UCP1 and AOX1a contribute to regulation of carbon and nitrogen metabolism and yield in Arabidopsis under low nitrogen stress

Cell Mol Life Sci. 2022 Jan 2;79(1):69. doi: 10.1007/s00018-021-04036-w.

Abstract

Nitrogen (N) availability is a critical factor for plant development and crop yield, and it closely correlates to carbon (C) metabolism. Uncoupling protein (UCP) and alternative oxidase (AOX) exhibit a strong correlation with N and C metabolism. Here, we investigated the functions of UCP1 and AOX1a using their mutants and complementation lines in Arabidopsis adaptation to low N. Low N markedly increased AOX1a and UCP1 expression, alternative pathway capacity and UCP activity. Eight-day-old aox1a/ucp1 seedlings were more sensitive to low N than Col-0 and single mutants, exhibiting lower primary root length and higher anthocyanin accumulation. The net photosynthetic rate, electron transport rate, PSII actual photochemical efficiency, stomatal conductance and carboxylation efficiency were markedly decreased in ucp1 and aox1a/ucp1 compared to those in Col-0 and aox1a under low N stress; comparatively, chlorophyll content and non-photochemical quenching coefficient were the lowest and highest in aox1a/ucp1, respectively. Nitrate acquisition rate was accelerated in aox1a/ucp1, but its transport activity was decreased, which resulted in low nitrate content and nitrate reductase activity under low N condition. The C/N ratio in seeds, but not in leaves, is higher in aox1a/ucp1 than that in Col-0, aox1a and ucp1 under low N condition. RNA-seq analysis revealed that many genes involved in photosynthesis and C/N metabolism were markedly down-regulated in aox1a/ucp1 under low N stress. These results highlight the key roles of UCP1 and AOX1a in modulating photosynthetic capacity, C/N assimilation and distribution under low N stress.

Keywords: C/N balance; Energy distribution; Macronutrient stress; Non-phosphorylating electron transport pathway.

MeSH terms

  • Anthocyanins / metabolism
  • Arabidopsis / metabolism*
  • Carbon / metabolism*
  • Chlorophyll / analysis
  • Mitochondrial Proteins / genetics
  • Mitochondrial Proteins / metabolism*
  • Nitrogen / metabolism*
  • Oxidoreductases / genetics
  • Oxidoreductases / metabolism*
  • Photosynthesis / genetics
  • Photosynthesis / physiology*
  • Plant Leaves / metabolism
  • Plant Proteins / genetics
  • Plant Proteins / metabolism*
  • Plant Roots / anatomy & histology
  • Plant Roots / physiology
  • RNA-Seq
  • Seedlings / metabolism
  • Seeds / metabolism
  • Stress, Physiological / genetics
  • Stress, Physiological / physiology
  • Uncoupling Protein 1 / genetics
  • Uncoupling Protein 1 / metabolism*

Substances

  • Anthocyanins
  • Mitochondrial Proteins
  • Plant Proteins
  • Uncoupling Protein 1
  • Chlorophyll
  • Carbon
  • Oxidoreductases
  • alternative oxidase
  • Nitrogen