also detects DNA footprints over cis-regulatory regions. Furthermore, using the single-molecule information provided by SAM-seq we identified extensive cellular heterogeneity at chromatin domains with antagonistic chromatin marks, suggesting that bivalency reflects cell-specific regulations. SAM-seq is a powerful approach to simultaneously study multiple epigenetic features over unique and repetitive sequences, opening new opportunities for the investigation of epigenetic mechanisms.

Indexed as

ArabidopsisChromatinDNA MethylationGenome, PlantZea maysCell NucleusDNA, PlantEpigenesis, GeneticHigh-Throughput Nucleotide SequencingNanopore SequencingNucleosomesSequence Analysis, DNAChromatinDNA, PlantNucleosomes

Identifiers

PMID38676941
PMCPMC11194078
OpenAlexW4395695971

What OpenQuestion holds

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LicenceCC BY-NC
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.