A dominant-interfering camta3 mutation compromises primary transcriptional outputs mediated by both cell surface and intracellular immune receptors in Arabidopsis thaliana

New Phytol. 2018 Mar;217(4):1667-1680. doi: 10.1111/nph.14943. Epub 2017 Dec 11.

Abstract

Pattern recognition receptors (PRRs) and nucleotide-binding domain and leucine-rich repeat (LRR)-containing proteins (NLRs) initiate pattern-triggered immunity (PTI) and effector-triggered immunity (ETI), respectively, each associated with the activation of an overlapping set of defence genes. The regulatory mechanism behind this convergence of PTI- and ETI-mediated defence gene induction remains elusive. We generated transgenic Arabidopsis plants that enable conditional NLR activation without pathogen infection to dissect NLR- and PRR-mediated transcriptional signals. A comparative analysis of over 40 transcriptome datasets linked calmodulin-binding transcription activators (CAMTAs) to the activation of overlapping defence genes in PTI and ETI. We used a dominant camta3 mutant (camta3-D) to assess CAMTA functions in the corresponding transcriptional regulation. Transcriptional regulation by NLRs, although highly similar to PTI responses, can be established independently of pathogen-associated molecular pattern (PAMP) perception, defence phytohormones and host cell death. Conditional expression of the N-terminal coiled-coil domain of the barley MLA (Mildew resistance locus A) NLR is sufficient to trigger similar transcriptional reprogramming as full-length NLRs. CAMTA-binding motifs are overrepresented in the 5' regulatory regions of the identified primary immune response genes, consistent with their altered expression and disease resistance responses in camta3-D plants. We propose that CAMTA-mediated transcriptional regulation defines an early convergence point in NLR- and PRR-mediated signalling.

Keywords: Arabidopsis thaliana; calmodulin-binding transcription activator (CAMTA); cross-tolerance; effector-triggered immunity (ETI); immediate early genes; nucleotide-binding domain and LRR-containing proteins (NLRs); pattern-triggered immunity (PTI); transcriptional responses.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Arabidopsis / genetics*
  • Arabidopsis / immunology
  • Arabidopsis / microbiology
  • Arabidopsis Proteins / genetics*
  • Arabidopsis Proteins / metabolism
  • Disease Resistance / genetics
  • Gene Expression Regulation, Plant
  • Genes, Dominant*
  • Genes, Plant
  • Intracellular Space / metabolism*
  • Mutation / genetics*
  • NLR Proteins / metabolism
  • Plant Diseases / genetics
  • Plant Diseases / immunology
  • Plant Diseases / microbiology
  • Plant Immunity
  • Receptors, Immunologic / metabolism*
  • Receptors, Pattern Recognition / metabolism
  • Signal Transduction
  • Stress, Physiological / genetics
  • Transcription Factors / genetics*
  • Transcription Factors / metabolism
  • Transcription, Genetic*
  • Transcriptome / genetics
  • Up-Regulation / genetics

Substances

  • AT2G22300 protein, Arabidopsis
  • Arabidopsis Proteins
  • NLR Proteins
  • Receptors, Immunologic
  • Receptors, Pattern Recognition
  • Transcription Factors