IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v14y2023i1d10.1038_s41467-023-41784-8.html
   My bibliography  Save this article

The admixed brushtail possum genome reveals invasion history in New Zealand and novel imprinted genes

Author

Listed:
  • Donna M. Bond

    (University of Otago)

  • Oscar Ortega-Recalde

    (University of Otago)

  • Melanie K. Laird

    (University of Otago)

  • Takashi Hayakawa

    (Hokkaido University)

  • Kyle S. Richardson

    (University of Otago
    University of Montana Western)

  • Finlay.C. B. Reese

    (University of Otago)

  • Bruce Kyle

    (University of Otago)

  • Brooke E. McIsaac-Williams

    (University of Otago)

  • Bruce C. Robertson

    (University of Otago)

  • Yolanda Heezik

    (University of Otago)

  • Amy L. Adams

    (University of Otago)

  • Wei-Shan Chang

    (The University of Sydney
    CSIRO)

  • Bettina Haase

    (The Rockefeller University)

  • Jacquelyn Mountcastle

    (The Rockefeller University)

  • Maximilian Driller

    (Leibniz Institute for Zoo and Wildlife Research)

  • Joanna Collins

    (Wellcome Sanger Institute)

  • Kerstin Howe

    (Wellcome Sanger Institute)

  • Yasuhiro Go

    (Hyogo University
    National Institutes of Natural Sciences
    National Institute for Physiological Sciences)

  • Francoise Thibaud-Nissen

    (National Institutes of Health)

  • Nicholas C. Lister

    (UNSW Sydney)

  • Paul D. Waters

    (UNSW Sydney)

  • Olivier Fedrigo

    (The Rockefeller University)

  • Erich D. Jarvis

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

  • Neil J. Gemmell

    (University of Otago)

  • Alana Alexander

    (University of Otago)

  • Timothy A. Hore

    (University of Otago)

Abstract

Combining genome assembly with population and functional genomics can provide valuable insights to development and evolution, as well as tools for species management. Here, we present a chromosome-level genome assembly of the common brushtail possum (Trichosurus vulpecula), a model marsupial threatened in parts of their native range in Australia, but also a major introduced pest in New Zealand. Functional genomics reveals post-natal activation of chemosensory and metabolic genes, reflecting unique adaptations to altricial birth and delayed weaning, a hallmark of marsupial development. Nuclear and mitochondrial analyses trace New Zealand possums to distinct Australian subspecies, which have subsequently hybridised. This admixture allowed phasing of parental alleles genome-wide, ultimately revealing at least four genes with imprinted, parent-specific expression not yet detected in other species (MLH1, EPM2AIP1, UBP1 and GPX7). We find that reprogramming of possum germline imprints, and the wider epigenome, is similar to eutherian mammals except onset occurs after birth. Together, this work is useful for genetic-based control and conservation of possums, and contributes to understanding of the evolution of novel mammalian epigenetic traits.

Suggested Citation

  • Donna M. Bond & Oscar Ortega-Recalde & Melanie K. Laird & Takashi Hayakawa & Kyle S. Richardson & Finlay.C. B. Reese & Bruce Kyle & Brooke E. McIsaac-Williams & Bruce C. Robertson & Yolanda Heezik & A, 2023. "The admixed brushtail possum genome reveals invasion history in New Zealand and novel imprinted genes," Nature Communications, Nature, vol. 14(1), pages 1-17, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-41784-8
    DOI: 10.1038/s41467-023-41784-8
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-023-41784-8
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-023-41784-8?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
    ---><---

    References listed on IDEAS

    as
    1. Tarjei S. Mikkelsen & Matthew J. Wakefield & Bronwen Aken & Chris T. Amemiya & Jean L. Chang & Shannon Duke & Manuel Garber & Andrew J. Gentles & Leo Goodstadt & Andreas Heger & Jerzy Jurka & Michael , 2007. "Genome of the marsupial Monodelphis domestica reveals innovation in non-coding sequences," Nature, Nature, vol. 447(7141), pages 167-177, May.
    2. 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.
    3. Jennifer Grant & Shantha K. Mahadevaiah & Pavel Khil & Mahesh N. Sangrithi & Hélène Royo & Janine Duckworth & John R. McCarrey & John L. VandeBerg & Marilyn B. Renfree & Willie Taylor & Greg Elgar & R, 2012. "Rsx is a metatherian RNA with Xist-like properties in X-chromosome inactivation," Nature, Nature, vol. 487(7406), pages 254-258, July.
    4. Norimasa Iwanami & Divine-Fondzenyuy Lawir & Katarzyna Sikora & Connor O´Meara & Kohei Takeshita & Michael Schorpp & Thomas Boehm, 2020. "Transgenerational inheritance of impaired larval T cell development in zebrafish," Nature Communications, Nature, vol. 11(1), pages 1-13, December.
    5. Ksenia Skvortsova & Katsiaryna Tarbashevich & Martin Stehling & Ryan Lister & Manuel Irimia & Erez Raz & Ozren Bogdanovic, 2019. "Retention of paternal DNA methylome in the developing zebrafish germline," Nature Communications, Nature, vol. 10(1), pages 1-13, December.
    Full references (including those not matched with items on IDEAS)

