VAMP711 Is Required for Abscisic Acid-Mediated Inhibition of Plasma Membrane H+-ATPase Activity

Plant Physiol. 2018 Nov;178(3):1332-1343. doi: 10.1104/pp.18.00499. Epub 2018 Sep 14.

Abstract

Drought stress is a limiting environmental factor that affects plant growth and development. The plant hormone abscisic acid (ABA) plays an important role in plant drought responses. Previous studies have indicated that ABA inhibits plasma membrane H+-ATPase (PM H+-ATPase) activity, and the decrease in PM H+-ATPase activity promotes stomatal closure under drought stress, thereby reducing water loss. However, the underlying molecular mechanisms are not well understood. In this study, we found that in Arabidopsis (Arabidopsis thaliana), ABA induces an N-ethylmaleimide-sensitive factor attachment protein receptor protein, namely, VESICLE-ASSOCIATED MEMBRANE PROTEIN 711 (VAMP711), to interact with the Arabidopsis PM H+-ATPases AHA1 and AHA2. The interaction occurs at their C-termini and inhibits PM H+-ATPase activity. Deletion of VAMP711 in Arabidopsis results in a higher PM H+-ATPase activity and slower stomatal closure in response to ABA and drought treatments. In addition, overexpression of VAMP711 partially rescues the drought-sensitive phenotype of ost2-2D, a mutation in AHA1 resulting in a constitutive activated PM H+-ATPase. Our results demonstrate that VAMP711 is involved in regulating ABA-mediated inhibition of PM H+-ATPase activity and stomatal closure in response to drought stress.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abscisic Acid / metabolism*
  • Amino Acid Sequence
  • Arabidopsis / genetics*
  • Arabidopsis / physiology
  • Arabidopsis Proteins / genetics
  • Arabidopsis Proteins / metabolism*
  • Cell Membrane / metabolism
  • Droughts
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Mutation
  • Phenotype
  • Plant Growth Regulators / metabolism*
  • Plant Leaves / genetics
  • Plant Leaves / physiology
  • Plant Stomata / genetics
  • Plant Stomata / physiology
  • Proton-Translocating ATPases / genetics
  • Proton-Translocating ATPases / metabolism*
  • R-SNARE Proteins / genetics
  • R-SNARE Proteins / metabolism
  • Sequence Alignment
  • Stress, Physiological

Substances

  • Arabidopsis Proteins
  • Membrane Proteins
  • Plant Growth Regulators
  • R-SNARE Proteins
  • VAMP711 protein, Arabidopsis
  • Abscisic Acid
  • Proton-Translocating ATPases
  • AHA1 protein, Arabidopsis
  • AHA2 protein, Arabidopsis