methyl-jasmonate and systemin

Topics: Acetates; Cyclopentanes; Ethylenes; Immunity, Innate; Oxylipins; Peptides; Plant Growth Regulators; Plant Proteins; Plants; Salicylates; Salicylic Acid; Signal Transduction

A gene encoding a preprohydroxyproline-rich systemin, SnpreproHypSys, was identified from the leaves of black nightshade (Solanum nigrum), which is a member of a small gene family of at least three genes that have orthologs in tobacco (Nicotiana tabacum; NtpreproHypSys), tomato (Solanum lycopersicum; SlpreproHypSys), petunia (Petunia hybrida; PhpreproHypSys), potato (Solanum tuberosum; PhpreproHypSys), and sweet potato (Ipomoea batatas; IbpreproHypSys). SnpreproHypSys was induced by wounding and by treatment with methyl jasmonate. The encoded precursor protein contained a signal sequence and was posttranslationally modified to produce three hydroxyproline-rich glycopeptide signals (HypSys peptides). The three HypSys peptides isolated from nightshade leaf extracts were called SnHypSys I (19 amino acids with six pentoses), SnHypSys II (20 amino acids with six pentoses), and SnHypSys III (20 amino acids with either six or nine pentoses) by their sequential appearance in SnpreproHypSys. The three SnHypSys peptides were synthesized and tested for their abilities to alkalinize suspension culture medium, with synthetic SnHypSys I demonstrating the highest activity. Synthetic SnHypSys I was capable of inducing alkalinization in other Solanaceae cell types (or species), indicating that structural conformations within the peptides are recognized by the different cells/species to initiate signal transduction pathways, apparently through recognition by homologous receptor(s). To further demonstrate the biological relevance of the SnHypSys peptides, the early defense gene lipoxygenase D was shown to be induced by all three synthetic peptides when supplied to excised nightshade plants.

Topics: Acetates; Amino Acid Sequence; Base Sequence; Cyclopentanes; DNA, Complementary; Gene Dosage; Glycoproteins; Lipoxygenase; Molecular Sequence Data; Multigene Family; Oxylipins; Peptides; Plant Leaves; Plant Proteins; RNA, Messenger; Signal Transduction; Solanum lycopersicum; Solanum nigrum

To determine whether the Nicotiana tabacum preproHypSys homolog in Nicotiana attenuata (NapreproHypSys) mediates anti-herbivore responses, we silenced (IRsys) and ectopically over-expressed (OVsys) NapreproHypSys in N. attenuata. Neither herbivore simulation nor methyl jasmonate (MeJA) application increased transcripts in wild-type (WT) or transformed lines. Compared to WT plants, OVsys plants had marginally higher constitutive levels but normally induced levels of trypsin proteinase inhibitors (TPIs) and nicotine; IRsys plants did not differ from WT plants. Herbivory-associated signalling [salicylic acid-induced protein kinase (SIPK) activity, jasmonic acid (JA), jasmonic acid-isoleucine/leucine (JA-Ile/Leu) and ethylene production or perception] did not differ strongly among the lines, but JA, JA-Ile/Leu and ethylene were marginally higher in OVsys plants. Manduca sexta larval performance did not differ among the lines, but feeding induced levels of TPI and nicotine in OVsys plants and decreased them in IRsys plants relative to WT. The secondary metabolite profiles of plants transplanted into N. attenuata's native habitat in the Great Basin Desert (UT, USA) mirrored those of glasshouse-grown plants, and compared to WT plants, OVsys plants suffered marginally less damage from grasshoppers, mirids and flea beetles but did not differ in their ability to attract Geocoris predators. We conclude that NapreproHypSys does not play a central role in anti-herbivore defense signalling in this native tobacco.

