Increase In ABA Research Articles

Transcriptional analysis of maize elite inbred line Jing24 and the function of ZmMAPKKK21 in the response to drought stress

Drought, one of the most devastating abiotic stresses to affect agricultural production worldwide, causes significant crop yield loss. In China, the yield and value of maize, a drought-sensitive staple crop, is significantly affected by drought. Jing24 (J24) is an elite, robust, and drought-resistant maize inbred line, but the underlying genetic basis for this resistance is imperfectly understood. We characterized the overall performance of three maize varieties (J24, B73, and X178) under moderate and severe drought conditions at seedling and flowering stages. RNA-Seq analysis revealed more genes to respond to drought treatment in J24 than either B73 or X178, and that some drought-responsive genes were common to each line in leaf and root tissues. Gene ontology analysis of common differentially expressed genes in J24 and X178 revealed membrane and transporter related genes to be significantly enriched in roots, whereas genes associated with photosynthesis and membrane were most-enriched in leaves. Because expression of ZmMAPKKK21 was significantly up-regulated in the root of J24 in the moderate drought treatment, we obtained transgenic Arabidopsis plants overexpressing ZmMAPKKK21 that showed a substantial reduction in ABA sensitivity but increase in drought tolerance. Maize plants in which ZmMAPKKK21 was knocked out were more sensitive to water deficiency and have a smaller root system and a lower survival rate after rewatering than wild type plants. These results suggest that ZmMAPKKK21 is a positive regulator for drought response in J24, which provides insights into the molecular mechanism of the strong drought resistance of J24.

The underlying molecular mechanisms of hormonal regulation of fruit color in fruit-bearing plants.

Fruit color is a key feature of fruit quality, primarily influenced by anthocyanin or carotenoid accumulation or chlorophyll degradation. Adapting the pigment content is crucial to improve the fruit's nutritional and commercial value. Genetic factors along with other environmental components (i.e., light, temperature, nutrition, etc.) regulate fruit coloration. The fruit coloration process is influenced by plant hormones, which alsoplay a vital role in various physiological and biochemical metabolic processes. Additionally, phytohormones play a role in the regulation of a highly conserved transcription factor complex, called MBW (MYB-bHLH-WD40). The MBW complex, which consists of myeloblastosis (MYB), basic helix-loop-helix (bHLH), and WD40 repeat (WDR) proteins, coordinates the expression of downstream structural genes associated with anthocyanin formation. In fruit production, the application of plant hormones may be important for promoting coloration. However, concerns such as improper concentration or application time must be addressed. This article explores the molecular processes underlying pigment formation and how they are influenced by various plant hormones. The ABA, jasmonate, and brassinosteroid increase anthocyanin and carotenoid formation, but ethylene, auxin, cytokinin, and gibberellin have positive as well as negative effects on anthocyanin formation. This article establishes the necessary groundwork for future studies into the molecular mechanisms of plant hormones regulating fruit color, ultimately aiding in their effective and scientific application towards fruit coloration.

Effects of exogenous GABA on physiological characteristics of licorice seedlings under saline-alkali stress

Licorice is widespread in arid and semi-arid areas, but high soil salinity has always been a limiting factor for vegetation growth in these areas. Gamma-aminobutyric acid (GABA) is a signaling molecule that can regulate tolerance in plant. However, the mechanism by which exogenous GABA regulates the response of licorice to saline-alkali stress is not yet clear. In this study, we investigated the effects of exogenous GABA on growth parameters, oxidative damage, hormone levels and photosynthetic indices of licorice seedlings under different combinations of saline and alkali stress conditions. The experiment involved eight treatments: CK, distilled water (control); CK + GABA, 0.1 mM GABA; salt stress (SS), 150 mM NaCl; SS + GABA, 150 mM NaCl + 0.1 mM GABA; alkali stress (AS), 10 mM Na2CO3; AS + GABA, 10 mM Na2CO3 + 0.1 mM GABA; mixed saline-alkali stress (MAS), 150 mM NaCl + 10 mM Na2CO3; MAS + GABA, 150 mM NaCl + 10 mM Na2CO3 + 0.1 mM GABA. Our results showed that the inhibitory effects of SS and MAS on the seedling height, root length and root-shoot ratio were significantly alleviated by exogenous GABA. Although soluble sugars, chlorophyll a, total chlorophyll, and superoxide dismutase (SOD) activity were lower in the leaves of the seedlings in the SS treatment compared with the control, these physiological parameters increased significantly after GABA application. Exogenous GABA improved glutathione (GSH) activity in both the leaves and roots of the seedlings during the AS treatment. Additionally, take advantage of GABA led to an increase in ABA, GA and IAA contents in leaves under SS, AS and MAS treatments. Furthermore, the photosynthetic parameters, including Pn, gs, Tr, ETR and qP, significantly increased following the utilization of GABA in both the SS and MAS treatments. Therefore, the application of exogenous GABA can reduce the accumulation of harmful substances, preserve cell morphology, and enhance cell function under saline, alkali, and saline-alkali stress. This enhances the resistance of licorice seedlings to stress conditions and reduces physiological damage.

