Signal transduction networks and the biology of plant cells.

The development of plant transformation in the mid-1980s and of many new tools for cell biology, molecular genetics, and biochemistry has resulted in enormous progress in plant biology in the past decade. With the completion of the genome sequence of Arabidopsis thaliana just around the corner, we can expect even faster progress in the next decade. The interface between cell biology and signal transduction is emerging as a new and important field of research. In the past we thought of cell biology strictly in terms of organelles and their biogenesis and function, and researchers focused on questions such as, how do proteins enter chloroplasts? or, what is the structure of the macromolecules of the cell wall and how are these molecules secreted? Signal transduction dealt primarily with the perception of light (photomorphogenesis) or hormones and with the effect such signals have on enhancing the activity of specific genes. Now we see that the fields of cell biology and signal transduction are merging because signals pass between organelles and a single signal transduction pathway usually involves multiple organelles or cellular structures. Here are some examples to illustrate this new paradigm. How does abscisic acid (ABA) regulate stomatal closure? This pathway involves not only ABA receptors whose location is not yet known, but cation and anion channels in the plasma membrane, changes in the cytoskeleton, movement of water through water channels in the tonoplast and the plasma membrane, proteins with a farnesyl tail that can be located either in the cytosol or attached to a membrane, and probably unidentified ion channels in the tonoplast. In addition there are highly localized calcium oscillations in the cytoplasm resulting from the release of calcium stored in various compartments. The activities of all these cellular structures need to be coordinated during ABA-induced stomatal closure. For another example of the interplay between the proteins of signal transduction pathways and cytoplasmic structures, consider how plants mount defense responses against pathogens. Elicitors produced by pathogens bind to receptors on the plant plasma membrane or in the cytosol and eventually activate a large number of genes. This results in the coordination of activities at the plasma membrane (production of reactive oxygen species), in the cytoskeleton, localized calcium oscillations, and the modulation of protein kinases and protein phosphatases whose locations remain to be determined. The movement of transcription factors into the nucleus to activate the defense genes requires their release from cytosolic anchors and passage through the nuclear pore complexes of the nuclear envelope. This review does not cover all the recent progress in plant signal transduction and cell biology; it is confined to the topics that were discussed at a recent (November 1998) workshop held in Santiago at which lecturers from Chile, the USA and the UK presented recent results from their laboratories.

[1]  M. Ishitani,et al.  Genetic analysis of osmotic and cold stress signal transduction in Arabidopsis: interactions and convergence of abscisic acid-dependent and abscisic acid-independent pathways. , 1997, The Plant cell.

[2]  Peter Agre,et al.  Appearance of Water Channels in Xenopus Oocytes Expressing Red Cell CHIP28 Protein , 1992, Science.

[3]  G. Pearce,et al.  A Polypeptide from Tomato Leaves Induces Wound-Inducible Proteinase Inhibitor Proteins , 1991, Science.

[4]  Jonathan D. G. Jones,et al.  Resistance gene-dependent plant defense responses. , 1996, The Plant cell.

[5]  Li-li Chen,et al.  A Receptor Kinase-Like Protein Encoded by the Rice Disease Resistance Gene, Xa21 , 1995, Science.

[6]  J. Joyard,et al.  Envelope Membranes from Spinach Chloroplasts Are a Site of Metabolism of Fatty Acid Hydroperoxides , 1996, Plant physiology.

[7]  A. Hodgkin,et al.  Movements of labelled calcium in squid giant axons , 1957, The Journal of physiology.

[8]  T. Valentine,et al.  Soluble Signals from Cells Identified at the Cell Wall Establish a Developmental Pathway in Carrot. , 1997, The Plant cell.

[9]  E. Farmer,et al.  Interplant communication: airborne methyl jasmonate induces synthesis of proteinase inhibitors in plant leaves. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[10]  A. Weig,et al.  The Major Intrinsic Protein Family of Arabidopsis Has 23 Members That Form Three Distinct Groups with Functional Aquaporins in Each Group , 1997, Plant Physiology.

[11]  B. Henrissat,et al.  Multidomain architecture of beta-glycosyl transferases: implications for mechanism of action , 1995, Journal of bacteriology.

[12]  Sorting of proteins to vacuoles in plant cells , 1998 .

[13]  L. Willmitzer,et al.  General roles of abscisic and jasmonic acids in gene activation as a result of mechanical wounding. , 1992, The Plant cell.

