The growth promoting effect of red light on internode elongation of Progress seedlings

Red light increased elongation of the apical 10 mm of epicotylsexcised from 7-day-old dark grown Progress seedlings. Removalof the basal portion of the plant appears to render the tissueinsensitive to the inhibitory influences of light. Additionof gibberellins A₁, A₃ or A₅ further increased elongation. Thered light growth response was independent of the gibberellinresponse; therefore, it was considered to be unrelated to anincrease in gibberellin biosynthesis. A study of the time course of growth in the presence of thegibberellins revealed that a 6–8 hr lag period was requiredbefore A₁ and A₅ became effective, while no lag period was associatedwith A₃. It was suggested that A₁ and A₅ were converted to anA₃-like gibberellin. (Received July 29, 1972; )     

Changes in Gibberellin Content during Seed Ripening in Grasses

Floret samples of Aberystwyth S. 321 perennial ryegrass andS. 352 timothy were analysed for gibberellin content at 2–5day intervals from inflorescence emergence to seed harvest.Both species had a high gibberellin content at emergence whichdiminished during anther formation. After anthesis there wasa sharp increase in gibberellin content with maxima of 256 and116 GA3 µ equivalents/Kg dry matter occurring in S. 321and S. 352 respectively. During the final stages of seed maturation,the level fell steadily to reach a stable content prior to harvest.Biological activity in ryegrass extracts was always identifiedchromatographically as gibberellin A₃, (GA₃), but in timothy,GA₃ was replaced after anthesis by a more mobile component,chromatographically similar to gibberellin A₃. The relationshipof these observations to seed formation and ripening is discussed.     

Inhibition of Gibberellin-Induced Elongation, Reorientation of Cortical Microtubules and Change of Isoform of Tubulin in Epicotyl Segments of Azuki Bean by Protein Kinase Inhibitors

When the segments of azuki bean were incubated with 3-indoleaceticacid (IAA) plus gibberellin A₃ (GA₃), one isoform of     

Effects of Gibberellin on Shoot Development in the dgt Mutant of Tomato

The morphological effects of gibberellin A₃ (GA₃) on the dgtmutant of tomato were investigated. The mutant effectively showedthe normal range of responses, including a promotion of stemlength due to an increased number of longer internodes, a dramaticincrease in apical dominance, and effects on leaf shape andcolour. In the case of stem elongation, the quantitative responseof the mutant was greater than normal. The morphological abnormalitiescharacteristic of the dgt mutant, such as horizontal growth,a thin stem and hyponastic leaves, were not normalized by GA₃. It is concluded that the demonstrated lack of response to auxinof the dgt mutant does not impair its gibberellin responses. Tomato, gibberellin, auxin, mutant, shoot development     

Auxin-gibberellin relationships in their effects on hypocotyl elongation of light-grown cucumber seedlings III. Gibberellin specificity in its enhancing effect on IAA-induced elongation

Pretreatment effects of different gibberellins, helminthosporicacid, cyclic AMP and Kinetin on subsequent IAA-induced elongationwere tested in cucumber hypocotyl sections. Gibberellin A₇ wasmore active than GA₃, while gibberellin A₃ was almost inactive.Both helminthosporic acid and cyclic AMP mimicked GA₃-action,though the degree of their activity was less. Kinetin pretreatmentresulted in marked inhibition of IAA-induced elongation. Thepretreatment effect of GA₃ was also reflected in a greater responceof the sections to synthetic auxins. (Received October 6, 1973; )     

Uptake of Gibberellin Methyl Esters by Spores and Induction of Dark Germination in Lygodium japonicum

In the fern Lygodium japonicum, the effect of the exogenousapplication of two gibberellin methyl esters, gibberellin A₄methyl ester (GA₄Me) and gibberellin A₂₀ methyl ester (GA₂₀Me)on spore germination in the dark and uptake of GA₄Me and GA₂₀Meby spores was investigated. Tritiated GA₄Me and GA₂₀Me wereprepared and used as radioactive tracers. The activity of GA₄Mewas more than 100-fold that of GA₂₀Me for the induction of sporegermination. When treated for 24 h, the activity for inducingspore germination remained after removal of the gibberellinmethyl esters from the medium. The amount of GA₄Me taken upby spores was more than three times that of GA₂₀Me throughoutthe 24 h time course of treatment. The uptake of both gibberellinmethyl esters was proportional to the external concentrationfor the range of concentrations between 10^–9 M and 10^–6M. When treated with the tritiated gibberellin methyl estersat 10^–6 M and 10^–7 M for 24 h, most of the gibberellinmethyl esters taken up by the spores were not metabolized. Althoughthe uptake of the two gibberellin methyl esters differed by3- to 5- fold, their abilities to induce spore germination differedby more than 100-fold. Therefore, the difference in the activityof the two gibberellin methyl esters regarding the inductionof spore germination could not be explained solely by the differencein their uptake. (Received January 11, 1988; Accepted May 26, 1988)     