Identification of osmotic stress resistance mediated by MdKAI2 in apple.

KAR (Karrikin), a novel plant growth regulator, can be recognized specifically by plants and can activate resistance responses. MdKAI2 is the natural receptor of KARs in apple. Here, we report the identification of osmotic stress resistance in MdKAI2 via the method of genetic transformation. The phenotypic traits, resistance indicators, and transcriptional and metabolic regulation of MdKAI2 were identified. KAR1, a highly active form of KAR, markedly promoted the root growth of Gala cultivar tissue culture‒generated plants, possibly through increases in ABA and TZR contents and decreases in the GA3 content. MdKAI2 was markedly upregulated by PEG stress and significantly promoted the growth of apple calli under nonstress conditions, whereas it was significantly inhibited under 20% PEG stress, as was cell death. MdKAI2 significantly increased the content of total flavonoids, the activity of reactive oxygen species (ROS)‒scavenging enzymes (SOD, POD and CAT), and the content of osmoregulatory substances (soluble protein, soluble sugars and proline). It also inhibited the MDA content and conductivity under osmotic stress. Differentially expressed genes (DEGs), including multiple transcription factors (TFs), such as MYB, bHLH and AP2‒EREBP, are significantly regulated by MdKAI2, and genes involved in the mitogen‒activated protein kinase (MAPK) signaling pathway play crucial roles in the regulation of plant resistance. In addition, pathways such as brassinosteroid (BR) biosynthesis and ABC transporters were downregulated, and the MAPK signaling pathway; plant‒pathogen interaction; cutin, suberin and wax biosynthesis; alpha‒linolenic acid metabolism; and phenylpropanoid biosynthesis were upregulated by MdKAI2. MdKAI2 significantly regulates the levels of lipids, amino acids, terpenoids, benzene, organic acids, carbohydrates, and alkaloids and is involved in the metabolic processes of amino acids, carbohydrates, nucleotides, lipids and secondary metabolites. Furthermore, MdKAI2 positively regulates fatty acids, esters, and terpenoids and negatively regulates metabolites of amino acids, amides and alcohols, and the MAPK signaling pathway may mediate this process. The study has provided a new direction for the industrial application of KAR1 in apples and resistance breeding based on the gene of MdKAI2.

14-3-3 Proteins and the Plasma Membrane H+-ATPase Are Involved in Maize (Zea mays) Magnetic Induction.

The geomagnetic field (GMF) is a natural component of the biosphere, and, during evolution, all organisms experienced its presence while some evolved the ability to perceive magnetic fields (MF). We studied the response of 14-3-3 proteins and the plasma membrane (PM) proton pump H+-ATPase to reduced GMF values by lowering the GMF intensity to a near-null magnetic field (NNMF). Seedling morphology, H+-ATPase activity and content, 14-3-3 protein content, binding to PM and phosphorylation, gene expression, and ROS quantification were assessed in maize (Zea mays) dark-grown seedlings. Phytohormone and melatonin quantification were also assessed by LG-MS/MS. Our results suggest that the GMF regulates the PM H+-ATPase, and that NNMF conditions alter the proton pump activity by reducing the binding of 14-3-3 proteins. This effect was associated with both a reduction in H2O2 and downregulation of genes coding for enzymes involved in ROS production and scavenging, as well as calcium homeostasis. These early events were followed by the downregulation of IAA synthesis and gene expression and the increase in both cytokinin and ABA, which were associated with a reduction in root growth. The expression of the homolog of the MagR gene, ZmISCA2, paralleled that of CRY1, suggesting a possible role of ISCA in maize magnetic induction. Interestingly, melatonin, a widespread molecule present in many kingdoms, was increased by the GMF reduction, suggesting a still unknown role of this molecule in magnetoreception.

