Arabidopsis Heterotrimeric G-protein Regulates Cell Wall Defense and Resistance to Necrotrophic Fungi

dc.contributor.authorDelgado Cerezo, Magdalena
dc.contributor.authorSánchez Rodríguez, Clara
dc.contributor.authorEscudero, Viviana
dc.contributor.authorMiedes, Eva
dc.contributor.authorFernández, Paula Virginia
dc.contributor.authorJordá, Lucía
dc.contributor.authorHernández Blanco, Camilo
dc.contributor.authorSánchez Vallet, Andrea
dc.contributor.authorBednarek, Pawel
dc.contributor.authorSchulze-Lefert, Paul
dc.contributor.authorSomerville, Shauna
dc.contributor.authorEstevez, José Manuel
dc.contributor.authorPersson, Staffan
dc.contributor.authorMolina, Antonio
dc.date.accessioned2024-12-18T07:52:40Z
dc.date.available2024-12-18T07:52:40Z
dc.date.created2012
dc.description.abstractThe Arabidopsis heterotrimeric G-protein controls defense responses to necrotrophic and vascular fungi. The agb1 mutant impaired in the Gb subunit displays enhanced susceptibility to these pathogens. Gb/AGB1 forms an obligate dimer with either one of the Arabidopsis Gg subunits (g1/AGG1 and g2/AGG2). Accordingly, we now demonstrate that the agg1 agg2 double mutant is as susceptible as agb1 plants to the necrotrophic fungus Plectosphaerella cucumerina. To elucidate the molecular basis of heterotrimeric G-protein-mediated resistance, we performed a comparative transcriptomic analysis of agb1-1 mutant and wild-type plants upon inoculation with P. cucumerina. This analysis, together with metab olomic studies, demonstrated that G-protein-mediated resistance was independent of defensive pathways required for resistance to necrotrophic fungi, such as the salicylic acid, jasmonic acid, ethylene, abscisic acid, and tryptophan-derived metabolites signaling, as these pathways were not impaired in agb1 and agg1 agg2 mutants. Notably, many mis-regulated genes in agb1 plants were related with cell wall functions, which was also the case in agg1 agg2 mutant. Biochemical analyses and Fourier Transform InfraRed (FTIR) spectroscopy of cell walls from G-protein mutants revealed that the xylose content was lower in agb1 and agg1 agg2 mutants than in wild-type plants, and that mutant walls had similar FTIR spec tratypes, which differed from that of wild-type plants. The data presented here suggest a canonical functionality of the Gb and Gg1/g2 subunits in the control of Arabidopsis immune responses and the regulation of cell wall composition. Key words: Plant immunity; cell wall; indole glucosinolates; xylose; necrotropic fungi; G-proteines_ES
dc.formatapplication/pdfes_ES
dc.identifier.locationN/Aes_ES
dc.identifier.urihttps://hdl.handle.net/20.500.12080/44972
dc.languageenges_ES
dc.rightsCC-BYes_ES
dc.rights.accessrightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.eses_ES
dc.titleArabidopsis Heterotrimeric G-protein Regulates Cell Wall Defense and Resistance to Necrotrophic Fungies_ES
dc.typeinfo:eu-repo/semantics/articlees_ES

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