Inference of Longevity-Related Genes from a Robust Coexpression Network of Seed Maturation Identifies Regulators Linking Seed Storability to Biotic Defense-Related Pathways

Seed longevity, the maintenance of viability during storage, is a crucial factor for preservation of genetic resources and ensuring proper seedling establishment and high crop yield. We used a systems biology approach to identify key genes regulating the acquisition of longevity during seed maturati...

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Published inThe Plant cell Vol. 27; no. 10; pp. 2692 - 2708
Main Authors Righetti, Karima, Vu, Joseph Ly, Pelletier, Sandra, Vu, Benoit Ly, Glaab, Enrico, Lalanne, David, Pasha, Asher, Patel, Rohan V., Provart, Nicholas J., Verdier, Jerome, Leprince, Olivier, Buitink, Julia
Format Journal Article
LanguageEnglish
Published England American Society of Plant Biologists 01.10.2015
American Society of Plant Biologists (ASPB)
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Summary:Seed longevity, the maintenance of viability during storage, is a crucial factor for preservation of genetic resources and ensuring proper seedling establishment and high crop yield. We used a systems biology approach to identify key genes regulating the acquisition of longevity during seed maturation of Medicago truncatula. Using 104 transcriptomes from seed developmental time courses obtained in five growth environments, we generated a robust, stable coexpression network (MatNet), thereby capturing the conserved backbone of maturation. Using a trait-based gene significance measure, a coexpression module related to the acquisition of longevity was inferred from MatNet. Comparative analysis of the maturation processes in M. truncatula and Arabidopsis thaliana seeds and mining Arabidopsis interaction databases revealed conserved connectivity for 87% of longevity module nodes between both species. Arabidopsis mutant screening for longevity and maturation phenotypes demonstrated high predictive power of the longevity cross-species network. Overrepresentation analysis of the network nodes indicated biological functions related to defense, light, and auxin. Characterization of defense-related wrky3 and nf-x1-like1 (nfxl1) transcription factor mutants demonstrated that these genes regulate some of the network nodes and exhibit impaired acquisition of longevity during maturation. These data suggest that seed longevity evolved by co-opting existing genetic pathways regulating the activation of defense against pathogens.
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PMCID: PMC4682330
www.plantcell.org/cgi/doi/10.1105/tpc.15.00632
The author responsible for the distribution of materials integral to the findings presented in this article in accordance with the policy described in the Instructions for Authors (www.plantcell.org) is: Julia Buitink (julia.buitink@angers.inra.fr).
ISSN:1040-4651
1532-298X
DOI:10.1105/tpc.15.00632