Species and Tissue Specificity of Jasmonate-induced Abundant Proteins

Herrmann, Gabriele; Lehmann, Jan; Peterson, Angela; Sembdner, G.; Weidhase, R; Parthier, B.

doi:10.1016/s0176-1617(89)80031-8

Cited by 62 publications

(41 citation statements)

References 19 publications

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“…Figure 1 illustrates the first two effects in the polypeptide patterns of MeJA-treated leaf tissues in plants as diverse as barley, Nicotiana plumbaginifolia, and Arabidopsis. Except for a few evolutionarily conserved polypeptides (see below), most JlPs appear to be expressed in a genus-and species-specific manner ( Figure 1; see also Herrmann et al, 1989). Their induction patterns differ markedly in both temporal and spatial aspects in different plant species (Müller-Uri et al, 1988;Herrmann et al, 1989;Farmer and Ryan, 1990;Staswick, 1990;Sánchez-Serrano et al, 1991;Gundlach et al, 1992;Reinbothe et al, 19924 1992~).…”

Section: Introductionmentioning

confidence: 99%

“…Except for a few evolutionarily conserved polypeptides (see below), most JlPs appear to be expressed in a genus-and species-specific manner ( Figure 1; see also Herrmann et al, 1989). Their induction patterns differ markedly in both temporal and spatial aspects in different plant species (Müller-Uri et al, 1988;Herrmann et al, 1989;Farmer and Ryan, 1990;Staswick, 1990;Sánchez-Serrano et al, 1991;Gundlach et al, 1992;Reinbothe et al, 19924 1992~). In addition, qualitative and quantitative differences exist in the extent to which MeJA represses the synthesis of preexisting proteins (Figure 1) Excised leaf tissues of barley (H.v.…”

Section: Introductionmentioning

confidence: 99%

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JIPs and RIPs: the regulation of plant gene expression by jasmonates in response to environmental cues and pathogens.

1994

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Section: Introductionmentioning

confidence: 99%

Section: Introductionmentioning

confidence: 99%

JIPs and RIPs: the regulation of plant gene expression by jasmonates in response to environmental cues and pathogens.

1994

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“…Since then it has been demonstrated that yeast cell wall preparations, bacterial antibiotics, plant cell wall-derived oligouronides, funga1 cell wallderived chitosan, N-acetylchitohepatose, wounding, and a variety of other stimuli lead to a rapid synthesis of endogenous JA (for review, see Mueller, 1997). This in turn activates defensive genes, eventually yielding a variety of jasmonate-induced proteins (Herrmann et al, 1989) and antibiotic secondary metabolites (Gundlach et al, 1992). Jasmonate-induced proteins fall into different categories.…”

mentioning

confidence: 99%

Induction of 12-Oxo-Phytodienoic Acid in Wounded Plants and Elicited Plant Cell Cultures

Parchmann¹,

Gundlach²,

Mueller³

1997

Plant Physiology

129

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Jasmonic acid (jA) is rapidly biosynthesized from a-linolenic acid in plants upon contact with pathogens or wounding, and triggers gene activation, leading to the synthesis of defensive secondary metabolites and proteins. Despite the recent finding that its precursor, 1 2-0x0-phytodienoic acid (PDA), is a more powerful inducer of gene activation, interest has focused so far almost exclusively on jA.A validated negative chemical ionization-gas chromatography-mass spectrometry method has been developed that allows the simultaneous quantification of endogenous 1 2-0x0-PDA and JA in plant tissues. In six out of eight plant species tested maximal levels of 12-0x0-PDA exceeded peak levels of JA by approximately 3-to 5-fold after elicitation with a yeast cell wall preparation or when plants were wounded. These experiments support the hypothesis that 12-0x0-PDA acts as the predominant jasmonate signal in most plants, whereas JA remains an active metabolite of its precursor. Furthermore, JA but not 12-0x0-PDA was shown to be secreted into the medium from cultured plant cells, suggesting that jA may also act as an intercellular signal.

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“…Leaf tissue of wheat (Triticum aestivum L.), as well as many other monocotyledon and dicotyledon species, induces proteins in response to MeJA treatment (6). The molecular mass and immunological properties of these induced proteins vary markedly among species, and considerable quantitative differences in the level of expression of MeJA-induced proteins apparently occur among barley (Hordeum vulgare L.) cultivars (6).…”

mentioning

confidence: 99%

“…The molecular mass and immunological properties of these induced proteins vary markedly among species, and considerable quantitative differences in the level of expression of MeJA-induced proteins apparently occur among barley (Hordeum vulgare L.) cultivars (6). In response to depodding, JA, MeJA, and other treatments given to soybean (Glycine max [L.] Merr.)…”

mentioning

confidence: 99%

Wheat Vegetative Nitrogen Compositional Changes in Response to Reduced Reproductive Sink Strength

MacKown¹,

Sanford²,

Zhang³

1992

Plant Physiol.

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N redistribution patterns and the N composition of vegetative tissues above the peduncle node of wheat (Triticum aestivum L.) plants with altered reproductive sink strength were evaluated to determine the role of vegetative storage proteins in the temporary storage of excess N destined for export. The degree of leaf senescence symptoms (loss of chlorophyll, total N, and ribulose-1,5-bisphosphate carboxylase/oxygenase) were quirements for N export or gene expression of VSP for the temporary storage of excess N.Leaf tissue of wheat (Triticum aestivum L.), as well as many other monocotyledon and dicotyledon species, induces proteins in response to MeJA treatment (6). The molecular mass and immunological properties of these induced proteins vary markedly among species, and considerable quantitative differences in the level of expression of MeJA-induced proteins apparently occur among barley (Hordeum vulgare L.) cultivars (6). In response to depodding, JA, MeJA, and other treatments given to soybean (Glycine max [L.] Merr.) plants, abundant levels of the same specific vegetative proteins (molecular masses of 27, 29, and 94 kD) accumulate predominantly in the vacuoles of PVM cells of leaves (5,7,18,19,21). The 94-kD protein was recently identified as a member of the vegetative lipoxygenase family and proposed to be a bifunctional zymogen capable of catalyzing the hydroperoxidation of lipids and storing excess N temporarily (21).The effects of an altered reproductive sink demand on accumulation of VSP have been limited to studies of soybean (5,18,19,25,26). Because depodding, JA, and MeJA elicit similar VSP accumulation responses in soybean, other monocarpic annuals that express MeJA-induced proteins also may accumulate proteins with VSP characteristics when reproductive sink demand is altered. In wheat, redistribution of vegetative N accumulated before anthesis normally provides the major source of grain N (1, 16, 22). During reproductive growth, the extent of vegetative N redistribution depends on sink size. Removal of all spikes from multiculm wheat plants delays physiological and biochemical processes associated with leaf senescence and net mobilization of N (2, 4, 15). Partial reduction of the reproductive sink, however, has a relatively small effect on the initiation and extent of N mobilization from the flag leaf of a partially degrained culm of wheat (9,10

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Species and Tissue Specificity of Jasmonate-induced Abundant Proteins

Cited by 62 publications

References 19 publications

JIPs and RIPs: the regulation of plant gene expression by jasmonates in response to environmental cues and pathogens.

JIPs and RIPs: the regulation of plant gene expression by jasmonates in response to environmental cues and pathogens.

Induction of 12-Oxo-Phytodienoic Acid in Wounded Plants and Elicited Plant Cell Cultures

Wheat Vegetative Nitrogen Compositional Changes in Response to Reduced Reproductive Sink Strength

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