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The Arabidopsis TIRome informs the design of artificial TIR (Toll/interleukin-1 receptor) domain proteins

拟南芥 伤亡人数 白细胞介素-1受体 Toll样受体 受体 领域(数学分析) 细胞生物学 计算生物学 白细胞介素 生物 神经科学 免疫学 遗传学 基因 细胞因子 先天免疫系统 数学 数学分析 突变体
作者
Adam M. Bayless,Lijiang Song,Mitchell Sorbello,Sam C. Ogden,T Todd,Andrew Flint,Natsumi Maruta,Jedidiah Tulu,Mikhail S. Drenichev,Vardis Ntoukakis,Thomas Ve,Mehdi Mobli,Li Wan,Qingli Liu,Jeffery L. Dangl,Boštjan Kobe,Murray Grant,Marc T. Nishimura
出处
期刊: [Cold Spring Harbor Laboratory]
被引量:2
标识
DOI:10.1101/2025.03.15.643477
摘要

Abstract The TIR (Toll/interleukin-1 receptor) domain is an ancient protein module that functions in immune and cell death responses across the Tree of Life. TIR domains encoded by plants and prokaryotes function as enzymes to produce diverse small molecule immune signals. Plant genomes can encode hundreds of TIR-domain containing proteins – many of which confer important agricultural disease resistance as TIR-NLR (nucleotide-binding, leucine-rich repeat) immune receptors. Despite their importance, how natural variation influences TIR enzymatic output and immunity-associated cell death is largely unexplored. We assayed a complete collection of the TIR domains of Arabidopsis thaliana Col-0 (the “AtTIRome”) to explore variation in TIR metabolite production and cell death signaling. Roughly half of the AtTIRome triggered cell death in transient assays. Artificial TIR proteins designed based on consensus sequences of the AtTIRome’s cell death phenotypic classes revealed polymorphisms controlling variation in TIR cell death elicitation and metabolite production. Structure-function analyses of artificial TIRs revealed that natural variation in the “BB-loop”, a flexible region overlying the catalytic pocket, determines differences in function across Arabidopsis TIR-containing proteins. We further demonstrate that artificial TIRs are functional on an NLR chassis and that BB-loop variation can tune the activity of a natural TIR-NLR protein. These findings shed light on the diversity of TIR outputs and reveal methods to design and engineer TIR-based immune receptors. Significance Statement TIR (Toll/interleukin-1 receptors) domain proteins perform immune signaling across the Tree of Life. TIR domains are enzymes that can process NAD + to generate diverse small molecule signals. In order to better understand TIR-based signaling, we leveraged Arabidopsis natural variation across ∼150 TIR proteins to inform the design of artificial TIRs, define features that control output, and tune the output of a natural TIR immune receptor. The engineering of plant immune pathways will enable the optimization of disease resistance to safeguard yields.
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