Cargando…
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...
Autores principales: | , , , , , , , , , , , , , , |
---|---|
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 |
_version_ | 1785093278404706304 |
---|---|
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. |
format | Online Article Text |
id | pubmed-10440993 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT liuxiong crisprcas9mediatedsimultaneousmutationofthreesalicylicacid5hydroxylaseoss5hgenesconfersbroadspectrumdiseaseresistanceinrice AT yuyan crisprcas9mediatedsimultaneousmutationofthreesalicylicacid5hydroxylaseoss5hgenesconfersbroadspectrumdiseaseresistanceinrice AT yaowei crisprcas9mediatedsimultaneousmutationofthreesalicylicacid5hydroxylaseoss5hgenesconfersbroadspectrumdiseaseresistanceinrice AT yinzhongliang crisprcas9mediatedsimultaneousmutationofthreesalicylicacid5hydroxylaseoss5hgenesconfersbroadspectrumdiseaseresistanceinrice AT wangyubo crisprcas9mediatedsimultaneousmutationofthreesalicylicacid5hydroxylaseoss5hgenesconfersbroadspectrumdiseaseresistanceinrice AT huangzijian crisprcas9mediatedsimultaneousmutationofthreesalicylicacid5hydroxylaseoss5hgenesconfersbroadspectrumdiseaseresistanceinrice AT zhoujieqiang crisprcas9mediatedsimultaneousmutationofthreesalicylicacid5hydroxylaseoss5hgenesconfersbroadspectrumdiseaseresistanceinrice AT liujinling crisprcas9mediatedsimultaneousmutationofthreesalicylicacid5hydroxylaseoss5hgenesconfersbroadspectrumdiseaseresistanceinrice AT luxuedan crisprcas9mediatedsimultaneousmutationofthreesalicylicacid5hydroxylaseoss5hgenesconfersbroadspectrumdiseaseresistanceinrice AT wangfeng crisprcas9mediatedsimultaneousmutationofthreesalicylicacid5hydroxylaseoss5hgenesconfersbroadspectrumdiseaseresistanceinrice AT zhangguilian crisprcas9mediatedsimultaneousmutationofthreesalicylicacid5hydroxylaseoss5hgenesconfersbroadspectrumdiseaseresistanceinrice AT chenguihua crisprcas9mediatedsimultaneousmutationofthreesalicylicacid5hydroxylaseoss5hgenesconfersbroadspectrumdiseaseresistanceinrice AT xiaoyunhua crisprcas9mediatedsimultaneousmutationofthreesalicylicacid5hydroxylaseoss5hgenesconfersbroadspectrumdiseaseresistanceinrice AT denghuabing crisprcas9mediatedsimultaneousmutationofthreesalicylicacid5hydroxylaseoss5hgenesconfersbroadspectrumdiseaseresistanceinrice AT tangwenbang crisprcas9mediatedsimultaneousmutationofthreesalicylicacid5hydroxylaseoss5hgenesconfersbroadspectrumdiseaseresistanceinrice |