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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...

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Autores principales: Ai, Yingfei, Li, Qinghong, Li, Chenying, Wang, Ran, Sun, Xun, Chen, Songyu, Cai, Xin-Zhong, Qi, Xingjiang, Liang, Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
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.
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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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