Evolutionary Trajectory of Pattern Recognition Receptors in Plants

Plants perceive pathogen-associated molecular patterns (PAMPs) via pattern recognition receptors (PRRs) to activate PRR-triggered immunity (PTI). Despite extensive research on PTI in model plant species, the evolutionary trajectory and emergence of PRRs remain elusive. Here we conducted a comparative genomic analysis of cell-surface receptors and downstream signalling components among 350 plant species. Our findings reveal that cell-surface receptors comprise two major classes, receptor-like proteins (RLPs) and receptor-like kinases (RLKs), with RLP being more ancient whereas RLK families have undergone significant expansion. We also demonstrate that multiple downstream signalling components have an ancient origin within the plant lineage. To shed light on the immune-specificity of PRRs, we traced the evolutionary origin of immune-specific leucine-rich repeat-RLPs (LRR-RLPs) in plants. Surprisingly, we discovered that the last four LRR motifs crucial for co-receptor interaction in LRR-RLPs are closely related to those of the LRR-RLK subgroup Xb, which primarily governs growth and development. Functional characterisation further reveals that LRR-RLPs initiate immune responses through their juxtamembrane and transmembrane regions, while LRR-RLK-Xb members regulate development through their cytosolic kinase domains. Our data suggest modular evolution of cell-surface receptors in which immunity- and development-specific cell-surface receptors share a common origin. After diversification, their ectodomains, juxtamembrane, transmembrane, and cytosolic regions have either diversified or stabilised to recognize ligands that activate different downstream responses. We propose that cell-surface receptors and downstream signalling components are ancient, and likely predate the emergence of land plants, subsequently evolving to exhibit greater complexity and specificity within the land plant lineage.