MicroRNA-like milR236, regulated by transcription factor MoMsn2, targets histone acetyltransferase MoHat1 to play a role in appressorium formation and virulence of the rice blast fungus Magnaporthe oryzae

Fungal Genet Biol. 2020 Apr:137:103349. doi: 10.1016/j.fgb.2020.103349. Epub 2020 Jan 29.

Abstract

MicroRNAs (miRNAs) play important roles in various cellular growth and developmental processes through post-transcriptional gene regulation via mRNA cleavage and degradation and the inhibition of protein translation. To explore if miRNAs play a role in appressoria formation and virulence that are also governed by the regulators of G-protein signaling (RGS) proteins in the rice blast fungus Magnaporthe oryzae, we have compared small RNA (sRNA) production between several ΔMorgs mutant and the wild-type strains. We have identified sRNA236 as a microRNA-like milR236 that targets the encoding sequence of MoHat1, a histone acetyltransferase type B catalytic subunit involved in appressorium function and virulence. We have also found that milR236 overexpression induces delayed appressorium formation and virulence attenuation, similar to those displayed by the ΔMohat1 mutant strain. Moreover, we have shown that the transcription factor MoMsn2 binds to the promoter sequence of milR236 to further suppress MoHAT1 transcription and MoHat1-regulated appressorium formation and virulence. In summary, by identifying a novel regulatory role of sRNA in the blast fungus, our studies reveal a new paradigm in the multifaceted regulatory pathways that govern the appressorium formation and virulence of M. oryzae.

Keywords: Appressorium; MicroRNA-like RNA; Transcription factor; Virulence.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Ascomycota / genetics*
  • Ascomycota / metabolism
  • Ascomycota / pathogenicity
  • DNA-Binding Proteins / metabolism
  • Fungal Proteins / genetics
  • Gene Expression Regulation, Fungal / genetics
  • Histone Acetyltransferases / genetics*
  • Histone Acetyltransferases / metabolism
  • Magnaporthe / genetics
  • Magnaporthe / pathogenicity
  • MicroRNAs / genetics
  • MicroRNAs / metabolism
  • Oryza / microbiology
  • Plant Diseases / microbiology
  • Saccharomyces cerevisiae Proteins / metabolism
  • Signal Transduction / genetics
  • Spores, Fungal / growth & development
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Virulence

Substances

  • DNA-Binding Proteins
  • Fungal Proteins
  • MSN2 protein, S cerevisiae
  • MicroRNAs
  • Saccharomyces cerevisiae Proteins
  • Transcription Factors
  • Histone Acetyltransferases
  • histone acetyltransferase type B complex

Supplementary concepts

  • Pyricularia oryzae