Alternative splicing of a potato disease resistance gene maintains homeostasis between development and immunity

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Abstract

Plants possess a robust and sophisticated innate immune system against pathogens. The intracellular receptors with nucleotide-binding, leucine-rich repeat (NLR) motifs recognize pathogen-derived effector proteins to trigger the immune response. To balance plant growth and rapid pathogen detection, NLR expression is precisely controlled in multifaceted ways. The role of post-transcriptional processing of NLRs, particularly alternative splicing (AS) of introns, in response to infection is recurrently observed but poorly understood. Here we report that the potato NLR geneRBundergoes AS of its intron, resulting in two transcriptional isoforms, which coordinately regulate plant immunity and growth homeostasis. During normal growth,RBpredominantly exists as intron-retained isoformRB_IR, encoding a truncated protein containing only the N-terminus of the NLR. Upon late blight infection, the causal pathogenPhytophthora infestansinduces intron splicing ofRB, increasing the abundance ofRB_CDS, which encodes a full-length, and active R protein. By deploying theRBsplicing isoforms fused with aluciferasereporter system, we identified IPI-O1 (also known as Avrblb1), the RB cognate effector, as a facilitator ofRBAS. Importantly, IPI-O1 directly interacts with potato splicing factor StCWC15 to promoteRBsplicing for activation ofRB-mediated resistance. Thus, our study reveals that StCWC15 serves as a surveillance facilitator sensing the pathogen-secreted effector, and regulates the trade-off betweenRB- mediated plant immunity and growth, expanding our understanding of molecular plant-microbe interactions.

One-sentence summary

Potato resistance geneRBbalances plant growth and immunity through AS (alternative splicing), while pathogen-secreted effector IPI-O1 mediates AS ofRBby targeting the conserved splicing factor StCWC15, further increasing theRB_CDSexpression level to activate immunity.

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