Plant growth regulators and the orchid cut-flower industry

Research involving plant growth regulators (PGRs) and orchids in areas of orchid growth and development are reviewed. For all areas covered in the review — seed germination and seedling growth, lateral shoot production, root production, flower initiation and development, postharvest physiology, and photosynthate partitioning — it was concluded that further studies would assist in clarifying potential uses for PGRs in the orchid cut-flower industry. It is suggested that extra PGR research on orchids is justified at the present time because of favourable prospects facing the orchid cut-flower industry.     

Arabidopsis ATM and ATR kinases prevent propagation of genome damage caused by telomere dysfunction

The ends of linear eukaryotic chromosomes are hidden in nucleoprotein structures called telomeres, and loss of the telomere structure causes inappropriate repair, leading to severe karyotypic and genomic instability. Although it has been shown that DNA damaging agents activate a DNA damage response (DDR), little is known about the signaling of dysfunctional plant telomeres. We show that absence of telomerase in Arabidopsis thaliana elicits an ATAXIA-TELANGIECTASIA MUTATED (ATM) and ATM AND RAD3-RELATED (ATR)-dependent DDR at telomeres, principally through ATM. By contrast, telomere dysfunction induces an ATR-dependent response in telomeric Conserved telomere maintenance component1 (Ctc1)-Suppressor of cdc thirteen (Stn1)-Telomeric pathways in association with Stn1 (CST)-complex mutants. These results uncover a new role for the CST complex in repressing the ATR-dependent DDR pathway in plant cells and show that plant cells use two different DNA damage surveillance pathways to signal telomere dysfunction. The absence of either ATM or ATR in ctc1 and stn1 mutants significantly enhances developmental and genome instability while reducing stem cell death. These data thus give a clear illustration of the action of ATM/ATR-dependent programmed cell death in maintaining genomic integrity through elimination of genetically unstable cells.     

Induction of water deficit tolerance in wheat due to exogenous application of plant growth regulators: membrane stability,water relations and photosynthesis

Our experiment was carried out in order to explore effects of plant growth regulators (PGR; thidiazuron, paclobutrazol, and ascorbic acid) on physiological traits of wheat genotypes under water surplus and deficit conditions. Study revealed that relative water content, membrane stability index, chlorophyll content, photosynthetic rate (P_N), and maximal quantum yield of PSII improved with PGRs application across the genotypes both under irrigation and water stress. The response of HD 2733 genotype was more positive toward PGRs treatment as compared to other genotypes under water stress. Higher P_N and chlorophyll contents were observed in HD 2987 followed by C 306 genotype under water-stress conditions. Moreover, Rubisco small subunit (SSU) expression was lower in wheat genotypes under water stress as compared to irrigated conditions. Application of PGRs led to upregulation of SSU under water stress, while no significant change was found in Rubisco level and activity under irrigated condition in dependence on PGRs treatments. Yield-related traits showed also significant reduction under water-stress conditions, while application of PGRs enhanced the yield and its components. Results indicated that the PGRs exhibited a positive interaction and synergetic effect on water stressed wheat plants in terms of photosynthetic machinery and yield.     

Starvation induced cell death in autophagy-defective yeast mutants is caused by mitochondria dysfunction

Autophagy is a highly-conserved cellular degradation and recycling system that is essential for cell survival during nutrient starvation. The loss of viability had been used as an initial screen to identify autophagy-defective (atg) mutants of the yeast Saccharomyces cerevisiae, but the mechanism of cell death in these mutants has remained unclear. When cells grown in a rich medium were transferred to a synthetic nitrogen starvation media, secreted metabolites lowered the extracellular pH below 3.0 and autophagy-defective mutants mostly died. We found that buffering of the starvation medium dramatically restored the viability of atg mutants. In response to starvation, wild-type (WT) cells were able to upregulate components of the respiratory pathway and ROS (reactive oxygen species) scavenging enzymes, but atg mutants lacked this synthetic capacity. Consequently, autophagy-defective mutants accumulated the high level of ROS, leading to deficient respiratory function, resulting in the loss of mitochondria DNA (mtDNA). We also showed that mtDNA deficient cells are subject to cell death under low pH starvation conditions. Taken together, under starvation conditions non-selective autophagy, rather than mitophagy, plays an essential role in preventing ROS accumulation, and thus in maintaining mitochondria function. The failure of response to starvation is the major cause of cell death in atg mutants.     

