Interacting TCP and NLP transcription factors control plant responses to nitrate availability

Proc Natl Acad Sci U S A. 2017 Feb 28;114(9):2419-2424. doi: 10.1073/pnas.1615676114. Epub 2017 Feb 15.

Abstract

Plants have evolved adaptive strategies that involve transcriptional networks to cope with and survive environmental challenges. Key transcriptional regulators that mediate responses to environmental fluctuations in nitrate have been identified; however, little is known about how these regulators interact to orchestrate nitrogen (N) responses and cell-cycle regulation. Here we report that teosinte branched1/cycloidea/proliferating cell factor1-20 (TCP20) and NIN-like protein (NLP) transcription factors NLP6 and NLP7, which act as activators of nitrate assimilatory genes, bind to adjacent sites in the upstream promoter region of the nitrate reductase gene, NIA1, and physically interact under continuous nitrate and N-starvation conditions. Regions of these proteins necessary for these interactions were found to include the type I/II Phox and Bem1p (PB1) domains of NLP6&7, a protein-interaction module conserved in animals for nutrient signaling, and the histidine- and glutamine-rich domain of TCP20, which is conserved across plant species. Under N starvation, TCP20-NLP6&7 heterodimers accumulate in the nucleus, and this coincides with TCP20 and NLP6&7-dependent up-regulation of nitrate assimilation and signaling genes and down-regulation of the G2/M cell-cycle marker gene, CYCB1;1 TCP20 and NLP6&7 also support root meristem growth under N starvation. These findings provide insights into how plants coordinate responses to nitrate availability, linking nitrate assimilation and signaling with cell-cycle progression.

Keywords: NIN-like protein; TCP; cell cycle; nitrate signaling; root growth.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Arabidopsis / drug effects
  • Arabidopsis / genetics*
  • Arabidopsis / growth & development
  • Arabidopsis / metabolism
  • Arabidopsis Proteins / genetics*
  • Arabidopsis Proteins / metabolism
  • Binding Sites
  • Cyclin B / genetics
  • Cyclin B / metabolism
  • G2 Phase Cell Cycle Checkpoints
  • Gene Expression Regulation, Developmental
  • Gene Expression Regulation, Plant*
  • Nitrate Reductase / genetics
  • Nitrate Reductase / metabolism
  • Nitrates / metabolism
  • Nitrates / pharmacology
  • Plant Roots / drug effects
  • Plant Roots / genetics*
  • Plant Roots / growth & development
  • Plant Roots / metabolism
  • Promoter Regions, Genetic
  • Protein Binding
  • Protein Isoforms / genetics
  • Protein Isoforms / metabolism
  • Sequence Alignment
  • Sequence Homology, Amino Acid
  • Signal Transduction
  • Transcription Factors / genetics*
  • Transcription Factors / metabolism
  • Transcription, Genetic

Substances

  • Arabidopsis Proteins
  • CycB1 protein, Arabidopsis
  • Cyclin B
  • NIN-LIKE PROTEIN7, Arabidopsis
  • Nitrates
  • Protein Isoforms
  • TCP20 protein, Arabidopsis
  • Transcription Factors
  • NIA1 protein, Arabidopsis
  • Nitrate Reductase