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Leucine-rich repeat receptor-like gene screen reveals that Nicotiana RXEG1 regulates glycoside hydrolase 12 MAMP detection.

Xiaobo ZhengYuanpeng XuYujing SunHuibin WangJiaming QiBowen WanWenwu YeYachun LinYuanyuan ShaoSuomeng DongBrett M TylerYuan-Chao Wang
Published in: Nature communications (2018)
Activation of innate immunity by membrane-localized receptors is conserved across eukaryotes. Plant genomes contain hundreds of such receptor-like genes and those encoding proteins with an extracellular leucine-rich repeat (LRR) domain represent the largest family. Here, we develop a high-throughput approach to study LRR receptor-like genes on a genome-wide scale. In total, 257 tobacco rattle virus-based constructs are generated to target 386 of the 403 identified LRR receptor-like genes in Nicotiana benthamiana for silencing. Using this toolkit, we identify the LRR receptor-like protein Response to XEG1 (RXEG1) that specifically recognizes the glycoside hydrolase 12 protein XEG1. RXEG1 associates with XEG1 via the LRR domain in the apoplast and forms a complex with the LRR receptor-like kinases BAK1 and SOBIR1 to transduce the XEG1-induced defense signal. Thus, this genome-wide silencing assay is demonstrated to be an efficient toolkit to pinpoint new immune receptors, which will contribute to developing durable disease resistance.
Keyphrases
  • genome wide
  • high throughput
  • dna methylation
  • binding protein
  • gene expression
  • small molecule
  • drug induced
  • high glucose
  • oxidative stress
  • single cell
  • genome wide analysis
  • label free