RESUMEN
In barley, incubation of primary dormant (D1) grains on water under conditions that do not allow germination, i.e. 30°C in air and 15°C or 30°C in 5% O2, induces a secondary dormancy (D2) expressed as a loss of the ability to germinate at 15°C in air. The aim of this study was to compare the proteome of barley embryos isolated from D1 grains and D2 ones after induction of D2 at 30°C or in hypoxia at 15°C or 30°C. Total soluble proteins were analyzed by 2DE gel-based proteomics, allowing the selection of 130 differentially accumulated proteins (DAPs) among 1,575 detected spots. According to the protein abundance profiles, the DAPs were grouped into six abundance-based similarity clusters. Induction of D2 is mainly characterized by a down-accumulation of proteins belonging to cluster 3 (storage proteins, proteases, alpha-amylase inhibitors and histone deacetylase HD2) and an up-accumulation of proteins belonging to cluster 4 (1-Cys peroxiredoxin, lipoxygenase2 and caleosin). The correlation-based network analysis for each cluster highlighted central protein hub. In addition, most of genes encoding DAPs display high co-expression degree with 19 transcription factors. Finally, this work points out that similar molecular events accompany the modulation of dormancy cycling by both temperature and oxygen, including post-translational, transcriptional and epigenetic regulation.
Asunto(s)
Hordeum , Ácido Abscísico/metabolismo , Epigénesis Genética , Germinación , Hordeum/metabolismo , Hipoxia/genética , Hipoxia/metabolismo , Oxígeno/metabolismo , Latencia en las Plantas/fisiología , Proteínas de Plantas/genética , Proteínas de Plantas/metabolismo , Proteómica , Semillas/metabolismo , TemperaturaRESUMEN
Well-aligned zinc oxide nanorods (WA-ZnO Nrods) with different lengths were synthesized and the effects of the growth times on the optical, morphological, and electrical properties of the WA-ZnO Nrods were examined. We also investigated the application of WA-ZnO Nrods as an electron transport layer (ETL) and tungsten trioxide (WO3) as a hole transport layer (HTL) to vacuum free hybrid photovoltaic (HPV) performance. The eutectic gallium-indium (EGaIn) alloy was used as a top electrode coated using a brush-painting method. A device with the structure of indium tin oxide (ITO)/WA-ZnO Nrods/(P3HT:PCBM)/WO3/EGaIn was optimized and fabricated. The maximum power conversion efficiency (PCE) was ~4.5%. Improvement of the device performance indicates that the well-aligned ZnO Nrods and WO3 can effectively be applied as charge carrier transport layer for vacuum free hybrid (HPV).
RESUMEN
Germination of primary dormant barley grains is promoted by darkness and temperatures below 20 °C, but is strongly inhibited by blue light. Exposure under blue light at 10 °C for periods longer than five days, results in a progressive inability to germinate in the dark, considered as secondary dormancy. We demonstrate that the inhibitory effect of blue light is reinforced in hypoxia. The inhibitory effect of blue light is associated with an increase in embryo abscisic acid (ABA) content (by 3.5- to 3.8-fold) and embryo sensitivity to both ABA and hypoxia. Analysis of expression of ABA metabolism genes shows that increase in ABA mainly results in a strong increase in HvNCED1 and HvNCED2 expression, and a slight decrease in HvABA8'OH-1. Among the gibberellins (GA) metabolism genes examined, blue light decreases the expression of HvGA3ox2, involved in GA synthesis, increases that of GA2ox3 and GA2ox5, involved in GA catabolism, and reduces the GA signalling evaluated by the HvExpA11 expression. Expression of secondary dormancy is associated with maintenance of high embryo ABA content and a low HvExpA11 expression. The partial reversion of the inhibitory effect of blue light by green light also suggests that cryptochrome might be involved in this hormonal regulation.
Asunto(s)
Germinación/efectos de la radiación , Hordeum/efectos de la radiación , Oxígeno/metabolismo , Reguladores del Crecimiento de las Plantas/metabolismo , Ácido Abscísico/metabolismo , Regulación de la Expresión Génica de las Plantas/efectos de la radiación , Giberelinas/metabolismo , Hordeum/crecimiento & desarrollo , Hordeum/metabolismo , Semillas/crecimiento & desarrollo , Semillas/efectos de la radiación , Transducción de Señal , TemperaturaRESUMEN
In barley, primary dormant grains did not germinate at 30 °C in air and at 15 °C in an atmosphere containing less than 10% O2, while they germinated easily at 15 °C in air. O2 tension in embryos measured with microsensors was 15.8% at 15 °C but only 0.3% at 30 °C. Incubation of grains at 30 °C is known to induce secondary dormancy in barley, and it was shown here that secondary dormancy was also induced by a 3 d treatment in O2 tensions lower than 10% at 15 °C. After such treatments, the grains lost their ability to germinate subsequently at 15 °C in air. During seed treatment in 5% O2, embryo abscisic acid (ABA) content decreased more slowly than in air and was not altered after transfer into air. Hypoxia did not alter the expression of ABA metabolism genes after 1 d, and induction of HvNCED2 occurred only after 3 d in hypoxia. Embryo sensitivity to ABA was similar in both primary and hypoxia-induced secondary dormant grains. Gibberellic acid (GA) metabolism genes were highly regulated and regulated earlier by the hypoxia treatment, with major changes in HvGA2ox3, HvGA3ox2 and HvGA20ox1 expression after 1 d, resulting in reduced GA signalling. Although a high temperature has an indirect effect on O2 availability, the data showed that it did not affect expression of prolyl-4-hydroxylases and that induction of secondary dormancy by hypoxia at 15 °C or by high temperature in air involved separate signalling pathways. Induction by hypoxia at 15 °C appears to be more regulated by GA and less by ABA than the induction by high temperature.
