Proteostatic regulation of MEP and shikimate pathways by redox-activated photosynthesis signaling in plants exposed to small fungal volatiles

Microorganisms produce volatile compounds (VCs) with molecular masses of less than 300 Da that promote plant growth and photosynthesis. Recently, we have shown that small VCs of less than 45 Da other than CO2 are major determinants of plant responses to fungal volatile emissions. However, the regulatory mechanisms involved in the plants’ responses to small microbial VCs remain unclear. In Arabidopsis thaliana plants exposed to small fungal VCs, growth promotion is accompanied by reduction of the thiol redox of Calvin-Benson cycle (CBC) enzymes and changes in the levels of shikimate and 2-C-methyl-D-erythritol 4-phosphate (MEP) pathway-related compounds. We hypothesized that plants’ responses to small microbial VCs involve post-translational modulation of enzymes of the MEP and shikimate pathways via mechanisms involving redox-activated photosynthesis signaling. To test this hypothesis, we compared the responses of wild-type (WT) plants and a cfbp1 mutant defective in a redox-regulated isoform of the CBC enzyme fructose-1,6-bisphosphatase to small VCs emitted by the fungal phytopathogen Alternaria alternata. Fungal VC-promoted growth and photosynthesis, as well as metabolic and proteomic changes, were substantially weaker in cfbp1 plants than in WT plants. In WT plants, but not in cfbp1 plants, small fungal VCs reduced the levels of both transcripts and proteins of the stromal Clp protease system and enhanced those of plastidial chaperonins and co-chaperonins. Consistently, small fungal VCs promoted the accumulation of putative Clp protease clients including MEP and shikimate pathway enzymes. clpr1-2 and clpc1 mutants with disrupted plastidial protein homeostasis responded weakly to small fungal VCs, strongly indicating that plant responses to microbial volatile emissions require a finely regulated plastidial protein quality control system. Our findings provide strong evidence that plant responses to fungal VCs involve chloroplast-to-nucleus retrograde signaling of redox-activated photosynthesis leading to proteostatic regulation of the MEP and shikimate pathways.

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Main Authors: Ameztoy, Kinia, Sánchez-López, Ángela María, Muñoz Pérez, Francisco José, Bahaji, Abdellatif, Almagro, Goizeder, Baroja-Fernández, Edurne, Gámez-Arcas, Samuel, Diego, Nuria de, Doležal, Karel, Nováck, Ondřej, Pěnčík, Ales, Alpízar, Adán, Rodríguez-Concepción, Manuel, Pozueta Romero, Javier
Other Authors: Agencia Estatal de Investigación (España)
Format: artículo biblioteca
Language:English
Published: Frontiers Media 2021-03-05
Subjects:Clp protease system, MEP pathway, Plant–microbe interaction, Proteostatic regulation, PQC system, Redox regulation, Chloroplast-to-nucleus retrograde signaling,
Online Access:http://hdl.handle.net/10261/237979
http://dx.doi.org/10.13039/501100004587
http://dx.doi.org/10.13039/501100011033
http://dx.doi.org/10.13039/501100000780
http://dx.doi.org/10.13039/501100002809
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id dig-idab-es-10261-237979
record_format koha
institution IDAB ES
collection DSpace
country España
countrycode ES
component Bibliográfico
access En linea
databasecode dig-idab-es
tag biblioteca
region Europa del Sur
libraryname Biblioteca del IDAB España
language English
topic Clp protease system
MEP pathway
Plant–microbe interaction
Proteostatic regulation
PQC system
Redox regulation
Chloroplast-to-nucleus retrograde signaling
Clp protease system
MEP pathway
Plant–microbe interaction
Proteostatic regulation
PQC system
Redox regulation
Chloroplast-to-nucleus retrograde signaling
spellingShingle Clp protease system
MEP pathway
Plant–microbe interaction
Proteostatic regulation
PQC system
Redox regulation
Chloroplast-to-nucleus retrograde signaling
Clp protease system
MEP pathway
Plant–microbe interaction
Proteostatic regulation
PQC system
Redox regulation
Chloroplast-to-nucleus retrograde signaling
Ameztoy, Kinia
Sánchez-López, Ángela María
Muñoz Pérez, Francisco José
Bahaji, Abdellatif
Almagro, Goizeder
Baroja-Fernández, Edurne
Gámez-Arcas, Samuel
Diego, Nuria de
Doležal, Karel
Nováck, Ondřej
Pěnčík, Ales
Alpízar, Adán
Rodríguez-Concepción, Manuel
Pozueta Romero, Javier
Proteostatic regulation of MEP and shikimate pathways by redox-activated photosynthesis signaling in plants exposed to small fungal volatiles
