Cargando…

Plant extracellular self-DNA inhibits growth and induces immunity via the jasmonate signaling pathway

Plants have evolved sophisticated mechanisms to detect various forms of danger. Damage-associated molecular patterns (DAMPs) are endogenous danger molecules that are released from damaged cells and activate the innate immunity. Recent evidence suggests that plant extracellular self-DNA (esDNA) can s...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhou, Xingang, Gao, Huan, Zhang, Xianhong, Khashi u Rahman, Muhammad, Mazzoleni, Stefano, Du, Minmin, Wu, Fengzhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10315318/
https://www.ncbi.nlm.nih.gov/pubmed/37002819
http://dx.doi.org/10.1093/plphys/kiad195
_version_ 1785067484024406016
author Zhou, Xingang
Gao, Huan
Zhang, Xianhong
Khashi u Rahman, Muhammad
Mazzoleni, Stefano
Du, Minmin
Wu, Fengzhi
author_facet Zhou, Xingang
Gao, Huan
Zhang, Xianhong
Khashi u Rahman, Muhammad
Mazzoleni, Stefano
Du, Minmin
Wu, Fengzhi
author_sort Zhou, Xingang
collection PubMed
description Plants have evolved sophisticated mechanisms to detect various forms of danger. Damage-associated molecular patterns (DAMPs) are endogenous danger molecules that are released from damaged cells and activate the innate immunity. Recent evidence suggests that plant extracellular self-DNA (esDNA) can serve as a DAMP molecule. However, the mechanisms by which esDNA functions are largely unknown. In this study, we confirmed that esDNA inhibits root growth and triggers reactive oxygen species (ROS) production in a concentration- and species-specific manner in Arabidopsis (Arabidopsis thaliana) and tomato (Solanum lycopersicum L.). Furthermore, by combining RNA sequencing, hormone measurement, and genetic analysis, we found that esDNA-mediated growth inhibition and ROS production are achieved through the jasmonic acid (JA) signaling pathway. Specifically, esDNA induces JA production and the expression of JA-responsive genes. The esDNA-mediated growth inhibition, ROS production, and gene expression are impaired in the JA-related mutants. Finally, we found that the JA signaling pathway is required for the esDNA-elicited resistance against the pathogens Botrytis cinerea and Pseudomonas syringae pv. tomato DC3000. This finding highlights the importance of JA signaling in esDNA-mediated biological effects, thereby providing insight into how esDNA functions as a DAMP.
format Online
Article
Text
id pubmed-10315318
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-103153182023-07-04 Plant extracellular self-DNA inhibits growth and induces immunity via the jasmonate signaling pathway Zhou, Xingang Gao, Huan Zhang, Xianhong Khashi u Rahman, Muhammad Mazzoleni, Stefano Du, Minmin Wu, Fengzhi Plant Physiol Research Article Plants have evolved sophisticated mechanisms to detect various forms of danger. Damage-associated molecular patterns (DAMPs) are endogenous danger molecules that are released from damaged cells and activate the innate immunity. Recent evidence suggests that plant extracellular self-DNA (esDNA) can serve as a DAMP molecule. However, the mechanisms by which esDNA functions are largely unknown. In this study, we confirmed that esDNA inhibits root growth and triggers reactive oxygen species (ROS) production in a concentration- and species-specific manner in Arabidopsis (Arabidopsis thaliana) and tomato (Solanum lycopersicum L.). Furthermore, by combining RNA sequencing, hormone measurement, and genetic analysis, we found that esDNA-mediated growth inhibition and ROS production are achieved through the jasmonic acid (JA) signaling pathway. Specifically, esDNA induces JA production and the expression of JA-responsive genes. The esDNA-mediated growth inhibition, ROS production, and gene expression are impaired in the JA-related mutants. Finally, we found that the JA signaling pathway is required for the esDNA-elicited resistance against the pathogens Botrytis cinerea and Pseudomonas syringae pv. tomato DC3000. This finding highlights the importance of JA signaling in esDNA-mediated biological effects, thereby providing insight into how esDNA functions as a DAMP. Oxford University Press 2023-04-01 /pmc/articles/PMC10315318/ /pubmed/37002819 http://dx.doi.org/10.1093/plphys/kiad195 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of American Society of Plant Biologists. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Research Article
Zhou, Xingang
Gao, Huan
Zhang, Xianhong
Khashi u Rahman, Muhammad
Mazzoleni, Stefano
Du, Minmin
Wu, Fengzhi
Plant extracellular self-DNA inhibits growth and induces immunity via the jasmonate signaling pathway
title Plant extracellular self-DNA inhibits growth and induces immunity via the jasmonate signaling pathway
title_full Plant extracellular self-DNA inhibits growth and induces immunity via the jasmonate signaling pathway
title_fullStr Plant extracellular self-DNA inhibits growth and induces immunity via the jasmonate signaling pathway
title_full_unstemmed Plant extracellular self-DNA inhibits growth and induces immunity via the jasmonate signaling pathway
title_short Plant extracellular self-DNA inhibits growth and induces immunity via the jasmonate signaling pathway
title_sort plant extracellular self-dna inhibits growth and induces immunity via the jasmonate signaling pathway
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10315318/
https://www.ncbi.nlm.nih.gov/pubmed/37002819
http://dx.doi.org/10.1093/plphys/kiad195
work_keys_str_mv AT zhouxingang plantextracellularselfdnainhibitsgrowthandinducesimmunityviathejasmonatesignalingpathway
AT gaohuan plantextracellularselfdnainhibitsgrowthandinducesimmunityviathejasmonatesignalingpathway
AT zhangxianhong plantextracellularselfdnainhibitsgrowthandinducesimmunityviathejasmonatesignalingpathway
AT khashiurahmanmuhammad plantextracellularselfdnainhibitsgrowthandinducesimmunityviathejasmonatesignalingpathway
AT mazzolenistefano plantextracellularselfdnainhibitsgrowthandinducesimmunityviathejasmonatesignalingpathway
AT duminmin plantextracellularselfdnainhibitsgrowthandinducesimmunityviathejasmonatesignalingpathway
AT wufengzhi plantextracellularselfdnainhibitsgrowthandinducesimmunityviathejasmonatesignalingpathway