Masaji Koshioka

slender Rice, a Constitutive Gibberellin Response Mutant, Is Caused by a Null Mutation of the SLR1 Gene, an Ortholog of the Height-Regulating Gene GAI/RGA/RHT/D8

The rice slender mutant (slr1-1) is caused by a single recessive mutation and results in a constitutive gibberellin (GA) response phenotype. The mutant elongates as if saturated with GAs. In this mutant, (1) elongation was unaffected by an inhibitor of GA biosynthesis, (2) GA-inducible α-amylase was produced by the aleurone layers without gibberellic acid application, and (3) endogenous GA content was lower than in the wild-type plant. These results indicate that the product of the SLR1 gene is an intermediate of the GA signal transduction pathway. SLR1 maps to OsGAI in rice and has significant homology with height-regulating genes, such as RHT-1Da in wheat, D8 in maize, and GAI and RGA in Arabidopsis. The GAI gene family is likely to encode transcriptional factors belonging to the GRAS gene superfamily. DNA sequence analysis revealed that the slr1-1 mutation is a single basepair deletion of the nuclear localization signal domain, resulting in a frameshift mutation that abolishes protein production. Furthermore, introduction of a 6-kb genomic DNA fragment containing the wild-type SLR1 gene into the slr1-1 mutant restored GA sensitivity to normal. These results indicate that the slr1-1 mutant is caused by a loss-of-function mutation of the SLR1 gene, which is an ortholog of GAI, RGA, RHT, and D8. We also succeeded in producing GA-insensitive dwarf rice by transforming wild-type rice with a modified SLR1 gene construct that has a 17–amino acid deletion affecting the DELLA region. Thus, we demonstrate opposite GA response phenotypes depending on the type of mutations in SLR1.

The Involvement of Gibberellin 20-Oxidase Genes in Phytochrome-Regulated Petiole Elongation of Arabidopsis

Long day (LD) exposure of rosette plants causes rapid stem/petiole elongation, a more vertical growth habit, and flowering; all changes are suggestive of a role for the gibberellin (GA) plant growth regulators. For Arabidopsis (Arabidopsis thaliana) L. (Heynh), we show that enhancement of petiole elongation by a far-red (FR)-rich LD is mimicked by a brief (10 min) end-of-day (EOD) FR exposure in short day (SD). The EOD response shows red (R)/FR photoreversibility and is not affected in a phytochrome (PHY) A mutant so it is mediated by PHYB and related PHYs. FR photoconversion of PHYB to an inactive form activates a signaling pathway, leading to increased GA biosynthesis. Of 10 GA biosynthetic genes, expression of the 20-oxidase, AtGA20ox2, responded most to FR (up to a 40-fold increase within 3 h). AtGA20ox1 also responded but to a lesser extent. Stimulation of petiole elongation by EOD FR is reduced in a transgenic AtGA20ox2 hairpin gene silencing line. By contrast, it was only in SD that a T-DNA insertional mutant of AtGA20ox1 (ga5-3) showed reduced response. Circadian entrainment to a daytime pattern provides an explanation for the SD expression of AtGA20ox1. Conversely, the strong EOD/LD FR responses of AtGA20ox2 may reflect its independence of circadian regulation. While FR acting via PHYB increases expression of AtGA20ox2, other GA biosynthetic genes are known to respond to R rather than FR light and/or to other PHYs. Thus, there must be different signal transduction pathways, one at least showing a positive response to active PHYB and another showing a negative response.

Identification of a triterpenoid saponin from a crucifer, Barbarea vulgaris, as a feeding deterrent to the diamondback moth, Plutella xylostella.

Larvae of the diamondback moth, Plutella xylostella, a crucifer specialist, refuse to feed on a crucifer, Barbarea vulgaris, because of the presence of a feeding deterrent, which is extractable with chloroform. We isolated a feeding deterrent from B. vulgaris leaves, by successive fractionations with silica-gel, ODS, i.e., C18 reversed phase, and Sephadex LH-20 column chromatographies, and ODS-HPLC, guided by a bioassay for feeding deterrent activity. The structure of the compound was determined to be a monodesmosidic triterpenoid saponin, 3-O-[O-β-D-glucopyranosyl-(1→4)-β-D-glucopyranosyl]-hederagenin, based on FAB-MS, 1H- and 13C-NMR spectra, and hydrolysis experiments. When the compound was applied to cabbage leaf disks at greater than 0.18 μg/mm2, consumption of the disks by third instars was less than 11% of control disks treated with the solvent alone. Furthermore, all first instars died on the disks treated with the same concentrations. Because the concentration of the compound in the fresh leaves of B. vulgaris was comparable to the effective dose in the cabbage leaf disk tested, we conclude that the unacceptability of B. vulgaris to P. xylostella larvae is primarily due to this saponin.

