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Genomics of cold adaptations in the Antarctic notothenioid fish radiation

Author

Listed:
  • Iliana Bista

    (Wellcome Genome Campus
    University of Cambridge
    University of Cambridge
    Naturalis Biodiversity Center)

  • Jonathan M. D. Wood

    (Wellcome Genome Campus)

  • Thomas Desvignes

    (University of Oregon, Institute of Neuroscience, 1254 University of Oregon)

  • Shane A. McCarthy

    (Wellcome Genome Campus
    University of Cambridge)

  • Michael Matschiner

    (University of Oslo, Natural History Museum, University of Oslo
    University of Zurich, Department of Palaeontology and Museum, University of Zurich)

  • Zemin Ning

    (Wellcome Genome Campus)

  • Alan Tracey

    (Wellcome Genome Campus)

  • James Torrance

    (Wellcome Genome Campus)

  • Ying Sims

    (Wellcome Genome Campus)

  • William Chow

    (Wellcome Genome Campus)

  • Michelle Smith

    (Wellcome Genome Campus)

  • Karen Oliver

    (Wellcome Genome Campus)

  • Leanne Haggerty

    (Wellcome Genome Campus)

  • Walter Salzburger

    (University of Basel, Zoological Institute, Department of Environmental Sciences)

  • John H. Postlethwait

    (University of Oregon, Institute of Neuroscience, 1254 University of Oregon)

  • Kerstin Howe

    (Wellcome Genome Campus)

  • Melody S. Clark

    (British Antarctic Survey, High Cross)

  • H. William Detrich

    (Northeastern University, Department of Marine and Environmental Sciences, Marine Science Centre)

  • C.-H. Christina Cheng

    (University of Illinois)

  • Eric A. Miska

    (Wellcome Genome Campus
    University of Cambridge)

  • Richard Durbin

    (Wellcome Genome Campus
    University of Cambridge)

Abstract

Numerous novel adaptations characterise the radiation of notothenioids, the dominant fish group in the freezing seas of the Southern Ocean. To improve understanding of the evolution of this iconic fish group, here we generate and analyse new genome assemblies for 24 species covering all major subgroups of the radiation, including five long-read assemblies. We present a new estimate for the onset of the radiation at 10.7 million years ago, based on a time-calibrated phylogeny derived from genome-wide sequence data. We identify a two-fold variation in genome size, driven by expansion of multiple transposable element families, and use the long-read data to reconstruct two evolutionarily important, highly repetitive gene family loci. First, we present the most complete reconstruction to date of the antifreeze glycoprotein gene family, whose emergence enabled survival in sub-zero temperatures, showing the expansion of the antifreeze gene locus from the ancestral to the derived state. Second, we trace the loss of haemoglobin genes in icefishes, the only vertebrates lacking functional haemoglobins, through complete reconstruction of the two haemoglobin gene clusters across notothenioid families. Both the haemoglobin and antifreeze genomic loci are characterised by multiple transposon expansions that may have driven the evolutionary history of these genes.

Suggested Citation

  • Iliana Bista & Jonathan M. D. Wood & Thomas Desvignes & Shane A. McCarthy & Michael Matschiner & Zemin Ning & Alan Tracey & James Torrance & Ying Sims & William Chow & Michelle Smith & Karen Oliver & , 2023. "Genomics of cold adaptations in the Antarctic notothenioid fish radiation," Nature Communications, Nature, vol. 14(1), pages 1-16, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-38567-6
    DOI: 10.1038/s41467-023-38567-6
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    References listed on IDEAS

    as
    1. Arang Rhie & Shane A. McCarthy & Olivier Fedrigo & Joana Damas & Giulio Formenti & Sergey Koren & Marcela Uliano-Silva & William Chow & Arkarachai Fungtammasan & Juwan Kim & Chul Lee & Byung June Ko &, 2021. "Towards complete and error-free genome assemblies of all vertebrate species," Nature, Nature, vol. 592(7856), pages 737-746, April.
    2. Chi-Hing C. Cheng & Liangbiao Chen, 1999. "Evolution of an antifreeze glycoprotein," Nature, Nature, vol. 401(6752), pages 443-444, September.
    3. Alexei J Drummond & Simon Y W Ho & Matthew J Phillips & Andrew Rambaut, 2006. "Relaxed Phylogenetics and Dating with Confidence," PLOS Biology, Public Library of Science, vol. 4(5), pages 1-1, March.
    4. Katie E. Davis & Jon Hill & Tim I. Astrop & Matthew A. Wills, 2016. "Global cooling as a driver of diversification in a major marine clade," Nature Communications, Nature, vol. 7(1), pages 1-8, December.
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    Cited by:

    1. M. S. Clark & J. I. Hoffman & L. S. Peck & L. Bargelloni & D. Gande & C. Havermans & B. Meyer & T. Patarnello & T. Phillips & K. R. Stoof-Leichsenring & D. L. J. Vendrami & A. Beck & G. Collins & M. W, 2023. "Multi-omics for studying and understanding polar life," Nature Communications, Nature, vol. 14(1), pages 1-12, December.

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