[14]  S. Luan,et al.  Voltage-Dependent K+ Channels as Targets of Osmosensing in Guard Cells , 1998, Plant Cell.

[15]  J. Ward,et al.  Perspectives on the physiology and structure of inward-rectifying K+ channels in higher plants: biophysical implications for K+ uptake. , 1994, Annual review of biophysics and biomolecular structure.

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

[17]  Abscisic Acid Mediates Wound Induction but Not Developmental-Specific Expression of the Proteinase Inhibitor II Gene Family. , 1991, The Plant cell.

[18]  H. Leyser,et al.  Ethylene as a Signal Mediating the Wound Response of Tomato Plants , 1996, Science.

[19]  G. Robertson,et al.  HERG, a human inward rectifier in the voltage-gated potassium channel family. , 1995, Science.

[20]  D. Bouchez,et al.  Identification and Disruption of a Plant Shaker-like Outward Channel Involved in K+ Release into the Xylem Sap , 1998, Cell.

[21]  X. Qin,et al.  Immediate early transcription activation by salicylic acid via the cauliflower mosaic virus as-1 element. , 1994, The Plant cell.

[22]  Jane Glazebrook,et al.  The Arabidopsis NPR1 Gene That Controls Systemic Acquired Resistance Encodes a Novel Protein Containing Ankyrin Repeats , 1997, Cell.

[23]  L. Willmitzer,et al.  Expression of a Flax Allene Oxide Synthase cDNA Leads to Increased Endogenous Jasmonic Acid (JA) Levels in Transgenic Potato Plants but Not to a Corresponding Activation of JA-Responding Genes. , 1995, The Plant cell.

[24]  C. Stange,et al.  Phosphorylation of nuclear proteins directs binding to salicylic acid-responsive elements. , 1997, The Plant journal : for cell and molecular biology.

[25]  M. Sussman,et al.  A role for the AKT1 potassium channel in plant nutrition. , 1998, Science.

[26]  Y. Jan,et al.  Tracing the roots of ion channels , 1992, Cell.

[27]  N. Raikhel,et al.  Transport to the vacuole: receptors and trans elements , 1998 .

[28]  N. Carpita,et al.  Structural models of primary cell walls in flowering plants: consistency of molecular structure with the physical properties of the walls during growth. , 1993, The Plant journal : for cell and molecular biology.

[29]  N. Raikhel,et al.  Xyloglucan fucosyltransferase, an enzyme involved in plant cell wall biosynthesis. , 1999, Science.

[30]  N. Raikhel,et al.  Short peptide domains target proteins to plant vacuoles , 1992, Cell.

[31]  Shiping Zhang,et al.  Xa21D Encodes a Receptor-like Molecule with a Leucine-Rich Repeat Domain That Determines Race-Specific Recognition and Is Subject to Adaptive Evolution , 1998, Plant Cell.

[32]  S. Assmann,et al.  Signal transduction in guard cells. , 1993, Annual review of cell biology.

[33]  W Herth,et al.  Molecular analysis of cellulose biosynthesis in Arabidopsis. , 1998, Science.

[34]  E. Farmer,et al.  Regulation of expression of proteinase inhibitor genes by methyl jasmonate and jasmonic Acid. , 1992, Plant physiology.

[35]  D. Klessig,et al.  Defense gene induction in tobacco by nitric oxide, cyclic GMP, and cyclic ADP-ribose. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[36]  A. Jagendorf,et al.  Signals involved in wound-induced proteinase inhibitor II gene expression in tomato and potato plants. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[37]  K. Shinozaki,et al.  A novel cis-acting element in an Arabidopsis gene is involved in responsiveness to drought, low-temperature, or high-salt stress. , 1994, The Plant cell.

[38]  N. Carpita,et al.  Dynamic changes in cell surface molecules are very early events in the differentiation of mesophyll cells from Zinnia elegans into tracheary elements , 1995 .

[39]  T. Kirchhausen,et al.  A putative vacuolar cargo receptor partially colocalizes with AtPEP12p on a prevacuolar compartment in Arabidopsis roots. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[40]  C. Maurel,et al.  The vacuolar membrane protein gamma‐TIP creates water specific channels in Xenopus oocytes. , 1993, The EMBO journal.

[41]  Jörg Durner,et al.  Salicylic acid and disease resistance in plants , 1997 .

[42]  A. Orellana,et al.  Evidence for a UDP-Glucose Transporter in Golgi Apparatus-Derived Vesicles from Pea and Its Possible Role in Polysaccharide Biosynthesis , 1996, Plant physiology.

