The ecology of palm genomes: repeat-associated genome size expansion is constrained by aridity.

Arecaceae (palms) adaptation ecology genome size phylogenetic regression plant evolution trait evolution transposable elements

Journal

The New phytologist
ISSN: 1469-8137
Titre abrégé: New Phytol
Pays: England
ID NLM: 9882884

Informations de publication

Date de publication:
10 2022
Historique:
received: 04 11 2021
accepted: 18 05 2022
pubmed: 20 6 2022
medline: 28 9 2022
entrez: 19 6 2022
Statut: ppublish

Résumé

Genome size varies 2400-fold across plants, influencing their evolution through changes in cell size and cell division rates which impact plants' environmental stress tolerance. Repetitive element expansion explains much genome size diversity, and the processes structuring repeat 'communities' are analogous to those structuring ecological communities. However, which environmental stressors influence repeat community dynamics has not yet been examined from an ecological perspective. We measured genome size and leveraged climatic data for 91% of genera within the ecologically diverse palm family (Arecaceae). We then generated genomic repeat profiles for 141 palm species, and analysed repeats using phylogenetically informed linear models to explore relationships between repeat dynamics and environmental factors. We show that palm genome size and repeat 'community' composition are best explained by aridity. Specifically, Ty3-gypsy and TIR elements were more abundant in palm species from wetter environments, which generally had larger genomes, suggesting amplification. By contrast, Ty1-copia and LINE elements were more abundant in drier environments. Our results suggest that water stress inhibits repeat expansion through selection on upper genome size limits. However, elements that may associate with stress-response genes (e.g. Ty1-copia) have amplified in arid-adapted palm species. Overall, we provide novel evidence of climate influencing the assembly of repeat 'communities'.

Identifiants

pubmed: 35717562
doi: 10.1111/nph.18323
pmc: PMC9796251
doi:

Substances chimiques

Retroelements 0

Banques de données

Dryad
['10.5061/dryad.4j0zpc8f4']

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

433-446

Subventions

Organisme : Biotechnology and Biological Sciences Research Council
ID : BB/S019669/1
Pays : United Kingdom

Informations de copyright

© 2022 The Authors. New Phytologist © 2022 New Phytologist Foundation.

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Auteurs

Rowan J Schley (RJ)

University of Exeter, Laver Building, North Park Road, Exeter, Devon, EX4 4QE, UK.
Royal Botanic Gardens, Kew, Surrey, TW9 3AB, UK.

Jaume Pellicer (J)

Royal Botanic Gardens, Kew, Surrey, TW9 3AB, UK.
Institut Botànic de Barcelona (IBB, CSIC-Ajuntament de Barcelona), Passeig del Migdia sn, 08038, Barcelona, Spain.

Xue-Jun Ge (XJ)

Key Laboratory of Plant Resources Conservation and Sustainable Utilization, South China Botanical Garden, Chinese Academy of Sciences, Guangzhou, 510650, China.

Craig Barrett (C)

Department of Biology, West Virginia University, Morgantown, WV, 26506, USA.

Sidonie Bellot (S)

Royal Botanic Gardens, Kew, Surrey, TW9 3AB, UK.

Maïté S Guignard (MS)

Royal Botanic Gardens, Kew, Surrey, TW9 3AB, UK.

Petr Novák (P)

Biology Centre, Institute of Plant Molecular Biology, Czech Academy of Sciences, 370 05, České Budějovice, Czech Republic.

Donald Fraser (D)

Royal Botanic Gardens, Kew, Surrey, TW9 3AB, UK.

William J Baker (WJ)

Royal Botanic Gardens, Kew, Surrey, TW9 3AB, UK.

Steven Dodsworth (S)

School of Biological Sciences, University of Portsmouth, Portsmouth, Hampshire, PO1 2DY, UK.

Jiří Macas (J)

Biology Centre, Institute of Plant Molecular Biology, Czech Academy of Sciences, 370 05, České Budějovice, Czech Republic.

Andrew R Leitch (AR)

Queen Mary University of London, Mile End Road, London, E1 4NS, UK.

Ilia J Leitch (IJ)

Royal Botanic Gardens, Kew, Surrey, TW9 3AB, UK.

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Classifications MeSH