Calcium signalling in Arabidopsis thaliana responding to drought and salinity.

Changes in cytosolic free calcium concentration ([Ca2+]cyt) in response to mannitol (drought) and salt treatments were detected in vivo in intact whole Arabidopsis seedlings. Transient elevations of [Ca2+]cyt to around 1.5 microM were observed, and these were substantially inhibited by pretreatment with the calcium-channel blocker lanthanum and to a lesser extent, the calcium-chelator EGTA. The expression of three genes, p5cs, which encodes delta(1)-pyrroline-5-carboxylate synthetase (P5CS), the first enzyme of the proline biosynthesis pathway, rab18 and Iti78 which both encode proteins of unknown function, was induced by mannitol and salt treatments. The induction of all three genes by mannitol was inhibited by pretreatment with lanthanum. Salt-induced p5cs, but not rab18 and Iti78, expression was also inhibited by lanthanum. Induction of p5cs by mannitol was also inhibited by the calcium channel-blockers gadolinium and verapamil and the calcium chelator EGTA, further suggesting the involvement of calcium signalling in this response. Mannitol induced greater levels of p5cs gene expression than an isoosmolar concentration of salt, at both relatively high and low concentrations. However, calcium transients were of a similar magnitude and duration in response to both mannitol and isoosmolar concentrations of salt, suggesting that a factor other than calcium is involved in the discrimination between drought and salinity signals in Arabidopsis. In order to gauge the involvement of the vacuole as an intracellular calcium store in the response of Arabidopsis to mannitol, [Ca2+]cyt was measured at the microdomain adjacent to the vacuolar membrane. The results obtained were consistent with a significant calcium release from the vacuole contributing to the overall mannitol-induced [Ca2+]cyt response. Data obtained by using inhibitors of inositol signalling suggested that this release was occurring through IP3-dependent calcium channels.

[1]  J. Williams,et al.  U73122 inhibits Ca2+ oscillations in response to cholecystokinin and carbachol but not to JMV-180 in rat pancreatic acinar cells. , 1992, The Journal of biological chemistry.

[2]  T. Flowers,et al.  Breeding for salinity resistance in crop plants: Where next? , 1995 .

[3]  D. Sanders,et al.  Release of Ca2+ from individual plant vacuoles by both InsP3 and cyclic ADP-ribose , 1995, Science.

[4]  A. Trewavas,et al.  Hypoosmotic Shock Induces Increases in Cytosolic Ca2+ in Tobacco Suspension-Culture Cells , 1997, Plant physiology.

[5]  A. Campbell,et al.  Transgenic plant aequorin reports the effects of touch and cold-shock and elicitors on cytoplasmic calcium , 1991, Nature.

[6]  J. Braam,et al.  Cold-Shock Regulation of the Arabidopsis TCH Genes and the Effects of Modulating Intracellular Calcium Levels , 1996, Plant physiology.

[7]  P. White Specificity of ion channel inhibitors for the maxi cation channel in rye root plasma membranes , 1996 .

[8]  K. Oda,et al.  Plant inositol monophosphatase is a lithium-sensitive enzyme encoded by a multigene family. , 1995, The Plant cell.

[9]  A. Galston,et al.  Chromosomal localization of osmotic and salt stress-induced differential alterations in polyamine content in wheat , 1993 .

[10]  Z. Hong,et al.  Overexpression of [delta]-Pyrroline-5-Carboxylate Synthetase Increases Proline Production and Confers Osmotolerance in Transgenic Plants , 1995, Plant physiology.

[11]  L. Erdei,et al.  Calcium‐dependent protein kinase in maize and sorghum induced by polyethylene glycol , 1996 .

[12]  J. Lynch,et al.  Salinity stress increases cytoplasmic ca activity in maize root protoplasts. , 1989, Plant physiology.

[13]  K. Skriver,et al.  Gene expression in response to abscisic acid and osmotic stress. , 1990, The Plant cell.

[14]  W. Busa,et al.  Lithium-sensitive production of inositol phosphates during amphibian embryonic mesoderm induction. , 1992, Science.

[15]  A. Trewavas,et al.  Cold calcium signaling in Arabidopsis involves two cellular pools and a change in calcium signature after acclimation. , 1996, The Plant cell.

[16]  E. Vierling,et al.  Plant responses to environmental stress , 1992, Current Biology.

[17]  D. Sanders,et al.  Osmotic stress enhances the competence of Beta vulgaris vacuoles to respond to inositol 1,4,5‐trisphosphate , 1994 .

[18]  F. Sachs,et al.  Block of stretch-activated ion channels in Xenopus oocytes by gadolinium and calcium ions. , 1989, Science.

