論文

査読有り
2019年4月

Disruption of the MAMP-Induced MEKK1-MKK1/MKK2-MPK4 Pathway Activates the TNL Immune Receptor SMN1/RPS6

Plant and Cell Physiology
  • Momoko Takagi
  • ,
  • Kohei Hamano
  • ,
  • Hiroki Takagi
  • ,
  • Takayuki Morimoto
  • ,
  • Kazuya Akimitsu
  • ,
  • Ryohei Terauchi
  • ,
  • Ken Shirasu
  • ,
  • Kazuya Ichimura

60
4
開始ページ
778
終了ページ
787
記述言語
掲載種別
研究論文(学術雑誌)
DOI
10.1093/pcp/pcy243

© The Author(s) 2019. Published by Oxford University Press on behalf of Japanese Society of Plant Physiologists. All rights reserved. Mitogen-activated protein kinase (MAPK) pathways have a pivotal role in innate immunity signaling in plants. In Arabidopsis, the MAPK pathway that consists of MEKK1, MKK1/MKK2 and MPK4 is involved in pattern-triggered immunity signaling upstream of defense gene expression. This pathway is partly guarded by SUMM2, a nucleotide-binding domain leucine-rich repeat (NLR) protein, which is activated by disruption of the MAPK pathway. To identify other components required for the guard mechanism, here we developed a new mutant screening system utilizing a dwarf autoimmune line that overexpressed the N-terminal regulatory domain of MEKK1. Mutants with suppression of the dwarf, autoimmune phenotypes were identified, and one locus responsible for the phenotype was designated as suppressor of MEKK1N overexpression-induced dwarf 1 (SMN1). MutMap analysis revealed that SMN1 encodes the Toll/ Interleukin-1 receptor (TIR)-class NLR protein RPS6, a previously identified resistant protein against bacterial pathogen Pseudomonas syringae pv. tomato expressing the HopA1 effector. Importantly, mutations in SMN1/RPS6 also partially suppressed the dwarf, autoimmune phenotypes of mekk1 and mpk4 plants. Our results suggest that the two structurally distinct NLR proteins, SMN1/RPS6 and SUMM2, monitor integrity of the MEKK1-MKK1/MKK2-MPK4 pathway.

リンク情報
DOI
https://doi.org/10.1093/pcp/pcy243
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/30590768
Scopus
https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85065728931&origin=inward
Scopus Citedby
https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=85065728931&origin=inward
ID情報
  • DOI : 10.1093/pcp/pcy243
  • ISSN : 0032-0781
  • eISSN : 1471-9053
  • PubMed ID : 30590768
  • SCOPUS ID : 85065728931

エクスポート
BibTeX RIS