The homeobox genes ATHB12 and ATHB7encode potential regulators of growth in response to water deficit in Arabidopsis

The Arabidopsis thaliana homeodomain leucine-zipper gene ATHB7, which is active specifically under water deficit conditions, is proposed to act as a negative regulator of growth (Söderman et al., 1996, Plant J. 10: 375 381; Hjellström et al., 2003, Plant Cell Environ 26: 1127 1136). In this report we demonstrate that the paralogous gene, ATHB12, has a similar expression pattern and function. ATHB12,like ATHB7,was up-regulated during water deficit conditions, the up-regulation being dependent on abscisic acid (ABA) and on the activity of the Ser/Thr phosphatases ABI1 and ABI2. Plants that are mutant for ATHB12, as a result of T-DNA insertions in the ATHB12 gene, showed a reduced sensitivity to ABA in root elongation assays, whereas transgenic Arabidopsis plants expressing ATHB12 and/orATHB7 as driven by the CaMV 35S promoter were hypersensitive in this response compared to wild-type. High-level expression of either gene also resulted in a delay in inflorescence stem elongation growth and caused plants to develop rosette leaves with a more rounded shape, shorter petioles, and increased branching of the inflorescence stem. Transgenic Arabidopsisplants expressing the reporter geneuidA under the control of the ATHB12promoter showed marker gene activity in axillary shoot primordia, lateral root primordia, inflorescence stems and in flower organs. Treatment of plants with ABA or water deficit conditions caused the activity of ATHB12to increase in the inflorescence stem, the flower organs and the leaves, and to expand into the vasculature of roots and the differentiation/elongation zone of root tips. Taken together, these results indicate that ATHB12 and ATHB7 act to mediate a growth response to water deficit by similar mechanisms.     

Plant growth regulators and virus infection: A critical review

Virus infection can severely inhibit plant growth and distort development. This article reviews changes in plant growth regulator metabolism caused by infection. In general, virus infection decreases auxin and gibberellin concentrations and increases abscisic acid concentration. Ethylene production is stimulated in necrotic or chlorotic reactions to infection, but not where the virus spreads systemically without necrosis. While these broad trends are true for most host-virus combinations studied, several situations are recorded where the virus had other effects on growth substance concentration. Cytokinin changes do not show any common pattern: both increases and decreases after infection have been reported.The extent to which virus-induced changes in growth substance concentration could be responsible for observed alterations in host growth and development is discussed. While changes in abscisic acid, gibberellin and ethylene production seem potentially important, the experimental evidence does not provide conclusive proof for control of growth by these changes.The numerous investigations of effects of exogenous regulators on virus multiplication and pathogenesis are reviewed. Different regulators, or the same regulator applied at different times or concentrations, had very diverse effects, and in some cases did significantly alter virus multiplication and pathogenesis. However, such studies seem to have yielded disappointingly little understanding of the biochemistry of the host-virus interaction, and the possible involvement of growth substances in this.Possible uses of plant growth regulators in chemotherapy of virus disease, and their possible involvement in natural or induced resistance mechanisms are discussed.     

Plant hormones and plant growth regulators in plant tissue culture

Summary This is a short review of the classical and new, natural and synthetic plant hormones and growth regulators (phytohormones) and highlights some of their uses in plant tissue culture. Plant hormones rarely act alone, and for most processes— at least those that are observed at the organ level—many of these regulators have interacted in order to produce the final effect. The following substances are discussed: (a) Classical plant hormones (auxins, cytokinins, gibberellins, abscisic acid, ethylene and growth regulatory substances with similar biological effects. New, naturally occurring substances in these categories are still being discovered. At the same time, novel structurally related compounds are constantly being synthesized. There are also many new but chemically unrelated compounds with similar hormone-like activity being produced. A better knowledge of the uptake, transport, metabolism, and mode of action of phytohormones and the appearance of chemicals that inhibit synthesis, transport, and action of the native plant hormones has increased our knowledge of the role of these hormones in growth and development. (b) More recently discovered natural growth substances that have phytohormonal-like regulatory roles (polyamines, oligosaccharins, salicylates, jasmonates, sterols, brassinosteroids, dehydrodiconiferyl alcohol glucosides, turgorins, systemin, unrelated natural stimulators and inhibitors), as well as myoinositol. Many of these growth active substances have not yet been examined in relation to growth and organized developmentin vitro.     