A role of OsGA20ox1 , encoding an isoform of gibberellin 20-oxidase, for regulation of plant stature in rice.

Gibberellin (GA) 20-oxidase (GA20ox) is a key enzyme that normally catalyzes the penultimate steps in GA biosynthesis. One of the GA20ox genes in rice (Oryza sativaL.), OsGA20ox2 (SD1), is well known as the ‘Green Revolution gene’, and loss-of function mutation in this locus causes semi-dwarfism. Another GA20ox gene, OsGA20ox1, has also been identified, but its contribution to plant stature has remained unclear because no suitable mutants have been available. We isolated a mutant, B142, tagged with a T-DNA containing three CaMV 35S promoters, which showed a tall, GA-overproduction phenotype. The final stature of the B142 mutant reflects internode overgrowth and is approximately twice that of its wild-type parent. This mutant responds to application of both GA3 and a GA biosynthesis inhibitor, indicating that it is a novel tall mutant of rice distinct from GA signaling mutants such as slr1. The integrated T-DNAs, which contain three CaMV 35S promoters, are located upstream of the OsGA20ox1 open reading frame (ORF) in the B142 mutant genome. Analysis of mRNA and the endogenous GAs reveal that biologically active GA level is increased by up-regulation of the OsGA20ox1 gene in B142. Introduction of OsGA20ox1 cDNA driven by 35S promoter into the wild type phenocopies the morphological characteristics of B142. These results indicate that the elongated phenotype of the B142 mutant is caused by up-regulation of the OsGA20ox1 gene. Moreover, the final stature of rice was reduced by specific suppression of the OsGA20ox1 gene expression. This result indicates that not only OsGA20ox2 but also OsGA20ox1 affects plant stature.

Reversed-phase C18 high-performance liquid chromatography of acidic and conjugated gibberellins

Abstract The retention times of gibberellins and their glucosyl esters and glucoside conjugates on C 18 reversed-phase high-performance liquid chromatographic (HPLC) columns were determined using gradient or isocratic elution with methanol—acetic acid 1% . The separation of double-bond gibberellin isomers was accomplished without the need for derivatization or the addition of salts. A combined HPLC—radiocounting with flow-through scintillation spectrometric procedure was suitable for the routine radioassay of acidic and conjugate-like metabolises from [ 3 H] gibberellin feeds. Similarly, HPLC—bioassay detection was suitable for purified plant extracts. The totally volatile methanol-1% acetic acid solvent in the gradient and/or isocratic mode should be capable of separating virtually any of the known gibberellins, their conjugates and their catabolites. However, retention time alone is inadequate and definitive detection techniques must be utilized.

Two Rice GRAS Family Genes Responsive to N-Acetylchitooligosaccharide Elicitor are Induced by Phytoactive Gibberellins: Evidence for Cross-Talk Between Elicitor and Gibberellin Signaling in Rice Cells

In this study, we present data showing that two members of the GRAS family of genes from rice, CIGR1 and CIGR2(chitin-inducible gibberellin-responsive), inducible by the potent elicitor N-acetylchitooligosaccharide (GN), are rapidly induced by exogenous gibberellins. The pattern of mRNA accumulation was dependent on the dose and biological activity of the gibberellins, suggesting that the induction of the genes by gibberellin is mediated by a biological receptor capable of specific recognition and signal transduction upon perception of the phytoactive compounds. Further pharmacological analysis revealed that the CIGR1 and CIGR2 mRNA accumulation by treatment with gibberellin is dependent upon protein phosphorylation/dephosphorylation events. In rice calli derived from slender rice 1, a constitutive gibberellin-responsive mutant, or d1, a mutant deficient in the α-subunit of the heterotrimeric G-protein, CIGR1 and CIGR2 were induced by a GN elicitor, yet not by gibberellin. Neither gibberellin nor GN showed related activities in defense or development, respectively. These results strongly suggested that the signal transduction cascade from gibberellin is independent of that from GN, and further implied that CIGR1 and CIGR2 have dual, distinct roles in defense and development.

Analysis of gibberellins in growing fruits of Lycopersicon esculentum after pollination or treatment with 4-chlorophenoxyacetic acid

SummaryIdentification and quantification of gibberellins (GAs) were conducted in tomato pistils (Lycopersicon esculentum Miller) two days before anthesis as well as in pollinated fruits and parthenocarpic fruits induced by 4-chlorophenoxyacetic acid (4-CPA) treatment at 1, 3,6,10 and 14 d after anthesis. GA1, GAg, GA17, GA19, GA20, GA29 and GA44 were identified by combined gas chromatography-mass spectrometry (GC-MS) in pollinated fruits and parthenocarpic fruits; pollinated fruits in addition contained GA9, GA15, GA24 and GA25. 2 β-OH-GA53 was also tentatively identified in both types of fruits. Activity of GAs could not be detected in emasculated pistils. In the early stage of growth of pollinated fruits between 1 and 6 d after anthesis, the biosynthetic pathway to the C20-GA precursor of GA1, GA19, was much more accelerated than in parthenocarpic fruits, indicating that pollination may stimulate the pathway more strongly than 4-CPA. Parthenocarpic fruit tissues had a much higher concentration of GA1 th...

