Phosphorylated nitrate reductase from spinach leaves is inhibited by 14-3-3 proteins and activated by fusicoccin

Curr Biol. 1996 Sep 1;6(9):1104-13. doi: 10.1016/s0960-9822(02)70677-5.

Abstract

Background: Nitrate reductase (NR) in leaves is rapidly inactivated in the dark by a two-step mechanism in which phosphorylation of NR on the serine at position 543 (Ser543) promotes binding to nitrate reductase inhibitor protein (NIP). The eukaryotic 14-3-3 proteins bind to many mammalian signalling components (Raf-1, Bcr, phosphoinositide 3-kinase, protein kinase C, polyomavirus middle-T antigen and Cdc25), and are implicated in the timing of mitosis, DNA-damage checkpoint control, exocytosis, and activation of the plant plasma-membrane H+-ATPase by fusicoccin. Their dimeric, saddle-shaped structures support the proposal that 14-3-3 proteins are 'adaptors' linking different signalling proteins, but their precise functions are still a mystery.

Results: We purified NIP to homogeneity and established by means of amino-acid sequencing that it is a mixture of several 14-3-3 isoforms. Mammalian and yeast 14-3-3 proteins were just as effective as NIP at inhibiting phosphorylated NR. The sequence around Ser543, the phosphorylation site in NR, is strikingly similar to the sequences around the phosphoserine residues (Ser259 and Ser621) of mammalian Raf-1 that interact with 14-3-3 proteins. We found that NIP activity was blocked by a synthetic phosphopeptide corresponding to residues 251-266 of Raf. Fusicoccin also blocked NIP activity, and plant plasma-membrane H+-ATPases were activated by either fusicoccin, the phosphoserine259-Raf-1 peptide, or protein phosphatase 2A.

Conclusions: Our findings establish that the mechanism of inactivation of NR involves the phosphorylation of Ser 543 followed by interaction with one or more plant 14-3-3 proteins. These results support the idea of a common mechanism for binding of 14-3-3 to its targets in all eukaryotes, and suggest that the phosphoserine259-Raf-1 peptide and fusicoccin may be of general use for disrupting the interaction of 14-3-3 with its target proteins. We propose that the plant plasma-membrane H+-ATPase is regulated in an analogous manner to NR-NIP, and speculate that 14-3-3 proteins provide a link between 'sensing' the activity state of NR and signalling to other cellular processes in plants.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 14-3-3 Proteins
  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Brassica / enzymology
  • Cell Membrane / enzymology
  • DNA Primers
  • Enzyme Activation
  • Glycosides / metabolism*
  • Molecular Sequence Data
  • Nitrate Reductase
  • Nitrate Reductases / antagonists & inhibitors*
  • Nitrate Reductases / metabolism*
  • Phosphoprotein Phosphatases / metabolism
  • Phosphorylation
  • Plant Leaves / enzymology
  • Plant Proteins / chemistry
  • Plant Proteins / metabolism
  • Protein Binding
  • Protein Phosphatase 2
  • Protein Serine-Threonine Kinases / metabolism
  • Proteins / chemistry
  • Proteins / metabolism*
  • Proto-Oncogene Proteins / metabolism
  • Proto-Oncogene Proteins c-raf
  • Proton-Translocating ATPases / metabolism
  • Spinacia oleracea / enzymology*
  • Tyrosine 3-Monooxygenase*

Substances

  • 14-3-3 Proteins
  • DNA Primers
  • Glycosides
  • NIP protein, Spinacia oleracea
  • Plant Proteins
  • Proteins
  • Proto-Oncogene Proteins
  • fusicoccin
  • Tyrosine 3-Monooxygenase
  • Nitrate Reductases
  • Nitrate Reductase
  • Protein Serine-Threonine Kinases
  • Proto-Oncogene Proteins c-raf
  • Phosphoprotein Phosphatases
  • Protein Phosphatase 2
  • Proton-Translocating ATPases