Plant growth regulators and amino acids released by Azospirillum sp in chemically defined media

AIMS: To investigate the ability of Azospirillum sp., a facultative endophitic diazotrophic bacterium, to release plant growth regulators (PGR) such as polyamines, ethylene, indoleacetic acid and amino acids in both combined-N and N-free cultures. METHODS AND RESULTS: The presence of those substances was analysed by HPLC. Azospirillum sp. is capable of releasing PGR and amino acids into the culture medium. CONCLUSIONS: The type and quantity of the released substances varied, depending on the presence of combined-N in the medium. SIGNIFICANCE AND IMPACT OF THE STUDY: A better knowledge of PGR produced by Azospirillum sp. has been gained.     

Root growth and water uptake during water deficit and recovering in wheat

Root growth and soil water content were measured in a field experiment with wheat subjected to two periods of water deficit. The first period was induced early in the season between the early vegetative stage (22 DAS) and late terminal spikelet (50 DAS), the second period at mid-season between terminal spikelet (42 DAS) and anthesis (74 DAS). Total root growth was reduced under water deficit by a reduction in the top 30 cm, while the root system continued to grow in the deeper soil profile between 30 and 60 cm. Shortly after rewatering, the growth pattern reverted to fastest root growth rates in the shallow soil layers. In relative terms, the total root system increased in relation to the above ground dry matter under water shortage. The early-, the mid-season water deficit treatments, and the control treatment had total root length of 27.4, 19.4 and 30.6 km m^-2, respectively, about 2 wk before maturity. Evapotranspiration declined under water deficit, but water uptake in deeper layers increased. Water uptake per unit root length was reduced with water deficit and was still low shortly after rewatering. Remarkable was the increase in water uptake at 2–3 weeks after rewatering, both deficit treatments exceeded the control by almost 100%. This increase in water uptake followed the burst of new root growth in the upper regions of the soil. However, water uptake rates subsequently declined towards maturity, being between 0.15 L km^-1 d^-1 and 0.17 L km^-1 d^-1 for the early and mid-season water deficit treatments, slightly higher than the control, 0.12 L km^-1 d^-1. The results showed that the crop subjected to early water deficit could compensate for some of the reductions in root growth during subsequent rewatering, but the impact of the mid-season water deficit treatment was more severe and permanent.     

Plant growth regulators from the fruiting bodies of Tricholoma flavovirens

A novel indole derivative (1) and three known compounds (2–4) were isolated from the fruiting bodies of Tricholoma flavovirens. Their structures were determined or identified by the interpretation of spectroscopic data. Compounds 1 and 2 promoted root growth of lettuce and inhibited hypocotyl growth at 1 μmol/paper. Compound 3 inhibited hypocotyl and root growth at 100 nmol/paper.     

Plant growth regulators and adventitious root development in relation to auxin

Adventitious root formation in stem cuttings of mung bean was enhanced by ethrel, which had an additive effect when employed simultaneously with indolebutyric acid (IBA). Abscisic acid (ABA) did not influence the number of roots per cutting whereas gibberellic acid (GA₃) and kinetin were without effect on rooting at lower concentrations but were inhibitory at higher concentrations. Nevertheless, all three of these chemicals showed synergistic interactions with IBA and/or indol-3-ylacetic acid (IAA) and thereby significantly promoted root formation. A localised application of morphactin to the epicotyl of cuttings totally inhibited root production irrespective of which of the foregoing growth regulators were suppliedvia the hypocotyl. Morphactin application also prevented root formation in cuttings treated with vitamin D₂. The various growth regulators employed had differing effects on growth of roots but there was no simple relationship between their effects on root formation and subsequent root growth.     

