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Alteration of cell wall xylan acetylation triggers defense responses that counterbalance the immune deficiencies of plants impaired in the b-subunit of the heterotrimeric G-protein

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Escudero, Viviana & Jordá, Lucía & Sopeña Torres, Sara & Melida, Hugo & Miedes, Eva & Muñoz Barrios, Antonio & Swami, Sanjay & Alexander, Danny & McKee, Lauren S. & Sanchez Vallet, Andrea & Bulone, Vincent & Jones, Alan M. & Molina, Antonio .Alteration of cell wall xylan acetylation triggers defense responses that counterbalance the immune deficiencies of plants impaired in the b-subunit of the heterotrimeric G-protein.

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Escudero, Viviana & Jordá, Lucía & Sopeña Torres, Sara & Melida, Hugo & Miedes, Eva & Muñoz Barrios, Antonio & Swami, Sanjay & Alexander, Danny & McKee, Lauren S. & Sanchez Vallet, Andrea & Bulone, Vincent & Jones, Alan M. & Molina, Antonio. Alteration of cell wall xylan acetylation triggers defense responses that counterbalance the immune deficiencies of plants impaired in the b-subunit of the heterotrimeric G-protein.

https://hdl.handle.net/20.500.12080/44976
dc.contributor.author Escudero, Viviana
dc.contributor.author Jordá, Lucía
dc.contributor.author Sopeña Torres, Sara
dc.contributor.author Melida, Hugo
dc.contributor.author Miedes, Eva
dc.contributor.author Muñoz Barrios, Antonio
dc.contributor.author Swami, Sanjay
dc.contributor.author Alexander, Danny
dc.contributor.author McKee, Lauren S.
dc.contributor.author Sanchez Vallet, Andrea
dc.contributor.author Bulone, Vincent
dc.contributor.author Jones, Alan M.
dc.contributor.author Molina, Antonio
dc.date.accessioned 2024-12-18T08:46:07Z
dc.date.available 2024-12-18T08:46:07Z
dc.date.created 2017
dc.identifier.uri https://hdl.handle.net/20.500.12080/44976
dc.description.abstract Arabidopsis heterotrimeric G-protein complex modulates pathogen-associated molecular pattern-triggered immunity (PTI) and disease resistance responses to different types of pathogens. It also plays a role in plant cell wall integrity as mutants impaired in the Gb- (agb1-2) or Gc-subunits have an altered wall composition compared with wild-type plants. Here we performed a mutant screen to identify suppressors of agb1-2 (sgb) that restore susceptibility to pathogens to wild-type levels. Out of the four sgb mutants (sgb10¿sgb13) identified, sgb11 is a new mutant allele of ESKIMO1 (ESK1), which encodes a plant-specific polysaccharide O-acetyltransferase involved in xylan acetylation. Null alleles (sgb11/esk1-7) of ESK1 restore to wild-type levels the enhanced susceptibility of agb1-2 to the necrotrophic fungus Plectosphaerella cucumerina BMM (PcBMM), but not to the bacterium Pseudomonas syringae pv. tomato DC3000 or to the oomycete Hyaloper onospora arabidopsidis. The enhanced resistance to PcBMM of the agb1-2 esk1-7 double mutant was not the result of the re-activation of deficient PTI responses in agb1-2. Alteration of cell wall xylan acetylation caused by ESK1 impairment was accompanied by an enhanced accumulation of abscisic acid, the constitu tive expression of genes encoding antibiotic peptides and enzymes involved in the biosynthesis of trypto phan-derived metabolites, and the accumulation of disease resistance-related secondary metabolites and different osmolites. These esk1-mediated responses counterbalance the defective PTI and PcBMM suscepti bility of agb1-2 plants, and explain the enhanced drought resistance of esk1 plants. These results suggest that a deficient PTI-mediated resistance is partially compensated by the activation of specific cell-wall-trig gered immune responses. Keywords: heterotrimeric G-protein, AGB1, agb1-2, plant cell wall, xylan, necrotrophic fungi, immunity, pathogen-associated molecular pattern, Plectosphaerella cucumerina, Arabidopsis thaliana es_ES
dc.format application/pdf es_ES
dc.language eng es_ES
dc.rights CC-BY es_ES
dc.rights.uri http://creativecommons.org/licenses/by/4.0/deed.es es_ES
dc.title Alteration of cell wall xylan acetylation triggers defense responses that counterbalance the immune deficiencies of plants impaired in the b-subunit of the heterotrimeric G-protein es_ES
dc.type info:eu-repo/semantics/article es_ES
dc.rights.accessrights info:eu-repo/semantics/openAccess es_ES
dc.identifier.location N/A es_ES


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