Evidence map›Paper›PMID 26494791›Full record

ArticleGenes & development2015

DNA methylation epigenetically silences crossover hot spots and controls chromosomal domains of meiotic recombination in Arabidopsis.

Nataliya E Yelina, Christophe Lambing, Thomas J Hardcastle, Xiaohui Zhao, Bruno Santos, Ian R Henderson

Open access · diamondAbstract read
In one paragraph

Article in Genes & development, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 111 papers.

0numbers the graph read from it
0cells of the map it votes in
111citing 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

111 citing papers in PubMed, 212 citations in OpenAlex.

  1. Article
  2. Review
  3. Why recombination hotspots?PLoS genetics · 2026
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Histone variant H2A.W7 represses meiotic crossover formation inProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  12. Review
  13. Article
  14. Dynamic changes in histone lysine lactylation during meiosis prophase I in mouse spermatogenesis.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  15. Heterochromatin in plant meiosis.Nucleus (Austin, Tex.) · 2024
    Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article

51 more citing papers are in PubMed but not listed here.

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

6 authors at 1 institution in 1 country.

Nataliya E YelinaDepartment of Plant Sciences, University of Cambridge, Cambridge CB2 3EA, United Kingdom.
Christophe LambingDepartment of Plant Sciences, University of Cambridge, Cambridge CB2 3EA, United Kingdom.
Thomas J HardcastleDepartment of Plant Sciences, University of Cambridge, Cambridge CB2 3EA, United Kingdom.
Xiaohui ZhaoDepartment of Plant Sciences, University of Cambridge, Cambridge CB2 3EA, United Kingdom.
Bruno SantosDepartment of Plant Sciences, University of Cambridge, Cambridge CB2 3EA, United Kingdom.
Ian R HendersonDepartment of Plant Sciences, University of Cambridge, Cambridge CB2 3EA, United Kingdom.
University of Cambridge · GB

Funding

Biotechnology and Biological Sciences Research Council BB/K007882/1Biotechnology and Biological Sciences Research Council BB/L006847/1Biotechnology and Biological Sciences Research Council BB/M004937/1
6 · The paper itself

Abstract

During meiosis, homologous chromosomes undergo crossover recombination, which is typically concentrated in narrow hot spots that are controlled by genetic and epigenetic information. Arabidopsis chromosomes are highly DNA methylated in the repetitive centromeres, which are also crossover-suppressed. Here we demonstrate that RNA-directed DNA methylation is sufficient to locally silence Arabidopsis euchromatic crossover hot spots and is associated with increased nucleosome density and H3K9me2. However, loss of CG DNA methylation maintenance in met1 triggers epigenetic crossover remodeling at the chromosome scale, with pericentromeric decreases and euchromatic increases in recombination. We used recombination mutants that alter interfering and noninterfering crossover repair pathways (fancm and zip4) to demonstrate that remodeling primarily involves redistribution of interfering crossovers. Using whole-genome bisulfite sequencing, we show that crossover remodeling is driven by loss of CG methylation within the centromeric regions. Using cytogenetics, we profiled meiotic DNA double-strand break (DSB) foci in met1 and found them unchanged relative to wild type. We propose that met1 chromosome structure is altered, causing centromere-proximal DSBs to be inhibited from maturation into interfering crossovers. These data demonstrate that DNA methylation is sufficient to silence crossover hot spots and plays a key role in establishing domains of meiotic recombination along chromosomes.

Indexed as

DNA MethylationEpigenomicsArabidopsisArabidopsis ProteinsCentromereChromosomes, PlantCrossing Over, GeneticDNA Breaks, Double-StrandedDNA (Cytosine-5-)-MethyltransferasesHomologous RecombinationMeiosisMutationNucleosomesArabidopsis ProteinsDNA (Cytosine-5-)-MethyltransferasesMET1 protein, ArabidopsisNucleosomescentromerescrossoverDNA methylationepigeneticshot spotsmeiosis

Identifiers

PMID26494791
PMCPMC4617981
OpenAlexW2144183172

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.