Effects of Interactions between Low-temperature Treatments, Gibberellin (GA3) and Photoperiod on Flowering and Stem Height of Spring Rape (Brassica napus var. annua)

Exogenous gibberellin A₃(GA₃) reduced the number of leaf nodesat flowering and time to flowering and increased the stem heightat flowering in three genotypes of spring rape (Brassica napusvar.annua L.). The responses to GA₃were similar to those forlong days (LD) and low-temperature treatments, suggesting thatthe effect of photoperiod and the vernalization response areprobably mediated through gibberellins. The response to exogenousGA₃was greatest in non-cold-treated plants in short days (SD)suggesting that endogenous GAs are limiting in these conditions.CCC, an inhibitor of gibberellin biosynthesis, caused a smallincrease in the number of leaf nodes at flowering and time toflowering and a small decrease in the stem height at flowering,but unexpectedly, its effect was hardly influenced by the applicationof exogenous GA₃. Genotypes that showed the clearest responsesto the treatments with regard to the number of leaf nodes atflowering and time to flowering did not show the clearest responseswith regard to the stem height at flowering; the pattern ofresponses of the number of leaf nodes at flowering and timeto flowering was distinct from that of stem height at flowering.This indicates that flower formation and stem elongation areseparable developmental processes which may be controlled bydifferent endogenous gibberellins, different levels of a specificendogenous gibberellin, or different responses to gibberellin.Copyright 1999 Annals of Botany Company Brassica napus var. annua, gibberellin, photoperiod, spring rape, vernalization.     

Studies on the Relationship between Gibberellin Metabolism and Daylength in Normal and Non-flowering Red Clover (Trifolium pratenseL.)

Feeding experiments on tillers of a non-flowering red cloversegregate indicated that the promotive effect of gibberellinupon stem extension and flowering occured only under inductivelong days (LD). Furthermore, floral initiation took place inLD only when free gibberellin exceeded an unspecified criticallevel. Various intermediates in fungal gibberellin synthesis were fedin a similar fashion but none exerted any effect upon reproductivegrowth. Studies using ³H-gibberellin A₃ (GA₃) showed that innormal (flowering) material GA₃ was more rapidly metabolizedin short days than in long days. Qualitative differences ingibberellin metabolism between normal and non-flowering genotypeswere revealed by radio-isotope studies. Non-flowering materialrapidly degraded GA₃ under LD conditions to a biologically inactivecompound chromatographically indentical with allo-gibberic acid,whereas normal plants metabolized GA₃ more slowly producinga compund similar to gibberellenic acid. The implications ofthese results are discussed in terms of the mechanism of stemelongation and floral initiation.     

Activity of Gibberellins A1 to A0 in the Avena First-leaf Bioassay, and Location after Chromatography

Activity curves are determined for gibberellins A₁ to A₀ bythe Avena first-leaf bioassay method. Gibberellins A¹, A₄ andA₅ can be detected at 10^-11 or 10^-10 g/ml and give optimum activityof approximately 230 per cent elongation (water controls = 100per cent). Gibberellins A²A³, and A⁹ can be detected at 10^-3g/mland give optimum activity of approximately 200 per cent. GibberellinsA₆ and A₇ can be detected at 10^-5g/ml; GA₇ gives optimum activityof around 190 per cent. All the gibberellins except GA₈ canbe detected by this bioassay method after chromatography inn-butanol: 1.5 N ammonia (3: 1) and benzene: acetic acid: water(4: 2: 1) when applied to the paper at concentrations from O.Ito µg. The sensitivity of the method is compared withthat of other gibberellin bioassay methods.     