Developed network between taxoid and phenylpropanoid pathways in Cryptosporiopsis tarraconensis, taxan-producing endophytic fungus by Debiased Sparse Partial Correlation (DSPC) algorithm.

Although bioproduction of Paclitaxel by endophytic fungi is highly considered as an alternative promising source, but its yield is usually very low in comparison with other taxoids. Different strategies i.e., chemical and physical elicitations have been developed in order to overcome the shortage of Paclitaxel production. Paclitaxel biosynthesis is started with terpenoid pathway followed by phenylpropanoid metabolism where a benzoylphenylisoserine moiety is attached to C13 of baccatin III skeleton. This point which is catalyzed by the function of PAM seems to be a bottleneck that limits the rate of Paclitaxel production. Whether phenylpropanoids pathway regulates the taxanes biosynthesis in Cryptosporiopsis tarraconensis endophytic fungus elicited with benzoic acid (BA) was hypothesized in the present paper. The involvement of certain signal molecules and key enzymes of terpenoid and phenylpropanoid metabolism were investigated. According to the results, application of BA promoted a signaling pathway which was started with increase of H2O2 and ABA and continued by increase of NO and MJ, and finally resulted in increase of both phenylpropanoids and taxanes. However, again the rate of Paclitaxel production was lower than other taxoids, and the latter was much lower than phenolics. Therefore, supplying benzoic acid provided the precursor for the common taxan ring production. It is unlikely that Paclitaxel production is merely controlled by side chain production stage. It is more likely that in C. tarraconensis endophytic fungus, similar to Taxus sp., the competition between phenylpropanoid and taxoid pathways for substrate ended in favor of the former. The interaction network which was constructed based on DSPC algorithm confirmed that most compounds with close proximity have shared metabolic pathway relationships. Therefore, it is unlikely that the feeding with a given precursor directly result in increase of a desired metabolite which is composed of different merits.

Atmospheric and soil water deficit induced changes in chemical and hydraulic signals in wheat (Triticum aestivum L.)

AbstractPlant responses to soil drying and the metabolic basis of drought‐induced limitations in stomatal opening are still being discussed. In this study, we investigate the roles of root‐born chemical and hydraulic signals on stomatal regulation in wheat genotypes as affected by soil drought and vapour pressure deficit. Twelve consecutive pot experiments were carried out in a glasshouse. Two bread wheat cultivars (Gönen and Basribey) were subjected to drought under high and low vapour pressure deficit (VPD) in a growth chamber. Total dry matter, specific leaf area, xylem ABA content, xylem osmotic potential, xylem pH, root water potential (RWP), stomatal conductance, leaf ABA content and photosynthetic activity were determined daily during 6 days after the onset of treatments (DAT). In the first phase of drought stress, soil drying induced an increase in the xylem ABA with a peak 3 DAT while RWP drastically decreased during the same period. Then the osmotic potential of leaves decreased and leaf ABA content increased 4 DAT. A similar peak was observed for stomatal conductance during the early stress phase, and it became stable and significantly higher than in well‐watered conditions especially in high vapour deficit conditions (H‐VPD). Furthermore, xylem pH and xylem osmotic potential appeared to be mostly associated with atmospheric moisture content than soil water availability. The results are discussed regarding possible drought adaptation of wheat under different atmospheric humidity.

Effect of Methyl Jasmonate in Gene Expression, and in Hormonal and Phenolic Profiles of Holm Oak Embryogenic Lines Before and After Infection With Phytophthora cinnamomi.

