Plant extracellular self-DNA inhibits growth and induces immunity via the jasmonate signaling pathway.
Xingang ZhouHuan GaoXianhong ZhangMuhammad Khashi U RahmanStefano MazzoleniMinmin DuFengzhi WuPublished in: Plant physiology (2023)
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.
Keyphrases
- signaling pathway
- reactive oxygen species
- induced apoptosis
- gene expression
- cell death
- dna damage
- arabidopsis thaliana
- pi k akt
- oxidative stress
- epithelial mesenchymal transition
- circulating tumor
- transcription factor
- cell free
- single cell
- single molecule
- immune response
- multidrug resistant
- poor prognosis
- long non coding rna
- cell proliferation
- binding protein
- cystic fibrosis
- cancer therapy
- escherichia coli
- circulating tumor cells
- biofilm formation