Evidence map›Paper›PMID 40856096›Full record

ArticleMolecular ecology2025

Whole Genome Sequencing Reveals How Plasticity and Genetic Differentiation Underlie Sympatric Morphs of Arctic Charr.

Khrystyna Kurta, Mariano Olivera Fedi, Kendall Baker, Tom Barker, Leah Catchpole, Claudio Ciofi, Arianna Cocco, Joanna Collins, Genevieve Diedericks, Maria Angela Diroma and 22 more

Abstract read
In one paragraph

Article in Molecular ecology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

32 authors.

Khrystyna KurtaDepartment of Medical Biochemistry and Microbiology, Uppsala University, Uppsala, Sweden.ORCID 0000-0002-9852-1896
Mariano Olivera FediEarlham Institute, Norwich, UK.
Kendall BakerEarlham Institute, Norwich, UK.
Tom BarkerEarlham Institute, Norwich, UK.
Leah CatchpoleEarlham Institute, Norwich, UK.
Claudio CiofiDepartment of Biology, University of Florence, Sesto Fiorentino, Italy.ORCID 0000-0001-8537-8659
Arianna CoccoDepartment of Medical Biochemistry and Microbiology, Uppsala University, Uppsala, Sweden.
Joanna CollinsTree of Life, Wellcome Sanger Institute, Hinxton, UK.
Genevieve DiedericksDepartment of Biology, University of Antwerp, Antwerp, Belgium.
Maria Angela DiromaDepartment of Biology, University of Florence, Sesto Fiorentino, Italy.
Alex DurrantEarlham Institute, Norwich, UK.
Kjetil HindarNorwegian Institute for Nature Research (NINA), Trondheim, Norway.ORCID 0000-0002-2769-2284
Alessio IannucciDepartment of Biology, University of Florence, Sesto Fiorentino, Italy.ORCID 0000-0001-7729-4412
Naomi IrishEarlham Institute, Norwich, UK.
Vanda KnitlhofferEarlham Institute, Norwich, UK.
Linda LaikreDepartment of Zoology, Stockholm University, Stockholm, Sweden.ORCID 0000-0001-9286-3361
Henrique G LeitãoDepartment of Biology, University of Antwerp, Antwerp, Belgium.
Sacha LucchiniEarlham Institute, Norwich, UK.
Seanna McTaggartEarlham Institute, Norwich, UK.
Arnar PálssonInstitute of Life- and Environmental Sciences, University of Iceland, Reykjavík, Iceland.ORCID 0000-0002-6525-8112
Mats E PetterssonDepartment of Medical Biochemistry and Microbiology, Uppsala University, Uppsala, Sweden.ORCID 0000-0002-7372-9076
Nils RymanDepartment of Zoology, Stockholm University, Stockholm, Sweden.ORCID 0000-0003-3342-8479
Sigurður S SnorrasonInstitute of Life- and Environmental Sciences, University of Iceland, Reykjavík, Iceland.
Hannes SvardalDepartment of Biology, University of Antwerp, Antwerp, Belgium.
David SwarbreckEarlham Institute, Norwich, UK.
Robert M WaterhouseDepartment of Ecology and Evolution, University of Lausanne, Lausanne, Switzerland.
Christopher WatkinsEarlham Institute, Norwich, UK.
Jonathan M D WoodTree of Life, Wellcome Sanger Institute, Hinxton, UK.ORCID 0000-0002-7545-2162
Han XiaoInstitute of Life- and Environmental Sciences, University of Iceland, Reykjavík, Iceland.ORCID 0009-0000-4699-5590
Karim GharbiEarlham Institute, Norwich, UK.
Zophonías O JónssonInstitute of Life- and Environmental Sciences, University of Iceland, Reykjavík, Iceland.ORCID 0000-0001-5798-9647
Leif AnderssonDepartment of Medical Biochemistry and Microbiology, Uppsala University, Uppsala, Sweden.ORCID 0000-0002-4085-6968

Funding

EPAKnut och Alice Wallenbergs Stiftelse KAW2023.0160Science for Life LaboratoryVetenskapsrådet 2017-02907
6 · The paper itself

Abstract

Salmonids have a remarkable ability to form sympatric morphs after postglacial colonisation of freshwater lakes. These morphs often differ in morphology, feeding and spawning behaviour. Here, we explored the genetic basis of morph differentiation in Arctic charr (n = 283) by first establishing a high-quality reference genome and then using this in whole genome sequencing of distinct morphs present in two Norwegian and two Icelandic lakes. The four lakes represent the spectrum of genetic differentiation between morphs from one lake with no genetic differentiation between morphs, implying phenotypic plasticity, to two lakes with locus-specific genetic differentiation, implying incomplete reproductive isolation, and one lake with strong genome-wide divergence consistent with complete reproductive isolation. As many as 12 putative inversions ranging from 0.45 to 3.25 Mbp in size segregated among the four morphs present in one lake, Thingvallavatn, and these contributed significantly to the genetic differentiation among morphs. None of the putative inversions were found in any of the other lakes, but there were cases of partial haplotype sharing in similar morph contrasts in other lakes. Our findings are consistent with a highly polygenic basis of morph differentiation with population-specific selection on alleles linked to the development of similar morph phenotypes. The results support a model where morph differentiation is first established through phenotypic plasticity, leading to niche expansion and separation. This may be followed by gradual development of reproductive isolation, locus-specific differentiation and eventually complete reproductive isolation and genome-wide divergence.

Indexed as

Genetic SpeciationGenetic VariationSympatryTroutWhole Genome SequencingAnimalsFemaleLakesMaleadaptationArctic charrgenetic differentiationphenotypic plasticitysympatric morphswhole genome sequencing

Identifiers

PMID40856096
PMCPMC12456120

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.