The Gibberellins of Developing Bean Seeds

Properties of gibberellin-like substances extracted from Frenchbean seeds during their development were studied. Two zonesof gibberellin-like activity were detected on paper chromatograms. Changes in activity of one of the zones correlated with changesin growth-rate of the seed. From considerations of Rf on paperchromatograms, and differential activity on dwarf peas, dwarf-1and dwarf-5 corn, it was deduced that activity of this zonewas due to substances resembling gibberellin A₁ and gibberellinA₅. Gibberellin A₅-like activity was highest in young seedsand disappeared after cell division in the cotyledons had ceased.Gibberellin A₁-like activity rose to its highest level duringthe period of rapid cell expansion in the cotyledons, afterthe disappearance of gibberellin A₅-like activity. The second zone of gibberellin-like activity was due mainlyto a non-acidic substance, which disappeared at the time GAj-likeactivity was rising to its highest level. A non-acidic substance that stimulated lateral bud growth ofdwarf peas also was detected in the extracts. It is presumedto be a cytokinin.     

Interactions of the Growth Retardants Daminozide and Piproctanyl Bromide, and Gibberellins A1, A3, A4+7, A5 and A13 in Stem Extension and Inflorescence Development in Chrysanthemum morifolium Ramat

Interactions between the growth retardants daminozide (a substitutedsuccinamic acid) or piproctanyl bromide (a quaternary ammonium,piperidinium compound), and a subsequent application of a singledose (40 µg) of either gibberellin A₁, A₃, A₄₊₇ or A₁₂,showed that, in Chrysanthemum morifolium Ramat. cv. Bright GoldenAnne, a strong interdependence exists between elongation ofthe lateral shoot and the rate of development of its terminalinflorescence. A₁, A₃, and A₄₊₇ were highly active in overcoming the restrictionson both internode extension and the rate of flower-bud developmentimposed by either retardant, suggesting that these two retardanteffects are caused by a deficiency of active gibberellins (GN).In the absence of retardant, A₁, A₃, and A₄₊₇ markedly increasedstem elongation, and flowering occurred earlier than in plantsreceiving neither retardant nor GN. A₁₃ the only 20-carbon GNtested, was much less active, while A₅ had a relatively greatereffect on the time of flowering than on shoot elongation. Thus,it is not necessarily the rate of stem extension which determinesthe rate of inflorescence development. The response to different amounts of A₁, A₃ or A₁₃ (1, 5, 10,20, or 50 µg per shoot) neither suggest that different‘threshold’ levels of a particular GN are requiredto induce increases in either stem elongation or in the rateat which inflorescences develop, nor did a change in the dosegiven lead to any consistent differential effect on these twoprocesses. Chrysanthemum morifolium Ramat., stem extension, inflorescence development, growth retardants, gibberellins     

REGULATION OF BUD REST IN TUBERS OF POTATO SOLANUM TUBEROSUM L.: I. EFFECT OF GROWTH SUBSTANCES ON EXCISED POTATO BUDS

Excised plugs containing buds from potato tubers were treatedwith 5-µliter droplets of a number of growth-regulatingsubstances. Gibberellin A₃ stimulated sprouting over a widerange of concentrations. Gibberellins A₃, A₄, A₅, and A₇ stimulatedsprouting, and A₆, A₈, and A₉ either had no effect or slightlyinhibited. Extracts of gibberellinlike substances from potatopeelings promoted sprouting. NAA and IAA both promoted sproutingslightly at low concentrations (4 x 10^–8M) but inhibitedsprouting at 4 x 10^–5M. Leaching of plugs resulted indelayed sprouting, and gibberellin restored total sproutingpotential. Plug size influenced rate of sprouting: small plugs(8 mm in diameter) sprouted faster than large (23 mm) plugs,and gibberellin stimulated sprouting slightly faster in thelarger than in the 8 mm plugs. None of the presumed componentsof ß, including cinnamic, chlorogenic, and caffeicacids, and coumarin, convincingly inhibited sprouting; in fact,they stimulated sprouting at almost all concentrations tested.5- Fluorouracil (5-FU) inhibited sprouting only slightly; andgibberellin completely or partially promoted sprouting in plugspreviously treated with 5-FU. Failure of 5-FU to inhibit sproutingwas considered to be the result of slow penetration of the inhibitorinto the potato bud. The potato "eye" bioassay is deficient in certain aspects, especiallyin view of the inconsistent rates of sprouting between experimentsand of nonspecificity. The results of this study, however, donot obviate the use of potato buds as a bioassay for inhibitorsof sprouting. ¹This research was supported in part by United States PublicHealth Service Grant EF-61. ²Present address: Department of Botany, Hebrew University, Jerusalem,Israel. ³Present address: U.S.D.A.-A.R.S., Department of Agronomy, Universityof California, Davis, California, U.S.A.     