Amelioration of growth reduction of lowland rice caused by a temporary loss of soil-water saturation

Decreases in nutrient availability after loss of soil-water saturation are significant constraints to productivity in lowland rainfed rice soils. The effectiveness of soil amendments like lime and straw in ameliorating these constraints are poorly understood. This pot experiment was conducted in Cambodia to investigate changes in soil chemical properties and nutrient uptake by rice after applying lime or straw to continuously flooded or intermittently flooded soil. In continuously flooded soils, exchangeable Al decreased to below 0.2 cmolc/kg. Liming (pH 6.5–6.8) the continuously flooded soil decreased the levels of acetate extractable Fe and P, plant P uptake and shoot dry matter, but had no effect on either Bray-1 or Olsen extractable P values. By contrast, the addition of straw (3.5 g dry straw/kg soil) increased Bray-1, Olsen, and acetate extractable P, plant P uptake, shoot P, and shoot dry matter. The non-amended soils became strongly acidic after loss of soil water saturation: extractable Al increased to 1.0 cmol_c/kg, a potentially harmful level for rice. By contrast, extractable P decreased markedly under loss of soil water saturation as did plant P uptake, shoot P, and shoot dry matter. With loss of soil water saturation, liming substantially depressed the levels of Al but it did not increase plant P uptake, shoot P, and shoot dry matter. Straw addition not only decreased extractable Al levels to well below 0.6 cmol_c/kg under loss of soil water saturation, but it also increased extractability of soil P, plant P uptake, shoot P, and shoot dry matter. Thus, in rainfed environments, the incorporation of straw may be more effective than liming to pH 6.8 for minimising the negative effects of temporary loss of soil-water saturation on P availability, P uptake, and growth of rice.     

α－synuclein对小剂量鱼藤酮导致的线粒体损伤的调控作用研究

建立稳定表达 -synuclein基因的人神经母细胞瘤细胞株SH-SY5Y细胞,,鱼藤酮作用1、2、4周后分别提取各组细胞线粒体,检测其complexⅠ功能、线粒体膜肿胀度和超氧阴离子的含量。结果显示在1、2周时过表达 -synuclein基因的细胞与对照组细胞相比,前者的complexⅠ的活性高,线粒体膜肿胀度轻,线粒体超氧阴离子的含量少。但4周后,前者的complexⅠ活性明显低于后者,且线粒体膜肿胀度及线粒体内超氧阴离子的含量均显示前者高于后者,也是前者多于后者。由此可见过表达 -synuclein基因的细胞在早期对鱼藤酮的损伤有一定的抵抗作用,但长期作用后可能有加重损伤的作用。提示PD患者多巴胺能神经元内 -synuclein的增高可能对小剂量鱼藤酮导致的线粒体损伤存在双重调节作用,初期可能由于 -synuclein上调引起的预适应改变起到一定的保护作用。而失代偿后,可能由于神经元内积累的 -synuclein聚变,对线粒体膜稳定性的损伤,导致神经元变性死亡。     

Ozone and water deficit reduced growth of Aleppo pine seedlings

The effects of ambient and elevated ozone (O₃) levels on photosynthesis, growth, pigment, biomass and element contents of Aleppo pine (Pinus halepensis Mill.) were studied for two growing seasons (1997, 1998). Two-year-old seedlings were exposed to elevated O₃ in open-top chambers. The treatments were charcoal-filtered air and non-filtered air + 50 nl l^–1 O₃ (24 h per day, 7 days per week). In summer 1998, half of the seedlings were drought-stressed (leaf water potential down to approximately –2 MPa), while the other half were kept well-watered. At the beginning of the season (1998), current (c) and previous-year (c + 1) needles under O₃ stress showed an increase in stomatal conductance and net photosynthesis. During the drought period, only stomatal conductance increased in both needle age-classes, whereas the net photosynthesis decreased. At the end of the measuring period, both parameters were reduced in the O₃ treatment. Both O₃ and drought decreased chlorophyll a and b concentrations, growth and biomass. A carry-over effect of O₃ on pigments was also observed. Needle K content was increased in the O₃ treatment. Drought protected Aleppo pine against O₃ (less chlorotic mottle and less decrease of stem and branch biomass).     