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. 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.
    2. Heiner Kuhl & Kang Du & Manfred Schartl & Lukáš Kalous & Matthias Stöck & Dunja K. Lamatsch, 2022. "Equilibrated evolution of the mixed auto-/allopolyploid haplotype-resolved genome of the invasive hexaploid Prussian carp," Nature Communications, Nature, vol. 13(1), pages 1-11, December.
    3. Ashley T. Sendell-Price & Frank J. Tulenko & Mats Pettersson & Du Kang & Margo Montandon & Sylke Winkler & Kathleen Kulb & Gavin P. Naylor & Adam Phillippy & Olivier Fedrigo & Jacquelyn Mountcastle & , 2023. "Low mutation rate in epaulette sharks is consistent with a slow rate of evolution in sharks," Nature Communications, Nature, vol. 14(1), pages 1-13, December.
    4. Zhen Huang & Ivanete De O. Furo & Jing Liu & Valentina Peona & Anderson J. B. Gomes & Wan Cen & Hao Huang & Yanding Zhang & Duo Chen & Ting Xue & Qiujin Zhang & Zhicao Yue & Quanxi Wang & Lingyu Yu & , 2022. "Recurrent chromosome reshuffling and the evolution of neo-sex chromosomes in parrots," Nature Communications, Nature, vol. 13(1), pages 1-11, December.
    5. Allegra Angeloni & Skye Fissette & Deniz Kaya & Jillian M. Hammond & Hasindu Gamaarachchi & Ira W. Deveson & Robert J. Klose & Weiming Li & Xiaotian Zhang & Ozren Bogdanovic, 2024. "Extensive DNA methylome rearrangement during early lamprey embryogenesis," Nature Communications, Nature, vol. 15(1), pages 1-14, December.
    6. Cassie L. Kemmler & Jana Smolikova & Hannah R. Moran & Brandon J. Mannion & Dunja Knapp & Fabian Lim & Anna Czarkwiani & Viviana Hermosilla Aguayo & Vincent Rapp & Olivia E. Fitch & Seraina Bötschi & , 2023. "Conserved enhancers control notochord expression of vertebrate Brachyury," Nature Communications, Nature, vol. 14(1), pages 1-18, December.
    7. Sarah Morrison-Smith & Christina Boucher & Aleksandra Sarcevic & Noelle Noyes & Catherine O’Brien & Nazaret Cuadros & Jaime Ruiz, 2022. "Challenges in large-scale bioinformatics projects," Palgrave Communications, Palgrave Macmillan, vol. 9(1), pages 1-9, December.
    8. Joanna Hård & Jeff E. Mold & Jesper Eisfeldt & Christian Tellgren-Roth & Susana Häggqvist & Ignas Bunikis & Orlando Contreras-Lopez & Chen-Shan Chin & Jessica Nordlund & Carl-Johan Rubin & Lars Feuk &, 2023. "Long-read whole-genome analysis of human single cells," Nature Communications, Nature, vol. 14(1), pages 1-12, December.
    9. Max Lundberg & Alexander Mackintosh & Anna Petri & Staffan Bensch, 2023. "Inversions maintain differences between migratory phenotypes of a songbird," Nature Communications, Nature, vol. 14(1), pages 1-15, December.
    10. Matteo Sebastianelli & Sifiso M. Lukhele & Simona Secomandi & Stacey G. Souza & Bettina Haase & Michaella Moysi & Christos Nikiforou & Alexander Hutfluss & Jacquelyn Mountcastle & Jennifer Balacco & S, 2024. "A genomic basis of vocal rhythm in birds," Nature Communications, Nature, vol. 15(1), pages 1-15, December.
    11. Xiao Luo & Xiongbin Kang & Alexander Schönhuth, 2022. "VeChat: correcting errors in long reads using variation graphs," Nature Communications, Nature, vol. 13(1), pages 1-12, December.
    12. Steen W. B. Bender & Marcus W. Dreisler & Min Zhang & Jacob Kæstel-Hansen & Nikos S. Hatzakis, 2024. "SEMORE: SEgmentation and MORphological fingErprinting by machine learning automates super-resolution data analysis," Nature Communications, Nature, vol. 15(1), pages 1-13, December.
    13. Lewis Stevens & Isaac Martínez-Ugalde & Erna King & Martin Wagah & Dominic Absolon & Rowan Bancroft & Pablo Gonzalez de la Rosa & Jessica L. Hall & Manuela Kieninger & Agnieszka Kloch & Sarah Pelan & , 2023. "Ancient diversity in host-parasite interaction genes in a model parasitic nematode," Nature Communications, Nature, vol. 14(1), pages 1-19, December.
    14. Alexander S. Leonard & Danang Crysnanto & Zih-Hua Fang & Michael P. Heaton & Brian L. Vander Ley & Carolina Herrera & Heinrich Bollwein & Derek M. Bickhart & Kristen L. Kuhn & Timothy P. L. Smith & Be, 2022. "Structural variant-based pangenome construction has low sensitivity to variability of haplotype-resolved bovine assemblies," Nature Communications, Nature, vol. 13(1), pages 1-13, December.

    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:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-41784-8. 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.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with 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.