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1.
Cells ; 10(9)2021 09 02.
Article in English | MEDLINE | ID: mdl-34571944

ABSTRACT

The remarkable desiccation tolerance of the vegetative tissues in the resurrection species Craterostigma plantagineum (Hochst.) is favored by its unique cell wall folding mechanism that allows the ordered and reversible shrinking of the cells without damaging neither the cell wall nor the underlying plasma membrane. The ability to withstand extreme drought is also maintained in abscisic acid pre-treated calli, which can be cultured both on solid and in liquid culture media. Cell wall research has greatly advanced, thanks to the use of inhibitors affecting the biosynthesis of e.g., cellulose, since they allowed the identification of the compensatory mechanisms underlying habituation. Considering the innate cell wall plasticity of C. plantagineum, the goal of this investigation was to understand whether habituation to the cellulose biosynthesis inhibitors dichlobenil and isoxaben entailed or not identical mechanisms as known for non-resurrection species and to decipher the cell wall proteome of habituated cells. The results showed that exposure of C. plantagineum calli/cells triggered abnormal phenotypes, as reported in non-resurrection species. Additionally, the data demonstrated that it was possible to habituate Craterostigma cells to dichlobenil and isoxaben and that gene expression and protein abundance did not follow the same trend. Shotgun and gel-based proteomics revealed a common set of proteins induced upon habituation, but also identified candidates solely induced by habituation to one of the two inhibitors. Finally, it is hypothesized that alterations in auxin levels are responsible for the increased abundance of cell wall-related proteins upon habituation.


Subject(s)
Benzamides/pharmacology , Cell Wall/metabolism , Craterostigma/metabolism , Gene Expression Regulation, Plant/drug effects , Nitriles/pharmacology , Plant Proteins/metabolism , Proteome/metabolism , Cell Membrane/metabolism , Cell Wall/drug effects , Craterostigma/drug effects , Craterostigma/growth & development , Droughts , Herbicides/pharmacology , Plant Proteins/genetics , Proteome/analysis , Proteome/drug effects
2.
PLoS Genet ; 11(12): e1005705, 2015 Dec.
Article in English | MEDLINE | ID: mdl-26633550

ABSTRACT

Global climate change, increasingly erratic weather and a burgeoning global population are significant threats to the sustainability of future crop production. There is an urgent need for the development of robust measures that enable crops to withstand the uncertainty of climate change whilst still producing maximum yields. Resurrection plants possess the unique ability to withstand desiccation for prolonged periods, can be restored upon watering and represent great potential for the development of stress tolerant crops. Here, we describe the remarkable stress characteristics of Tripogon loliiformis, an uncharacterised resurrection grass and close relative of the economically important cereals, rice, sorghum, and maize. We show that T. loliiformis survives extreme environmental stress by implementing autophagy to prevent Programmed Cell Death. Notably, we identified a novel role for trehalose in the regulation of autophagy in T.loliiformis. Transcriptome, Gas Chromatography Mass Spectrometry, immunoblotting and confocal microscopy analyses directly linked the accumulation of trehalose with the onset of autophagy in dehydrating and desiccated T. loliiformis shoots. These results were supported in vitro with the observation of autophagosomes in trehalose treated T. loliiformis leaves; autophagosomes were not detected in untreated samples. Presumably, once induced, autophagy promotes desiccation tolerance in T.loliiformis, by removal of cellular toxins to suppress programmed cell death and the recycling of nutrients to delay the onset of senescence. These findings illustrate how resurrection plants manipulate sugar metabolism to promote desiccation tolerance and may provide candidate genes that are potentially useful for the development of stress tolerant crops.


Subject(s)
Autophagy/genetics , Craterostigma/growth & development , Transcriptome/genetics , Trehalose/metabolism , Climate Change , Craterostigma/genetics , Desiccation , Oryza , Plant Leaves/genetics , Plant Leaves/metabolism , Poaceae/genetics , Stress, Physiological/genetics , Trehalose/genetics , Water
4.
New Phytol ; 179(3): 877-887, 2008.
Article in English | MEDLINE | ID: mdl-18482228

ABSTRACT

* Craterostigma plantagineum can lose up to 96% of its water content but fully recover within hours after rehydration. The callus tissue of the plant becomes desiccation tolerant upon pre-incubation with abscisic acid (ABA). In callus and vegetative organs, ABA addition and water depletion induce a set of dehydration-responsive genes. * Previously, activation tagging led to the isolation of Craterostigma desiccation tolerant (CDT-1), a dehydration-related ABA-inducible gene which renders callus desiccation tolerant without ABA pre-treatment. This gene belongs to a family of retroelements, members of which are inducible by dehydration. * Craterostigma plantagineum transformation with mutated versions of CDT-1 indicated that protein is not required for the induction of callus desiccation tolerance. Northern analysis and protoplast transfection indicated that CDT-1 directs the synthesis of a double-stranded 21-bp short interfering RNA (siRNA), which opens the metabolic pathway for desiccation tolerance. * Via transposition, these retroelements have progressively increased the capacity of the species to synthesize siRNA and thus recover after dehydration. This may be a case of evolution towards the acquisition of a new trait, stimulated by the environment acting directly on intra-genomic DNA replication.


