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Gene expression evolution in pattern-triggered immunity within Arabidopsis thaliana and across Brassicaceae species

Plants recognize surrounding microbes by sensing microbe-associated molecular patterns (MAMPs) to activate pattern-triggered immunity (PTI). Despite their significance for microbial control, the evolution of PTI responses remains largely uncharacterized. Here, by employing comparative transcriptomic...

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Detalles Bibliográficos
Autores principales: Winkelmüller, Thomas M, Entila, Frederickson, Anver, Shajahan, Piasecka, Anna, Song, Baoxing, Dahms, Eik, Sakakibara, Hitoshi, Gan, Xiangchao, Kułak, Karolina, Sawikowska, Aneta, Krajewski, Paweł, Tsiantis, Miltos, Garrido-Oter, Ruben, Fukushima, Kenji, Schulze-Lefert, Paul, Laurent, Stefan, Bednarek, Paweł, Tsuda, Kenichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8290292/
https://www.ncbi.nlm.nih.gov/pubmed/33751107
http://dx.doi.org/10.1093/plcell/koab073
Descripción
Sumario:Plants recognize surrounding microbes by sensing microbe-associated molecular patterns (MAMPs) to activate pattern-triggered immunity (PTI). Despite their significance for microbial control, the evolution of PTI responses remains largely uncharacterized. Here, by employing comparative transcriptomics of six Arabidopsis thaliana accessions and three additional Brassicaceae species to investigate PTI responses, we identified a set of genes that commonly respond to the MAMP flg22 and genes that exhibit species-specific expression signatures. Variation in flg22-triggered transcriptome responses across Brassicaceae species was incongruent with their phylogeny, while expression changes were strongly conserved within A. thaliana. We found the enrichment of WRKY transcription factor binding sites in the 5′-regulatory regions of conserved and species-specific responsive genes, linking the emergence of WRKY-binding sites with the evolution of gene expression patterns during PTI. Our findings advance our understanding of the evolution of the transcriptome during biotic stress.