Mitogen-activated protein kinases play an essential role in oxidative burst-independent expression of pathogenesis-related genes in parsley

J Biol Chem. 2003 Jan 24;278(4):2256-64. doi: 10.1074/jbc.M208200200. Epub 2002 Nov 7.

Abstract

Plants are continuously exposed to attack by potential phytopathogens. Disease prevention requires pathogen recognition and the induction of a multifaceted defense response. We are studying the non-host disease resistance response of parsley to the oomycete, Phytophthora sojae using a cell culture-based system. Receptor-mediated recognition of P. sojae may be achieved through a thirteen amino acid peptide sequence (Pep-13) present within an abundant cell wall transglutaminase. Following recognition of this elicitor molecule, parsley cells mount a defense response, which includes the generation of reactive oxygen species (ROS) and transcriptional activation of genes encoding pathogenesis-related (PR) proteins or enzymes involved in the synthesis of antimicrobial phytoalexins. Treatment of parsley cells with the NADPH oxidase inhibitor, diphenylene iodonium (DPI), blocked both Pep-13-induced phytoalexin production and the accumulation of transcripts encoding enzymes involved in their synthesis. In contrast, DPI treatment had no effect upon Pep-13-induced PR gene expression, suggesting the existence of an oxidative burst-independent mechanism for the transcriptional activation of PR genes. The use of specific antibodies enabled the identification of three parsley mitogen-activated protein kinases (MAPKs) that are activated within the signal transduction pathway(s) triggered following recognition of Pep-13. Other environmental challenges failed to activate these kinases in parsley cells, suggesting that their activation plays a key role in defense signal transduction. Moreover, by making use of a protoplast co-transfection system overexpressing wild-type and loss-of-function MAPK mutants, we show an essential role for post-translational phosphorylation and activation of MAPKs for oxidative burst-independent PR promoter activation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptation, Physiological / physiology*
  • Amino Acid Sequence
  • Blotting, Western
  • Cell Line
  • DNA, Complementary / metabolism
  • Enzyme Activation
  • Gene Expression Regulation, Plant*
  • MAP Kinase Signaling System*
  • Molecular Sequence Data
  • Mutagenesis, Site-Directed
  • Petroselinum / enzymology
  • Petroselinum / microbiology*
  • Phytophthora / metabolism
  • Plant Physiological Phenomena
  • Plant Proteins / metabolism
  • Precipitin Tests
  • Promoter Regions, Genetic
  • Protoplasts / metabolism
  • Respiratory Burst*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sequence Homology, Amino Acid
  • Time Factors
  • Transfection

Substances

  • DNA, Complementary
  • Plant Proteins

Associated data

  • GENBANK/AY173414
  • GENBANK/AY173415
  • GENBANK/Y12875