Asunto(s)
Hordeum/metabolismo , Hordeum/fisiología , Semillas/metabolismo , Semillas/fisiología , Ácido Abscísico/farmacología , Hipoxia de la Célula/efectos de los fármacos , Hipoxia de la Célula/fisiología , Germinación/efectos de los fármacos , Germinación/genética , Giberelinas/farmacología , Hordeum/efectos de los fármacos , Proteínas de Plantas/genética , Proteínas de Plantas/metabolismo , Semillas/efectos de los fármacos , Transducción de Señal/efectos de los fármacos , TemperaturaRESUMEN
Primary dormant barley (Hordeum vulgare) grains germinate at 10-15°C but not at 30°C, and there exist a positive correlation between embryo ABA content after 24 h on water and the depth of dormancy. Incubation at 30°C results in a progressive loss of the ability to germinate at 15°C. This induction of a secondary dormancy is optimal after 3 days and requires an embryo water content higher than 0.50 g H2O g⻹ DW, this corresponding with activation of the cell cycle. There exists no correlation between ABA content after 3 days at 30°C and the induction of secondary dormancy. However, at high water content (1.60-1.87 g H2O g⻹ DW), secondary dormancy is associated with an high embryo ABA content after transfer to 15°C, resulting from an increase in HvNCED1 and HvNCED2 expression and a decrease in HvABA8'OH-1. Such changes are not observed at 0.45 g H2O g⻹ DW. Incubation at 30°C also results in an increase in expression of genes involved in GA catabolism (HvGA2ox1, HvGA2ox3 and HvGA2ox5) and synthesis (HvGA3ox2, HvGA20ox1 and HvGA20ox3). The HvGA3ox2/HvGA2ox3 transcript ratio remains low (0.27-0.37) at 30°C and after transfer to 15°C in secondary dormant seeds, but it is higher than two when secondary dormancy is not induced. Changes in HvExpA11 expression indicate that GA signaling decreases when a secondary dormancy is expressed. Our results clearly indicate that expression of genes involved in ABA and GA metabolism differs in primary and secondary dormancies and furthermore, their expression is related to embryo water content.
Asunto(s)
Ácido Abscísico/metabolismo , Giberelinas/metabolismo , Hordeum/fisiología , Reguladores del Crecimiento de las Plantas/metabolismo , Semillas/fisiología , Agua/fisiología , Regulación de la Expresión Génica de las Plantas , Germinación/fisiología , Hordeum/genética , Hordeum/metabolismo , Latencia en las Plantas/fisiología , Proteínas de Plantas/genética , Proteínas de Plantas/metabolismo , ARN Mensajero/genética , ARN Mensajero/metabolismo , ARN de Planta/genética , Semillas/genética , Semillas/metabolismo , Transducción de Señal , Temperatura , Agua/análisisRESUMEN
Freshly harvested seeds of Arabidopsis thaliana, Columbia (Col) accession were dormant when imbibed at 25°C in the dark. Their dormancy was alleviated by continuous light during imbibition or by 5 weeks of storage at 20°C (after-ripening). We investigated the possible role of reactive oxygen species (ROS) in the regulation of Col seed dormancy. After 24 h of imbibition at 25°C, non-dormant seeds produced more ROS than dormant seeds, and their catalase activity was lower. In situ ROS localization revealed that germination was associated with an accumulation of superoxide and hydrogen peroxide in the radicle. ROS production was temporally and spatially regulated: ROS were first localized within the cytoplasm upon imbibition of non-dormant seeds, then in the nucleus and finally in the cell wall, which suggests that ROS play different roles during germination. Imbibition of dormant and non-dormant seeds in the presence of ROS scavengers or donors, which inhibited or stimulated germination, respectively, confirmed the role of ROS in germination. Freshly harvested seeds of the mutants defective in catalase (cat2-1) and vitamin E (vte1-1) did not display dormancy; however, seeds of the NADPH oxidase mutants (rbohD) were deeply dormant. Expression of a set of genes related to dormancy upon imbibition in the cat2-1 and vet1-1 seeds revealed that their non-dormant phenotype was probably not related to ABA or gibberellin metabolism, but suggested that ROS could trigger germination through gibberellin signaling activation.