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AtBBX29 integrates photomorphogenesis and defense responses in Arabidopsis
Light is an environmental signal that modulates plant defenses against attackers. Recent research has focused on the effects of light on defense hormone signaling; however, the connections between light signaling pathways and the biosynthesis of specialized metabolites involved in plant defense have...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10310583/ https://www.ncbi.nlm.nih.gov/pubmed/36807054 http://dx.doi.org/10.1007/s43630-023-00391-8 |
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author | Medina-Fraga, Ana L. Chinen, Lucas A. Demkura, Patricia V. Lichy, Micaela Z. Gershenzon, Jonathan Ballaré, Carlos L. Crocco, Carlos D. |
author_facet | Medina-Fraga, Ana L. Chinen, Lucas A. Demkura, Patricia V. Lichy, Micaela Z. Gershenzon, Jonathan Ballaré, Carlos L. Crocco, Carlos D. |
author_sort | Medina-Fraga, Ana L. |
collection | PubMed |
description | Light is an environmental signal that modulates plant defenses against attackers. Recent research has focused on the effects of light on defense hormone signaling; however, the connections between light signaling pathways and the biosynthesis of specialized metabolites involved in plant defense have been relatively unexplored. Here, we show that Arabidopsis BBX29, a protein that belongs to the B-Box transcription factor (TF) family, integrates photomorphogenic signaling with defense responses by promoting flavonoid, sinapate and glucosinolate accumulation in Arabidopsis leaves. AtBBX29 transcript levels were up regulated by light, through photoreceptor signaling pathways. Genetic evidence indicated that AtBBX29 up-regulates MYB12 gene expression, a TF known to induce genes related to flavonoid biosynthesis in a light-dependent manner, and MYB34 and MYB51, which encode TFs involved in the regulation of glucosinolate biosynthesis. Thus, bbx29 knockout mutants displayed low expression levels of key genes of the flavonoid biosynthetic pathway, and the opposite was true in BBX29 overexpression lines. In agreement with the transcriptomic data, bbx29 mutant plants accumulated lower levels of kaempferol glucosides, sinapoyl malate, indol-3-ylmethyl glucosinolate (I3M), 4-methylsulfinylbutyl glucosinolate (4MSOB) and 3-methylthiopropyl glucosinolate (3MSP) in rosette leaves compared to the wild-type, and showed increased susceptibility to the necrotrophic fungus Botrytis cinerea and to the herbivore Spodoptera frugiperda. In contrast, BBX29 overexpressing plants displayed increased resistance to both attackers. In addition, we found that AtBBX29 plays an important role in mediating the effects of ultraviolet-B (UV-B) radiation on plant defense against B. cinerea. Taken together, these results suggest that AtBBX29 orchestrates the accumulation of specific light-induced metabolites and regulates Arabidopsis resistance against pathogens and herbivores. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s43630-023-00391-8. |
format | Online Article Text |
id | pubmed-10310583 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-103105832023-07-01 AtBBX29 integrates photomorphogenesis and defense responses in Arabidopsis Medina-Fraga, Ana L. Chinen, Lucas A. Demkura, Patricia V. Lichy, Micaela Z. Gershenzon, Jonathan Ballaré, Carlos L. Crocco, Carlos D. Photochem Photobiol Sci Original Papers Light is an environmental signal that modulates plant defenses against attackers. Recent research has focused on the effects of light on defense hormone signaling; however, the connections between light signaling pathways and the biosynthesis of specialized metabolites involved in plant defense have been relatively unexplored. Here, we show that Arabidopsis BBX29, a protein that belongs to the B-Box transcription factor (TF) family, integrates photomorphogenic signaling with defense responses by promoting flavonoid, sinapate and glucosinolate accumulation in Arabidopsis leaves. AtBBX29 transcript levels were up regulated by light, through photoreceptor signaling pathways. Genetic evidence indicated that AtBBX29 up-regulates MYB12 gene expression, a TF known to induce genes related to flavonoid biosynthesis in a light-dependent manner, and MYB34 and MYB51, which encode TFs involved in the regulation of glucosinolate biosynthesis. Thus, bbx29 knockout mutants displayed low expression levels of key genes of the flavonoid biosynthetic pathway, and the opposite was true in BBX29 overexpression lines. In agreement with the transcriptomic data, bbx29 mutant plants accumulated lower levels of kaempferol glucosides, sinapoyl malate, indol-3-ylmethyl glucosinolate (I3M), 4-methylsulfinylbutyl glucosinolate (4MSOB) and 3-methylthiopropyl glucosinolate (3MSP) in rosette leaves compared to the wild-type, and showed increased susceptibility to the necrotrophic fungus Botrytis cinerea and to the herbivore Spodoptera frugiperda. In contrast, BBX29 overexpressing plants displayed increased resistance to both attackers. In addition, we found that AtBBX29 plays an important role in mediating the effects of ultraviolet-B (UV-B) radiation on plant defense against B. cinerea. Taken together, these results suggest that AtBBX29 orchestrates the accumulation of specific light-induced metabolites and regulates Arabidopsis resistance against pathogens and herbivores. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s43630-023-00391-8. Springer International Publishing 2023-02-18 2023 /pmc/articles/PMC10310583/ /pubmed/36807054 http://dx.doi.org/10.1007/s43630-023-00391-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Papers Medina-Fraga, Ana L. Chinen, Lucas A. Demkura, Patricia V. Lichy, Micaela Z. Gershenzon, Jonathan Ballaré, Carlos L. Crocco, Carlos D. AtBBX29 integrates photomorphogenesis and defense responses in Arabidopsis |
title | AtBBX29 integrates photomorphogenesis and defense responses in Arabidopsis |
title_full | AtBBX29 integrates photomorphogenesis and defense responses in Arabidopsis |
title_fullStr | AtBBX29 integrates photomorphogenesis and defense responses in Arabidopsis |
title_full_unstemmed | AtBBX29 integrates photomorphogenesis and defense responses in Arabidopsis |
title_short | AtBBX29 integrates photomorphogenesis and defense responses in Arabidopsis |
title_sort | atbbx29 integrates photomorphogenesis and defense responses in arabidopsis |
topic | Original Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10310583/ https://www.ncbi.nlm.nih.gov/pubmed/36807054 http://dx.doi.org/10.1007/s43630-023-00391-8 |
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