Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8645375 | Gene | 2018 | 14 Pages |
Abstract
In Arabidopsis and certain other plant species, the type 2C protein phosphatases (PP2Cs) of the clade A class have been demonstrated to act as negative regulators in ABA-induced stress responses, such as stomatal closure. The present study reports the identification of a PP2C ortholog from the ancient desert shrub Ammopiptanthus mongolicus (Maxim.) Cheng f. (AmPP2C), which is functionally conserved over its counterparts reported from other plant species. AmPP2C was primarily expressed in leaves, with strong transcriptional accumulation being observed in the guard cells. The expression of AmPP2C was induced in response to PEG or ABA treatments, implying the potential involvement in ABA-induced stress responses. The GFP-tagging observation revealed that AmPP2C was predominantly localized to the nuclei and partly to the cytoplasm. Furthermore, BiFC assays demonstrated an interaction between AmPP2C and the typical protein kinase SnRK2.6 (AmOST1). Overexpression of AmPP2C in Arabidopsis significantly overcame the inhibition of seed germination by ABA. The transgenic Arabidopsis lines exhibited larger stomatal apertures and significantly reduced sensitivity to ABA-induced stomatal closure, which subsequently led to greater water loss and decreased biomass under PEG-simulated drought stress treatments. Under limited nitrogen or potassium supplements, plants overexpressing AmPP2C obtained a superior capability of nitrogen (N) and potassium (K) acquisition in the green parts. Therefore, the impairment of ABA-induced stomatal closure rendered by the function of PP2C helped to identify a potential survival strategy in plants suffering persistent drought stress via the maintenance of the necessary mineral nutrient acquisition driven by transpirational solute flow.
Keywords
PP2CqRT-PCRGUSBiFCCPKSPSSX-GlucYFPGFPPYRDREBLSDAbi1Ammopiptanthus mongolicusrCARSnRKOST1ABAopen stomata 1SLAC1DNAArabidopsis thalianadeoxyribonucleic acidabscisic acidRNAribonucleic acidPhotosynthetically active radiationTranspirationParbimolecular fluorescence complementationleast significant differenceDroughtstandard errorStatistical Product and Service SolutionsLuria-BertaniMeSwild typelow nitrogenpolymerase chain reactionquantitative real-time PCRPCRlow potassiumprotein phosphatase 2CGreen fluorescence proteinyellow fluorescent proteinCalcium-dependent protein kinasepolyethylene glycolPEGPylGlucuronidaseGORK
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Authors
Lei Han, Junlin Li, Man Jin, Yanhua Su,