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CRISPR/Cas9‐mediated simultaneous mutation of three salicylic acid 5‐hydroxylase (OsS5H) genes confers broad‐spectrum disease resistance in rice

Salicylic acid (SA) is an essential plant hormone that plays critical roles in basal defence and amplification of local immune responses and establishes resistance against various pathogens. However, the comprehensive knowledge of the salicylic acid 5‐hydroxylase (S5H) in rice‐pathogen interaction i...

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Autores principales: Liu, Xiong, Yu, Yan, Yao, Wei, Yin, Zhongliang, Wang, Yubo, Huang, Zijian, Zhou, Jie‐Qiang, Liu, Jinling, Lu, Xuedan, Wang, Feng, Zhang, Guilian, Chen, Guihua, Xiao, Yunhua, Deng, Huabing, Tang, Wenbang
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/PMC10440993/
https://www.ncbi.nlm.nih.gov/pubmed/37323119
http://dx.doi.org/10.1111/pbi.14099
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author Liu, Xiong
Yu, Yan
Yao, Wei
Yin, Zhongliang
Wang, Yubo
Huang, Zijian
Zhou, Jie‐Qiang
Liu, Jinling
Lu, Xuedan
Wang, Feng
Zhang, Guilian
Chen, Guihua
Xiao, Yunhua
Deng, Huabing
Tang, Wenbang
author_facet Liu, Xiong
Yu, Yan
Yao, Wei
Yin, Zhongliang
Wang, Yubo
Huang, Zijian
Zhou, Jie‐Qiang
Liu, Jinling
Lu, Xuedan
Wang, Feng
Zhang, Guilian
Chen, Guihua
Xiao, Yunhua
Deng, Huabing
Tang, Wenbang
author_sort Liu, Xiong
collection PubMed
description Salicylic acid (SA) is an essential plant hormone that plays critical roles in basal defence and amplification of local immune responses and establishes resistance against various pathogens. However, the comprehensive knowledge of the salicylic acid 5‐hydroxylase (S5H) in rice‐pathogen interaction is still elusive. Here, we reported that three OsS5H homologues displayed salicylic acid 5‐hydroxylase activity, converting SA into 2,5‐dihydroxybenzoic acid (2,5‐DHBA). OsS5H1, OsS5H2, and OsS5H3 were preferentially expressed in rice leaves at heading stage and responded quickly to exogenous SA treatment. We found that bacterial pathogen Xanthomonas oryzae pv. oryzae (Xoo) strongly induced the expression of OsS5H1, OsS5H2, and OsS5H3. Rice plants overexpressing OsS5H1, OsS5H2, and OsS5H3 showed significantly decreased SA contents and increased 2,5‐DHBA levels, and were more susceptible to bacterial blight and rice blast. A simple single guide RNA (sgRNA) was designed to create oss5h1oss5h2oss5h3 triple mutants through CRISPR/Cas9‐mediated gene mutagenesis. The oss5h1oss5h2oss5h3 exhibited stronger resistance to Xoo than single oss5h mutants. And oss5h1oss5h2oss5h3 plants displayed enhanced rice blast resistance. The conferred pathogen resistance in oss5h1oss5h2oss5h3 was attributed to the significantly upregulation of OsWRKY45 and pathogenesis‐related (PR) genes. Besides, flg22‐induced reactive oxygen species (ROS) burst was enhanced in oss5h1oss5h2oss5h3. Collectively, our study provides a fast and effective approach to generate rice varieties with broad‐spectrum disease resistance through OsS5H gene editing.
