Abstract

Two related tree species, Norway maple (Acer platanoides L.) and sycamore (Acer pseudoplatanus L.), produce desiccation-tolerant (orthodox) and desiccation-sensitive (recalcitrant) seeds, respectively. We compared the seeds of these two species to characterize the developmentally driven changes in the levels of peptide-bound methionine sulfoxide (MetO) and the abundance of methionine sulfoxide reductases (Msrs) B1 and B2, with respect to the cellular redox environment. Protein oxidation at the Met level was dynamic only in Norway maple seeds, and the reduced MsrB2 form was detected only in this species. Cell redox status, characterized by the levels of reduced and oxidized ascorbate, glutathione, and nicotinamide adenine dinucleotide (NAD)/phosphate (NADP), was clearly more reduced in the Norway maple seeds than in the sycamore seeds. Clear correlations between MetO levels, changes in water content and redox status were reported in orthodox Acer seeds. The abundance of Msrs was correlated in both species with redox determinants, mainly ascorbate and glutathione. Our data suggest that MsrB2 is associated with the acquisition of desiccation tolerance and that ascorbate might be involved in the redox pathway enabling the regeneration of Msr via intermediates that are not known yet.

Highlights

  • Seeds are reproductive structures that evolved to successfully colonize the terrestrial environment by developing important features, including desiccation tolerance and seed dormancy

  • Controlled oxidation is critical for developmental transitions in plants, such as those occurring in seeds

  • In addition to cysteine redox switches, the reversible oxidation of Met to methionine sulfoxide (MetO) is an important protein posttranslational modification involved in redox signaling [33]

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Summary

Introduction

Seeds are reproductive structures that evolved to successfully colonize the terrestrial environment by developing important features, including desiccation tolerance and seed dormancy. Desiccation tolerance involves the ability to withstand extreme dehydration and to repair damage upon rehydration by activation of protective mechanisms. It is based on the ability of the cell to enter into a quiescent state, fill the vacuole, accumulate protective molecules (sugars, late embryogenesis abundant proteins, heat-shock proteins) and produce antioxidants (reviewed in Dekkers et al [2]). Orthodox and recalcitrant seeds differ in terms of several characteristics, e.g., the structural integrity of membranes and organelles after water removal, metabolic shutdown, the antioxidant system, the availability of protectants including sucrose, oligosaccharides, and late embryogenic abundant proteins [4,10]

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