The Plasma Membrane Purinoreceptor P2K1/DORN1 Is Essential in Stomatal Closure Evoked by Extracellular Diadenosine Tetraphosphate (Ap<sub>4</sub>A) in <i>Arabidopsis thaliana</i>

oleh: Jędrzej Dobrogojski, Van Hai Nguyen, Joanna Kowalska, Sławomir Borek, Małgorzata Pietrowska-Borek

Format: Article
Diterbitkan: MDPI AG 2023-11-01

Deskripsi

Dinucleoside polyphosphates (Np<sub>n</sub>Ns) are considered novel signalling molecules involved in the induction of plant defence mechanisms. However, Np<sub>n</sub>N signal recognition and transduction are still enigmatic. Therefore, the aim of our research was the identification of the Np<sub>n</sub>N receptor and signal transduction pathways evoked by these nucleotides. Earlier, we proved that purine and pyrimidine Np<sub>n</sub>Ns differentially affect the phenylpropanoid pathway in <i>Vitis vinifera</i> suspension-cultured cells. Here, we report, for the first time, that both diadenosine tetraphosphate (Ap<sub>4</sub>A) and dicytidine tetraphosphate (Cp<sub>4</sub>C)-induced stomatal closure in <i>Arabidopsis thaliana</i>. Moreover, we showed that plasma membrane purinoreceptor P2K1/DORN1 (does not respond to nucleotide 1) is essential for Ap<sub>4</sub>A-induced stomata movements but not for Cp<sub>4</sub>C. Wild-type Col-0 and the <i>dorn1-3 A. thaliana</i> knockout mutant were used. Examination of the leaf epidermis <i>dorn1-3</i> mutant provided evidence that P2K1/DORN1 is a part of the signal transduction pathway in stomatal closure evoked by extracellular Ap<sub>4</sub>A but not by Cp<sub>4</sub>C. Reactive oxygen species (ROS) are involved in signal transduction caused by Ap<sub>4</sub>A and Cp<sub>4</sub>C, leading to stomatal closure. Ap<sub>4</sub>A induced and Cp<sub>4</sub>C suppressed the transcriptional response in wild-type plants. Moreover, in <i>dorn1-3</i> leaves, the effect of Ap<sub>4</sub>A on gene expression was impaired. The interaction between P2K1/DORN1 and Ap<sub>4</sub>A leads to changes in the transcription of signalling hubs in signal transduction pathways.