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The pivotal ripening gene SlDML2 participates in regulating disease resistance in tomato

Fruit ripening and disease resistance are two essential biological processes for quality formation and maintenance. DNA methylation, in the form of 5‐methylcytosine (5mC), has been elucidated to modulate fruit ripening, but its role in regulating fruit disease resistance remains poorly understood. I...

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Autores principales: Zhou, Leilei, Gao, Guangtong, Li, Xiaojing, Wang, Weihao, Tian, Shiping, Qin, Guozheng
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/PMC10579708/
https://www.ncbi.nlm.nih.gov/pubmed/37466912
http://dx.doi.org/10.1111/pbi.14130
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author Zhou, Leilei
Gao, Guangtong
Li, Xiaojing
Wang, Weihao
Tian, Shiping
Qin, Guozheng
author_facet Zhou, Leilei
Gao, Guangtong
Li, Xiaojing
Wang, Weihao
Tian, Shiping
Qin, Guozheng
author_sort Zhou, Leilei
collection PubMed
description Fruit ripening and disease resistance are two essential biological processes for quality formation and maintenance. DNA methylation, in the form of 5‐methylcytosine (5mC), has been elucidated to modulate fruit ripening, but its role in regulating fruit disease resistance remains poorly understood. In this study, we show that mutation of SlDML2, the DNA demethylase gene essential for fruit ripening, affects multiple developmental processes of tomato besides fruit ripening, including seed germination, leaf length and width and flower branching. Intriguingly, loss of SlDML2 function decreased the resistance of tomato fruits against the necrotrophic fungal pathogen Botrytis cinerea. Comparative transcriptomic analysis revealed an obvious transcriptome reprogramming caused by SlDML2 mutation during B. cinerea invasion. Among the thousands of differentially expressed genes, SlβCA3 encoding a β‐carbonic anhydrase and SlFAD3 encoding a ω‐3 fatty acid desaturase were demonstrated to be transcriptionally activated by SlDML2‐mediated DNA demethylation and positively regulate tomato resistance to B. cinerea probably in the same genetic pathway with SlDML2. We further show that the pericarp tissue surrounding B. cinerea infection exhibited a delay in ripening with singnificant decrease in expression of ripening genes that are targeted by SlDML2 and increase in expression of SlβCA3 and SlFAD3. Taken together, our results uncover an essential layer of gene regulation mediated by DNA methylation upon B. cinerea infection and raise the possible that the DNA demethylase gene SlDML2, as a multifunctional gene, participates in modulating the trade‐off between fruit ripening and disease resistance.
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spelling pubmed-105797082023-10-18 The pivotal ripening gene SlDML2 participates in regulating disease resistance in tomato Zhou, Leilei Gao, Guangtong Li, Xiaojing Wang, Weihao Tian, Shiping Qin, Guozheng Plant Biotechnol J Research Articles Fruit ripening and disease resistance are two essential biological processes for quality formation and maintenance. DNA methylation, in the form of 5‐methylcytosine (5mC), has been elucidated to modulate fruit ripening, but its role in regulating fruit disease resistance remains poorly understood. In this study, we show that mutation of SlDML2, the DNA demethylase gene essential for fruit ripening, affects multiple developmental processes of tomato besides fruit ripening, including seed germination, leaf length and width and flower branching. Intriguingly, loss of SlDML2 function decreased the resistance of tomato fruits against the necrotrophic fungal pathogen Botrytis cinerea. Comparative transcriptomic analysis revealed an obvious transcriptome reprogramming caused by SlDML2 mutation during B. cinerea invasion. Among the thousands of differentially expressed genes, SlβCA3 encoding a β‐carbonic anhydrase and SlFAD3 encoding a ω‐3 fatty acid desaturase were demonstrated to be transcriptionally activated by SlDML2‐mediated DNA demethylation and positively regulate tomato resistance to B. cinerea probably in the same genetic pathway with SlDML2. We further show that the pericarp tissue surrounding B. cinerea infection exhibited a delay in ripening with singnificant decrease in expression of ripening genes that are targeted by SlDML2 and increase in expression of SlβCA3 and SlFAD3. Taken together, our results uncover an essential layer of gene regulation mediated by DNA methylation upon B. cinerea infection and raise the possible that the DNA demethylase gene SlDML2, as a multifunctional gene, participates in modulating the trade‐off between fruit ripening and disease resistance. John Wiley and Sons Inc. 2023-07-19 2023-11 /pmc/articles/PMC10579708/ /pubmed/37466912 http://dx.doi.org/10.1111/pbi.14130 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/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Zhou, Leilei
Gao, Guangtong
Li, Xiaojing
Wang, Weihao
Tian, Shiping
Qin, Guozheng
The pivotal ripening gene SlDML2 participates in regulating disease resistance in tomato
title The pivotal ripening gene SlDML2 participates in regulating disease resistance in tomato
title_full The pivotal ripening gene SlDML2 participates in regulating disease resistance in tomato
title_fullStr The pivotal ripening gene SlDML2 participates in regulating disease resistance in tomato
title_full_unstemmed The pivotal ripening gene SlDML2 participates in regulating disease resistance in tomato
title_short The pivotal ripening gene SlDML2 participates in regulating disease resistance in tomato
title_sort pivotal ripening gene sldml2 participates in regulating disease resistance in tomato
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10579708/
https://www.ncbi.nlm.nih.gov/pubmed/37466912
http://dx.doi.org/10.1111/pbi.14130
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