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 effectsABSTRACT
Craterostigma plantagineum tolerates extreme desiccation. Leaves of this plant shrink and extensively fold during dehydration and expand again during rehydration, preserving their structural integrity. Genes were analysed that may participate in the reversible folding mechanism. Analysis of transcripts abundantly expressed in desiccated leaves identified a gene putatively coding for an apoplastic glycine-rich protein (CpGRP1). We studied the expression, regulation and subcellular localization of CpGRP1 and its ability to interact with a cell wall-associated protein kinase (CpWAK1) to understand the role of CpGRP1 in the cell wall during dehydration. The CpGRP1 protein accumulates in the apoplast of desiccated leaves. Analysis of the promoter revealed that the gene expression is mainly regulated at the transcriptional level, is independent of abscisic acid (ABA) and involves a drought-responsive cis-element (DRE). CpGRP1 interacts with CpWAK1 which is down-regulated in response to dehydration. Our data suggest a role of the CpGRP1-CpWAK1 complex in dehydration-induced morphological changes in the cell wall during dehydration in C. plantagineum. Cell wall pectins and dehydration-induced pectin modifications are predicted to be involved in the activity of the CpGRP1-CpWAK1 complex.
Subject(s)
Cell Wall/metabolism , Craterostigma/metabolism , Glycine/metabolism , Plant Leaves/metabolism , Plant Proteins/metabolism , Protein Kinases/metabolism , Abscisic Acid/pharmacology , Amino Acid Sequence , Arabidopsis Proteins/metabolism , Base Sequence , Cell Wall/drug effects , Craterostigma/drug effects , Craterostigma/genetics , DNA, Complementary/genetics , DNA, Complementary/isolation & purification , Dehydration , Down-Regulation/drug effects , Droughts , Electrophoresis, Gel, Two-Dimensional , Gene Expression Regulation, Plant/drug effects , Green Fluorescent Proteins/metabolism , Models, Biological , Plant Leaves/drug effects , Plant Proteins/chemistry , Plant Proteins/genetics , Promoter Regions, Genetic/genetics , Protein Binding/drug effects , Recombinant Fusion Proteins/metabolism , Saccharomyces cerevisiae/metabolism , Sequence Analysis, DNAABSTRACT
The resurrection plant Craterostigma plantagineum is able to withstand desiccation of its vegetative tissues and is found in areas with variable water availability. The closely related species Lindernia brevidens and Lindernia subracemosa are both endemic to montane rainforests of coastal Africa, but remarkably L. brevidens is tolerant to desiccation. We studied the regulation of the desiccation-related LEA-like 11-24 gene at multiple levels in closely related species in order to investigate the conservation of mechanisms involved in desiccation tolerance. The dehydration-responsive transcription of the LEA-like 11-24 gene is differentially regulated in these plants. Comparison of the LEA-like 11-24 core promoter regions revealed that promoters have different activities, but some functional cis-acting elements are conserved between species. Upon dehydration, LEA-like 11-24 proteins are phosphorylated at different levels and phosphorylation sites are not conserved among the three LEA-like 11-24 proteins. Differences in the regulation of the LEA-like 11-24 gene in the studied plant species appear to be the result of mutations that occurred during evolution. We postulate that L. brevidens will eventually lose the ability to survive vegetative desiccation, given that this trait appears not to be essential for survival.
Subject(s)
Adaptation, Physiological/genetics , Craterostigma/genetics , Craterostigma/physiology , Desiccation , Gene Expression Regulation, Plant , Lamiaceae/genetics , Lamiaceae/physiology , Abscisic Acid/pharmacology , Adaptation, Physiological/drug effects , Base Sequence , Craterostigma/drug effects , Gene Expression Regulation, Plant/drug effects , Lamiaceae/drug effects , Molecular Sequence Data , Mutagenesis/genetics , Nucleotide Motifs/genetics , Osmotic Pressure/drug effects , Phosphorylation/drug effects , Phylogeny , Plant Proteins/genetics , Plant Proteins/metabolism , Promoter Regions, Genetic , RNA, Messenger/genetics , RNA, Messenger/metabolism , Species SpecificityABSTRACT
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.