Topics: Acetates; Animals; Cyclopentanes; Ethylenes; Feeding Behavior; Gene Expression Regulation, Plant; Glycopeptides; Hydroxyproline; Larva; Manduca; Nicotiana; Oxylipins; Peptides; Plants, Genetically Modified; RNA, Messenger; Signal Transduction

Two hydroxyproline-rich glycopeptide systemin (TobHS) precursor proteins known as preproTobHypSys-A and B were recently discovered in tobacco (Nicotiana tabacum L.) [Pearce et al. in Nature 411:817-820, 2001]. In this work, the effect of elicitors, insect damage, and abiotic stress on the expression of preproTobHypSys-A ppTobHS-A) in tobacco plants was evaluated. Foliar application of methyl jasmonate preferentially induced the systemic expression of ppTobHS-A in leaves phyllotactically one position above-treated leaves. Abscisic acid strongly induced ppTobHS-A, but water-stress did not. Mechanical wound-induction of ppTobHS-A in young plantlets was rapidly (1 h) and simultaneously detected in wounded and upper unwounded leaves, whereas in older plants induction was slow (12 h) and localized. ppTobHS-A was induced in plants infested with Bemisia tabaci or damaged by herbivory with Manduca sexta larvae. Compared to mechanical wounding, larval herbivory induced a stronger and more stable expression of ppTobHS-A. Moreover, exposure to Manduca-damaged plants induced its expression in neighboring intact plants. In most treatments, the expression patterns of ppTobHS-A coincided with those of selected wound-responsive (WR) genes (e.g., PIOX, NtPI-I, TPI). This correlation was tighter in the wounded and MeJA-treated leaves, whereas in distal, undamaged leaves, it appeared to depend on the type of WR gene examined and on the type of damage sustained by the plant. These results are consistent with the perceived role of the TobHS in defense signaling.

Topics: Abscisic Acid; Acetates; Animals; Base Sequence; Cyclopentanes; DNA, Plant; Gene Expression; Hemiptera; Manduca; Nicotiana; Oxylipins; Peptides; Plant Growth Regulators; Plant Proteins; Protein Precursors; RNA, Messenger; RNA, Plant

The systemic accumulation of both hydrogen peroxide (H(2)O(2)) and proteinase inhibitor proteins in tomato leaves in response to wounding was inhibited by the NADPH oxidase inhibitors diphenylene iodonium (DPI), imidazole, and pyridine. The expression of several defense genes in response to wounding, systemin, oligosaccharides, and methyl jasmonate also was inhibited by DPI. These genes, including those of four proteinase inhibitors and polyphenol oxidase, are expressed within 4 to 12 hr after wounding. However, DPI did not inhibit the wound-inducible expression of genes encoding prosystemin, lipoxygenase, and allene oxide synthase, which are associated with the octadecanoid signaling pathway and are expressed 0.5 to 2 hr after wounding. Accordingly, treatment of plants with the H(2)O(2)-generating enzyme glucose oxidase plus glucose resulted in the induction of only the later-expressed defensive genes and not the early-expressed signaling-related genes. H(2)O(2) was cytochemically detected in the cell walls of vascular parenchyma cells and spongy mesophyll cells within 4 hr after wounding of wild-type tomato leaves, but not earlier. The cumulative results suggest that active oxygen species are generated near cell walls of vascular bundle cells by oligogalacturonide fragments produced by wound-inducible polygalacturonase and that the resulting H(2)O(2) acts as a second messenger for the activation of defense genes in mesophyll cells. These data provide a rationale for the sequential, coordinated, and functional roles of systemin, jasmonic acid, oligogalacturonides, and H(2)O(2) signals for systemic signaling in tomato plants in response to wounding.

