2009
DOI: 10.1016/j.tplants.2008.11.007
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Towards a systems-based understanding of plant desiccation tolerance

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Cited by 166 publications
(130 citation statements)
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“…Interestingly, exactly the same band was shown to be shifted during desiccation-induced conformational changes of a recombinant LEA (Late embryogenesis abundant) protein (Tolleter et al 2007). Structurally considered to be random coil, LEA proteins have been shown to form stabilized structures in the vicinity of membranes and they can act as antiaggregants, protecting the proteomes against water loss induced aggregation (Moore et al 2009). LEA are extremely hydrophilic proteins produced at high levels in seeds and pollen grains during the latter stages of maturation and desiccation that are ubiquitously produced by plants, algae and cyanobacteria in response to water stress (Rascio & La Rocca 2005), where LEA proteins can reach as much as 40% of the dry weight in some resurrection plants (Gechev et al 2012).…”
Section: Discussionmentioning
confidence: 92%
See 1 more Smart Citation
“…Interestingly, exactly the same band was shown to be shifted during desiccation-induced conformational changes of a recombinant LEA (Late embryogenesis abundant) protein (Tolleter et al 2007). Structurally considered to be random coil, LEA proteins have been shown to form stabilized structures in the vicinity of membranes and they can act as antiaggregants, protecting the proteomes against water loss induced aggregation (Moore et al 2009). LEA are extremely hydrophilic proteins produced at high levels in seeds and pollen grains during the latter stages of maturation and desiccation that are ubiquitously produced by plants, algae and cyanobacteria in response to water stress (Rascio & La Rocca 2005), where LEA proteins can reach as much as 40% of the dry weight in some resurrection plants (Gechev et al 2012).…”
Section: Discussionmentioning
confidence: 92%
“…Poikilochlorophyllous resurrection plants degrade their chlorophyll and resynthesize it after rehydration. Homoiochlorophyllous are subjected to a greater risk of photo-oxidative and metabolic damage occurring because active photosystems can be uncoupled from metabolic dissipation mechanisms, resulting in oxidative damage (Moore et al 2009), which is minimized by additional morphological and biochemical mechanisms such as leaf folding to reduce absorbed radiation or/and accumulation of anthocyanins and other phenolic compounds to protect against solar radiation (Farrant & Moore 2011).…”
Section: Introductionmentioning
confidence: 99%
“…It is also necessary to understand how the system might be affected by the interplay of external factors (e.g., water availability) and internal factors (developmental triggers). Therefore, analyses of the system structures (e.g., gene interactions) and dynamics (e.g., metabolic fluxes) become important (Kitano 2002;Moore et al 2009). Correlation of next-generation sequencing, genomescale molecular analysis, modeling of physiological and molecular data to the physiology of the plant leads to new data about adaptability and improved traits which can ultimately be incorporated in crop plants to improve productivity under stress (weckwerth 2011).…”
Section: Introductionmentioning
confidence: 99%
“…In lichens, both desiccation and rehydration occur rapidly due to the absence of a waxy cuticullar barrier to water exchanges, making both processes potentially more harmful than in plants. For example, some desiccation-tolerant vascular plants ("resurrection plants") degrade their chlorophyll during dehydration and resynthesize it after rehydration [31], thus preventing unbalanced ROS production. However, lichen photobionts do not significantly alter their content of photosynthetic pigments during their rapid and cyclic changes in water content.…”
Section: Introductionmentioning
confidence: 99%