[43]  Neckelmann,et al.  Metabolism of uridine 5'-diphosphate-glucose in golgi vesicles from pea stems , 1998, Plant physiology.

[44]  Chaumont,et al.  High expression of the tonoplast aquaporin ZmTIP1 in epidermal and conducting tissues of maize , 1998, Plant physiology.

[45]  Roles of Ion Channels in Initiation of Signal Transduction in Higher Plants. , 1995 .

[46]  A. Trewavas,et al.  Elevation of cytoplasmic calcium by caged calcium or caged inositol trisphosphate initiates stomatal closure , 1990, Nature.

[47]  Colin W. Taylor,et al.  Cooperative activation of IP3 receptors by sequential binding of IP3 and Ca2+ safeguards against spontaneous activity , 1997, Current Biology.

[48]  D. Inzé,et al.  H2O2 and NO: redox signals in disease resistance , 1998 .

[49]  S. Luan Protein phosphatases and signaling cascades in higher plants , 1998 .

[50]  J. Fisahn,et al.  Electric signaling and pin2 gene expression on different abiotic stimuli depend on a distinct threshold level of endogenous abscisic acid in several abscisic acid-deficient tomato mutants , 1999, Plant physiology.

[51]  Piotr Mikolajczyk,et al.  A+A+C , 1964 .

[52]  N. Chua,et al.  Activation of the CaMV as‐1 cis‐element by salicylic acid: differential DNA‐binding of a factor related to TGA1a. , 1996, The EMBO journal.

[53]  J.-H. Sheen,et al.  Ca2+-Dependent Protein Kinases and Stress Signal Transduction in Plants , 1996, Science.

[54]  B. Gerhardt,et al.  Glyoxysomal β-oxidation of long-chain fatty acids: completeness of degradation , 1998, Planta.

[55]  D. Delmer,et al.  Higher plants contain homologs of the bacterial celA genes encoding the catalytic subunit of cellulose synthase. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[56]  J. Fisahn,et al.  Localized Wounding by Heat Initiates the Accumulation of Proteinase Inhibitor II in Abscisic Acid-Deficient Plants by Triggering Jasmonic Acid Biosynthesis , 1996, Plant physiology.

[57]  Bratislav Stankovic,et al.  Surface potentials and hydraulic signals in wheat leaves following localized wounding by heat , 1991 .

[58]  J. Fisahn,et al.  Proteinase Inhibitor II Gene Expression Induced by Electrical Stimulation and Control of Photosynthetic Activity in Tomato Plants , 1995 .

[59]  L. Willmitzer,et al.  Abscisic acid is involved in the wound-induced expression of the proteinase inhibitor II gene in potato and tomato. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[60]  Xin Li,et al.  Generation of broad-spectrum disease resistance by overexpression of an essential regulatory gene in systemic acquired resistance. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[61]  H. Hirt,et al.  MP2C, a plant protein phosphatase 2C, functions as a negative regulator of mitogen-activated protein kinase pathways in yeast and plants. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[62]  M. Guerinot,et al.  MOLECULAR BIOLOGY OF CATION TRANSPORT IN PLANTS. , 1998, Annual review of plant physiology and plant molecular biology.

[63]  S. Luan,et al.  Identification of a dual-specificity protein phosphatase that inactivates a MAP kinase from Arabidopsis. , 1998, The Plant journal : for cell and molecular biology.

[64]  Y. Jan,et al.  Sequence of a probable potassium channel component encoded at Shaker locus of Drosophila. , 1987, Science.

[65]  R. Malhó Spatial characteristics to calcium signalling; the calcium wave as a basic unit in plant cell calcium signalling , 1998 .

[66]  F. Gaymard,et al.  Plant K+ channels: structure, activity and function. , 1996, Biochemical Society transactions.

[67]  Dianna J. Bowles,et al.  Systemic responses arising from localized heat stimuli in tomato plants , 1989 .

[68]  F. Bezanilla,et al.  How Does an Ion Channel Sense Voltage , 1997 .

[69]  B. Chait,et al.  The structure of the potassium channel: molecular basis of K+ conduction and selectivity. , 1998, Science.

[70]  D. Klessig,et al.  Signal perception and transduction in plant defense responses. , 1997, Genes & development.

[71]  H. Hirt,et al.  Stress signaling in plants: a mitogen-activated protein kinase pathway is activated by cold and drought. , 1996, Proceedings of the National Academy of Sciences of the United States of America.