Stimulation of oat and rice mesocotyl growth by ethylene

A low concentration of ethylene stimulated growth of intactoat and rice mesocotyls in darkness. Combined application ofethylene and gibberellin A₃ produced an evident additive effecton the elongation of rice mesocotyls. (Received April 9, 1971; )     

EFFECTS OF VARIOUS FACTORS ON THE INCREASE OF {alpha}-AMYLASE ACTIVITY IN RICE ENDOSPERM INDUCED BY GIBBERELLIN A3

The increase of -amylase activity in embryoless rice endosperminduced by the addition of gibberellin A₃ was examined undervarious conditions with an aim to establish a bioassay methodfor gibberellins. Sterilized embryoless rice endosperms were incubated in a testtube containing 0.2–1.0 ml of test solution for 4 daysat 30. -Amylase activity in the endosperm was determined bymeasuring digestion of added starch. The increase of amylaseactivity during the incubation was not affected by the additionof various vitamins, amino acids, organic acids, protease, sucrose,indoleacetic acid or kinetin. Helminthosporol, helminthosporicacid and sclerin (1–10 µg/ml) had weak promotingeffects. Under appropriate conditions, 10^–5 µg/mlof gibberellin A₃ could be detected. In double logarithmic plot,the increase in the enzyme activity was proportional to thegibberellin A₃ concentration in the range from 10^–5 to10^–2 µg/ml. (Received April 13, 1966; )     

The Relationship of Endogenous Gibberellins to Light-regulated Stem Elongation Rates in Dwarf and Normal Cultivars of Pisum sativum L.

Dwarf cultivar Progress No. 9 and normal cultivar Alaska ofPisum sativum L. were grown under conditions of darkness orred light. Red light decreased the stem elongation rate of bothcultivars. Gibberellins present during the linear phase of stemelongation were isolated and the two main components were tentativelyidentified by gas chromato-chromatography and mass spectrometryas Gibberellin A₁ and A₅. Both gibberellins varied quantitativelywithin and between cultivar and treatment groups, and the amountspresent were inversely related to stem elongation rate. Althoughthe stem elongation rate of plants grown under red light wasrepressed, endogenous gibberellin was not limiting and was asmuch as two-fold higher in red light-grown plants than in dark-grownplants. The levels of endogenous gibberellin in dawrf plantsindicated that the genetic growth limitation was not due toa gibberellin deficiency. (Received May 26, 1981; Accepted January 28, 1982)     

Gibberellin-Induced Flowering in Cordyline (Agavaceae)

Normal, terminal inflorescences of Cordyline terminalis, a woodymonocotyledon, appeared 4–6 weeks after apical buds weretreated with gibberellin A₃ (GA₃) or GA₄₊₇. There was no responseto GA₁₃. Large plants, newly rooted cuttings, and seedlingsall responded, although there were clonal differences. Floweringwas induced under natural day lengths throughout the year. Untreatedcontrol plants in all experiments remained vegetative. Dracaenaspp. did not respond to the three gibberellins.     

Distribution of Radioactivity from Exogenously Supplied [1-14C]Indol-3-yl-acetic Acid and [3, 4-3H (N)] Gibberellin A, in Geotropically-stimulated Picea abies (L.) Karst. Roots

The distribution of exogenously-supplied radioactive labelledindol-3-yl-acetic acid (IAA) and gibberellin A₁ (GA₁) in geotropicallystimulated roots of Norway spruce (Picea abies (L.) Karst.)has been demonstrated. Seedlings were positioned with theirroot tips in 2.1 x 10^–6 M [¹⁴C]IAA or 1.3 x 10^–8m ³H-GA₁ for 4 and 20 h, respectively. After geotropic stimulationfor 90 min in the horizontal position the root tips were cutlongitudinally in 50 µm thick sections, using a freeze-microtome.The radioactivity in the ¹⁴C-IAA treated roots occurred in higherconcentration in the lower than in the upper halves (ratio 1.25:1). A similar trend was observed in the [³H]GA₁-treated rootswhere the ratio lower: upper halves was 2.04: 1. The ratio ofradioactivity in right and left halves of vertical roots wasapproximately the same in roots supplied with [¹⁴C]IAA and [³H]GA₁(1.09: 1). The supplied radioactive compounds were analysed chromatographicallyafter extraction in methanol of 6 mm apical root segments. Onlya small fraction (7–8 per cent) of the supplied [¹⁴C]IAAwas revealed unchanged in the segments. The major part of thechromatographed, labelled compound has not been identified,but on basis of its R_F value it is suggested that it may beindol-3-acetyl-aspartic acid (IAAasp). The chromatographic analysis of the [³H]GA,-treated segmentsshowed that only small fractions of this gibberellin has beenconverted to other compounds. These results have been discussed and correlated with knowledgeof plant growth regulators and their participation in root geotropism. Picea abies, spruce, geotropism, gibberellin A₁, indol-3-yl-acetic acid, growth regulators, redistribution in roots     

