The Regulatory Network of CMPG1-V in Wheat- Blumeria graminis f. sp. tritici Interaction Revealed by Temporal Profiling Using RNA-Seq

Int J Mol Sci. 2020 Aug 19;21(17):5967. doi: 10.3390/ijms21175967.

Abstract

Wheat powdery mildew (Pm), caused by Blumeria graminis f. sp. tritici (Bgt), is a prevalent fungal disease. The diploid wheat relative Haynaldia villosa (H. villosa) showed broad-spectrum resistance (BSR) to Pm. A previous study reported an E3 ligase gene, CMPG1-V from H. villosa, showing BSR to Pm. To elucidate the regulatory network mediated by CMPG1-V, in this study, gene expression profiling of CMPG1-V transgenic plant (CMPG1-VOE) and its receptor Yangmai 158 was analyzed and compared after Bgt inoculation at four infection stages. GO and KEGG analysis revealed obvious reprogramming of SA and ABA signaling, starch/sucrose metabolism, and photosynthesis in CMPG1-VOE, compared with those in Yangmai 158. Transcripts of SA synthesis genes SARD1 and UGT, signaling factors TGA and PRs, and SnRKs in ABA signaling were specifically upregulated in CMPG1-VOE rather than Yangmai 158. Transcripts of LHCII in photosynthesis, GLUC and TPP in starch/sucrose metabolism were also induced distinctly in CMPG1-VOE. WGCNA analysis showed crucial regulatory candidates of CMPG1-V, involving serine/threonine-protein kinase in phosphorylation, glucosyltransferase in flavonoid biosynthesis, defense factor WRKYs, and peroxidase in oxidative stress. Our results facilitate the deciphering of the resistant regulatory network of CMPG1-V and the identification of key candidates which might be employed in breeding programs.

Keywords: CMPG1-V; Haynaldia villosa; RNA-seq; hormone signaling; metabolism process; wheat powdery mildew.

MeSH terms

  • Abscisic Acid / metabolism
  • Ascomycota / pathogenicity*
  • Disease Resistance*
  • Gene Expression Regulation, Plant
  • Gene Regulatory Networks*
  • Plant Proteins / genetics
  • Plant Proteins / metabolism*
  • Salicylic Acid / metabolism
  • Sucrose / metabolism
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Transcriptome
  • Transgenes
  • Triticum / genetics*
  • Triticum / microbiology
  • Ubiquitin-Protein Ligases / genetics
  • Ubiquitin-Protein Ligases / metabolism*

Substances

  • Plant Proteins
  • Transcription Factors
  • Sucrose
  • Abscisic Acid
  • Ubiquitin-Protein Ligases
  • Salicylic Acid

Supplementary concepts

  • Blumeria graminis