Abstract

The combination of robust physiological models with “omics” studies holds promise for the discovery of genes and pathways linked to how organisms deal with drying. Here we used a transcriptomics approach in combination with an in vivo physiological model of re-establishment of desiccation tolerance (DT) in Arabidopsis thaliana seeds. We show that the incubation of desiccation sensitive (DS) germinated Arabidopsis seeds in a polyethylene glycol (PEG) solution re-induces the mechanisms necessary for expression of DT. Based on a SNP-tile array gene expression profile, our data indicates that the re-establishment of DT, in this system, is related to a programmed reversion from a metabolic active to a quiescent state similar to prior to germination. Our findings show that transcripts of germinated seeds after the PEG-treatment are dominated by those encoding LEA, seed storage and dormancy related proteins. On the other hand, a massive repression of genes belonging to many other classes such as photosynthesis, cell wall modification and energy metabolism occurs in parallel. Furthermore, comparison with a similar system for Medicago truncatula reveals a significant overlap between the two transcriptomes. Such overlap may highlight core mechanisms and key regulators of the trait DT. Taking into account the availability of the many genetic and molecular resources for Arabidopsis, the described system may prove useful for unraveling DT in higher plants.

Highlights

  • Desiccation tolerance (DT), or anhydrobiosis, can be conceptually defined as the ability to survive, by reversible cessation of metabolism, the removal of almost all cellular free water when in equilibrium with moderately dry air and resume normal function when re-hydrated [1]

  • Assessment of the re-establishment of desiccation tolerance Previous reports have shown that DT can be fully rescued in germinated seeds [10,14,16]

  • It was tested whether DT could be re-induced in Arabidopsis seeds by treating them in a polyethylene glycol (PEG) (2.5 MPa) solution for three days at 22uC

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Summary

Introduction

Desiccation tolerance (DT), or anhydrobiosis, can be conceptually defined as the ability to survive, by reversible cessation of metabolism, the removal of almost all cellular free water when in equilibrium with moderately dry air and resume normal function when re-hydrated [1]. Desiccation tolerance is the ability of living organisms to deal with water losses below 0.1 g H2O g21 dry weight and survive the re-hydration process without permanent damage [2]. DT in (orthodox) seeds is based on a range of relatively complex protection mechanisms that accompany dehydration [4]. A strong correlation between protective mechanisms activated during dehydration, such as the accumulation of Late embryogenesis abundant (LEA) proteins and dehydrins, non-reducing sugars, sucrose, reactive oxygen species (ROS) scavenging, as well as switching off of metabolism, have been so far postulated as playing major roles in this phenomenon [5]. The mechanisms involved in DT may be roughly divided in three groups: 1) signalling mechanisms, gene regulation and functional proteomics; 2) metabolic adjustment and antioxidant systems; and 3) macromolecular and mechanical stability [8]

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