Discovery of nitrate-CPK-NLP signalling in central nutrient-growth networks

Nature. 2017 May 18;545(7654):311-316. doi: 10.1038/nature22077. Epub 2017 May 10.

Abstract

Nutrient signalling integrates and coordinates gene expression, metabolism and growth. However, its primary molecular mechanisms remain incompletely understood in plants and animals. Here we report unique Ca2+ signalling triggered by nitrate with live imaging of an ultrasensitive biosensor in Arabidopsis leaves and roots. A nitrate-sensitized and targeted functional genomic screen identifies subgroup III Ca2+-sensor protein kinases (CPKs) as master regulators that orchestrate primary nitrate responses. A chemical switch with the engineered mutant CPK10(M141G) circumvents embryo lethality and enables conditional analyses of cpk10 cpk30 cpk32 triple mutants to define comprehensive nitrate-associated regulatory and developmental programs. Nitrate-coupled CPK signalling phosphorylates conserved NIN-LIKE PROTEIN (NLP) transcription factors to specify the reprogramming of gene sets for downstream transcription factors, transporters, nitrogen assimilation, carbon/nitrogen metabolism, redox, signalling, hormones and proliferation. Conditional cpk10 cpk30 cpk32 and nlp7 mutants similarly impair nitrate-stimulated system-wide shoot growth and root establishment. The nutrient-coupled Ca2+ signalling network integrates transcriptome and cellular metabolism with shoot-root coordination and developmental plasticity in shaping organ biomass and architecture.

Publication types

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

MeSH terms

  • Amidohydrolases / genetics
  • Amidohydrolases / metabolism*
  • Amino Acid Sequence
  • Arabidopsis / genetics
  • Arabidopsis / growth & development*
  • Arabidopsis / metabolism*
  • Arabidopsis Proteins / chemistry
  • Arabidopsis Proteins / genetics
  • Arabidopsis Proteins / metabolism
  • Biomass
  • Calcium / metabolism*
  • Calcium Signaling
  • Calcium-Binding Proteins / chemistry
  • Calcium-Binding Proteins / genetics
  • Calcium-Binding Proteins / metabolism
  • Calcium-Calmodulin-Dependent Protein Kinases / chemistry
  • Calcium-Calmodulin-Dependent Protein Kinases / genetics
  • Calcium-Calmodulin-Dependent Protein Kinases / metabolism
  • Carbon / metabolism
  • Cellular Reprogramming
  • Food
  • Gene Expression Regulation, Plant
  • Nitrates / metabolism*
  • Nitrogen / metabolism
  • Oxidation-Reduction
  • Phosphorylation
  • Plant Roots / growth & development
  • Plant Roots / metabolism
  • Plant Shoots / growth & development
  • Plant Shoots / metabolism
  • Plants, Genetically Modified
  • Protein Kinases / chemistry
  • Protein Kinases / genetics
  • Protein Kinases / metabolism*
  • Signal Transduction*
  • Transcription, Genetic
  • Transcriptome

Substances

  • ATCDPK1 protein, Arabidopsis
  • Arabidopsis Proteins
  • Calcium-Binding Proteins
  • Nitrates
  • Carbon
  • CPK32 protein, Arabidopsis
  • Protein Kinases
  • CPK30 protein, Arabidopsis
  • Calcium-Calmodulin-Dependent Protein Kinases
  • Amidohydrolases
  • Nitrogen
  • Calcium