Evidence map›Paper›PMID 24416374›Full record

ArticlePloS one2014

Karyotypic changes through dysploidy persist longer over evolutionary time than polyploid changes.

Marcial Escudero, Santiago Martín-Bravo, Itay Mayrose, Mario Fernández-Mazuecos, Omar Fiz-Palacios, Andrew L Hipp, Manuel Pimentel, Pedro Jiménez-Mejías, Virginia Valcárcel, Pablo Vargas and 1 more

Abstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing 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

33 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Plants (Basel, Switzerland) · 2023
    Article
  11. Using ChromEvol to Determine the Mode of Chromosomal Evolution.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  12. Review
  13. Mixed-Ploidy and Dysploidy inPlants (Basel, Switzerland) · 2022
    Article
  14. Article
  15. Review
  16. Article
  17. Polyploidy Expands the Range ofFrontiers in plant science · 2021
    Article
  18. Article
  19. Article
  20. 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

11 authors.

Marcial EscuderoMolecular Biology and Biochemical Engineering, Pablo de Olavide University, Seville, Spain ; Herbarium, The Morton Arboretum, Lisle, Illinois, United States of America ; Botany, The Field Museum, Chicago, Illinois, United States of America.
Santiago Martín-BravoMolecular Biology and Biochemical Engineering, Pablo de Olavide University, Seville, Spain.
Itay MayroseMolecular Biology and Ecology of Plants, Tel Aviv University, Tel Aviv, Israel.
Mario Fernández-MazuecosBiodiversity and Conservation, Real Jardín Botánico CSIC, Madrid, Spain.
Omar Fiz-PalaciosSystematic Biology, Uppsala University, Uppsala, Sweden.
Andrew L HippHerbarium, The Morton Arboretum, Lisle, Illinois, United States of America ; Botany, The Field Museum, Chicago, Illinois, United States of America.
Manuel PimentelPlant and Animal Biology and Ecology, University of A Coruña, A Coruña, Spain.
Pedro Jiménez-MejíasMolecular Biology and Biochemical Engineering, Pablo de Olavide University, Seville, Spain ; Biodiversity and Conservation, Real Jardín Botánico CSIC, Madrid, Spain.
Virginia ValcárcelBiology, Universidad Autónoma de Madrid, Madrid, Spain.
Pablo VargasBiodiversity and Conservation, Real Jardín Botánico CSIC, Madrid, Spain.
Modesto LuceñoMolecular Biology and Biochemical Engineering, Pablo de Olavide University, Seville, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chromosome evolution has been demonstrated to have profound effects on diversification rates and speciation in angiosperms. While polyploidy has predated some major radiations in plants, it has also been related to decreased diversification rates. There has been comparatively little attention to the evolutionary role of gains and losses of single chromosomes, which may or not entail changes in the DNA content (then called aneuploidy or dysploidy, respectively). In this study we investigate the role of chromosome number transitions and of possible associated genome size changes in angiosperm evolution. We model the tempo and mode of chromosome number evolution and its possible correlation with patterns of cladogenesis in 15 angiosperm clades. Inferred polyploid transitions are distributed more frequently towards recent times than single chromosome gains and losses. This is likely because the latter events do not entail changes in DNA content and are probably due to fission or fusion events (dysploidy), as revealed by an analysis of the relationship between genome size and chromosome number. Our results support the general pattern that recently originated polyploids fail to persist, and suggest that dysploidy may have comparatively longer-term persistence than polyploidy. Changes in chromosome number associated with dysploidy were typically observed across the phylogenies based on a chi-square analysis, consistent with these changes being neutral with respect to diversification.

Indexed as

AneuploidyGenome, PlantChromosomes, PlantDNA, PlantGenetic SpeciationGenome SizeKaryotypingMagnoliopsidaPhylogenyPolyploidyDNA, Plant

Identifiers

PMID24416374
PMCPMC3887030

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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.