Topics: Acetates; Cyclopentanes; Gene Expression Regulation, Plant; Hydrogen Peroxide; Oxylipins; Peptides; Second Messenger Systems; Solanum lycopersicum

Seven small (approximately 6,000 D) wound-inducible proteinase inhibitor proteins were isolated from leaves of pepper (Capsicum annuum) plants that are members of the potato inhibitor II family. N-terminal sequences obtained indicated that the pepper leaf proteinase inhibitors (PLPIs) exhibit homology to two GenBank accessions that code for preproteins containing three isoinhibitors domains each that, when post-translationally processed, can account for the mixture of isoinhibitors that are reported herein from pepper leaves. A constitutive level of PLPI proteins was found in pepper leaves, and these levels increased up to 2.6-fold upon wounding of the lower leaves. Exposing intact plants to methyl jasmonate vapors induced the accumulation of PLPIs. Supplying excised young pepper plants with water through the cut stems induced PLPI proteins to levels higher than those found in intact plants, but with high variability. Supplying the excised plants with systemin did not result in an increase of PLPI levels that were statistically higher than levels found in excised plants. Gel-blot analyses of PLPI induction revealed the presence of two mRNA bands, having slightly different mobilities in agarose gels. Only the low M(r) mRNA is present in untreated control plants, and it appears to be responsible for the constitutive levels of PLPI found in leaves. Both mRNA species are wound- and methyl jasmonate-inducible. Only the low- M(r) species is weakly induced by systemin, indicating a differential expression of the two PLPI species.

Topics: Acetates; Amino Acid Sequence; Capsicum; Chromatography, High Pressure Liquid; Cyclopentanes; Electrophoresis, Polyacrylamide Gel; Gene Expression Regulation, Plant; Molecular Sequence Data; Oxylipins; Peptides; Plants, Medicinal; Protease Inhibitors; Sequence Homology, Amino Acid

We investigated the relationship between the expression of lipoxygenase (LOX) genes and the systemin-dependent wound response in tomato (Lycopersicon esculentum) leaves. A polymerase chain reaction-based approach was used to isolate two tomato Lox cDNAs, called TomLoxC and TomLoxD. Both TomLOXC and TomLOXD amino acid sequences possess an N-terminal extension of about 60 residues that were shown by in vitro uptake to function as transit peptides, targeting these proteins into the chloroplast. Within 30 to 50 min following wounding or systemin or methyl jasmonate treatments, the TomLoxD mRNA level increased and reached a maximum between 1 and 2 h. TomLoxC mRNA was not detectable in leaves and was not found following wounding, but it was found in ripening fruits, indicating that the two tomato Lox genes are regulated in different tissues by different processes. The results suggest that the TomLoxD gene is up-regulated in leaves in response to wounding and encodes a chloroplast LOX that may play a role as a component of the octadecanoid defense-signaling pathway.

Topics: Acetates; Amino Acid Sequence; Chloroplasts; Cyclopentanes; Enzyme Induction; Gene Expression Regulation, Plant; Genes, Plant; Kinetics; Lipoxygenase; Molecular Sequence Data; Oxylipins; Peptides; Plant Growth Regulators; Plant Proteins; RNA, Messenger; Sequence Alignment; Sequence Homology, Amino Acid; Solanum lycopersicum; Time Factors; Transcription, Genetic; Wounds and Injuries

A full-length cDNA encoding an aspartic protease (LeAspP) has been cloned from a tomato leaf cDNA library. Using LeAspP cDNA as a probe in gel blots, LeAspP mRNA was shown to be systemically induced in tomato leaves by wounding. Application of methyl jasmonate to leaves of intact tomato plants, or supplying systemin to young tomato plants through their cut stems, induces synthesis of LeAspP mRNA. LeAspP message is regulated in tomato similar to several systemic wound response proteins (swrps) that are part of the defense response in tomato plants directed against herbivore attacks.

Topics: Acetates; Amino Acid Sequence; Aspartic Acid Endopeptidases; Base Sequence; Binding Sites; Cloning, Molecular; Cyclopentanes; DNA, Complementary; Gene Expression; Molecular Sequence Data; Oxylipins; Peptides; Plant Growth Regulators; Plant Leaves; Plant Proteins; RNA, Plant; Sequence Homology, Amino Acid; Solanum lycopersicum