Evidence map›Paper›PMID 28615063›Full record

ArticleGenome biology2017

Lineage-specific rediploidization is a mechanism to explain time-lags between genome duplication and evolutionary diversification.

Fiona M Robertson, Manu Kumar Gundappa, Fabian Grammes, Torgeir R Hvidsten, Anthony K Redmond, Sigbjørn Lien, Samuel A M Martin, Peter W H Holland, Simen R Sandve, Daniel J Macqueen

Abstract read
In one paragraph

Article in Genome biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 113 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
113citing papers in PubMed, 1 pooled it
–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

113 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  12. The molecular evolution of vertebrate organs.Nature ecology & evolution · 2026
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53 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

10 authors.

Fiona M RobertsonInstitute of Biological and Environmental Sciences, University of Aberdeen, Aberdeen, AB24 2TZ, UK.
Manu Kumar GundappaInstitute of Biological and Environmental Sciences, University of Aberdeen, Aberdeen, AB24 2TZ, UK.
Fabian GrammesCentre for Integrative Genetics (CIGENE), Faculty of Biosciences, Norwegian University of Life Sciences, Ås, NO-1432, Norway.
Torgeir R HvidstenDepartment of Chemistry, Biotechnology and Food Science, Norwegian University of Life Sciences, 1432, Ås, Norway.
Anthony K RedmondInstitute of Biological and Environmental Sciences, University of Aberdeen, Aberdeen, AB24 2TZ, UK.
Sigbjørn LienCentre for Integrative Genetics (CIGENE), Faculty of Biosciences, Norwegian University of Life Sciences, Ås, NO-1432, Norway.
Samuel A M MartinInstitute of Biological and Environmental Sciences, University of Aberdeen, Aberdeen, AB24 2TZ, UK.
Peter W H HollandDepartment of Zoology, University of Oxford, South Parks Road, Oxford, OX1 3PS, UK.
Simen R SandveCentre for Integrative Genetics (CIGENE), Faculty of Biosciences, Norwegian University of Life Sciences, Ås, NO-1432, Norway.
Daniel J MacqueenInstitute of Biological and Environmental Sciences, University of Aberdeen, Aberdeen, AB24 2TZ, UK. daniel.macqueen@abdn.ac.uk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe functional divergence of duplicate genes (ohnologues) retained from whole genome duplication (WGD) is thought to promote evolutionary diversification. However, species radiation and phenotypic diversification are often temporally separated from WGD. Salmonid fish, whose ancestor underwent WGD by autotetraploidization ~95 million years ago, fit such a 'time-lag' model of post-WGD radiation, which occurred alongside a major delay in the rediploidization process. Here we propose a model, 'lineage-specific ohnologue resolution' (LORe), to address the consequences of delayed rediploidization. Under LORe, speciation precedes rediploidization, allowing independent ohnologue divergence in sister lineages sharing an ancestral WGD event.

resultsUsing cross-species sequence capture, phylogenomics and genome-wide analyses of ohnologue expression divergence, we demonstrate the major impact of LORe on salmonid evolution. One-quarter of each salmonid genome, harbouring at least 4550 ohnologues, has evolved under LORe, with rediploidization and functional divergence occurring on multiple independent occasions >50 million years post-WGD. We demonstrate the existence and regulatory divergence of many LORe ohnologues with functions in lineage-specific physiological adaptations that potentially facilitated salmonid species radiation. We show that LORe ohnologues are enriched for different functions than 'older' ohnologues that began diverging in the salmonid ancestor.

conclusionsLORe has unappreciated significance as a nested component of post-WGD divergence that impacts the functional properties of genes, whilst providing ohnologues available solely for lineage-specific adaptation. Under LORe, which is predicted following many WGD events, the functional outcomes of WGD need not appear 'explosively', but can arise gradually over tens of millions of years, promoting lineage-specific diversification regimes under prevailing ecological pressures.

Indexed as

Evolution, MolecularAdaptation, PhysiologicalAnimalsGenes, DuplicateGenetic SpeciationGenomeGenomicsPhylogenySalmonidaeSyntenyAutotetraploidizationDuplicate genesFunctional divergenceLineage-specific Ohnologue Resolution (LORe)RediploidizationSalmonid fishSpecies radiationWhole genome duplication

Identifiers

PMID28615063
PMCPMC5470254

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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.