The dieback syndrome affecting Quercus ilex and other oak species impels the search for tolerant plant genotypes, as well as methods of plant immunization against such infections. Elicitation treatments can be an effective strategy to activate plant defense response and embryogenic lines represent a promising tool to generate new tolerant genotypes and also to study early markers involved in defense response. The aim of the presented work was to investigate changes in gene expression, and in hormonal and phenolic profiles induced in three holm oak embryogenic lines (ELs) elicited with methyl jasmonate (MeJA) before and after infection with the oomycete Phytophthora cinnamomi, which is the main biotic agent involved in this pathogenic process. The three ELs, derived from three genotypes, showed different basal profiles in all tested parameters, noting that the VA5 naïve genotype from a scape tree was characterized by a basal higher expression in NADPH-dependent cinnamyl alcohol dehydrogenase (CAD) and chalcone synthase (CHS) genes and also by higher caffeic acid content. Our work also identifies changes triggered by MeJA elicitation in holm oak embryogenic lines, such as increases in ABA and JA contents, as well as in levels of most of the determined phenolic compounds, especially in caffeic acid in Q8 and E00 ELs, but not in their biosynthesis genes. Irrespective of the EL, the response to oomycete infection in holm oak elicited plant material was characterized by a further increase in JA. Since JA and phenols have been described as a part of the Q. ilex defense response against P. cinnamomi, we propose that MeJA may act as an induced resistance (IR) stimulus and that in our embryogenic material induced both direct (detected prior to any challenge) and primed (detected after subsequent challenge) defense responses.

Regulation of the Bud Dormancy Development and Release in Micropropagated Rhubarb 'Malinowy'.

Culinary rhubarb is a vegetable crop, valued for its stalks, very rich in different natural bioactive ingredients. In commercial rhubarb stalk production, the bud dormancy development and release are crucial processes that determine the yields and quality of stalks. To date, reports on rhubarb bud dormancy regulation, however, are lacking. It is known that dormancy status depends on cultivars. The study aimed to determine the dormancy regulation in a valuable selection of rhubarb ‘Malinowy’. Changes in carbohydrate, total phenolic, endogenous hormone levels, and gene expression levels during dormancy development and release were studied in micropropagated rhubarb plantlets. Dormancy developed at high temperature (25.5 °C), and long day. Leaf senescence and dying were consistent with a significant increase in starch, total phenolics, ABA, IAA and SA levels. Five weeks of cooling at 4 °C were sufficient to break dormancy, but rhizomes stored for a longer duration showed faster and more uniformity leaf growing, and higher stalk length. No growth response was observed for non-cooled rhizomes. The low temperature activated carbohydrate and hormone metabolism and signalling in the buds. The increased expression of AMY3, BMY3, SUS3, BGLU17, GAMYB genes were consistent with a decrease in starch and increase in soluble sugars levels during dormancy release. Moreover, some genes (ZEP, ABF2, GASA4, GA2OX8) related to ABA and GA metabolism and signal transduction were activated. The relationship between auxin (IAA, IBA, 5-Cl-IAA), and phenolic, including SA levels and dormancy status was also observed.

Alterations in endogenous hormone levels and energy metabolism promoted the induction, differentiation and maturation of Begonia somatic embryos under clinorotation

The present study provides a visual insight into the effects of simulated microgravity (MG) on somatic embryogenesis (SE) in Begonia through the analysis of phytohormone fluctuations and energy metabolism. To investigate this relationship, thin cell layer culture model was first used. The results showed that MG changed the phytohormone content and stimulated starch biosynthesis to convert into sugar to release energy needed for regeneration and proliferation. Moreover, from the results it is likely that MG accelerated the initiation and subsequently maturation and aging of SE via decrease of AUX and increase of ABA. High content of GA, CKs, starch, sugar and low ABA as well as high CKs/ABA ratio were responsible for the increase in the number of embryos under clinorotation which was 1.57-fold higher than control after 90 days. The increase in fresh and dry weight of somatic embryos and chlorophyll content under MG were confirmed as their adaptive responses to gravitational stress. However, long-term exposure to MG (120 days) stimulated biosynthesis of ABA levels 1.85-fold higher than controls, which resulted in a decrease in chlorophyll content, increase in number of mature embryos and stomata length. These results revealed that MG regulated the induction, differentiation and senescence of somatic embryos via a biochemical interaction pathway.

