RIN4 Functions with Plasma Membrane H+-ATPases to Regulate Stomatal Apertures during Pathogen Attack

Pathogen perception by the plant innate immune system is of central importance to plant survival and productivity. The Arabidopsis protein RIN4 is a negative regulator of plant immunity. In order to identify additional proteins involved in RIN4-mediated immune signal transduction, we purified compon...

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Published inPLoS biology Vol. 7; no. 6; p. e1000139
Main Authors Liu, Jun, Elmore, James M., Fuglsang, Anja T., Palmgren, Michael G., Staskawicz, Brian J., Coaker, Gitta
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 30.06.2009
Public Library of Science (PLoS)
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Summary:Pathogen perception by the plant innate immune system is of central importance to plant survival and productivity. The Arabidopsis protein RIN4 is a negative regulator of plant immunity. In order to identify additional proteins involved in RIN4-mediated immune signal transduction, we purified components of the RIN4 protein complex. We identified six novel proteins that had not previously been implicated in RIN4 signaling, including the plasma membrane (PM) H(+)-ATPases AHA1 and/or AHA2. RIN4 interacts with AHA1 and AHA2 both in vitro and in vivo. RIN4 overexpression and knockout lines exhibit differential PM H(+)-ATPase activity. PM H(+)-ATPase activation induces stomatal opening, enabling bacteria to gain entry into the plant leaf; inactivation induces stomatal closure thus restricting bacterial invasion. The rin4 knockout line exhibited reduced PM H(+)-ATPase activity and, importantly, its stomata could not be re-opened by virulent Pseudomonas syringae. We also demonstrate that RIN4 is expressed in guard cells, highlighting the importance of this cell type in innate immunity. These results indicate that the Arabidopsis protein RIN4 functions with the PM H(+)-ATPase to regulate stomatal apertures, inhibiting the entry of bacterial pathogens into the plant leaf during infection.
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The author(s) have made the following declarations about their contributions: Conceived and designed the experiments: JL MGP BJS GC. Performed the experiments: JL JME ATF GC. Analyzed the data: JL GC. Contributed reagents/materials/analysis tools: BJS. Wrote the paper: JL JME ATF MGP BJS GC.
ISSN:1545-7885
1544-9173
1545-7885
DOI:10.1371/journal.pbio.1000139