description Microorganisms produce volatile compounds (VCs) with molecular masses of less than 300 Da that promote plant growth and photosynthesis. Recently, we have shown that small VCs of less than 45 Da other than CO2 are major determinants of plant responses to fungal volatile emissions. However, the regulatory mechanisms involved in the plants’ responses to small microbial VCs remain unclear. In Arabidopsis thaliana plants exposed to small fungal VCs, growth promotion is accompanied by reduction of the thiol redox of Calvin-Benson cycle (CBC) enzymes and changes in the levels of shikimate and 2-C-methyl-D-erythritol 4-phosphate (MEP) pathway-related compounds. We hypothesized that plants’ responses to small microbial VCs involve post-translational modulation of enzymes of the MEP and shikimate pathways via mechanisms involving redox-activated photosynthesis signaling. To test this hypothesis, we compared the responses of wild-type (WT) plants and a cfbp1 mutant defective in a redox-regulated isoform of the CBC enzyme fructose-1,6-bisphosphatase to small VCs emitted by the fungal phytopathogen Alternaria alternata. Fungal VC-promoted growth and photosynthesis, as well as metabolic and proteomic changes, were substantially weaker in cfbp1 plants than in WT plants. In WT plants, but not in cfbp1 plants, small fungal VCs reduced the levels of both transcripts and proteins of the stromal Clp protease system and enhanced those of plastidial chaperonins and co-chaperonins. Consistently, small fungal VCs promoted the accumulation of putative Clp protease clients including MEP and shikimate pathway enzymes. clpr1-2 and clpc1 mutants with disrupted plastidial protein homeostasis responded weakly to small fungal VCs, strongly indicating that plant responses to microbial volatile emissions require a finely regulated plastidial protein quality control system. Our findings provide strong evidence that plant responses to fungal VCs involve chloroplast-to-nucleus retrograde signaling of redox-activated photosynthesis leading to proteostatic regulation of the MEP and shikimate pathways.
author2 Agencia Estatal de Investigación (España)
author_facet Agencia Estatal de Investigación (España)
Ameztoy, Kinia
Sánchez-López, Ángela María
Muñoz Pérez, Francisco José
Bahaji, Abdellatif
Almagro, Goizeder
Baroja-Fernández, Edurne
Gámez-Arcas, Samuel
Diego, Nuria de
Doležal, Karel
Nováck, Ondřej
Pěnčík, Ales
Alpízar, Adán
Rodríguez-Concepción, Manuel
Pozueta Romero, Javier
format artículo
topic_facet Clp protease system
MEP pathway
Plant–microbe interaction
Proteostatic regulation
PQC system
Redox regulation
Chloroplast-to-nucleus retrograde signaling
author Ameztoy, Kinia
Sánchez-López, Ángela María
Muñoz Pérez, Francisco José
Bahaji, Abdellatif
Almagro, Goizeder
Baroja-Fernández, Edurne
Gámez-Arcas, Samuel
Diego, Nuria de
Doležal, Karel
Nováck, Ondřej
Pěnčík, Ales
Alpízar, Adán
Rodríguez-Concepción, Manuel
Pozueta Romero, Javier
author_sort Ameztoy, Kinia
title Proteostatic regulation of MEP and shikimate pathways by redox-activated photosynthesis signaling in plants exposed to small fungal volatiles
title_short Proteostatic regulation of MEP and shikimate pathways by redox-activated photosynthesis signaling in plants exposed to small fungal volatiles
title_full Proteostatic regulation of MEP and shikimate pathways by redox-activated photosynthesis signaling in plants exposed to small fungal volatiles
title_fullStr Proteostatic regulation of MEP and shikimate pathways by redox-activated photosynthesis signaling in plants exposed to small fungal volatiles
title_full_unstemmed Proteostatic regulation of MEP and shikimate pathways by redox-activated photosynthesis signaling in plants exposed to small fungal volatiles
title_sort proteostatic regulation of mep and shikimate pathways by redox-activated photosynthesis signaling in plants exposed to small fungal volatiles
publisher Frontiers Media
publishDate 2021-03-05
url http://hdl.handle.net/10261/237979
http://dx.doi.org/10.13039/501100004587
http://dx.doi.org/10.13039/501100011033
http://dx.doi.org/10.13039/501100000780
http://dx.doi.org/10.13039/501100002809
