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SlBBX20 attenuates JA signalling and regulates resistance to Botrytis cinerea by inhibiting SlMED25 in tomato

Jasmonic acid (JA) plays an important role in regulating plant growth and defence responses. Here, we show that a transcription factor that belongs to the B‐box (BBX) family named SlBBX20 regulates resistance to Botrytis cinerea in tomato by modulating JA signalling. The response to JA was significa...

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Autores principales: Luo, Dan, Sun, Wenhui, Cai, Jun, Hu, Guoyu, Zhang, Danqiu, Zhang, Xiaoyan, Larkin, Robert M., Zhang, Junhong, Yang, Changxian, Ye, Zhibiao, Wang, Taotao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10037119/
https://www.ncbi.nlm.nih.gov/pubmed/36582069
http://dx.doi.org/10.1111/pbi.13997
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author Luo, Dan
Sun, Wenhui
Cai, Jun
Hu, Guoyu
Zhang, Danqiu
Zhang, Xiaoyan
Larkin, Robert M.
Zhang, Junhong
Yang, Changxian
Ye, Zhibiao
Wang, Taotao
author_facet Luo, Dan
Sun, Wenhui
Cai, Jun
Hu, Guoyu
Zhang, Danqiu
Zhang, Xiaoyan
Larkin, Robert M.
Zhang, Junhong
Yang, Changxian
Ye, Zhibiao
Wang, Taotao
author_sort Luo, Dan
collection PubMed
description Jasmonic acid (JA) plays an important role in regulating plant growth and defence responses. Here, we show that a transcription factor that belongs to the B‐box (BBX) family named SlBBX20 regulates resistance to Botrytis cinerea in tomato by modulating JA signalling. The response to JA was significantly suppressed when SlBBX20 was overexpressed in tomato. By contrast, the JA response was enhanced in SlBBX20 knockout lines. RNA sequencing analysis provided more evidence that SlBBX20 modulates the expression of genes that are involved in JA signalling. We found that SlBBX20 interacts with SlMED25, a subunit of the Mediator transcriptional co‐activator complex, and prevents the accumulation of the SlMED25 protein and transcription of JA‐responsive genes. JA contributes to the defence response against necrotrophic pathogens. Knocking out SlBBX20 or overexpressing SlMED25 enhanced tomato resistance to B. cinerea. The resistance was impaired when SlBBX20 was overexpressed in plants that also overexpressed SlMED25. These data show that SlBBX20 attenuates JA signalling by regulating SlMED25. Interestingly, in addition to developing enhanced resistance to B. cinerea, SlBBX20‐KO plants also produced higher fruit yields. SlBBX20 is a potential target gene for efforts that aim to develop elite crop varieties using gene editing technologies.
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spelling pubmed-100371192023-03-25 SlBBX20 attenuates JA signalling and regulates resistance to Botrytis cinerea by inhibiting SlMED25 in tomato Luo, Dan Sun, Wenhui Cai, Jun Hu, Guoyu Zhang, Danqiu Zhang, Xiaoyan Larkin, Robert M. Zhang, Junhong Yang, Changxian Ye, Zhibiao Wang, Taotao Plant Biotechnol J Research Articles Jasmonic acid (JA) plays an important role in regulating plant growth and defence responses. Here, we show that a transcription factor that belongs to the B‐box (BBX) family named SlBBX20 regulates resistance to Botrytis cinerea in tomato by modulating JA signalling. The response to JA was significantly suppressed when SlBBX20 was overexpressed in tomato. By contrast, the JA response was enhanced in SlBBX20 knockout lines. RNA sequencing analysis provided more evidence that SlBBX20 modulates the expression of genes that are involved in JA signalling. We found that SlBBX20 interacts with SlMED25, a subunit of the Mediator transcriptional co‐activator complex, and prevents the accumulation of the SlMED25 protein and transcription of JA‐responsive genes. JA contributes to the defence response against necrotrophic pathogens. Knocking out SlBBX20 or overexpressing SlMED25 enhanced tomato resistance to B. cinerea. The resistance was impaired when SlBBX20 was overexpressed in plants that also overexpressed SlMED25. These data show that SlBBX20 attenuates JA signalling by regulating SlMED25. Interestingly, in addition to developing enhanced resistance to B. cinerea, SlBBX20‐KO plants also produced higher fruit yields. SlBBX20 is a potential target gene for efforts that aim to develop elite crop varieties using gene editing technologies. John Wiley and Sons Inc. 2023-02-07 2023-04 /pmc/articles/PMC10037119/ /pubmed/36582069 http://dx.doi.org/10.1111/pbi.13997 Text en © 2022 The Authors. Plant Biotechnology Journal published by Society for Experimental Biology and The Association of Applied Biologists and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Luo, Dan
Sun, Wenhui
Cai, Jun
Hu, Guoyu
Zhang, Danqiu
Zhang, Xiaoyan
Larkin, Robert M.
Zhang, Junhong
Yang, Changxian
Ye, Zhibiao
Wang, Taotao
SlBBX20 attenuates JA signalling and regulates resistance to Botrytis cinerea by inhibiting SlMED25 in tomato
title SlBBX20 attenuates JA signalling and regulates resistance to Botrytis cinerea by inhibiting SlMED25 in tomato
title_full SlBBX20 attenuates JA signalling and regulates resistance to Botrytis cinerea by inhibiting SlMED25 in tomato
title_fullStr SlBBX20 attenuates JA signalling and regulates resistance to Botrytis cinerea by inhibiting SlMED25 in tomato
title_full_unstemmed SlBBX20 attenuates JA signalling and regulates resistance to Botrytis cinerea by inhibiting SlMED25 in tomato
title_short SlBBX20 attenuates JA signalling and regulates resistance to Botrytis cinerea by inhibiting SlMED25 in tomato
title_sort slbbx20 attenuates ja signalling and regulates resistance to botrytis cinerea by inhibiting slmed25 in tomato
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10037119/
https://www.ncbi.nlm.nih.gov/pubmed/36582069
http://dx.doi.org/10.1111/pbi.13997
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