Landscape genomic prediction for restoration of a Eucalyptus foundation species under climate change

  1. Megan Ann Supple  Is a corresponding author
  2. Jason G Bragg
  3. Linda M Broadhurst
  4. Adrienne B Nicotra
  5. Margaret Byrne
  6. Rose L Andrew
  7. Abigail Widdup
  8. Nicola C Aitken
  9. Justin O Borevitz
  1. The Australian National University, Australia
  2. Commonwealth Scientific and Industrial Research Organisation, Australia
  3. Department of Parks and Wildlife Western Australia, Australia
  4. University of New England, Australia

Abstract

As species face rapid environmental change, we can build resilient populations through restoration projects that incorporate predicted future climates into seed sourcing decisions. Eucalyptus melliodora is a foundation species of a critically endangered community in Australia that is a target for restoration. We examined genomic and phenotypic variation to make empirical based recommendations for seed sourcing. We examined isolation by distance and isolation by environment, determining high levels of gene flow extending for 500 km and correlations with climate and soil variables. Growth experiments revealed extensive phenotypic variation both within and among sampling sites, but no site-specific differentiation in phenotypic plasticity. Model predictions suggest that seed can be sourced broadly across the landscape, providing ample diversity for adaptation to environmental change. Application of our landscape genomic model to E. melliodora restoration projects can identify genomic variation suitable for predicted future climates, thereby increasing the long term probability of successful restoration.

Data availability

The following data sets were generated
The following previously published data sets were used

Article and author information

Author details

  1. Megan Ann Supple

    Research School of Biology, The Australian National University, Canberra, Australia
    For correspondence
    megan.a.supple@gmail.com
    Competing interests
    The authors declare that no competing interests exist.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-0204-7852
  2. Jason G Bragg

    Research School of Biology, The Australian National University, Canberra, Australia
    Competing interests
    The authors declare that no competing interests exist.
  3. Linda M Broadhurst

    Centre for Australian National Biodiversity Research, Commonwealth Scientific and Industrial Research Organisation, Canberra, Australia
    Competing interests
    The authors declare that no competing interests exist.
  4. Adrienne B Nicotra

    Research School of Biology, The Australian National University, Canberra, Australia
    Competing interests
    The authors declare that no competing interests exist.
  5. Margaret Byrne

    Science and Conservation Division, Department of Parks and Wildlife Western Australia, Perth, Australia
    Competing interests
    The authors declare that no competing interests exist.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0002-7197-5409
  6. Rose L Andrew

    School of Environmental and Rural Science, University of New England, Armidale, Australia
    Competing interests
    The authors declare that no competing interests exist.
  7. Abigail Widdup

    Research School of Biology, The Australian National University, Canberra, Australia
    Competing interests
    The authors declare that no competing interests exist.
  8. Nicola C Aitken

    Research School of Biology, The Australian National University, Canberra, Australia
    Competing interests
    The authors declare that no competing interests exist.
  9. Justin O Borevitz

    Research School of Biology, The Australian National University, Canberra, Australia
    Competing interests
    The authors declare that no competing interests exist.

Funding

Australian Research Council (Linkage Grant LP130100455)

  • Jason G Bragg
  • Linda M Broadhurst
  • Adrienne B Nicotra
  • Margaret Byrne
  • Justin O Borevitz

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.

Reviewing Editor

  1. Daniel J Kliebenstein, University of California, Davis, United States

Version history

  1. Received: September 10, 2017
  2. Accepted: April 7, 2018
  3. Accepted Manuscript published: April 24, 2018 (version 1)
  4. Version of Record published: May 14, 2018 (version 2)

Copyright

© 2018, Supple et al.

This article is distributed under the terms of the Creative Commons Attribution License permitting unrestricted use and redistribution provided that the original author and source are credited.

Metrics

  • 3,319
    views
  • 400
    downloads
  • 52
    citations

Views, downloads and citations are aggregated across all versions of this paper published by eLife.

Download links

A two-part list of links to download the article, or parts of the article, in various formats.

