TaAP2-15, An AP2/ERF Transcription Factor, Is Positively Involved in Wheat Resistance to Puccinia striiformis f. sp. tritici

Int J Mol Sci. 2021 Feb 19;22(4):2080. doi: 10.3390/ijms22042080.

Abstract

AP2 transcription factors play a crucial role in plant development and reproductive growth, as well as response to biotic and abiotic stress. However, the role of TaAP2-15, in the interaction between wheat and the stripe fungus, Puccinia striiformis f. sp. tritici (Pst), remains elusive. In this study, we isolated TaAP2-15 and characterized its function during the interaction. TaAP2-15 was localized in the nucleus of wheat and N. benthamiana. Silencing of TaAP2-15 by barley stripe mosaic virus (BSMV)-mediated VIGS (virus-induced gene silencing) increased the susceptibility of wheat to Pst accompanied by enhanced growth of the pathogen (number of haustoria, haustorial mother cells and hyphal length). We confirmed by quantitative real-time PCR that the transcript levels of pathogenesis-related genes (TaPR1 and TaPR2) were down-regulated, while reactive oxygen species (ROS)-scavenging genes (TaCAT3 and TaFSOD3D) were induced accompanied by reduced accumulation of H2O2. Furthermore, we found that TaAP2-15 interacted with a zinc finger protein (TaRZFP34) that is a homolog of OsRZFP34 in rice. Together our findings demonstrate that TaAP2-15 is positively involved in resistance of wheat to the stripe rust fungus and provides new insights into the roles of AP2 in the host-pathogen interaction.

Keywords: Puccinia striiformis f. sp. tritici; TaAP2; VIGS; resistance; salicylic acid; transcription factor; wheat.

MeSH terms

  • Amino Acid Sequence
  • Base Sequence
  • Cell Nucleus / drug effects
  • Cell Nucleus / metabolism
  • Disease Resistance*
  • Gene Expression Regulation, Plant / drug effects
  • Gene Silencing / drug effects
  • Plant Diseases / microbiology*
  • Promoter Regions, Genetic / genetics
  • Protein Binding / drug effects
  • Puccinia / physiology*
  • Reactive Oxygen Species / metabolism
  • Salicylic Acid / pharmacology
  • Stress, Physiological / drug effects
  • Stress, Physiological / genetics
  • Transcription Factor AP-2 / chemistry
  • Transcription Factor AP-2 / genetics
  • Transcription Factor AP-2 / metabolism*
  • Triticum / drug effects
  • Triticum / genetics
  • Triticum / metabolism*
  • Triticum / microbiology*

Substances

  • Reactive Oxygen Species
  • Transcription Factor AP-2
  • Salicylic Acid