The protein phosphatase 2C clade A TaPP2CA interact with calcium-dependent protein kinases, TaCDPK5/TaCDPK9-1, that phosphorylate TabZIP60 transcription factor from wheat (Triticum aestivum L.)

Plant Sci. 2022 Aug:321:111304. doi: 10.1016/j.plantsci.2022.111304. Epub 2022 May 6.

Abstract

Previously we have found that TabZIP60 from the ABF/AREB (ABRE-binding factor/ABA-responsive element-binding protein) subfamily of bZIP transcription factor (TF) was involved in salt stress response. However, the regulatory mechanism of TabZIP60 is unknown. In the present study, we identified two calcium-dependent protein kinase (CDPK) genes, TaCDPK5/TaCDPK9-1, which were clustered into group Ⅰ and were induced by salt, abscisic acid (ABA), and polyethylene glycol (PEG) treatments. RT-qPCR results showed that the expression level of salt-induced TabZIP60 was drastically inhibited by Ca2+ channel blocker LaCl3. TaCDPK5/TaCDPK9-1 were involved in interaction with TabZIP60 protein in vivo and in vitro. And TaCDPK5/TaCDPK9-1 could autophosphorylate and phosphorylate TabZIP60 protein in a Ca2+-dependent way. Mutational analysis indicated that Serine-110 of TabZIP60 was essential for TaCDPK5/TaCDPK9-1-TabZIP60 interaction and was the phosphorylation site of TaCDPK5/TaCDPK9-1 kinases. Yeast two-hybrid assay results showed the interactions between TaCDPK5/TaCDPK9-1 and wheat protein phosphatase 2 C clade A TaPP2CA116/ TaPP2CA121 separately. These findings demonstrate that the phosphorylation status of TabZIP60 controlled by TaPP2CA116/ TaPP2CA121 and TaCDPK5/TaCDPK9-1 might play a crucial role in wheat during salt stress.

Keywords: Phosphorylation; TaCDPK5/TaCDPK9–1; TaPP2CA116/ TaPP2CA 121; TabZIP60 TF; Wheat.

MeSH terms

  • Abscisic Acid / metabolism
  • Gene Expression Regulation, Plant
  • Phosphoprotein Phosphatases / genetics
  • Phosphoprotein Phosphatases / metabolism
  • Plant Proteins / genetics
  • Plant Proteins / metabolism
  • Protein Kinases
  • Protein Phosphatase 2C / genetics
  • Protein Phosphatase 2C / metabolism
  • Transcription Factors* / genetics
  • Transcription Factors* / metabolism
  • Triticum* / metabolism

Substances

  • Plant Proteins
  • Transcription Factors
  • Abscisic Acid
  • Protein Kinases
  • calcium-dependent protein kinase
  • Phosphoprotein Phosphatases
  • Protein Phosphatase 2C