GARP transcription factors repress Arabidopsis nitrogen starvation response via ROS-dependent and -independent pathways

J Exp Bot. 2021 May 4;72(10):3881-3901. doi: 10.1093/jxb/erab114.

Abstract

Plants need to cope with strong variations of nitrogen availability in the soil. Although many molecular players are being discovered concerning how plants perceive NO3- provision, it is less clear how plants recognize a lack of nitrogen. Following nitrogen removal, plants activate their nitrogen starvation response (NSR), which is characterized by the activation of very high-affinity nitrate transport systems (NRT2.4 and NRT2.5) and other sentinel genes involved in N remobilization such as GDH3. Using a combination of functional genomics via transcription factor perturbation and molecular physiology studies, we show that the transcription factors belonging to the HHO subfamily are important regulators of NSR through two potential mechanisms. First, HHOs directly repress the high-affinity nitrate transporters, NRT2.4 and NRT2.5. hho mutants display increased high-affinity nitrate transport activity, opening up promising perspectives for biotechnological applications. Second, we show that reactive oxygen species (ROS) are important to control NSR in wild-type plants and that HRS1 and HHO1 overexpressors and mutants are affected in their ROS content, defining a potential feed-forward branch of the signaling pathway. Taken together, our results define the relationships of two types of molecular players controlling the NSR, namely ROS and the HHO transcription factors. This work (i) up opens perspectives on a poorly understood nutrient-related signaling pathway and (ii) defines targets for molecular breeding of plants with enhanced NO3- uptake.

Keywords: Cell sorting; GARP transcription factors; ROS; TARGET; nitrogen starvation response; plant growth; root nitrate uptake; root protoplasts.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anion Transport Proteins / genetics
  • Anion Transport Proteins / metabolism
  • Arabidopsis Proteins* / genetics
  • Arabidopsis Proteins* / metabolism
  • Arabidopsis* / genetics
  • Arabidopsis* / metabolism
  • Gene Expression Regulation, Plant
  • Nitrates / metabolism
  • Nitrogen / metabolism
  • Plant Roots / metabolism
  • Reactive Oxygen Species
  • Transcription Factors / genetics
  • Transcription Factors / metabolism

Substances

  • Anion Transport Proteins
  • Arabidopsis Proteins
  • Nitrates
  • Reactive Oxygen Species
  • Transcription Factors
  • Nitrogen