Abscisic acid signaling negatively regulates nitrate uptake via phosphorylation of NRT1.1 by SnRK2s in Arabidopsis

J Integr Plant Biol. 2021 Mar;63(3):597-610. doi: 10.1111/jipb.13057.

Abstract

Nitrogen (N) is a limiting nutrient for plant growth and productivity. The phytohormone abscisic acid (ABA) has been suggested to play a vital role in nitrate uptake in fluctuating N environments. However, the molecular mechanisms underlying the involvement of ABA in N deficiency responses are largely unknown. In this study, we demonstrated that ABA signaling components, particularly the three subclass III SUCROSE NON-FERMENTING1 (SNF1)-RELATED PROTEIN KINASE 2S (SnRK2) proteins, function in root foraging and uptake of nitrate under N deficiency in Arabidopsis thaliana. The snrk2.2snrk2.3snrk2.6 triple mutant grew a longer primary root and had a higher rate of nitrate influx and accumulation compared with wild-type plants under nitrate deficiency. Strikingly, SnRK2.2/2.3/2.6 proteins interacted with and phosphorylated the nitrate transceptor NITRATE TRANSPORTER1.1 (NRT1.1) in vitro and in vivo. The phosphorylation of NRT1.1 by SnRK2s resulted in a significant decrease of nitrate uptake and impairment of root growth. Moreover, we identified NRT1.1Ser585 as a previously unknown functional site: the phosphomimetic NRT1.1S585D was impaired in both low- and high-affinity transport activities. Taken together, our findings provide new insight into how plants fine-tune growth via ABA signaling under N deficiency.

Keywords: NRT1.1; SnRK2.2/2.3/2.6; abscisic acid; nitrogen deficiency.

MeSH terms

  • Abscisic Acid / metabolism*
  • Anion Transport Proteins / metabolism*
  • Arabidopsis / metabolism*
  • Arabidopsis Proteins / metabolism*
  • Models, Biological
  • Mutation / genetics
  • Nitrates / metabolism*
  • Nitrogen / pharmacology
  • Phenotype
  • Phosphorylation
  • Plant Proteins / metabolism*
  • Plant Roots / drug effects
  • Plant Roots / growth & development
  • Protein Binding / drug effects
  • Protein Serine-Threonine Kinases / metabolism*
  • Signal Transduction*

Substances

  • Anion Transport Proteins
  • Arabidopsis Proteins
  • NRT1.1 protein, Arabidopsis
  • Nitrates
  • Plant Proteins
  • SnRK2 protein, Arabidopsis
  • Abscisic Acid
  • Protein Serine-Threonine Kinases
  • Nitrogen