De-regulated expression of the plant glutamate receptor homolog AtGLR3.1 impairs long-term Ca2+-programmed stomatal closure

Daeshik Cho, Sun A. Kim, Yoshiyuki Murata, Sangmee Lee, Seul Ki Jae, Hong Gil Nam, June M. Kwak

Research output: Contribution to journalArticlepeer-review

56 Citations (Scopus)

Abstract

Cytosolic Ca2+ ([Ca2+]cyt) mediates diverse cellular responses in both animal and plant cells in response to various stimuli. Calcium oscillation amplitude and frequency control gene expression. In stomatal guard cells, [Ca2+]cyt has been shown to regulate stomatal movements, and a defined window of Ca2+ oscillation kinetic parameters encodes necessary information for long-term stomatal movements. However, it remains unknown how the encrypted information in the cytosolic Ca2+ signature is decoded to maintain stomatal closure. Here we report that the Arabidopsis glutamate receptor homolog AtGLR3.1 is preferentially expressed in guard cells compared to mesophyll cells. Furthermore, over-expression of AtGLR3.1 using a viral promoter resulted in impaired external Ca2+-induced stomatal closure. Cytosolic Ca 2+ activation of S-type anion channels, which play a central role in Ca2+-reactive stomatal closure, was normal in the AtGLR3.1 over-expressing plants. Interestingly, AtGLR3.1 over-expression did not affect Ca2+-induced Ca2+ oscillation kinetics, but resulted in a failure to maintain long-term 'Ca2+-programmed' stomatal closure when Ca2+ oscillations containing information for maintaining stomatal closure were imposed. By contrast, prompt short-term Ca2+-reactive closure was not affected in AtGLR3.1 over-expressing plants. In wild-type plants, the translational inhibitor cyclohexamide partially inhibited Ca 2+-programmed stomatal closure induced by experimentally imposed Ca2+ oscillations without affecting short-term Ca2+- reactive closure, mimicking the guard cell behavior of the AtGLR3.1 over-expressing plants. Our results suggest that over-expression of AtGLR3.1 impairs Ca2+ oscillation-regulated stomatal movements, and that de novo protein synthesis contributes to the maintenance of long-term Ca 2+-programmed stomatal closure.

Original languageEnglish
Pages (from-to)437-449
Number of pages13
JournalPlant Journal
Volume58
Issue number3
DOIs
Publication statusPublished - May 2009

Keywords

  • Anion channel
  • Calcium oscillation
  • Gene expression
  • Glutamate receptor homolog
  • Guard cells

ASJC Scopus subject areas

  • Genetics
  • Plant Science
  • Cell Biology

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