Abstract

Important functions of the plant hormone abscisic acid (ABA) in stress reactions, growth and photosynthetic processes are extensively studied in the model plant Arabidopsis thaliana. This paper investigates the importance of Moco-sulphurase ABA3 and aldehyde oxidase (AO) on ABA-biosynthesis in Populus × canescens. ABA3 is essential for activation of the molybdenum enzymes AO and xanthine dehydrogenase (XDH). AO itself catalyzes the last step in ABA-biosynthesis. Generation of transgenic poplar plants altered in ABA3 and AO-activity using RNAi knock down and overexpression was performed. Whereas RNAi-AO plants show a specific loss of AO activity, the RNAi-ABA3 plants has a strongly reduced activity of both molybdenum enzymes: AO and XDH. Constructs of AO and ABA3-promoters fused to β-glucuronidase provide the basis to investigate transcriptional regulation of ABA-biosynthetic processes under stress conditions. Application of high salt concentrations and different drought stress intensities does change the endogenous AO or XDH neither on the side of transcription nor on protein activity. On phytohormone level however, water loss leads to increased ABA-amounts regardless of whether transgenic or wildtype plants are studied. Salt application resulted in higher ABA-levels in all analyzed plant lines. The down regulation of AO in the two different RNAi-plant lines strongly prevented a wildtype-like increase of ABA-levels. Whereas the WT plants accumulated up to 6000 ng ABA g-1 FW-1 after 16 h of salt stress exposure, plants of the RNAi lines revealed a markedly lower increase of only up to 2000 ng ABA g-1 FW-1. Opposing to these observations, ABA-levels increased during drought without any influence by the RNAi-effect. These results revealed that although stresses did not result in a visible increased AO-activity, ABA-production was influenced by AO and ABA3 at least under salinity.

Highlights

  • IntroductionPlant cell expansion and vegetative growth are heavily dependent upon a positive water-generated turgor pressure which is maintained by keeping a constant osmotic potential

  • Every organism depends to some extend on water supply

  • In Arabidopsis, the molybdenum cofactor (Moco) sulphurating enzyme ABA3 (At1g16540) regulates the activation of aldehyde oxidase (AO) and xanthine dehydrogenase (XDH) by inserting a sulphur atom into the Moco to generate its sulphurized form, which is required by AO and XDH to accomplish their tasks in drought and salt stress reactions [13] [30]. ptaba3 is described in the P. trichocarpa database as POPTR_0007s08330/PtABA3 (“similar to abscisic acid (ABA) DEFICIENT 3”) representing an ‘ortholog of Arabidopsis At1g16540’

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Summary

Introduction

Plant cell expansion and vegetative growth are heavily dependent upon a positive water-generated turgor pressure which is maintained by keeping a constant osmotic potential Abiotic factors such as high salinity and drought cause shifts in this osmotic potential. ABA is further needed to induce the transcription of dehydration tolerance genes [4]-[6] These signals and reactions are extended in secondary responses by triggering the already generated signals to gain maximal efficiency. Both salinity and drought lead to ABA release, a further upstream component involved in salinity response makes these stresses distinguishable: the SOS pathway (Salt Overly Sensitive, [4]). This results in activation of membrane associated Na+/H+ antiporters, which are directly involved in recovering ion homeostasis [1] [4] [7] [8]

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