An hydraulic interpretation of rapid, long-distance wound signalling in the tomato

Localised wounding causes rapid and systemic induction of proteinase inhibitors in tomato (Lycopersicon esculentum L.). The signalling system which coordinates this response is not known. Recent work has shown that systemic hydraulic signals are transmitted from wound sites in tomato, but that these cannot by themselves induce proteinase inhibitors. Here, it is demonstrated that the hydraulic signal is nevertheless an essential requirement for the systemic induction of proteinase inhibitors by localised treatments. It is also shown that mass flows similar to those associated with the wound-induced hydraulic signal, can convey a variety of solutes rapidly throughout the shoot. It is concluded that long-distance wound signalling in the tomato occurs by xylem transmission of soluble elicitors in the mass flows induced by wounding.

[1]  K. Bradford,et al.  Xylem Transport of 1-Aminocyclopropane-1-carboxylic Acid, an Ethylene Precursor, in Waterlogged Tomato Plants. , 1980, Plant physiology.

[2]  G. Pearce,et al.  A sycamore cell wall polysaccharide and a chemically related tomato leaf polysaccharide possess similar proteinase inhibitor-inducing activities. , 1981, Plant physiology.

[3]  M. Malone Kinetics of wound-induced hydraulic signals and variation potentials in wheat seedlings , 1992, Planta.

[4]  J. Huet,et al.  Movement of elicitins, necrosis-inducing proteins secreted by Phytophthora sp., in tobacco , 1992, Planta.

[5]  R. M. Spanswick,et al.  Sink to source translocation in soybean. , 1984, Plant physiology.

[6]  C. Ryan Assay and Biochemical Properties of the Proteinase Inhibitor-inducing Factor, a Wound Hormone. , 1974, Plant physiology.

[7]  A. Brun,et al.  Long distance transport of 14C-putrescine in potato plantlets (Solanum tuberosum cv. Bintje) , 1992 .

[8]  J. Oertli Water Transport in Plants under Climatic Stress: Effect of cavitation on the status of water in plants , 1993 .

[9]  William J. Davies,et al.  Xylem‐transported abscisic acid: the relative importance of its mass and its concentration in the control of stomatal aperture , 1993 .

[10]  J. Graham,et al.  Regulation of synthesis of proteinase inhibitors I and II mRNAs in leaves of wounded tomato plants , 1986, Planta.

[11]  M. Canny Tansley Review No. 22 What becomes of the transpiration stream? , 1990, The New phytologist.

[12]  M. Bruin,et al.  Non‐steady state xylem transport of fifteen elements into the tomato leaf as measured by gamma‐ray spectroscopy: A model , 1984 .

[13]  M. Tepfer,et al.  The Permeability of Plant Cell Walls as Measured by Gel Filtration Chromatography , 1981, Science.

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

[15]  G. Pearce,et al.  Structure, expression, and antisense inhibition of the systemin precursor gene. , 1992, Science.

[16]  P. Minchin,et al.  Xylem Transport of Recently Fixed Carbon within Lupin , 1987 .

[17]  G. Pearce,et al.  Purification and Characterization from Tobacco (Nicotiana tabacum) Leaves of Six Small, Wound-Inducible, Proteinase Isoinhibitors of the Potato Inhibitor II Family , 1993, Plant physiology.

[18]  P. Morey,et al.  An Application of the Prussian Blue Technique to a Light Microscope Study of Water Movement in Transpiring Leaves of Cotton (Gossypium hirsutum L.) , 1976 .

[19]  L. Noodén,et al.  Transmission of the Monocarpic Senescence Signal via the Xylem in Soybean. , 1982, Plant physiology.

[20]  M. Malone,et al.  Wound-Induced Hydraulic Signals: Survey of Occurrence in a Range of Species , 1993 .

[21]  L. Willmitzer,et al.  Both wound‐inducible and tuber‐specific expression are mediated by the promoter of a single member of the potato proteinase inhibitor II gene family , 1989, The EMBO journal.

[22]  S. Fry,et al.  The immobility of pectic substances in injured tomato leaves and its bearing on the identity of the wound hormone , 1985, Planta.

[23]  P. Albersheim,et al.  Structure of Plant Cell Walls: X. RHAMNOGALACTURONAN I, A STRUCTURALLY COMPLEX PECTIC POLYSACCHARIDE IN THE WALLS OF SUSPENSION-CULTURED SYCAMORE CELLS. , 1980, Plant physiology.

[24]  L. Willmitzer,et al.  Systemic induction of proteinase-inhibitor-II gene expression in potato plants by wounding , 1988, Planta.

[25]  L. Marcelis,et al.  Apical application of aqueous solutions to roses via flower tubes: a technique with possibilities. , 1988 .

[26]  P. Minchin,et al.  Electrical signalling and systemic proteinase inhibitor induction in the wounded plant , 1992, Nature.

[27]  H. Jones,et al.  The relationship between wound‐induced proteinase inhibitors and hydraulic signals in tomato seedlings , 1994 .

[28]  H. Barlow Sectorial Patterns in Leaves on Fruit Tree Shoots Produced by Radioactive Assimilates and Solutions , 1979 .

[29]  M. Gordon,et al.  Systemically wound-responsive genes in poplar trees encode proteins similar to sweet potato sporamins and legume Kunitz trypsin inhibitors , 2004, Plant Molecular Biology.

[30]  C. Ryan The search for the proteinase inhibitor-inducing factor, PIIF , 1992, Plant Molecular Biology.