Retardation of leaf senescence by urea cytokinins in Raphanus sativus

Approximately 500 urea derivatives and related compounds were tested for ability to retard leaf senescence as measured by chlorophyll retention in radish (Raphanus sativus) leaf discs. Of the 90 compounds found to be active, some had activity at 10^?6 M of the same order as kinetin. There was a high correlation between ability to promote chlorophyll retention and initiation of cell division. Highly active compounds had a planar ring and a HNCONH bridge; substitution with a HNCSNH bridge reduced activity and all other tested arrangements of the bridge gave inactive compounds. Substitution of both amino hydrogen atoms on one or both sides of the bridge reduced or removed activity. Some N′-substituted phenyl ureas were highly active. Introduction of a N-phenyl ring to a N-phenyl urea increased activity except where one ring was substituted in the para position with chloro, bromo or iodo. The activities of symmetrical disubstituted ureas were generally less than the corresponding N-monosubstituted derivative. The results suggest that the receptor site for cytokinin activity is the same for senescence retadation and cell division initiation.     

Differential changes in the synthesis and steady-state levels of thylakoid proteins during bean leaf senescence

During senescence of primary bean leaves (Phaseolus vulgaris), there are differential changes in the rates at which thylakoid proteins are synthesized. In particular, synthesis of the 32 kD herbicide-binding protein continues throughout senescence, whereas formation of the and subunits of ATPase, the 68 kD photosystem I reaction center polypeptide, cytochrome f, cytochrome b₆ and the structural apoprotein of the lightharvesting chlorophyll protein complex (LHCP) declines. Pulse-chase experiments with intact leaves indicated rapid degradation of the 32 kD protein, which is consistent with its known rapid rate of turnover. This degradation was light-dependent and inhibited by DCMU, and the kinetics of degradation were similar for young and senescent membranes. In Coomassie-stained gels, the 68 kD reaction center polypeptide of photosystem I, the and subunits of ATPase and the LHCP were the dominant proteins for all ages of membranes. Western blot analysis indicated that cytochrome f and cytochrome b₆ are selectively depleted during senescence. The data have been interpreted as indicating that translational disruptions in both the cytoplasmic and chloroplastic compartments may contribute to the decline in photosynthetic electron transport in the senescing leaf.     

Altered protein synthesis during in situ oat leaf senescence

Quantitative and qualitative changes in protein synthesis during in situ senescence of oat ( Avena saliva L. cv. Victory) leaf have been examined. The rate of protein synthesis shows a transitory increase during early stages of senescence. This increase is not accompanied by a corresponding increase in amino acid uptake and is smaller when expressed on a dry weight rather than a protein basis. Total protein, total RNA and poly(A)⁺-RNA decline rapidly during senescence. Analysis of protein populations with 2-D SDS-PAGE shows that while some proteins decline sharply during leaf senescence, the synthesis of several others is induced or enhanced. Synthesis of new proteins shown in this study may explain the reported requriement for protein synthesis in leaf senescence.     

Retardation of Leaf Senescence by Triadimefon Treatment in Mung Bean Seedling

Treatment of triadimefon on detached leaves of mung bean (Phaseolus radiatus L. ) seedlings increased the levels of chlorophyll and soluble proteins. Declined activities of superoxide dismutase (SOD), peroxidase (POD), catalase (CAT) and ascorbate-peroxidase (AsA-POD) and contents of ascorbate (ASA) and glutathione (GSH) were observed during the senescence of detached young leaves. Triadimefon at concentration of 20 mg/L promoted the activities of POD, AsA-POD and levels of AsA and GSH, but had no effect on the activities of SOD and CAT. On the other hand, the levels of malondialdehyde (MDA) were increased and the increase of which was markedly negative correlated with the activities of POD, AsA-POD and with the contents of AsA and GSH during the senescence of leaves. MDA contents were decreased by triadimefon treatment. These resuits suggested that triadimefon retarded the senescence of leaves in mung bean seedlings in terms of enhancing the protective ability of plant tissues against membrane lipid peroxidation.     

