Evidence map›Paper›PMID 33502506›Full record

ArticleMolecular biology and evolution2021

De Novo Mutation and Rapid Protein (Co-)evolution during Meiotic Adaptation in Arabidopsis arenosa.

Magdalena Bohutínská, Vinzenz Handrick, Levi Yant, Roswitha Schmickl, Filip Kolář, Kirsten Bomblies, Pirita Paajanen

Open access · goldAbstract read
In one paragraph

Article in Molecular biology and evolution, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

15 citing papers in PubMed, 29 citations in OpenAlex.

  1. Whole-genome duplication increases genetic diversity and load in outcrossingProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  2. Article
  3. Improved synapsis dynamics accompany meiotic stability inProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Article
  5. Review
  6. Article
  7. Partial cytological diploidization of neoautotetraploid meiosis by induced cross-over rate reduction.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  8. Review
  9. Meiosis in allopolyploid Arabidopsis suecica.The Plant journal : for cell and molecular biology · 2022
    Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Genomic basis of parallel adaptation varies with divergence inProceedings of the National Academy of Sciences of the United States of America · 2021
    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

7 authors at 3 institutions in 4 countries.

Magdalena BohutínskáDepartment of Botany, Faculty of Science, Charles University, Prague, Czech Republic.
Vinzenz HandrickDepartment of Cell and Developmental Biology, John Innes Centre, Norwich, United Kingdom.
Levi YantDepartment of Cell and Developmental Biology, John Innes Centre, Norwich, United Kingdom.
Roswitha SchmicklDepartment of Botany, Faculty of Science, Charles University, Prague, Czech Republic.
Filip KolářDepartment of Botany, Faculty of Science, Charles University, Prague, Czech Republic.
Kirsten BombliesDepartment of Cell and Developmental Biology, John Innes Centre, Norwich, United Kingdom.
Pirita PaajanenDepartment of Cell and Developmental Biology, John Innes Centre, Norwich, United Kingdom.ORCID 0000-0002-0561-3717
John Innes Centre · GBCharles University · CZUniversität Innsbruck · AT

Funding

Biotechnology and Biological Sciences Research Council BB/P013511/1
6 · The paper itself

Abstract

A sudden shift in environment or cellular context necessitates rapid adaptation. A dramatic example is genome duplication, which leads to polyploidy. In such situations, the waiting time for new mutations might be prohibitive; theoretical and empirical studies suggest that rapid adaptation will largely rely on standing variation already present in source populations. Here, we investigate the evolution of meiosis proteins in Arabidopsis arenosa, some of which were previously implicated in adaptation to polyploidy, and in a diploid, habitat. A striking and unexplained feature of prior results was the large number of amino acid changes in multiple interacting proteins, especially in the relatively young tetraploid. Here, we investigate whether selection on meiosis genes is found in other lineages, how the polyploid may have accumulated so many differences, and whether derived variants were selected from standing variation. We use a range-wide sample of 145 resequenced genomes of diploid and tetraploid A. arenosa, with new genome assemblies. We confirmed signals of positive selection in the polyploid and diploid lineages they were previously reported in and find additional meiosis genes with evidence of selection. We show that the polyploid lineage stands out both qualitatively and quantitatively. Compared with diploids, meiosis proteins in the polyploid have more amino acid changes and a higher proportion affecting more strongly conserved sites. We find evidence that in tetraploids, positive selection may have commonly acted on de novo mutations. Several tests provide hints that coevolution, and in some cases, multinucleotide mutations, might contribute to rapid accumulation of changes in meiotic proteins.

Indexed as

Evolution, MolecularTetraploidyAdaptation, BiologicalArabidopsisBiological CoevolutionMeiosisMutationcoevolutionde novo mutationsmeiosispolyploidystanding variation

Identifiers

PMID33502506
PMCPMC8097281
OpenAlexW3121291548

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.