Respiration metabolism in mitochondria of pea seedlings of different age under water deficit and rewatering

The effects of an osmoticum (mannitol) on growth, water content, respiration, and proline content in epicotyls of etiolated two-day-old (S₂) and three-day-old (S₃) pea (Pisum sativum L., cv. Flora-2) seedlings were studied. Water deficit was produced by placing plant roots in 0.6 M mannitol for 2–4 days. Control S₃ epicotyls contained more water than S₂ epicotyls; they were also characterized by more intense mitochondrial activity (in state 3, V ₃) and by the higher value of the respiratory control (RC) due to a fourfold decrease of proportion of weakly phosphorylating cyanide-resistant respiration (CRR). After 2-day-long treatment with the osmoticum, S₂ epicotyls lost more water than S₃; water deficit in them attained 40% (28% in S₃). In S₃ treatment, epicotyls continued to grow at the almost unchanged rate, and the content of proline in them changed insignificantly, whereas in S₂ seedlings epicotyl growth stopped, and proline accumulated in them. In the presence of the osmoticum, V ₃ and RC reduced, but in S₃ treatment they retained higher than in treatment S₂. In mitochondria of S₃ subjected to dehydration, the proportion of the cytochromic pathway of oxidation (V _cyt) remained high, but the absolute values of the respiration rate reduced, whereas in S₂ both these indices reduced and the proportion of CRR increased. After rewatering, indices of mitochondrial activity (the rate of substrate oxidation, RC value) were restored, but in S₃ they were higher. The ratio of V _cyt to CRR in S₃ shifted toward CRR, whereas in S₂, in contrast, it was shifted toward V _cyt. When temperature during seedling growth and experiment performing was declined from 22°C (in control) to 18°C, growth of S₃ epicotyls was retarded to the rate characteristic of S₂ at 22°C. Under the effect of osmoticum, they, like S₂, acquired a capacity to accumulate proline. Nevertheless, mitochondrial activity in such S₃ turned out to be higher than in S₂ grown at 22°C. The results obtained than, as distinct from traditional notes, 3-day-old pea seedlings manifested the higher tolerance to water deficit than 2-day-old seedlings.     

Inhibitors of protein synthesis and RNA synthesis prevent neuronal death caused by nerve growth factor deprivation

We have developed an experimental paradigm to study the mechanism by which nerve growth factor (NGF) allows the survival of sympathetic neurons. Dissociated sympathetic neurons from embryonic day-21 rats were grown in vitro for 7 d in the presence of NGF. Neurons were then deprived of trophic support by adding anti-NGF antiserum, causing them to die between 24 and 48 h later. Ultrastructural changes included disruption of neurites, followed by cell body changes characterized by an accumulation of lipid droplets, changes in the nuclear membrane, and dilation of the rough endoplasmic reticulum. No primary alterations of mitochondria or lysosomes were observed. The death of NGF-deprived neurons was characterized biochemically by assessing [35S]methionine incorporation into TCA precipitable protein and by measuring the release of the cytosolic enzyme adenylate kinase into the culture medium. Methionine incorporation began to decrease approximately 18 h post-deprivation and was maximally depressed by 36 h. Adenylate kinase began to appear in the culture medium approximately 30 h after deprivation, reaching a maximum by 54 h. The death of NGF-deprived neurons was entirely prevented by inhibiting protein or RNA synthesis. Cycloheximide, puromycin, anisomycin, actinomycin-D, and dichlorobenzimidazole riboside all prevented neuronal death subsequent to NGF deprivation as assessed by the above morphologic and biochemical criteria. The fact that sympathetic neurons must synthesize protein and RNA to die when deprived of NGF indicates that NGF, and presumably other neurotrophic factors, maintains neuronal survival by suppressing an endogenous, active death program.