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Tomato LysM receptor kinase 4 mediates chitin-elicited fungal resistance in both leaves and fruit
Fungal infection is a major cause of crop and fruit losses. Recognition of chitin, a component of fungal cell walls, endows plants with enhanced fungal resistance. Here, we found that mutation of tomato LysM receptor kinase 4 (SlLYK4) and chitin elicitor receptor kinase 1 (SlCERK1) impaired chitin-i...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10266952/ https://www.ncbi.nlm.nih.gov/pubmed/37323235 http://dx.doi.org/10.1093/hr/uhad082 |
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author | Ai, Yingfei Li, Qinghong Li, Chenying Wang, Ran Sun, Xun Chen, Songyu Cai, Xin-Zhong Qi, Xingjiang Liang, Yan |
author_facet | Ai, Yingfei Li, Qinghong Li, Chenying Wang, Ran Sun, Xun Chen, Songyu Cai, Xin-Zhong Qi, Xingjiang Liang, Yan |
author_sort | Ai, Yingfei |
collection | PubMed |
description | Fungal infection is a major cause of crop and fruit losses. Recognition of chitin, a component of fungal cell walls, endows plants with enhanced fungal resistance. Here, we found that mutation of tomato LysM receptor kinase 4 (SlLYK4) and chitin elicitor receptor kinase 1 (SlCERK1) impaired chitin-induced immune responses in tomato leaves. Compared with the wild type, sllyk4 and slcerk1 mutant leaves were more susceptible to Botrytis cinerea (gray mold). SlLYK4 extracellular domain showed strong binding affinity to chitin, and the binding of SlLYK4 induced SlLYK4-SlCERK1 association. Remarkably, qRT–PCR analysis indicated that SlLYK4 was highly expressed in tomato fruit, and β-GLUCURONIDASE (GUS) expression driven by the SlLYK4 promoter was observed in tomato fruit. Furthermore, SlLYK4 overexpression enhanced disease resistance not only in leaves but also in fruit. Our study suggests that chitin-mediated immunity plays a role in fruit, providing a possible way to reduce fungal infection-related fruit losses by enhancing the chitin-induced immune responses. |
format | Online Article Text |
id | pubmed-10266952 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-102669522023-06-15 Tomato LysM receptor kinase 4 mediates chitin-elicited fungal resistance in both leaves and fruit Ai, Yingfei Li, Qinghong Li, Chenying Wang, Ran Sun, Xun Chen, Songyu Cai, Xin-Zhong Qi, Xingjiang Liang, Yan Hortic Res Article Fungal infection is a major cause of crop and fruit losses. Recognition of chitin, a component of fungal cell walls, endows plants with enhanced fungal resistance. Here, we found that mutation of tomato LysM receptor kinase 4 (SlLYK4) and chitin elicitor receptor kinase 1 (SlCERK1) impaired chitin-induced immune responses in tomato leaves. Compared with the wild type, sllyk4 and slcerk1 mutant leaves were more susceptible to Botrytis cinerea (gray mold). SlLYK4 extracellular domain showed strong binding affinity to chitin, and the binding of SlLYK4 induced SlLYK4-SlCERK1 association. Remarkably, qRT–PCR analysis indicated that SlLYK4 was highly expressed in tomato fruit, and β-GLUCURONIDASE (GUS) expression driven by the SlLYK4 promoter was observed in tomato fruit. Furthermore, SlLYK4 overexpression enhanced disease resistance not only in leaves but also in fruit. Our study suggests that chitin-mediated immunity plays a role in fruit, providing a possible way to reduce fungal infection-related fruit losses by enhancing the chitin-induced immune responses. Oxford University Press 2023-04-25 /pmc/articles/PMC10266952/ /pubmed/37323235 http://dx.doi.org/10.1093/hr/uhad082 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Nanjing Agricultural University. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Article Ai, Yingfei Li, Qinghong Li, Chenying Wang, Ran Sun, Xun Chen, Songyu Cai, Xin-Zhong Qi, Xingjiang Liang, Yan Tomato LysM receptor kinase 4 mediates chitin-elicited fungal resistance in both leaves and fruit |
title | Tomato LysM receptor kinase 4 mediates chitin-elicited fungal resistance in both leaves and fruit |
title_full | Tomato LysM receptor kinase 4 mediates chitin-elicited fungal resistance in both leaves and fruit |
title_fullStr | Tomato LysM receptor kinase 4 mediates chitin-elicited fungal resistance in both leaves and fruit |
title_full_unstemmed | Tomato LysM receptor kinase 4 mediates chitin-elicited fungal resistance in both leaves and fruit |
title_short | Tomato LysM receptor kinase 4 mediates chitin-elicited fungal resistance in both leaves and fruit |
title_sort | tomato lysm receptor kinase 4 mediates chitin-elicited fungal resistance in both leaves and fruit |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10266952/ https://www.ncbi.nlm.nih.gov/pubmed/37323235 http://dx.doi.org/10.1093/hr/uhad082 |
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