Phase Change in Hedera helix L.: III. THE EFFECTS OF GIBBERELLINS, ABSCISIC ACID AND GROWTH RETARDANTS ON JUVENILE AND ADULT IVY

Gibberellic acid, applied to delaminated petioles of rootedcuttings of juvenile and adult ivy initially induced internodeelongation and abnormal leaf development, and suppressed apicaldominance. Juvenile cuttings were affected only transientlyand soon reverted to normal growth. Adult cuttings, insteadof resuming normal growth after this initial response to GA₃,gradually developed many juvenile characteristics. Approximately16 weeks after treatment at 25 ?C nearly all shoots of adultcuttings had undergone complete rejuvenation. Lower temperaturereduced the speed of response to GA₃. A mixture of gibberellinsA₄ and A₇ had effects similar to those of GA₃ on the growthof juvenile and adult cuttings. Treatment of both phases ofivy with abscisic acid (ABA) induced no visible effects andwhen ABA was applied with GA₃ it did not reduce the responseof either phase to the gibberellin. CCC had a marked dwarfingeffect on juvenile ivy but did not induce pre-maturation. However,extraction of gibberellin-like substances from severely dwarfedplants suggested that CCC was not exerting its growth retardingeffect through an inhibition of gibberellin biosynthesis. AMO1618 did not retard growth of juvenile ivy cuttings.     

Gibberellin-colchicine interaction in elongation of azuki bean epicotyl sections

In azuki bean (Azukia angularis = Vigna angularis) epicotylsections, gibberellin A₃ (GA₃) enhanced the growth promotingeffect of indoleacetic acid (IAA), but showed no growth effectwhen applied alone. Sections showed practically no cell division.The promoting effect of GA₃ on section growth seems to be dueto its promoting effect on cell elongation. The diameters of sections treated with IAA increased, but thediameters of sections treated with GA₃ together with IAA remainedconstant. GA₃ seems to suppress cell expansion in a directiontransverse to the cell axis. Colchicine at a concentration with no inhibiting effect on IAA-inducedelongation almost completely reversed the effect of GA₃ On the basis of these results, the participation of wall microtubulesin GA₃-induced elongation is discussed. (Received October 22, 1971; )     

Studies of Growth and Flowering in Picea sitchensis (Bong.) Carr. 1. Effects of Growth Regulator Applications to Mature Scions on Seedling Rootstocks

Effects of growth regulator applications on the flowering of5-years-grafted mature scions of Picea sitchensis (Bong.) Carr.were assessed. Growth regulators were applied to the bud surfacein droplets of ethanol during July, August and September ina polythene house or glasshouse. A mixture of gibberellins A₄and A₇ applied alone, and in combination with gibberellins A₃and A₅, significantly increased numbers by up to seven timesfor male and by up to eight times for female strobili, gibberellinA, gave relatively the strongest response, and gibberellin A₄was inactive. Phosphon D and abscisic acid each reversed thepromotion of flowering by gibberellins, whilst kinetin and N,N-diphenylureahad no effect. The number of female strobili was negativelycorrelated with vegetative shoot length in the year after treatment. Under field conditions hormones were applied in July and Augustunder flaps of bark on the branches of 10-years-grafted maturescions. Gibberellin applications caused a 5-fold increase inflowering and N⁶-benzyladenine further increased the response.Naphth-lyl-acetic acid reduced female and increased male flowering.Bark removal near the base of the branch further enhanced hormone-inducedstrobilus production. The usefulness of these findings for thebreeding of Picea sitchensis is discussed.