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MYC transcription factors coordinate tryptophan‐dependent defence responses and compromise seed yield in Arabidopsis
Robust plant immunity negatively affects other fitness traits, including growth and seed production. Jasmonate (JA) confers broad‐spectrum protection against plant consumers by stimulating the degradation of JASMONATE ZIM‐DOMAIN (JAZ) proteins, which in turn relieves repression on transcription fact...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9541860/ https://www.ncbi.nlm.nih.gov/pubmed/35642375 http://dx.doi.org/10.1111/nph.18293 |
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author | Guo, Qiang Major, Ian T. Kapali, George Howe, Gregg A. |
author_facet | Guo, Qiang Major, Ian T. Kapali, George Howe, Gregg A. |
author_sort | Guo, Qiang |
collection | PubMed |
description | Robust plant immunity negatively affects other fitness traits, including growth and seed production. Jasmonate (JA) confers broad‐spectrum protection against plant consumers by stimulating the degradation of JASMONATE ZIM‐DOMAIN (JAZ) proteins, which in turn relieves repression on transcription factors (TFs) coincident with reduced growth and fecundity. The molecular mechanisms underlying JA‐mediated decreases in fitness remain largely unknown. To assess the contribution of MYC TFs to growth and reproductive fitness at high levels of defence, we mutated three MYC genes in a JAZ‐deficient mutant (jazD) of Arabidopsis thaliana that exhibits strong defence and low seed yield. Genetic epistasis analysis showed that de‐repression of MYC TFs in jazD not only conferred strong resistance to insect herbivory but also reduced shoot and root growth, fruit size and seed yield. We also provided evidence that the JAZ–MYC module coordinates the supply of tryptophan with the production of indole glucosinolates and the proliferation of endoplasmic reticulum bodies that metabolise glucosinolates through the action of β‐glucosidases. Our results establish MYCs as major regulators of growth‐ and reproductive–defence trade‐offs and further indicate that these factors coordinate tryptophan availability with the production of amino acid‐derived defence compounds. |
format | Online Article Text |
id | pubmed-9541860 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95418602022-10-14 MYC transcription factors coordinate tryptophan‐dependent defence responses and compromise seed yield in Arabidopsis Guo, Qiang Major, Ian T. Kapali, George Howe, Gregg A. New Phytol Research Robust plant immunity negatively affects other fitness traits, including growth and seed production. Jasmonate (JA) confers broad‐spectrum protection against plant consumers by stimulating the degradation of JASMONATE ZIM‐DOMAIN (JAZ) proteins, which in turn relieves repression on transcription factors (TFs) coincident with reduced growth and fecundity. The molecular mechanisms underlying JA‐mediated decreases in fitness remain largely unknown. To assess the contribution of MYC TFs to growth and reproductive fitness at high levels of defence, we mutated three MYC genes in a JAZ‐deficient mutant (jazD) of Arabidopsis thaliana that exhibits strong defence and low seed yield. Genetic epistasis analysis showed that de‐repression of MYC TFs in jazD not only conferred strong resistance to insect herbivory but also reduced shoot and root growth, fruit size and seed yield. We also provided evidence that the JAZ–MYC module coordinates the supply of tryptophan with the production of indole glucosinolates and the proliferation of endoplasmic reticulum bodies that metabolise glucosinolates through the action of β‐glucosidases. Our results establish MYCs as major regulators of growth‐ and reproductive–defence trade‐offs and further indicate that these factors coordinate tryptophan availability with the production of amino acid‐derived defence compounds. John Wiley and Sons Inc. 2022-06-21 2022-10 /pmc/articles/PMC9541860/ /pubmed/35642375 http://dx.doi.org/10.1111/nph.18293 Text en © 2022 The Authors. New Phytologist © 2022 New Phytologist Foundation. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Guo, Qiang Major, Ian T. Kapali, George Howe, Gregg A. MYC transcription factors coordinate tryptophan‐dependent defence responses and compromise seed yield in Arabidopsis |
title |
MYC transcription factors coordinate tryptophan‐dependent defence responses and compromise seed yield in Arabidopsis |
title_full |
MYC transcription factors coordinate tryptophan‐dependent defence responses and compromise seed yield in Arabidopsis |
title_fullStr |
MYC transcription factors coordinate tryptophan‐dependent defence responses and compromise seed yield in Arabidopsis |
title_full_unstemmed |
MYC transcription factors coordinate tryptophan‐dependent defence responses and compromise seed yield in Arabidopsis |
title_short |
MYC transcription factors coordinate tryptophan‐dependent defence responses and compromise seed yield in Arabidopsis |
title_sort | myc transcription factors coordinate tryptophan‐dependent defence responses and compromise seed yield in arabidopsis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9541860/ https://www.ncbi.nlm.nih.gov/pubmed/35642375 http://dx.doi.org/10.1111/nph.18293 |
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