Cargando…
Crosstalk between heterotrimeric G protein-coupled signaling pathways and WRKY transcription factors modulating plant responses to suboptimal micronutrient conditions
Nutrient stresses induce foliar chlorosis and growth defects. Here we propose heterotrimeric G proteins as signaling mediators of various nutrient stresses, through meta-analyses of >20 transcriptomic data sets associated with nutrient stresses or G protein mutations. Systematic comparison of tra...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7260721/ https://www.ncbi.nlm.nih.gov/pubmed/32107545 http://dx.doi.org/10.1093/jxb/eraa108 |
_version_ | 1783540377329860608 |
---|---|
author | Wu, Ting-Ying Krishnamoorthi, Shalini Goh, Honzhen Leong, Richalynn Sanson, Amy Catherine Urano, Daisuke |
author_facet | Wu, Ting-Ying Krishnamoorthi, Shalini Goh, Honzhen Leong, Richalynn Sanson, Amy Catherine Urano, Daisuke |
author_sort | Wu, Ting-Ying |
collection | PubMed |
description | Nutrient stresses induce foliar chlorosis and growth defects. Here we propose heterotrimeric G proteins as signaling mediators of various nutrient stresses, through meta-analyses of >20 transcriptomic data sets associated with nutrient stresses or G protein mutations. Systematic comparison of transcriptomic data yielded 104 genes regulated by G protein subunits under common nutrient stresses: 69 genes under Gβ subunit (AGB1) control and 35 genes under Gα subunit (GPA1) control. Quantitative real-time PCR experiments validate that several transcription factors and metal transporters changed in expression level under suboptimal iron, zinc, and/or copper concentrations, while being misregulated in the Arabidopsis Gβ-null (agb1) mutant. The agb1 mutant had altered metal ion profiles and exhibited severe growth arrest under zinc stress, and aberrant root waving under iron and zinc stresses, while the Gα-null mutation attenuated leaf chlorosis under iron deficiency in both Arabidopsis and rice. Our transcriptional network analysis inferred computationally that WRKY-family transcription factors mediate the AGB1-dependent nutrient responses. As corroborating evidence of our inference, ectopic expression of WRKY25 or WRKY33 rescued the zinc stress phenotypes and the expression of zinc transporters in the agb1-2 background. These results, together with Gene Ontology analyses, suggest two contrasting roles for G protein-coupled signaling pathways in micronutrient stress responses: one enhancing general stress tolerance and the other modulating ion homeostasis through WRKY transcriptional regulatory networks. In addition, tolerance to iron stress in the rice Gα mutant provides an inroad to improve nutrient stress tolerance of agricultural crops by manipulating G protein signaling. |
format | Online Article Text |
id | pubmed-7260721 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-72607212020-06-03 Crosstalk between heterotrimeric G protein-coupled signaling pathways and WRKY transcription factors modulating plant responses to suboptimal micronutrient conditions Wu, Ting-Ying Krishnamoorthi, Shalini Goh, Honzhen Leong, Richalynn Sanson, Amy Catherine Urano, Daisuke J Exp Bot Research Papers Nutrient stresses induce foliar chlorosis and growth defects. Here we propose heterotrimeric G proteins as signaling mediators of various nutrient stresses, through meta-analyses of >20 transcriptomic data sets associated with nutrient stresses or G protein mutations. Systematic comparison of transcriptomic data yielded 104 genes regulated by G protein subunits under common nutrient stresses: 69 genes under Gβ subunit (AGB1) control and 35 genes under Gα subunit (GPA1) control. Quantitative real-time PCR experiments validate that several transcription factors and metal transporters changed in expression level under suboptimal iron, zinc, and/or copper concentrations, while being misregulated in the Arabidopsis Gβ-null (agb1) mutant. The agb1 mutant had altered metal ion profiles and exhibited severe growth arrest under zinc stress, and aberrant root waving under iron and zinc stresses, while the Gα-null mutation attenuated leaf chlorosis under iron deficiency in both Arabidopsis and rice. Our transcriptional network analysis inferred computationally that WRKY-family transcription factors mediate the AGB1-dependent nutrient responses. As corroborating evidence of our inference, ectopic expression of WRKY25 or WRKY33 rescued the zinc stress phenotypes and the expression of zinc transporters in the agb1-2 background. These results, together with Gene Ontology analyses, suggest two contrasting roles for G protein-coupled signaling pathways in micronutrient stress responses: one enhancing general stress tolerance and the other modulating ion homeostasis through WRKY transcriptional regulatory networks. In addition, tolerance to iron stress in the rice Gα mutant provides an inroad to improve nutrient stress tolerance of agricultural crops by manipulating G protein signaling. Oxford University Press 2020-05-30 2020-02-28 /pmc/articles/PMC7260721/ /pubmed/32107545 http://dx.doi.org/10.1093/jxb/eraa108 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Experimental Biology. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Papers Wu, Ting-Ying Krishnamoorthi, Shalini Goh, Honzhen Leong, Richalynn Sanson, Amy Catherine Urano, Daisuke Crosstalk between heterotrimeric G protein-coupled signaling pathways and WRKY transcription factors modulating plant responses to suboptimal micronutrient conditions |
title | Crosstalk between heterotrimeric G protein-coupled signaling pathways and WRKY transcription factors modulating plant responses to suboptimal micronutrient conditions |
title_full | Crosstalk between heterotrimeric G protein-coupled signaling pathways and WRKY transcription factors modulating plant responses to suboptimal micronutrient conditions |
title_fullStr | Crosstalk between heterotrimeric G protein-coupled signaling pathways and WRKY transcription factors modulating plant responses to suboptimal micronutrient conditions |
title_full_unstemmed | Crosstalk between heterotrimeric G protein-coupled signaling pathways and WRKY transcription factors modulating plant responses to suboptimal micronutrient conditions |
title_short | Crosstalk between heterotrimeric G protein-coupled signaling pathways and WRKY transcription factors modulating plant responses to suboptimal micronutrient conditions |
title_sort | crosstalk between heterotrimeric g protein-coupled signaling pathways and wrky transcription factors modulating plant responses to suboptimal micronutrient conditions |
topic | Research Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7260721/ https://www.ncbi.nlm.nih.gov/pubmed/32107545 http://dx.doi.org/10.1093/jxb/eraa108 |
work_keys_str_mv | AT wutingying crosstalkbetweenheterotrimericgproteincoupledsignalingpathwaysandwrkytranscriptionfactorsmodulatingplantresponsestosuboptimalmicronutrientconditions AT krishnamoorthishalini crosstalkbetweenheterotrimericgproteincoupledsignalingpathwaysandwrkytranscriptionfactorsmodulatingplantresponsestosuboptimalmicronutrientconditions AT gohhonzhen crosstalkbetweenheterotrimericgproteincoupledsignalingpathwaysandwrkytranscriptionfactorsmodulatingplantresponsestosuboptimalmicronutrientconditions AT leongrichalynn crosstalkbetweenheterotrimericgproteincoupledsignalingpathwaysandwrkytranscriptionfactorsmodulatingplantresponsestosuboptimalmicronutrientconditions AT sansonamycatherine crosstalkbetweenheterotrimericgproteincoupledsignalingpathwaysandwrkytranscriptionfactorsmodulatingplantresponsestosuboptimalmicronutrientconditions AT uranodaisuke crosstalkbetweenheterotrimericgproteincoupledsignalingpathwaysandwrkytranscriptionfactorsmodulatingplantresponsestosuboptimalmicronutrientconditions |