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spelling dig-idab-es-10261-2379792021-12-27T15:38:24Z Proteostatic regulation of MEP and shikimate pathways by redox-activated photosynthesis signaling in plants exposed to small fungal volatiles Ameztoy, Kinia Sánchez-López, Ángela María Muñoz Pérez, Francisco José Bahaji, Abdellatif Almagro, Goizeder Baroja-Fernández, Edurne Gámez-Arcas, Samuel Diego, Nuria de Doležal, Karel Nováck, Ondřej Pěnčík, Ales Alpízar, Adán Rodríguez-Concepción, Manuel Pozueta Romero, Javier Agencia Estatal de Investigación (España) Ministerio de Ciencia, Innovación y Universidades (España) European Commission Ministry of Education, Youth and Sports (Czech Republic) Instituto de Salud Carlos III Generalitat de Catalunya CSIC - Unidad de Recursos de Información Científica para la Investigación (URICI) Clp protease system MEP pathway Plant–microbe interaction Proteostatic regulation PQC system Redox regulation Chloroplast-to-nucleus retrograde signaling Microorganisms produce volatile compounds (VCs) with molecular masses of less than 300 Da that promote plant growth and photosynthesis. Recently, we have shown that small VCs of less than 45 Da other than CO2 are major determinants of plant responses to fungal volatile emissions. However, the regulatory mechanisms involved in the plants’ responses to small microbial VCs remain unclear. In Arabidopsis thaliana plants exposed to small fungal VCs, growth promotion is accompanied by reduction of the thiol redox of Calvin-Benson cycle (CBC) enzymes and changes in the levels of shikimate and 2-C-methyl-D-erythritol 4-phosphate (MEP) pathway-related compounds. We hypothesized that plants’ responses to small microbial VCs involve post-translational modulation of enzymes of the MEP and shikimate pathways via mechanisms involving redox-activated photosynthesis signaling. To test this hypothesis, we compared the responses of wild-type (WT) plants and a cfbp1 mutant defective in a redox-regulated isoform of the CBC enzyme fructose-1,6-bisphosphatase to small VCs emitted by the fungal phytopathogen Alternaria alternata. Fungal VC-promoted growth and photosynthesis, as well as metabolic and proteomic changes, were substantially weaker in cfbp1 plants than in WT plants. In WT plants, but not in cfbp1 plants, small fungal VCs reduced the levels of both transcripts and proteins of the stromal Clp protease system and enhanced those of plastidial chaperonins and co-chaperonins. Consistently, small fungal VCs promoted the accumulation of putative Clp protease clients including MEP and shikimate pathway enzymes. clpr1-2 and clpc1 mutants with disrupted plastidial protein homeostasis responded weakly to small fungal VCs, strongly indicating that plant responses to microbial volatile emissions require a finely regulated plastidial protein quality control system. Our findings provide strong evidence that plant responses to fungal VCs involve chloroplast-to-nucleus retrograde signaling of redox-activated photosynthesis leading to proteostatic regulation of the MEP and shikimate pathways. [One Sentence Summary] We provide strong evidence that plant responses to volatile compounds emitted by the fungal phytopathogen Alternaria alternata involve chloroplast-to-nucleus retrograde signaling of redox-activated photosynthesis leading to proteostatic regulation of the MEP and shikimate pathways. This work was supported by the Agencia Estatal de Investigación (AEI) and Fondo Europeo de Desarrollo Regional (Spain) (Grants BIO2016-78747-P, BIO2017-84041-P, BIO2017-90877-REDT, and PID2019-104685GB-100) and the Ministry of Education, Youth and Sport of the Czech Republic and ERDF project “Plants as a tool for sustainable global development” (No. CZ.02.1.01/0.0/0.0/16_019/0000827). Proteomic Unit, National Biotechnology Center was a member of Proteored, PRB3 and was supported by grant PT17/0019 of the PE I + D + i 2013–2016, funded by ISCIII and ERDF. Funding from Generalitat de Catalunya (2017SGR-710) and European Union’s Horizon 2020 (EU-H2020) COST Action CA15136 (EuroCaroten) was also acknowledged. We acknowledge support of the publication fee by the CSIC Open Access Publication Support Initiative through its Unit of Information Resources for Research (URICI). Peer reviewed 2021-04-14T09:07:18Z 2021-04-14T09:07:18Z 2021-03-05 artículo http://purl.org/coar/resource_type/c_6501 Frontiers in Plant Science 12: 637976 (2021) http://hdl.handle.net/10261/237979 10.3389/fpls.2021.637976 1664-462X http://dx.doi.org/10.13039/501100004587 http://dx.doi.org/10.13039/501100011033 http://dx.doi.org/10.13039/501100000780 http://dx.doi.org/10.13039/501100002809 33747018 en #PLACEHOLDER_PARENT_METADATA_VALUE# #PLACEHOLDER_PARENT_METADATA_VALUE# #PLACEHOLDER_PARENT_METADATA_VALUE# #PLACEHOLDER_PARENT_METADATA_VALUE# info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/BIO2016-78747-P info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/BIO2017-84041-P info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/BIO2017-90877-REDT info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2019-104685GB-100 Publisher's version https://doi.org/10.3389/fpls.2021.637976 Sí open Frontiers Media