Morpho-Physiological and Transcriptome Changes in Tomato Anthers of Different Developmental Stages under Drought Stress.

Drought limits the growth and productivity of plants. Reproductive development is sensitive to drought but the underlying physiological and molecular mechanisms remain unclear in tomatoes. Here, we investigated the effect of drought on tomato floral development using morpho-physiological and transcriptome analyses. Drought-induced male sterility through abnormal anther development includes pollen abortion, inadequate pollen starch accumulation and anther indehiscence which caused floral bud and opened flower abortions and reduced fruit set/yield. Under drought stress (DS), pollen mother cell to meiotic (PMC-MEI) anthers survived whereas tetrad to vacuolated uninucleate microspore (TED-VUM) anthers aborted. PMC-MEI anthers had lower ABA increase, reduced IAA and elevated sugar contents under DS relative to well-watered tomato plants. However, TED-VUM anthers had higher ABA increase and IAA levels, and lower accumulation of soluble sugars, indicating abnormal carbohydrate and hormone metabolisms when exposed to drought-stress conditions. Moreover, RNA-Seq analysis identified altogether >15,000 differentially expressed genes that were assigned to multiple pathways, suggesting that tomato anthers utilize complicated mechanisms to cope with drought. In particular, we found that tapetum development and ABA homeostasis genes were drought-induced while sugar utilization and IAA metabolic genes were drought-repressed in PMC-MEI anthers. Our results suggest an important role of phytohormones metabolisms in anther development under DS and provide novel insight into the molecular mechanism underlying drought resistance in tomatoes.

Elevating Ascorbate in Arabidopsis Stimulates the Production of Abscisic Acid, Phaseic Acid, and to a Lesser Extent Auxin (IAA) and Jasmonates, Resulting in Increased Expression of DHAR1 and Multiple Transcription Factors Associated with Abiotic Stress Tolerance.

Gene expression and phytohormone contents were measured in response to elevating ascorbate in the absence of other confounding stimuli such as high light and abiotic stresses. Young Arabidopsis plants were treated with 25 mM solutions of l-galactose pathway intermediates l-galactose (l-gal) or l-galactono-1,4-lactone (l-galL), as well as L-ascorbic acid (AsA), with 25 mM glucose used as control. Feeding increased rosette AsA 2- to 4-fold but there was little change in AsA biosynthetic gene transcripts. Of the ascorbate recycling genes, only Dehydroascorbate reductase 1 expression was increased. Some known regulatory genes displayed increased expression and included ANAC019, ANAC072, ATHB12, ZAT10 and ZAT12. Investigation of the ANAC019/ANAC072/ATHB12 gene regulatory network revealed a high proportion of ABA regulated genes. Measurement of a subset of jasmonate, ABA, auxin (IAA) and salicylic acid compounds revealed consistent increases in ABA (up to 4.2-fold) and phaseic acid (PA; up to 5-fold), and less consistently certain jasmonates, IAA, but no change in salicylic acid levels. Increased ABA is likely due to increased transcripts for the ABA biosynthetic gene NCED3. There were also smaller increases in transcripts for transcription factors ATHB7, ERD1, and ABF3. These results provide insights into how increasing AsA content can mediate increased abiotic stress tolerance.

Timing-dependent effects of salicylic acid treatment on phytohormonal changes, ROS regulation, and antioxidant defense in salinized barley (Hordeum vulgare L.)