镍对离体玉米叶片衰老的调节作用

本文研究了镍对离体玉米叶片衰老的调节作用。研究结果表明,玉米叶片在衰老过程中,超氧化物歧化酶（ＳＯＤ）、过氧化物酶（ＰＯＤ）过氧化氢酶（ＣＡＴ）、抗坏血酸过氧化物酶（ＡsＳ－ＰＯＤ）活性和抗坏血酸（ＡsA)含量显著降低,超氧阴离子自由基（Ｏ^-2)产生率显著增加,脂质过氧化作用加剧,丙二醛（ＭＤＡ）含量升高,细胞质膜透性增大。而１０^-2、１０^-3mol.L^-1Ni^2 处理能增强上述保护酶活性和抗氧化剂ＡsA的含量从而能减轻细胞膜脂过氧化使用。２０^-3、１０^-2mol.L^-1Ni^2 处理能显著延缓蛋白质和叶绿素 降解。因此镍能延缓离体玉米叶片的衰老,尤其是以１０^-2mol.L^-1Ni^2 对衰老的延缓作用更大。动态测定结果表明,１０^-2mol.L^-1Ni^2 处理能使衰老滞后２－天。     

Effect of source-sink relations and nitrogen nutrition on senescence and N remobilization in the flag leaf of wheat

The relation between the source-sink ratio and nitrogen nutrition on grain yield of wheat ( Triticum aestivum L. cv. Klein Chamaco) was studied in a greenhouse experiment. Plants were grown until anthesis in pots with soil fertilized with 0.16 mmol N per plant twice a week. At anthesis, all leaves but the flag leaf were excised in a group of plants. In another group the treatment consisted in a similar defoliation plus the longitudinal excision of half the ear, while a third group was left untouched as a control. At the same time, the N supply to half of the plants in each group was interrupted, while the other half continued receiving 16 m M N. The defoliated plants showed a longer functional life of the flag leaf than the control, retaining the chlorophyll, soluble proteins and total reduced nitrogen for a longer time. The ear-excised plants showed an intermediate behavior. The plants with the interrupted N supply showed a faster leaf senescence than the N supplied ones, and this coincided with an increase in the proteolytic activity and nitrogen transport to the ear. However there were no differences in ear weight between the two nitrogen treatments. It is concluded that leaves and ear compete for the nitrogen, and that a low level of carbohydrates in the flag leaf, due to a low source-sink ratio, delays leaf senescence.     

Retardation of leaf senescence by benzyladenine in intact bean plants

Summary Benzyladenine (BA) applied to primary leaves of intact bean plants delayed the senescence of both the leaves and the entire shoot. The retardation of senescence was manifested in higher levels of chlorophyll, protein, RNA and ribonuclease activity at all stages of development. Also, the levels of incorporation of labelled precursors into protein and RNA were enhanced. The effect of BA was largely independent of light intensity and the compound did not act merely as a nitrogen source.     

Iron deficiency in rice shoots: identification of novel induced genes using RDA and possible relation to leaf senescence

Rice plants are highly susceptible to Fe-deficiency. Under nutrient deprivation, plant cells undergo extensive metabolic changes for their continued survival. To provide further insight into the pathways induced during Fe-deficiency, rice seedlings were grown for 3, 6 and 9 days in the presence or absence of Fe. Using RDA (Representational Difference Analysis), sequences of 32 induced genes in rice shoots under Fe-deficiency were identified. About 30% of the sequences found have been previously reported as responsive to other abiotic and even biotic stresses. However, this is the first report that indicates their relation to Fe deprivation. Differential expression of selected genes was confirmed by semi-quantitative RT-PCR analysis. The identification of classical senescence-related sequences, such as lipase EC 3.1.1.-, ubiquitin-conjugating enzyme EC 6.3.2.19, beta-Glucosidase EC 3.2.1.21 and cysteine synthase EC 2.5.1.47, besides the higher accumulation of total soluble sugars prior to the decrease of total chlorophyll content in Fe-deficient leaves, indicate that sugar accumulation may be one of the factors leading to premature leaf senescence induced by Fe-deficiency.     

Time-course of programmed cell death during leaf senescence in <Emphasis Type="Italic">Eucommia ulmoides</Emphasis>

Leaves of Eucommia ulmoides Oliv. harvested between April to November were examined for programmed cell death (PCD) during growth and senescence. Leaves developed in April, becoming fully expanded in late May, remaining unchanged until November when they started to dehisce. Falling leaves retained a green color. Our results showed that (1) mesophyll cells gradually reduced their nuclei from September to November, (2) positive TUNEL signals appeared on the nuclei from August, (3) ladder-like DNA fragmentation occurred in September and October, and (4) a 20-kDa Ca²⁺-dependent DNase appeared in these same months. In fallen leaves, intact mesophyll cell nuclei could not be detected, but a few cells around the vascular bundle had nuclei. Therefore, (1) programmed cell death (PCD) of leaf cells occurred in the leaves of E. ulmoides, (2) the progress of mesophyll cell PCD lasted for more than 2 months, and (3) PCD of leaf cells was asynchronous in natural senescing leaves. Electronic Publication     

Identification and functional characterization of a leucine-rich repeat receptor-like kinase gene that is involved in regulation of soybean leaf senescence

