AtTGA4, a bZIP transcription factor, confers drought resistance by enhancing nitrate transport and assimilation in Arabidopsis thaliana

Biochem Biophys Res Commun. 2015 Feb 13;457(3):433-9. doi: 10.1016/j.bbrc.2015.01.009. Epub 2015 Jan 13.

Abstract

To cope with environmental stress caused by global climate change and excessive nitrogen application, it is important to improve water and nitrogen use efficiencies in crop plants. It has been reported that higher nitrogen uptake could alleviate the damaging impact of drought stress. However, there is scant evidence to explain how nitrogen uptake affects drought resistance. In this study we observed that bZIP transcription factor AtTGA4 (TGACG motif-binding factor 4) was induced by both drought and low nitrogen stresses, and that overexpression of AtTGA4 simultaneously improved drought resistance and reduced nitrogen starvation in Arabidopsis. Following drought stress there were higher nitrogen and proline contents in transgenic AtTGA4 plants than in wild type controls, and activity of the key enzyme nitrite reductase (NIR) involved in nitrate assimilation processes was also higher. Expressions of the high-affinity nitrate transporter genes NRT2.1 and NRT2.2 and nitrate reductase genes NIA1 and NIA2 in transgenic plants were all higher than in wild type indicating that higher levels of nitrate transport and assimilation activity contributed to enhanced drought resistance of AtTGA4 transgenic plants. Thus genetic transformation with AtTGA4 may provide a new approach to simultaneously improve crop tolerance to drought and low nitrogen stresses.

Keywords: Arabidopsis thaliana; Drought stress; Low nitrogen stress; Nitrogen absorption; Transcription factor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anion Transport Proteins / genetics
  • Anion Transport Proteins / metabolism
  • Arabidopsis / genetics
  • Arabidopsis / metabolism*
  • Arabidopsis Proteins / genetics
  • Arabidopsis Proteins / metabolism*
  • Basic-Leucine Zipper Transcription Factors / genetics
  • Basic-Leucine Zipper Transcription Factors / metabolism*
  • Climate Change
  • Droughts
  • Gene Expression Regulation, Plant
  • Genes, Plant
  • Nitrate Transporters
  • Nitrates / metabolism*
  • Nitrite Reductases / genetics
  • Nitrite Reductases / metabolism
  • Plants, Genetically Modified
  • Stress, Physiological

Substances

  • Anion Transport Proteins
  • Arabidopsis Proteins
  • AtNRT2.1 protein, Arabidopsis
  • Basic-Leucine Zipper Transcription Factors
  • NRT2.2 protein, Arabidopsis
  • Nitrate Transporters
  • Nitrates
  • TGA4 protein, Arabidopsis
  • Nitrite Reductases