Matching NLR Immune Receptors to Autoimmunity in camta3 Mutants Using Antimorphic NLR Alleles

Cell Host Microbe. 2017 Apr 12;21(4):518-529.e4. doi: 10.1016/j.chom.2017.03.005.

Abstract

To establish infection, pathogens deploy effectors to modify or remove host proteins. Plant immune receptors with nucleotide-binding, leucine-rich repeat domains (NLRs) detect these modifications and trigger immunity. Plant NLRs thus guard host "guardees." A corollary is that autoimmunity may result from inappropriate NLR activation because mutations in plant guardees could trigger corresponding NLR guards. To explore these hypotheses, we expressed 108 dominant-negative (DN) Arabidopsis NLRs in various lesion mimic mutants, including camta3, which exhibits autoimmunity. CAMTA3 was previously described as a negative regulator of immunity, and we find that autoimmunity in camta3 is fully suppressed by expressing DNs of two NLRs, DSC1 and DSC2. Additionally, expression of either NLR triggers cell death that can be suppressed by CAMTA3 expression. These findings support a model in which DSC1 and DSC2 guard CAMTA3, and they suggest that other negative regulators of immunity may similarly represent guardees.

MeSH terms

  • Alleles
  • Arabidopsis / immunology*
  • Arabidopsis Proteins / genetics
  • Arabidopsis Proteins / metabolism*
  • Autoimmunity*
  • Mutant Proteins / genetics
  • Mutant Proteins / metabolism
  • NLR Proteins / genetics
  • NLR Proteins / metabolism*
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*

Substances

  • AT2G22300 protein, Arabidopsis
  • Arabidopsis Proteins
  • DSC1 protein, Arabidopsis
  • DSC2 protein, Arabidopsis
  • Mutant Proteins
  • NLR Proteins
  • Transcription Factors