Abstract
Plants perceive pathogenic threats through receptors localized at the plasma membrane and inside cells to initiate pattern-triggered immunity (PTI) and effector-triggered immunity (ETI), respectively. PTI and ETI pathways are interconnected and partially converge on the EDS1-PAD4-ADR1 branch which stimulates anti-pathogen defence. Besides these canonical immune pathways, proteolysis plays a pivotal role in immunity by regulating the abundance and activities of diverse components. We previously identified Arabidopsis papain-like cysteine protease RD19 as a PAD4 interactor and showed that RD19 promotes resistance to host-adapted pathogens. Here, we investigated the contribution of RD19 to bacterial flg22 and nlp20 elicited PTI responses which exhibit, respectively, partial and high PAD4 dependence. We show that although PAD4 and RD19 both promote PTI, they have separate functions. In resting (non-triggered) and nlp20-triggered tissues, RD19 limits RBOHD protein accumulation and consequently ROS production. Using N-terminomic enrichment and protease cleavage site identification methods we identify candidate RD19 substrates in resting and nlp20-responding tissues. Our analysis shows that two immune-related aspartyl proteases AED3 and AED2/ASPG1 are likely direct RD19 targets. This study reveals a role of RD19 in ROS regulation and advances our understanding of proteolysis and dynamic RD19 substrate targeting in plant immunity.