A previously unrecognized AAA+ ATPase–F-box module that controls receptor homeostasis is revealed and StGCN4 is identified as a promising molecular target for breeding high-yielding and late blight resistant potato cultivars.
Abstract
Fine-tuning immune receptor stability is essential for maintaining the balance between defense and growth in crops. Here, we identify an AAA+ ATPase–F-box regulatory module that negatively regulates potato immunity by promoting the degradation of the immune co-receptor StSOBIR1. The AAA+ ATPase StGCN4 functions as a negative regulator of potato immunity. Silencing of StGCN4 markedly enhanced resistance to Phytophthora infestans without affecting plant growth, while overexpression increased susceptibility. StGCN4 interacts with the PP2-type F-box protein StPFB1 and stabilizes it at the plasma membrane, which also negatively regulate immunity and together they facilitate proteasomal degradation of StSOBIR1, thereby dampening receptor-mediated defense signaling. Suppression of StGCN4 or StPFB1 enhances reactive oxygen species (ROS) production, salicylic acid accumulation, and expression of defense-related genes, resulting in strong resistance to P. infestans without growth penalty. These findings reveal a previously unrecognized AAA+ ATPase–F-box module that controls receptor homeostasis and identify StGCN4 as a promising molecular target for breeding high-yielding and late blight resistant potato cultivars.
An RLCK-V subfamily member in potato is reported, StSOAK1, which negatively regulates disease resistance to the oomycete Phytophthora infestans and the fungus Botrytis cinerea and reveals a regulatory mechanism of potato StRBOHB, which occurs in parallel with its paradigmatic AtPBL13-mediated regulation in Arabidopsis.
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It is found that the amino-terminal domain of TOE3 (T3N) inhibits abscisic acid (ABA) signaling, which reveals how TOE3 uncoupling to provide strategies for breeding crops with strong growth and antiviral immunity.
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Abstract Plant responses to pathogens often rely on receptor-like cytoplasmic kinases (RLCKs) that mediate signaling through interactions with receptor kinases and downstream components. Here, we studied the tomato RLCK, TPK1b Related Protein Kinase (TPK09), and demonstrate its function in integrating defense with ligh...
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