Cross-talk between exogenous salicylic acid (SA) and endogenous phytohormone pathways affects the antioxidant defense system and its response to salt stress. The study presented here investigated the effects of SA treatment before and during salt stress on the levels of endogenous plant growth regulators in three barley cultivars with different salinity tolerances: Hordeum vulgare L. cvs. Akhisar (sensitive), Erginel (moderate), and Kalaycı (tolerant). The cultivars’ relative leaf water contents, growth parameters, proline contents, chlorophyll a/b ratios, and lipid peroxidation levels were measured, along with the activities of enzymes involved in detoxifying reactive oxygen species (ROS) including superoxide-dismutase, peroxidase, catalase, ascorbate-peroxidase, and glutathione-reductase. In addition, levels of several endogenous phytohormones (indole-3-acetic-acid, cytokinins, abscisic acid, jasmonic acid, and ethylene) were measured. Barley is known to be more salt tolerant than related plant species. Accordingly, none of the studied cultivars exhibited changes in membrane lipid peroxidation under salt stress. However, they responded differently to salt-stress with respect to their accumulation of phytohormones and antioxidant enzyme activity. The strongest and weakest increases in ABA and proline accumulation were observed in Kalaycı and Akhisar, respectively, suggesting that salt-stress was more effectively managed in Kalaycı. The effects of exogenous SA treatment depended on both the timing of the treatment and the cultivar to which it was applied. In general, however, where SA helped mitigate salt stress, it appeared to do so by increasing ROS scavenging capacity and antioxidant enzyme activity. SA treatment also induced changes in phytohormone levels, presumably as a consequence of SA-phytohormone salt-stress cross-talk.

The control of red colour by a family of MYB transcription factors in octoploid strawberry (Fragaria×ananassa) fruits.

SummaryOctoploid strawberry (Fragaria × ananassa Duch.) is a model plant for research and one of the most important non‐climacteric fruit crops throughout the world. The associations between regulatory networks and metabolite composition were explored for one of the most critical agricultural properties in octoploid strawberry, fruit colour. Differences in the levels of flavonoids are due to the differences in the expression of structural and regulatory genes involved in flavonoid biosynthesis. The molecular mechanisms underlying differences in fruit colour were compared between red and white octoploid strawberry varieties. FaMYB genes had combinatorial effects in determining the red colour of fruit through the regulation of flavonoid biosynthesis in response to the increase in endogenous ABA at the final stage of fruit development. Analysis of alleles of FaMYB10 and FaMYB1 in red and white strawberry varieties led to the discovery of a white‐specific variant allele of FaMYB10, FaMYB10‐2. Its coding sequence possessed an ACTTATAC insertion in the genomic region encoding the C‐terminus of the protein. This insertion introduced a predicted premature termination codon, which suggested the loss of intact FaMYB10 protein playing a critical role in the loss of red colour in white octoploid strawberry.

Involvement of putrescine in osmotic stress-induced ABA signaling in leaves of wheat seedlings

To elucidate one mechanism by which putrescine (Put) functions in plant signaling under osmotic stress, Put and ABA contents, and plasma membrane-NADPH oxidase (PM-NOX) activity were detected in wheat seedling leaves. Under osmotic stress, ABA and Put contents, PM-NOX activity, and PM-NOX-dependent O2.- production all increased. The inhibitor tungstate (T) of ABA bio-synthesis reduced the increases in ABA and Put contents under osmotic stress. The inhibitor D-arginine (D-Arg) of Put bio-synthesis didn't reduce osmotic-induced increase of ABA, but it inhibited the increases of PM-NOX activity and O2 . - production, and the inhibitory effects were reversed by exogenous Put. These findings suggested that ABA might regulate Put biosynthesis, and Put might regulate PM-NOX activity. Treatments with three inhibitors imidazole (I), diphenylene iodonium (DPI) and pyridine (P) of PM-NOX reduced significantly not only O2 . - production, but also the stress-induced increase of Put content, which indicated that O2 . - production might regulate Put biosynthesis. Treatments with EGTA (Ca2+ chelator), La3+ and verapamil (V) (Ca2+ channel blockers) reduced significantly the stress-induced increase of Put content, which suggested that Ca2+ might regulate Put biosynthesis. With these findings, it could be concluded that Put was involved in ABA signaling induced by osmotic stress via regulating PM-NOX activity in wheat seedling leaves.

