Adenosine 5'-monophosphate inhibits the association of 14-3-3 proteins with the plant plasma membrane H(+)-ATPase

J Biol Chem. 2001 Aug 24;276(34):31709-12. doi: 10.1074/jbc.M104194200. Epub 2001 Jun 21.

Abstract

Although a well ascertained evidence proves that the activity of the plant plasma membrane H(+)-ATPase is regulated by 14-3-3 proteins, information about physiological factors modulating the phosphorylation-dependent association between 14-3-3 proteins and the proton pump is largely incomplete. In this paper we show that the 5'-AMP-mimetic, 5-aminoimidazole-4-carboxamide ribonucleoside (AICAR), inhibits the fusicoccin-promoted proton extrusion in maize roots. We also demonstrate that 5'-AMP inhibits the association of 14-3-3 proteins with the C-terminal domain of the H(+)-ATPase in an overlay assay as well as the 14-3-3-dependent stimulation of the Arabidopsis thaliana H(+)-ATPase AHA1 isoform expressed in yeast membranes. Finally, by means of affinity chromatography with immobilized 5'-AMP and trinitrophenyl-AMP fluorescence analysis, we demonstrate that the 14-3-3 isoform GF14-6 from maize is able to bind 5'-AMP. The possible role of 5'-AMP as a general regulator of 14-3-3 functions in the plant cell is discussed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 14-3-3 Proteins
  • Adenosine Monophosphate / pharmacology*
  • Amino Acid Sequence
  • Arabidopsis / enzymology*
  • Cell Membrane / enzymology
  • Molecular Sequence Data
  • Proton-Translocating ATPases / antagonists & inhibitors*
  • Proton-Translocating ATPases / metabolism
  • Spectrometry, Fluorescence
  • Tyrosine 3-Monooxygenase / antagonists & inhibitors*
  • Tyrosine 3-Monooxygenase / metabolism
  • Zea mays / enzymology*

Substances

  • 14-3-3 Proteins
  • Adenosine Monophosphate
  • Tyrosine 3-Monooxygenase
  • Proton-Translocating ATPases