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

Karima Righetti(Institut de Recherche en Horticulture et Semences), Joseph Ly Vu(Institut de Recherche en Horticulture et Semences), Sandra Pelletier(Institut de Recherche en Horticulture et Semences), Benoît Ly Vu(Institut de Recherche en Horticulture et Semences), Enrico Glaab(University of Luxembourg), David Lalanne(Institut de Recherche en Horticulture et Semences), Asher Pasha(University of Toronto), Rohan Patel(University of Toronto), Nicholas J. Provart(University of Toronto), Jérôme Verdier(Chinese Academy of Sciences), Olivier Leprince(Institut de Recherche en Horticulture et Semences), Julia Buitink(Institut de Recherche en Horticulture et Semences)
The Plant Cell
September 26, 2015
Cited by 185Open Access
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Abstract

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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