[19]  B. Sundberg,et al.  Alterations in Water Status, Endogenous Abscisic Acid Content, and Expression of rab18 Gene during the Development of Freezing Tolerance in Arabidopsis thaliana , 1994, Plant physiology.

[20]  A. Bennett,et al.  Higher plant Ca(2+)-ATPase: primary structure and regulation of mRNA abundance by salt. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[21]  A. Campbell Chemiluminescence : principles and applications in biology and medicine , 1988 .

[22]  D. E. Nelson,et al.  Approaches to improve stress tolerance using molecular genetics , 1994 .

[23]  J. Cairney,et al.  Osmotic regulation of gene expression: ionic strength as an intracellular signal? , 1987 .

[24]  S. Nakashima,et al.  Neomycin is a potent agent for arachidonic acid release in human platelets. , 1987, Biochemical and biophysical research communications.

[25]  J. Lassalles,et al.  Hydrostatic and osmotic pressure activated channel in plant vacuole. , 1991, Biophysical journal.

[26]  J. A. Smith,et al.  Salt regulation of transcript levels for the c subunit of a leaf vacuolar H(+)-ATPase in the halophyte Mesembryanthemum crystallinum. , 1996, The Plant journal : for cell and molecular biology.

[27]  R. Finkelstein,et al.  Arabidopsis mutants with reduced response to NaCl and osmotic stress [rss] , 1995 .

[28]  Michael J. Berridge,et al.  Inositol trisphosphate, a novel second messenger in cellular signal transduction , 1984, Nature.

[29]  K. Takeda,et al.  Effects of osmotic and salt stresses on the accumulation of polyamines in leaf segments from wheat varieties differing in salt and drought tolerance , 1990 .

[30]  D. Verma,et al.  PROLINE BIOSYNTHESIS AND OSMOREGULATION IN PLANTS , 1993 .

[31]  E. T. Palva,et al.  Role of Abscisic Acid in Drought-Induced Freezing Tolerance, Cold Acclimation, and Accumulation of LT178 and RAB18 Proteins in Arabidopsis thaliana , 1995, Plant physiology.

[32]  R. Kado,et al.  Opening of Ca2+ channels in isolated red beet root vacuole membrane by inositol 1,4,5-trisphosphate , 1990, Nature.

[33]  K. Shinozaki,et al.  Correlation between the induction of a gene for delta 1-pyrroline-5-carboxylate synthetase and the accumulation of proline in Arabidopsis thaliana under osmotic stress. , 1995, The Plant journal : for cell and molecular biology.

[34]  Heather Knight,et al.  Recombinant aequorin methods for intracellular calcium measurement in plants. , 1995, Methods in cell biology.

[35]  D. Pasternak Salt Tolerance and Crop Production-A Comprehensive Approach , 1987 .

[36]  M. Van Montagu,et al.  Isolation, characterization, and chromosomal location of a gene encoding the Δ 1‐pyrroline‐5‐carboxylate synthetase in Arabidopsis thaliana , 1995, FEBS letters.

[37]  E. Blumwald,et al.  Calcium Retrieval from Vacuolar Pools (Characterization of a Vacuolar Calcium Channel) , 1993, Plant physiology.

[38]  Michael J. Berridge,et al.  Neural and developmental actions of lithium: A unifying hypothesis , 1989, Cell.

[39]  J. Lynch,et al.  Salinity affects intracellular calcium in corn root protoplasts. , 1988, Plant physiology.

[40]  G Boheim,et al.  Gadolinium‐sensitive, voltage‐dependent calcium release channels in the endoplasmic reticulum of a higher plant mechanoreceptor organ. , 1995, The EMBO journal.

[41]  C. Larsson,et al.  The major integral proteins of spinach leaf plasma membranes are putative aquaporins and are phosphorylated in response to Ca2+ and apoplastic water potential. , 1996, The Plant cell.

[42]  D. Sanders,et al.  Two Voltage-Gated, Calcium Release Channels Coreside in the Vacuolar Membrane of Broad Bean Guard Cells. , 1994, The Plant cell.

[43]  M. Zoratti,et al.  Gadolinium ion inhibits loss of metabolites induced by osmotic shock and large stretch-activated channels in bacteria. , 1992, European journal of biochemistry.

[44]  L. Ding,et al.  SOS1, a Genetic Locus Essential for Salt Tolerance and Potassium Acquisition. , 1996, The Plant cell.

[45]  F. Skoog,et al.  A revised medium for rapid growth and bio assays with tobacco tissue cultures , 1962 .