IDEAS home Printed from https://ideas.repec.org/a/nat/nature/v583y2020i7817d10.1038_s41586-020-2486-3.html
   My bibliography  Save this article

Six reference-quality genomes reveal evolution of bat adaptations

Author

Listed:
  • David Jebb

    (Max Planck Institute of Molecular Cell Biology and Genetics
    Max Planck Institute for the Physics of Complex Systems
    Center for Systems Biology Dresden)

  • Zixia Huang

    (University College Dublin)

  • Martin Pippel

    (Max Planck Institute of Molecular Cell Biology and Genetics
    Center for Systems Biology Dresden)

  • Graham M. Hughes

    (University College Dublin)

  • Ksenia Lavrichenko

    (Max Planck Institute for Psycholinguistics)

  • Paolo Devanna

    (Max Planck Institute for Psycholinguistics)

  • Sylke Winkler

    (Max Planck Institute of Molecular Cell Biology and Genetics)

  • Lars S. Jermiin

    (University College Dublin
    Australian National University
    University College Dublin)

  • Emilia C. Skirmuntt

    (University of Oxford)

  • Aris Katzourakis

    (University of Oxford)

  • Lucy Burkitt-Gray

    (University College Dublin)

  • David A. Ray

    (Texas Tech University)

  • Kevin A. M. Sullivan

    (Texas Tech University)

  • Juliana G. Roscito

    (Max Planck Institute of Molecular Cell Biology and Genetics
    Max Planck Institute for the Physics of Complex Systems
    Center for Systems Biology Dresden)

  • Bogdan M. Kirilenko

    (Max Planck Institute of Molecular Cell Biology and Genetics
    Max Planck Institute for the Physics of Complex Systems
    Center for Systems Biology Dresden)

  • Liliana M. Dávalos

    (Stony Brook University
    Stony Brook University)

  • Angelique P. Corthals

    (John Jay College of Criminal Justice)

  • Megan L. Power

    (University College Dublin)

  • Gareth Jones

    (University of Bristol)

  • Roger D. Ransome

    (University of Bristol)

  • Dina K. N. Dechmann

    (Max Planck Institute of Animal Behavior
    University of Konstanz
    Smithsonian Tropical Research Institute)

  • Andrea G. Locatelli

    (University College Dublin)

  • Sébastien J. Puechmaille

    (ISEM, University of Montpellier
    University of Greifswald)

  • Olivier Fedrigo

    (The Rockefeller University)

  • Erich D. Jarvis

    (The Rockefeller University
    The Rockefeller University
    Howard Hughes Medical Institute)

  • Michael Hiller

    (Max Planck Institute of Molecular Cell Biology and Genetics
    Max Planck Institute for the Physics of Complex Systems
    Center for Systems Biology Dresden)

  • Sonja C. Vernes

    (Max Planck Institute for Psycholinguistics
    Cognition and Behaviour)

  • Eugene W. Myers

    (Max Planck Institute of Molecular Cell Biology and Genetics
    Center for Systems Biology Dresden
    Technical University Dresden)

  • Emma C. Teeling

    (University College Dublin)

Abstract

Bats possess extraordinary adaptations, including flight, echolocation, extreme longevity and unique immunity. High-quality genomes are crucial for understanding the molecular basis and evolution of these traits. Here we incorporated long-read sequencing and state-of-the-art scaffolding protocols1 to generate, to our knowledge, the first reference-quality genomes of six bat species (Rhinolophus ferrumequinum, Rousettus aegyptiacus, Phyllostomus discolor, Myotis myotis, Pipistrellus kuhlii and Molossus molossus). We integrated gene projections from our ‘Tool to infer Orthologs from Genome Alignments’ (TOGA) software with de novo and homology gene predictions as well as short- and long-read transcriptomics to generate highly complete gene annotations. To resolve the phylogenetic position of bats within Laurasiatheria, we applied several phylogenetic methods to comprehensive sets of orthologous protein-coding and noncoding regions of the genome, and identified a basal origin for bats within Scrotifera. Our genome-wide screens revealed positive selection on hearing-related genes in the ancestral branch of bats, which is indicative of laryngeal echolocation being an ancestral trait in this clade. We found selection and loss of immunity-related genes (including pro-inflammatory NF-κB regulators) and expansions of anti-viral APOBEC3 genes, which highlights molecular mechanisms that may contribute to the exceptional immunity of bats. Genomic integrations of diverse viruses provide a genomic record of historical tolerance to viral infection in bats. Finally, we found and experimentally validated bat-specific variation in microRNAs, which may regulate bat-specific gene-expression programs. Our reference-quality bat genomes provide the resources required to uncover and validate the genomic basis of adaptations of bats, and stimulate new avenues of research that are directly relevant to human health and disease1.

Suggested Citation

  • David Jebb & Zixia Huang & Martin Pippel & Graham M. Hughes & Ksenia Lavrichenko & Paolo Devanna & Sylke Winkler & Lars S. Jermiin & Emilia C. Skirmuntt & Aris Katzourakis & Lucy Burkitt-Gray & David , 2020. "Six reference-quality genomes reveal evolution of bat adaptations," Nature, Nature, vol. 583(7817), pages 578-584, July.
  • Handle: RePEc:nat:nature:v:583:y:2020:i:7817:d:10.1038_s41586-020-2486-3
    DOI: 10.1038/s41586-020-2486-3
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41586-020-2486-3
    File Function: Abstract
    Download Restriction: Access to the full text of the articles in this series is restricted.

    File URL: https://libkey.io/10.1038/s41586-020-2486-3?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    As the access to this document is restricted, you may want to search for a different version of it.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:nature:v:583:y:2020:i:7817:d:10.1038_s41586-020-2486-3. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.