4.8 Article

Extracellular Nucleotides and Apyrases Regulate Stomatal Aperture in Arabidopsis

Journal

PLANT PHYSIOLOGY
Volume 156, Issue 4, Pages 1740-1753

Publisher

AMER SOC PLANT BIOLOGISTS
DOI: 10.1104/pp.111.174466

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Funding

  1. National Science Foundation [0718890, 1027514]
  2. German Research Foundation [STE 1455/3-1]
  3. Direct For Biological Sciences
  4. Division Of Integrative Organismal Systems [0718890] Funding Source: National Science Foundation

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This study investigates the role of extracellular nucleotides and apyrase enzymes in regulating stomatal aperture. Prior data indicate that the expression of two apyrases in Arabidopsis (Arabidopsis thaliana), APY1 and APY2, is strongly correlated with cell growth and secretory activity. Both are expressed strongly in guard cell protoplasts, as determined by reverse transcription-polymerase chain reaction and immunoblot analyses. Promoter activity assays for APY1 and APY2 show that expression of both apyrases correlates with conditions that favor stomatal opening. Correspondingly, immunoblot data indicate that APY expression in guard cell protoplasts rises quickly when these cells are moved from darkness into light. Both short-term inhibition of ectoapyrase activity by polyclonal antibodies and long-term suppression of APY1 and APY2 transcript levels significantly disrupt normal stomatal behavior in light. Stomatal aperture shows a biphasic response to applied adenosine 5'-[gamma-thio]triphosphate (ATP gamma S) or adenosine 5'-[beta-thio] diphosphate, with lower concentrations inducing stomatal opening and higher concentrations inducing closure. Equivalent concentrations of adenosine 5'-O-thiomonophosphate have no effect on aperture. Two mammalian purinoceptor inhibitors block ATP gamma S- and adenosine 5'-[beta-thio] diphosphate-induced opening and closing and also partially block the ability of abscisic acid to induce stomatal closure and of light to induce stomatal opening. Treatment of epidermal peels with ATP gamma S induces increased levels of nitric oxide and reactive oxygen species, and genetically suppressing the synthesis of these agents blocks the effects of nucleotides on stomatal aperture. A luciferase assay indicates that treatments that induce either the closing or opening of stomates also induce the release of ATP from guard cells. These data favor the novel conclusion that ectoapyrases and extracellular nucleotides play key roles in regulating stomatal functions.

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