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spelling pubmed-104409932023-08-22 CRISPR/Cas9‐mediated simultaneous mutation of three salicylic acid 5‐hydroxylase (OsS5H) genes confers broad‐spectrum disease resistance in rice Liu, Xiong Yu, Yan Yao, Wei Yin, Zhongliang Wang, Yubo Huang, Zijian Zhou, Jie‐Qiang Liu, Jinling Lu, Xuedan Wang, Feng Zhang, Guilian Chen, Guihua Xiao, Yunhua Deng, Huabing Tang, Wenbang Plant Biotechnol J Research Articles Salicylic acid (SA) is an essential plant hormone that plays critical roles in basal defence and amplification of local immune responses and establishes resistance against various pathogens. However, the comprehensive knowledge of the salicylic acid 5‐hydroxylase (S5H) in rice‐pathogen interaction is still elusive. Here, we reported that three OsS5H homologues displayed salicylic acid 5‐hydroxylase activity, converting SA into 2,5‐dihydroxybenzoic acid (2,5‐DHBA). OsS5H1, OsS5H2, and OsS5H3 were preferentially expressed in rice leaves at heading stage and responded quickly to exogenous SA treatment. We found that bacterial pathogen Xanthomonas oryzae pv. oryzae (Xoo) strongly induced the expression of OsS5H1, OsS5H2, and OsS5H3. Rice plants overexpressing OsS5H1, OsS5H2, and OsS5H3 showed significantly decreased SA contents and increased 2,5‐DHBA levels, and were more susceptible to bacterial blight and rice blast. A simple single guide RNA (sgRNA) was designed to create oss5h1oss5h2oss5h3 triple mutants through CRISPR/Cas9‐mediated gene mutagenesis. The oss5h1oss5h2oss5h3 exhibited stronger resistance to Xoo than single oss5h mutants. And oss5h1oss5h2oss5h3 plants displayed enhanced rice blast resistance. The conferred pathogen resistance in oss5h1oss5h2oss5h3 was attributed to the significantly upregulation of OsWRKY45 and pathogenesis‐related (PR) genes. Besides, flg22‐induced reactive oxygen species (ROS) burst was enhanced in oss5h1oss5h2oss5h3. Collectively, our study provides a fast and effective approach to generate rice varieties with broad‐spectrum disease resistance through OsS5H gene editing. John Wiley and Sons Inc. 2023-06-15 2023-09 /pmc/articles/PMC10440993/ /pubmed/37323119 http://dx.doi.org/10.1111/pbi.14099 Text en © 2023 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
Liu, Xiong
Yu, Yan
Yao, Wei
Yin, Zhongliang
Wang, Yubo
Huang, Zijian
Zhou, Jie‐Qiang
Liu, Jinling
Lu, Xuedan
Wang, Feng
Zhang, Guilian
Chen, Guihua
Xiao, Yunhua
Deng, Huabing
Tang, Wenbang
CRISPR/Cas9‐mediated simultaneous mutation of three salicylic acid 5‐hydroxylase (OsS5H) genes confers broad‐spectrum disease resistance in rice
title CRISPR/Cas9‐mediated simultaneous mutation of three salicylic acid 5‐hydroxylase (OsS5H) genes confers broad‐spectrum disease resistance in rice
title_full CRISPR/Cas9‐mediated simultaneous mutation of three salicylic acid 5‐hydroxylase (OsS5H) genes confers broad‐spectrum disease resistance in rice
title_fullStr CRISPR/Cas9‐mediated simultaneous mutation of three salicylic acid 5‐hydroxylase (OsS5H) genes confers broad‐spectrum disease resistance in rice
title_full_unstemmed CRISPR/Cas9‐mediated simultaneous mutation of three salicylic acid 5‐hydroxylase (OsS5H) genes confers broad‐spectrum disease resistance in rice
title_short CRISPR/Cas9‐mediated simultaneous mutation of three salicylic acid 5‐hydroxylase (OsS5H) genes confers broad‐spectrum disease resistance in rice
title_sort crispr/cas9‐mediated simultaneous mutation of three salicylic acid 5‐hydroxylase (oss5h) genes confers broad‐spectrum disease resistance in rice
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10440993/
https://www.ncbi.nlm.nih.gov/pubmed/37323119
http://dx.doi.org/10.1111/pbi.14099
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