Fruit Development and ABA Biosynthesis During Caryocar brasiliense (Caryocaraceae) Seed Maturation

Little is currently known about the interactions between structural and physiological factors in Neotropical fruit development. We sought to characterize fruit development and the dynamics of ABA biosynthesis during seed maturation in Caryocar brasiliense, a tree species endemic to the Cerrado biome of Brazil. Biometric evaluations were made of both the pericarp and seed during fruit development. ABA1, NCED4, and NCED9 expression were evaluated in embryonic tissues during seed maturation, as well as anatomical, histochemical, and ultrastructural evaluations, in vitro and ex vitro embryo cultures, and ABA quantifications. Fruit development demonstrated three stages: histodifferentiation (0–40 days after anthesis—DAA); endocarp maturation (40–60 DAA); and the conclusion of mesocarp and seed maturation (60–90 DAA). The embryos showed early degrees of differentiation: hypocotyl expansion, development of the leaf primordia, and vascularization. Seed maturation occurred (from 40 DAA) concomitantly with the development of endocarp aculei in four phases influenced by ABA dynamics. The beginning of reserve deposition and the acquisition of dehydration tolerance were related to increases in extra-embryonic ABA. ABA biosynthesis at the radicular pole was related to increased reserve deposition and dehydration tolerance (which was not associated with the occurrence of a desiccation phase). The maturation of C. brasiliense seeds is influenced by embryonic and extra-embryonic ABA, and the dormancy of the pyrenes results from the interaction of the effects of that hormone and pericarp tissue.

Effects of CEPA and 1-MCP on Flower Bud Differentiation of Apple cv. ‘Nagafu No.2’ Grafted on Different Rootstocks

The apple (Malus domestica Borkh.) has a relatively long sapling stage which prevents fruit breeding. The understanding of the flowering system is important to improve breeding efficiency in apple. In this context, 2-year-old “Fuji” apple cv. “Nagafu No.2” trees were grafted onto dwarf self-rooted rootstock M.26, vigorous rootstock M. sieversii and interstock M.26/M. sieversii, respectively. Trees were sprayed with clean water (as controls), 800 mg·L−1 2-chloroethylphosphonic acid (CEPA), and 2 µL·L−1 1-methylcyclopropene (1-MCP). The results showed that CEPA significantly repressed the vegetative growth attributed to the increase of ABA and ZT synthesis, and the decrease of IAA synthesis in leaves and buds. However, there was no significant difference or significant inverse effect between 1-MCP and control. Furthermore, CEPA promoted flower formation, increased the flowering rate, and advanced the blossom period for 2 days compared with the control, which was accompanied by the accumulation of soluble sugar, glucose, and sucrose; and the increase of α-amylase and sucrose phosphate synthase activities; and the decrease of starch contents and sucrose synthase activities in leaves and buds. However, the blossom period was delayed for 2 days after spraying with 1-MCP. Finally, the expression of TFL1 was significantly repressed, whereas AP1 was significantly promoted in buds from M.26 and M.26/M. sieversii after spraying with CEPA, whereas the effect was not significant from M. sieversii. However, the expression levels of TFL1 and AP1 were not significantly different from the control after the application of 1-MCP. In spite of this, CEPA was more susceptible to easy-flowering M.26, followed by M.26/M. sieversii, and still less susceptible to difficult-flowering rootstock M. sieversii.

Physiological and Metabolic Responses Triggered by Omeprazole Improve Tomato Plant Tolerance to NaCl Stress.

