Abstract

The stromal ascorbate peroxidase (sAPX) functions as central element of the chloroplast antioxidant defense system. Its expression is under retrograde control of chloroplast signals including redox- and reactive oxygen species-linked cues. The sAPX promoter of Arabidopsis thaliana was dissected in transient reporter assays using mesophyll protoplasts. The study revealed regulatory elements up to –1868 upstream of the start codon. By yeast-one-hybrid screening, the transcription factor ANAC089 was identified to bind to the promoter fragment 2 (–1262 to –1646 bp upstream of translational initiation). Upon mutation of the cis-acting element CACG, binding of ANAC089 was abolished. Expression of a fused fluorescent protein version and comparison with known endomembrane markers localized ANAC089 to the trans-Golgi network and the ER. The transcription factor was released upon treatment with reducing agents and targeted to the nucleus. Transactivation assays using wild type and mutated versions of the promoter showed a partial suppression of reporter expression. The data indicate that ANAC089 functions in a negative retrograde loop, lowering sAPX expression if the cell encounters a highly reducing condition. This conclusion was supported by reciprocal transcript accumulation of ANAC089 and sAPX during acclimation to low, normal, and high light conditions.

Highlights

  • Photosynthetic metabolism involves light driven electron transfer reactions, production of metabolic intermediates with high reducing potential and the generation of reactive oxygen species (ROS)

  • The promoter region of sapx was cloned as assumed full length or truncated form and fused to enhanced yellow fluorescent protein (YFP) as reporter gene

  • The selected sapx1 DNA sequence started from −1868 bp upstream of the translational initiation site down to −1, sapx3 from −1321 to −1, sapx5 from −691 to −1 and sapx6 from −263 to −1

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Summary

Introduction

Photosynthetic metabolism involves light driven electron transfer reactions, production of metabolic intermediates with high reducing potential and the generation of reactive oxygen species (ROS). Appropriate sensing allows for using redox and ROS information to adjust photosynthetic metabolism and tune gene expression in the plastids and in the nuclear genome by retrograde signal transfer from the chloroplast to the nucleus (Baier and Dietz, 2005). Operational control coordinates nuclear gene expression with the actual needs of photosynthetic metabolism. Accumulation of singlet oxygen, changes in redox state of intersystem electron transport chain, redox state of metabolites or proteins as Abbreviations: 3-AT, 3-amino-1,2,4-triazol; DTT, dithiothreitol; CFP, (enhanced) cyan fluorescent protein; EMSA, electrophoretic mobility shift assay; FRET, Förster/fluorescence resonance energy transfer; MTTF, membrane-tethered transcription factors; ROS, reactive oxygen species; sAPX, stromal ascorbate peroxidase; SOD, superoxide dismutase; TF, transcription factor; YFP, (enhanced) yellow fluorescent protein

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