A CNL protein forms an NLR pair with NRCX to modulate plant immunity.

IF 5.8
Xiaohua Dong, Xiaoyan Zhang, Xu Lu, Yufeng Yang, Chuyan Xia, Weiye Pan, Zhiyuan Yin, Yaning Zhao, Gan Ai, Daolong Dou
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引用次数: 0

Abstract

Nucleotide-binding leucine-rich repeat (NLR) proteins assemble into genetically linked pairs to mediate effector-triggered immunity (ETI) in plants. Here, we characterize the paired NLRs NRCX and NARY (NRCX adjacent resistance gene Y) in Nicotiana benthamiana. CRISPR/Cas9 knockout of NRCX caused severe dwarfism and constitutively activated immunity, marked by PR1 upregulation and enhanced resistance to Phytophthora capsici. Co-silencing or double knockout of the adjacent NLR NARY partially rescued the nrcx phenotype, revealing NARY as a compensatory regulator that modulates growth and immunity. Structural analysis revealed that NARY harbors non-canonical Walker B and MHD motifs, which lack autoactivation capacity despite their divergence from canonical NLR executors. Split-luciferase and co-immunoprecipitation assays showed that NRCX and NARY interact exclusively through their CC domains, forming a non-canonical regulatory complex. Notably, simultaneous silencing of NRC2/3 and NARY incompletely restored growth in nrcx mutants, implicating additional factors in immune modulation. Our findings establish NARY as a compensatory NLR partner of NRCX that fine-tunes immunity without triggering cell death, revealing a novel mechanism for balancing growth and defense in Solanaceae.

CNL蛋白与NRCX形成NLR对,调节植物免疫。
核苷酸结合的富含亮氨酸重复序列(NLR)蛋白组装成遗传连锁对,介导植物的效应触发免疫(ETI)。本研究中,我们对本烟中NLRs NRCX和NRCX相邻抗性基因Y的配对进行了表征。CRISPR/Cas9敲除NRCX导致严重的侏儒症和组成性免疫激活,其标志是PR1上调和对辣椒疫霉的抗性增强。共沉默或双敲除邻近NLR的NARY部分挽救了nrx表型,揭示了NARY作为调节生长和免疫的代偿调节因子。结构分析表明,尽管与NLR执行子存在差异,但其包含非规范的Walker B和MHD基序,缺乏自激活能力。分裂荧光素酶和共免疫沉淀实验表明,NRCX和NARY仅通过其CC结构域相互作用,形成非规范调节复合物。值得注意的是,同时沉默NRC2/3和NARY不能完全恢复nrcx突变体的生长,这暗示了免疫调节中的其他因素。我们的研究结果表明,在不引发细胞死亡的情况下,NRCX作为NLR的补偿性伴侣,可以对免疫进行微调,从而揭示了茄科植物平衡生长和防御的新机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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