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BRASSINOSTEROID‐SIGNALLING KINASES 7 and 8 associate with the FLS2 immune receptor and are required for flg22‐induced PTI responses

Pattern‐triggered immunity (PTI) is typically initiated in plants by recognition of pathogen‐ or damage‐associated molecular patterns (PAMP/DAMPs) by cell surface‐localized pattern recognition receptors (PRRs). Here, we investigated the role in PTI of Arabidopsis thaliana brassinosteroid‐signalling...

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Autores principales: Majhi, Bharat Bhusan, Sobol, Guy, Gachie, Sarah, Sreeramulu, Shivakumar, Sessa, Guido
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8232025/
https://www.ncbi.nlm.nih.gov/pubmed/33955635
http://dx.doi.org/10.1111/mpp.13062
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author Majhi, Bharat Bhusan
Sobol, Guy
Gachie, Sarah
Sreeramulu, Shivakumar
Sessa, Guido
author_facet Majhi, Bharat Bhusan
Sobol, Guy
Gachie, Sarah
Sreeramulu, Shivakumar
Sessa, Guido
author_sort Majhi, Bharat Bhusan
collection PubMed
description Pattern‐triggered immunity (PTI) is typically initiated in plants by recognition of pathogen‐ or damage‐associated molecular patterns (PAMP/DAMPs) by cell surface‐localized pattern recognition receptors (PRRs). Here, we investigated the role in PTI of Arabidopsis thaliana brassinosteroid‐signalling kinases 7 and 8 (BSK7 and BSK8), which are members of the receptor‐like cytoplasmic kinase subfamily XII. BSK7 and BSK8 localized to the plant cell periphery and interacted in yeast and in planta with FLS2, but not with other PRRs. Consistent with a role in FLS2 signalling, bsk7 and bsk8 single and bsk7,8 double mutant plants were impaired in several immune responses induced by flg22, but not by other PAMP/DAMPs. These included resistance to Pseudomonas syringae and Botrytis cinerea, reactive oxygen species accumulation, callose deposition at the cell wall, and expression of the defence‐related gene PR1, but not activation of MAP kinases and expression of the FRK1 and WRKY29 genes. bsk7, bsk8, and bsk7,8 plants also displayed enhanced susceptibility to P. syringae and B. cinerea. Finally, BSK7 and BSK8 variants mutated in their myristoylation site or in the ATP‐binding site failed to complement defective phenotypes of the corresponding mutants, suggesting that localization to the cell periphery and kinase activity are critical for BSK7 and BSK8 functions. Together, these findings demonstrate that BSK7 and BSK8 play a role in PTI initiated by recognition of flg22 by interacting with the FLS2 immune receptor.
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spelling pubmed-82320252021-06-29 BRASSINOSTEROID‐SIGNALLING KINASES 7 and 8 associate with the FLS2 immune receptor and are required for flg22‐induced PTI responses Majhi, Bharat Bhusan Sobol, Guy Gachie, Sarah Sreeramulu, Shivakumar Sessa, Guido Mol Plant Pathol Original Articles Pattern‐triggered immunity (PTI) is typically initiated in plants by recognition of pathogen‐ or damage‐associated molecular patterns (PAMP/DAMPs) by cell surface‐localized pattern recognition receptors (PRRs). Here, we investigated the role in PTI of Arabidopsis thaliana brassinosteroid‐signalling kinases 7 and 8 (BSK7 and BSK8), which are members of the receptor‐like cytoplasmic kinase subfamily XII. BSK7 and BSK8 localized to the plant cell periphery and interacted in yeast and in planta with FLS2, but not with other PRRs. Consistent with a role in FLS2 signalling, bsk7 and bsk8 single and bsk7,8 double mutant plants were impaired in several immune responses induced by flg22, but not by other PAMP/DAMPs. These included resistance to Pseudomonas syringae and Botrytis cinerea, reactive oxygen species accumulation, callose deposition at the cell wall, and expression of the defence‐related gene PR1, but not activation of MAP kinases and expression of the FRK1 and WRKY29 genes. bsk7, bsk8, and bsk7,8 plants also displayed enhanced susceptibility to P. syringae and B. cinerea. Finally, BSK7 and BSK8 variants mutated in their myristoylation site or in the ATP‐binding site failed to complement defective phenotypes of the corresponding mutants, suggesting that localization to the cell periphery and kinase activity are critical for BSK7 and BSK8 functions. Together, these findings demonstrate that BSK7 and BSK8 play a role in PTI initiated by recognition of flg22 by interacting with the FLS2 immune receptor. John Wiley and Sons Inc. 2021-05-06 /pmc/articles/PMC8232025/ /pubmed/33955635 http://dx.doi.org/10.1111/mpp.13062 Text en © 2021 The Authors. Molecular Plant Pathology published by British Society for Plant Pathology 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 Original Articles
Majhi, Bharat Bhusan
Sobol, Guy
Gachie, Sarah
Sreeramulu, Shivakumar
Sessa, Guido
BRASSINOSTEROID‐SIGNALLING KINASES 7 and 8 associate with the FLS2 immune receptor and are required for flg22‐induced PTI responses
title BRASSINOSTEROID‐SIGNALLING KINASES 7 and 8 associate with the FLS2 immune receptor and are required for flg22‐induced PTI responses
title_full BRASSINOSTEROID‐SIGNALLING KINASES 7 and 8 associate with the FLS2 immune receptor and are required for flg22‐induced PTI responses
title_fullStr BRASSINOSTEROID‐SIGNALLING KINASES 7 and 8 associate with the FLS2 immune receptor and are required for flg22‐induced PTI responses
title_full_unstemmed BRASSINOSTEROID‐SIGNALLING KINASES 7 and 8 associate with the FLS2 immune receptor and are required for flg22‐induced PTI responses
title_short BRASSINOSTEROID‐SIGNALLING KINASES 7 and 8 associate with the FLS2 immune receptor and are required for flg22‐induced PTI responses
title_sort brassinosteroid‐signalling kinases 7 and 8 associate with the fls2 immune receptor and are required for flg22‐induced pti responses
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8232025/
https://www.ncbi.nlm.nih.gov/pubmed/33955635
http://dx.doi.org/10.1111/mpp.13062
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