A high-throughput screen of cell-death-inducing factors in Nicotiana benthamiana identifies a novel MAPKK that mediates INF1-induced cell death signaling and non-host resistance to Pseudomonas cichorii

Plant J. 2007 Mar;49(6):1030-40. doi: 10.1111/j.1365-313X.2006.03022.x. Epub 2007 Feb 2.

Abstract

A high-throughput overexpression screen of Nicotiana benthamiana cDNAs identified a gene for a mitogen-activated protein kinase kinase (MAPKK) as a potent inducer of the hypersensitive response (HR)-like cell death. NbMKK1 protein is localized to the nucleus, and the N-terminal putative MAPK docking site of NbMKK1 is required for its function as a cell-death inducer. NbMKK1-mediated leaf-cell death was compromised in leaves where NbSIPK expression was silenced by virus-induced gene silencing. A yeast two-hybrid assay showed that NbMKK1 and NbSIPK physically interact, suggesting that NbSIPK is one of the downstream targets of NbMKK1. Phytophthora infestans INF1 elicitor-mediated HR was delayed in NbMKK1-silenced plants, indicating that NbMKK1 is involved in this HR pathway. Furthermore, the resistance of N. benthamiana to a non-host pathogen Pseudomonas cichorii was compromised in NbMKK1-silenced plants. These results demonstrate that MAPK cascades involving NbMKK1 control non-host resistance including HR cell death.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Death / physiology*
  • Cell Nucleus / metabolism
  • Gene Expression
  • Hydrogen Peroxide / metabolism
  • Immunity, Innate / physiology*
  • MAP Kinase Signaling System / physiology
  • Mitogen-Activated Protein Kinase Kinases / physiology*
  • Nicotiana
  • Plant Diseases
  • Pseudomonas / physiology*
  • Signal Transduction / physiology*

Substances

  • Hydrogen Peroxide
  • Mitogen-Activated Protein Kinase Kinases