Subject(s)
Biological Evolution , Craterostigma/genetics , RNA, Small Interfering/physiology , Retroelements/physiology , Abscisic Acid/metabolism , Adaptation, Biological , Craterostigma/growth & development , Craterostigma/physiology , Desiccation , Environment , Epigenesis, Genetic , Gene Expression Regulation, Plant , In Situ Hybridization , Plant Proteins/genetics , Protein Biosynthesis , Transformation, Genetic
5.
Plant Cell Rep ; 25(5): 442-9, 2006 May.
Article in English | MEDLINE | ID: mdl-16362301

ABSTRACT

In this paper we describe the first procedure for Agrobacterium tumefaciens-mediated genetic transformation of the desiccation tolerant plant Ramonda myconi (L.) Rchb. Previously, we reported the establishment of a reliable and effective tissue culture system based on the integrated optimisation of antioxidant and growth regulator composition and the stabilisation of the pH of the culture media by means of a potassium phosphate buffer. This efficient plant regeneration via callus phase provided a basis for the optimisation of the genetic transformation in R. myconi. For gene delivery, both a standard (method A) and a modified protocol (method B) have been applied. Since the latter has previously resulted in successful transformation of another resurrection plant, Craterostigma plantagineum, an identical protocol was utilized in transformation of R. myconi, as this method may prove general for dicotyledonous resurrection plants. On this basis, physical and biochemical key variables in transformation were evaluated such as mechanical microwounding of plant explants and in vitro preinduction of vir genes. While the physical enhancement of bacterial penetration was proved to be essential for successful genetic transformation of R. myconi, an additional two-fold increase in the transformation frequency was obtained when the above physical and biochemical treatments were applied in combination. All R0 and R1 transgenic plants were fertile, and no morphological abnormalities were observed on the whole-plant level.


Subject(s)
Craterostigma/genetics , Plant Leaves/genetics , Agrobacterium tumefaciens/genetics , Anti-Bacterial Agents/pharmacology , Cefotaxime/pharmacology , Clavulanic Acids/pharmacology , Craterostigma/drug effects , Craterostigma/growth & development , Dehydration , Gene Transfer Techniques , Plant Leaves/drug effects , Plant Leaves/growth & development , Plant Leaves/microbiology , Plants, Genetically Modified , Ticarcillin/pharmacology , Transformation, Genetic
6.
J Exp Bot ; 54(391): 2313-21, 2003 Oct.
Article in English | MEDLINE | ID: mdl-12947051

ABSTRACT

The ability of the root system of the poikilohydric plant Craterostigma plantagineum to survive dehydration was investigated. The data presented here reveal that the root system is capable of surviving dehydration, but shortly after rehydration the root system senesces. Two weeks after rehydration the growth of a complete new root system is initiated. During dehydration sucrose accumulates from 36 to a maximum of 111 micromol g-1 DW in the roots. It is suggested that the accumulation of sucrose protects the root system during dehydration. There are major stores of stachyose in the roots of Craterostigma (making up over 40% of the dry weight of the tissue) and during dehydration these stores are metabolized. It is suggested that these stachyose stores act as carbohydrate reserves for the synthesis of sucrose. However, over 350 micromol g-1 DW stachyose is metabolized in the roots, which is well in excess of that required for the accumulation of sucrose observed. It is likely that the stachyose reserves in the root system are translocated to other regions of the plant to support carbohydrate metabolism during dehydration of the tissue. During rehydration, the stachyose reserves return to their original level within 96 h. There is no change in the elevated sucrose content of the roots over this period. Thus the roots maintain the protective properties of sucrose much longer than they are needed. The maintenance of high sucrose contents in rehydrating roots is discussed as a possible survival strategy against recurrent desiccation events.


Subject(s)
Carbohydrate Metabolism , Craterostigma/growth & development , Plant Roots/growth & development , Water/physiology , Craterostigma/metabolism , Dehydration , Oligosaccharides/metabolism , Plant Roots/drug effects , Plant Roots/metabolism , Sucrose/metabolism , Water/pharmacology
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