Evidence map›Paper›PMID 29374461›Full record

ArticleBMC evolutionary biology2018

Allele phasing is critical to revealing a shared allopolyploid origin of Medicago arborea and M. strasseri (Fabaceae).

Jonna S Eriksson, Filipe de Sousa, Yann J K Bertrand, Alexandre Antonelli, Bengt Oxelman, Bernard E Pfeil

Open access · goldAbstract read
In one paragraph

Article in BMC evolutionary biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
7.4field-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

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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

12 citing papers in PubMed, 38 citations in OpenAlex.

  1. Phylogenetic networks empower biodiversity research.Proceedings of the National Academy of Sciences of the United States of America · 2025
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  7. flopp: Extremely Fast Long-Read Polyploid Haplotype Phasing by Uniform Tree Partitioning.Journal of computational biology : a journal of computational molecular cell biology · 2022
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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 2 institutions in 1 country.

Jonna S ErikssonDepartment of Biological and Environmental Sciences, University of Gothenburg, Box 461, 40530, Gothenburg, Sweden. jonna.eriksson@bioenv.gu.se.
Filipe de SousaDepartment of Biological and Environmental Sciences, University of Gothenburg, Box 461, 40530, Gothenburg, Sweden.
Yann J K BertrandDepartment of Biological and Environmental Sciences, University of Gothenburg, Box 461, 40530, Gothenburg, Sweden.
Alexandre AntonelliDepartment of Biological and Environmental Sciences, University of Gothenburg, Box 461, 40530, Gothenburg, Sweden.
Bengt OxelmanDepartment of Biological and Environmental Sciences, University of Gothenburg, Box 461, 40530, Gothenburg, Sweden.
Bernard E PfeilDepartment of Biological and Environmental Sciences, University of Gothenburg, Box 461, 40530, Gothenburg, Sweden.
Göteborgs Stads · SEUniversity of Gothenburg · SE

Funding

European Research Council 331024Royal Swedish Academy of Sciences 2009-5206
6 · The paper itself

Abstract

backgroundWhole genome duplication plays a central role in plant evolution. There are two main classes of polyploid formation: autopolyploids which arise within one species by doubling of similar homologous genomes; in contrast, allopolyploidy (hybrid polyploidy) arise via hybridization and subsequent doubling of nonhomologous (homoeologous) genomes. The distinction between polyploid origins can be made using gene phylogenies, if alleles from each genome can be correctly retrieved. We examined whether two closely related tetraploid Mediterranean shrubs (Medicago arborea and M. strasseri) have an allopolyploid origin - a question that has remained unsolved despite substantial previous research. We sequenced and analyzed ten low-copy nuclear genes from these and related species, phasing all alleles. To test the efficacy of allele phasing on the ability to recover the evolutionary origin of polyploids, we compared these results to analyses using unphased sequences.

resultsIn eight of the gene trees the alleles inferred from the tetraploids formed two clades, in a non-sister relationship. Each of these clades was more closely related to alleles sampled from other species of Medicago, a pattern typical of allopolyploids. However, we also observed that alleles from one of the remaining genes formed two clades that were sister to one another, as is expected for autopolyploids. Trees inferred from unphased sequences were very different, with the tetraploids often placed in poorly supported and different positions compared to results obtained using phased alleles.

conclusionsThe complex phylogenetic history of M. arborea and M. strasseri is explained predominantly by shared allotetraploidy. We also observed that an increase in woodiness is correlated with polyploidy in this group of species and present a new possibility that woodiness could be a transgressive phenotype. Correctly phased homoeologues are likely to be critical for inferring the hybrid origin of allopolyploid species, when most genes retain more than one homoeologue. Ignoring homoeologous variation by merging the homoeologues can obscure the signal of hybrid polyploid origins and produce inaccurate results.

Indexed as

AllelesPolyploidyBase SequenceEvolution, MolecularGenes, PlantHybridization, GeneticMedicagoPhylogenyPopulation DensitySpecies SpecificityAllele phasingAllopolyploidyAlloppNETAutopolyploidyGene treeHybridizationLegumesMedicagoNetworkNGSPhylogenyWoody

Identifiers

PMID29374461
PMCPMC5787288
OpenAlexW2795018838

What OpenQuestion holds

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LicenceCC BY
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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.