Antagonistic control of rice immunity against distinct pathogens by the two transcription modules via salicylic acid and jasmonic acid pathways

Dev Cell. 2024 Jun 17;59(12):1609-1622.e4. doi: 10.1016/j.devcel.2024.03.033. Epub 2024 Apr 18.

Abstract

Although the antagonistic effects of host resistance against biotrophic and necrotrophic pathogens have been documented in various plants, the underlying mechanisms are unknown. Here, we investigated the antagonistic resistance mediated by the transcription factor ETHYLENE-INSENSITIVE3-LIKE 3 (OsEIL3) in rice. The Oseil3 mutant confers enhanced resistance to the necrotroph Rhizoctonia solani but greater susceptibility to the hemibiotroph Magnaporthe oryzae and biotroph Xanthomonas oryzae pv. oryzae. OsEIL3 directly activates OsERF040 transcription while repressing OsWRKY28 transcription. The infection of R. solani and M. oryzae or Xoo influences the extent of binding of OsEIL3 to OsWRKY28 and OsERF040 promoters, resulting in the repression or activation of both salicylic acid (SA)- and jasmonic acid (JA)-dependent pathways and enhanced susceptibility or resistance, respectively. These results demonstrate that the distinct effects of plant immunity to different pathogen types are determined by two transcription factor modules that control transcriptional reprogramming and the SA and JA pathways.

Keywords: EIN3; Magnaporthe oryzae; Rhizoctonia solani; Xanthomonas oryzae pv. oryzae; jasmonic acid; plant immunity; rice; salicylic acid; transcriptional regulation.

MeSH terms

  • Cyclopentanes* / metabolism
  • Disease Resistance / genetics
  • Gene Expression Regulation, Plant*
  • Magnaporthe
  • Oryza* / genetics
  • Oryza* / immunology
  • Oryza* / metabolism
  • Oryza* / microbiology
  • Oxylipins* / metabolism
  • Plant Diseases* / immunology
  • Plant Diseases* / microbiology
  • Plant Immunity* / genetics
  • Plant Proteins* / genetics
  • Plant Proteins* / metabolism
  • Promoter Regions, Genetic / genetics
  • Rhizoctonia
  • Salicylic Acid* / metabolism
  • Signal Transduction
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Transcription, Genetic
  • Xanthomonas* / pathogenicity

Substances

  • Cyclopentanes
  • Oxylipins
  • jasmonic acid
  • Salicylic Acid
  • Plant Proteins
  • Transcription Factors

Supplementary concepts

  • Xanthomonas oryzae
  • Rhizoctonia solani