Ectopic Expression of Pumpkin Gibberellin Oxidases Alters Gibberellin Biosynthesis and Development of Transgenic Arabidopsis Plants

Immature pumpkin (Cucurbita maxima) seeds contain gibberellin (GA) oxidases with unique catalytic properties resulting in GAs of unknown function for plant growth and development. Overexpression of pumpkin GA 7-oxidase (CmGA7ox) in Arabidopsis (Arabidopsis thaliana) resulted in seedlings with elongated roots, taller plants that flower earlier with only a little increase in bioactive GA4 levels compared to control plants. In the same way, overexpression of the pumpkin GA 3-oxidase1 (CmGA3ox1) resulted in a GA overdose phenotype with increased levels of endogenous GA4. This indicates that, in Arabidopsis, 7-oxidation and 3-oxidation are rate-limiting steps in GA plant hormone biosynthesis that control plant development. With an opposite effect, overexpression of pumpkin seed-specific GA 20-oxidase1 (CmGA20ox1) in Arabidopsis resulted in dwarfed plants that flower late with reduced levels of GA4 and increased levels of physiological inactive GA17 and GA25 and unexpected GA34 levels. Severe dwarfed plants were obtained by overexpression of the pumpkin GA 2-oxidase1 (CmGA2ox1) in Arabidopsis. This dramatic change in phenotype was accompanied by a considerable decrease in the levels of bioactive GA4 and an increase in the corresponding inactivation product GA34 in comparison to control plants. In this study, we demonstrate the potential of four pumpkin GA oxidase-encoding genes to modulate the GA plant hormone pool and alter plant stature and development.

Gibberellins do not act against abscisic acid in the regulation of bulb dormancy of Allium wakegi Araki

Abscisic acid (ABA) is involved in bulb dormancy of Alliumwakegi Araki. We examined the antagonistic role of gibberellins(GAs)against ABA in the regulation of this dormancy. The concentrations of ABA andGAs in the basal leaf sheaths or bulbs of A. wakegi cv.Kiharawase were investigated during growth in the field and postharveststorage.The concentration of ABA in the basal leaf sheaths began to increase about onemonth before they began to swell, reached a maximum shortly after bulbharvesting, and decreased during postharvest storage. The plants showed bulbdormancy accompanied with the change in ABA concentration. GA1,GA3, GA4, GA12, GA15, GA19, and GA20 were identified in the basal leaf sheaths of A. wakegi from Kovats retention indices (KRI) andfull-scan mass spectra by gas chromatography - mass spectrometry (GC-MS)analysis. The concentrations of all classes of GAs in the basal leaf sheathsestimated by the dwarf rice micro-drop assay increased transitorily shortlybefore they began to swell, and decreased rapidly during bulb development. Bulbdormancy had already been induced when the concentration of the GAs becamemaximum. All the GAs in the bulbs remained at a low level during postharveststorage, when bulbs were gradually released from dormancy. The concentrationsof GA1+3, GA4, GA15, and GA20 inthe bulbs increased after sprouting of the bulbs planted in moist vermiculite.Hence, the state of bulb dormancy is considered to be independent of the GAconcentrations of in the basal leaf sheaths or bulbs of A.wakegi.

Metabolism of [3H]gibberellin A4 in somatic suspension cultures of anise

Abstract The native gibberellin A4 (GA4) was fed as [1, 2-3H]GA4 (1.3 Ci/mmol) to anise somatic cultures maintained either at a proembryo-like stage with 2,4-dichlorophenoxyacetic acid (2,4-D), or allowed to undergo embryogenic development on a - 2,4-D medium. Proembryos, although only 20% of the dry wt of embryos, absorbed 1.4-times more [3H]GA4/g dry wt than embryos. The [3H]GA4 was metabolized to GA1 and GA8, and at least six conjugates [GA4-glucoside (GA4-G), GA4 glucosyl ester (GA4-GE), GA1-0(3)-G, GA1-0(13)-G, GA1-GE and a GA8-glucosyl conjugate]. The major metabolite was GA4-G at each of two, 204 and 348 hr harvests (56–71 %), with GA8-G increasing from