Downloads (link to download the article as PDF)

Open citations (links to open the citations from this article in various online reference manager services)

Cite this article (links to download the citations from this article in formats compatible with various reference manager tools)

  1. Megan Ann Supple
  2. Jason G Bragg
  3. Linda M Broadhurst
  4. Adrienne B Nicotra
  5. Margaret Byrne
  6. Rose L Andrew
  7. Abigail Widdup
  8. Nicola C Aitken
  9. Justin O Borevitz
(2018)
Landscape genomic prediction for restoration of a Eucalyptus foundation species under climate change
eLife 7:e31835.
https://doi.org/10.7554/eLife.31835

Share this article

https://doi.org/10.7554/eLife.31835

Further reading

    1. Biochemistry and Chemical Biology
    2. Plant Biology
    Dietmar Funck, Malte Sinn ... Jörg S Hartig
    Research Article

    Metabolism and biological functions of the nitrogen-rich compound guanidine have long been neglected. The discovery of four classes of guanidine-sensing riboswitches and two pathways for guanidine degradation in bacteria hint at widespread sources of unconjugated guanidine in nature. So far, only three enzymes from a narrow range of bacteria and fungi have been shown to produce guanidine, with the ethylene-forming enzyme (EFE) as the most prominent example. Here, we show that a related class of Fe2+- and 2-oxoglutarate-dependent dioxygenases (2-ODD-C23) highly conserved among plants and algae catalyze the hydroxylation of homoarginine at the C6-position. Spontaneous decay of 6-hydroxyhomoarginine yields guanidine and 2-aminoadipate-6-semialdehyde. The latter can be reduced to pipecolate by pyrroline-5-carboxylate reductase but more likely is oxidized to aminoadipate by aldehyde dehydrogenase ALDH7B in vivo. Arabidopsis has three 2-ODD-C23 isoforms, among which Din11 is unusual because it also accepted arginine as substrate, which was not the case for the other 2-ODD-C23 isoforms from Arabidopsis or other plants. In contrast to EFE, none of the three Arabidopsis enzymes produced ethylene. Guanidine contents were typically between 10 and 20 nmol*(g fresh weight)-1 in Arabidopsis but increased to 100 or 300 nmol*(g fresh weight)-1 after homoarginine feeding or treatment with Din11-inducing methyljasmonate, respectively. In 2-ODD-C23 triple mutants, the guanidine content was strongly reduced, whereas it increased in overexpression plants. We discuss the implications of the finding of widespread guanidine-producing enzymes in photosynthetic eukaryotes as a so far underestimated branch of the bio-geochemical nitrogen cycle and propose possible functions of natural guanidine production.

    1. Plant Biology
    Ivan Kulich, Julia Schmid ... Jiří Friml
    Research Article

    Root gravitropic bending represents a fundamental aspect of terrestrial plant physiology. Gravity is perceived by sedimentation of starch-rich plastids (statoliths) to the bottom of the central root cap cells. Following gravity perception, intercellular auxin transport is redirected downwards leading to an asymmetric auxin accumulation at the lower root side causing inhibition of cell expansion, ultimately resulting in downwards bending. How gravity-induced statoliths repositioning is translated into asymmetric auxin distribution remains unclear despite PIN auxin efflux carriers and the Negative Gravitropic Response of roots (NGR) proteins polarize along statolith sedimentation, thus providing a plausible mechanism for auxin flow redirection. In this study, using a functional NGR1-GFP construct, we visualized the NGR1 localization on the statolith surface and plasma membrane (PM) domains in close proximity to the statoliths, correlating with their movements. We determined that NGR1 binding to these PM domains is indispensable for NGR1 functionality and relies on cysteine acylation and adjacent polybasic regions as well as on lipid and sterol PM composition. Detailed timing of the early events following graviperception suggested that both NGR1 repolarization and initial auxin asymmetry precede the visible PIN3 polarization. This discrepancy motivated us to unveil a rapid, NGR-dependent translocation of PIN-activating AGCVIII kinase D6PK towards lower PMs of gravity-perceiving cells, thus providing an attractive model for rapid redirection of auxin fluxes following gravistimulation.