Interest in the role of small bioactive molecules (< 500 Da) in plants is on the rise, compelled by plant scientists' attempt to unravel their mode of action implicated in stimulating growth and enhancing tolerance to environmental stressors. The current study aimed at elucidating the morphological, physiological and metabolomic changes occurring in greenhouse tomato (cv. Seny) treated with omeprazole (OMP), a benzimidazole inhibitor of animal proton pumps. The OMP was applied at three rates (0, 10, or 100 μM) as substrate drench for tomato plants grown under nonsaline (control) or saline conditions sustained by nutrient solutions of 1 or 75 mM NaCl, respectively. Increasing NaCl concentration from 1 to 75 mM decreased the tomato shoot dry weight by 49% in the 0 μM OMP treatment, whereas the reduction was not significant at 10 or 100 μM of OMP. Treatment of salinized (75 mM NaCl) tomato plants with 10 and especially 100 μM OMP decreased Na+ and Cl− while it increased Ca2+ concentration in the leaves. However, OMP was not strictly involved in ion homeostasis since the K+ to Na+ ratio did not increase under combined salinity and OMP treatment. OMP increased root dry weight, root morphological characteristics (total length and surface), transpiration, and net photosynthetic rate independently of salinity. Metabolic profiling of leaves through UHPLC liquid chromatography coupled to quadrupole-time-of-flight mass spectrometry facilitated identification of the reprogramming of a wide range of metabolites in response to OMP treatment. Hormonal changes involved an increase in ABA, decrease in auxins and cytokinin, and a tendency for GA down accumulation. Cutin biosynthesis, alteration of membrane lipids and heightened radical scavenging ability related to the accumulation of phenolics and carotenoids were observed. Several other stress-related compounds, such as polyamine conjugates, alkaloids and sesquiterpene lactones, were altered in response to OMP. Although a specific and well-defined mechanism could not be posited, the metabolic processes involved in OMP action suggest that this small bioactive molecule might have a hormone-like activity that ultimately elicits an improved tolerance to NaCl salinity stress.

Overexpression of RcFUSCA3, a B3 transcription factor from the PLB in Rosa canina, activates starch accumulation and induces male sterility in Arabidopsis

A homologue of the Arabidopsis gene FUSCA3 (FUS3), isolated from the protocorm-like body (PLB) of Rosa canina and designated RcFUS3, encodes 331 amino acid residues. It was shown that RcFUS3 is specifically expressed in the PLB of R. canina and that its subcellular localization is in the nucleus. The Arabidopsis fus3-3 mutant phenotype could be rescued by over-expression of RcFUS3, suggesting that RcFUS3 has a function similar to that of Arabidopsis FUS3. Over-expression of RcFUS3 in wild type Arabidopsis resulted in a decrease in endogenous GA and CTK levels, an increase in ABA and IAA contents, starch grain accumulation in the cotyledon and hypocotyl, failure of cotyledon extension and abnormal elongation of the hypocotyl, abnormal stomatal and pavement cells, an increase in branch numbers, prolongation of the growth cycle, and morphological changes in floral organs. Interestingly, over-expression of RcFUS3 in homozygous form resulted in premature degradation of the tapetum, indehiscent anthers and hypogenetic stamens, causing complete male sterility in Arabidopsis; this is the first observation that over-expression of a gene (RcFUS3) homologous to FUS3 can lead to male sterility and starch grain accumulation in Arabidopsis.

Wheat and rye genome confer specific phytohormone profile features and interplay under water stress in two phenotypes of triticale

The aim of the experiment was to determine phytohormone profile of triticale and quality-based relationships between the analyzed groups of phytohormones. The study involved two triticale phenotypes, a long-stemmed one and a semi-dwarf one with Dw1 gene, differing in mechanisms of acclimation to drought and controlled by wheat or rye genome.Water deficit in the leaves triggered a specific phytohormone response in both winter triticale phenotypes attributable to the dominance of wheat (semi-dwarf cultivar) or rye (long-stemmed cultivar) genome. Rye genome in long-stemmed triticale was responsible for specific increase (tillering: gibberellic acid; heading: N6-isopentenyladenine, trans-zeatin-9-riboside, cis-zeatin-9-riboside; flowering: N6-isopentenyladenine, indolebutyric acid, salicylic acid) or decrease (heading: trans-zeatin) in the content of some phytohormones. Wheat genome in semi-dwarf triticale controlled a specific increase in trans-zeatin content at heading and anthesis in gibberellin A1 during anthesis. The greatest number of changes in the phytohormone levels was observed in the generative phase. In both triticale types, the pool of investigated phytohormones was dominated by abscisic acid and gibberellins. The semi-dwarf cultivar with Dw1 gene was less sensitive to gibberellins and its mechanisms of acclimation to water stress were mainly ABA-dependent. An increase in ABA and gibberellins during drought and predominance of these hormones in the total pool of analyzed phytohormones indicated their equal share in drought acclimation mechanisms in long-stemmed cultivar.