We report here the cloning and characterization of a soybean receptor-like kinase (RLK) gene, designated GmSARK (Glycine max senescence-associated receptor-like kinase), which is involved in regulating leaf senescence. The conceptual protein product of GmSARK contains typical domains of LRR receptor-like kinases: a cytoplasmic domain with all the 11 kinase subdomains, a transmembrane domain and an extracelullar domain containing 9 Leucine-Rich Repeat (LRR) units that may act as a receptor. The expression of GmSARK in soybean leaves was up-regulated in all the three tested senescence systems: senescing cotyledons, dark-induced primary leaf senescence and the natural leaf senescence process after florescence. Furthermore, the RNA interference (RNAi)-mediated knocking-down of GmSARK dramatically retarded soybean leaf senescence. A more complex thylakoid membrane system, higher foliar level of chlorophyll content and a very remarkable delay of senescence-induced disintegration of chloroplast structure were observed in GmSARK-RNAi transgenic leaves. A homolog of maize lethal leaf-spot 1 gene, which has been suggested to encode a key enzyme catalyzing chlorophyll breakdown, was isolated and nominated Gmlls1. The expression level of Gmgtr1 gene, which encodes a key enzyme of chlorophyll synthesis, was also analyzed. It was found that Gmlls1 was up-regulated and Gmgtr1 was down-regulated during senescence in wild-type soybean leaves. However, both of the up-regulation of Gmlls1 and down-regulation of Gmgtr1 were retarded during senescence of GmSARK-RNAi transgenic leaves. In addition, over-expression of the GmSARK gene greatly accelerated the senescence progression of CaMV 35S:GmSARK transgenic plants. Taken together, these results strongly suggested the involvement of this LRR-RLK in regulation of soybean leaf senescence, maybe via regulating chloroplast development and chlorophyll accumulation. Multiple functions of GmSARK besides its regulation of leaf senescence were also discussed. Electronic Supplementary Material Supplementary material is available for this article at Rui Gan, Peng-Li Li and Yuan-Yuan Ma contributed equally to this work.     

Retardation of bean leaf senescence by benzyladenine and its influence on phosphate metabolism

The levels of glucose, sugar phosphates, and adenosine phosphates were determined in primary leaves of intact bean plants during normal senescence and compared to leaves in which senescence was delayed by application of benzyladenine (BA). In both cases there was a rise with time in the levels of glucose 1-phosphate, glucose 6-phosphate, and fructose 6-phosphate, and a decline in 2-phosphoglyceric acid, inorganic phosphate, and the adenosine phosphates (AMP, ADP, ATP). The levels of fructose 1,6-diphosphate remained fairly constant. Although the levels of hexose phosphates, adenosine phosphates, and inorganic phosphate were lower in the BA-treated leaves, the incorporation of ³²P into these compounds by 3- and 6-week-old plants was higher than in the controls. These results suggest that the retardation of leaf senescence by BA in intact bean plants is associated with increased utilization of metabolites, indicating a more rapid turnover of the adenosine phosphates. It is concluded that this effect is brought about by a regulatory coordination of metabolic processes in relation to energy production and utilization.     

Earlier leaf senescence dates are constrained by soil moisture

The unprecedented warming that has occurred in recent decades has led to later autumn leaf senescence dates (LSD) throughout the Northern Hemisphere. Yet, great uncertainties still exist regarding the strength of these delaying trends, especially in terms of how soil moisture affects them. Here we show that changes in soil moisture in 1982–2015 had a substantial impact on autumn LSD in one-fifth of the vegetated areas in the Northern Hemisphere (>30° N), and how it contributed more to LSD variability than either temperature, precipitation or radiation. We developed a new model based on soil-moisture-constrained cooling degree days (CDD_SM) to characterize the effects of soil moisture on LSD and compared its performance with the CDD, Delpierre and spring-influenced autumn models. We show that the CDD_SM model with inputs of temperature and soil moisture outperformed the three other models for LSD modelling and had an overall higher correlation coefficient (R), a lower root mean square error and lower Akaike information criterion (AIC) between observations and model predictions. These improvements were particularly evident in arid and semi-arid regions. We studied future LSD using the CDD_SM model under two scenarios (SSP126 and SSP585) and found that predicted LSD was 4.1 ± 1.4 days and 5.8 ± 2.8 days earlier under SSP126 and SSP585, respectively, than other models for the end of this century. Our study therefore reveals the importance of soil moisture in regulating autumn LSD and, in particular, highlights how coupling this effect with LSD models can improve simulations of the response of vegetation phenology to future climate change.     

Effects of growth temperature and winter duration on leaf phenology of Erythronium japonicum,a forest spring geophyte

The effects of growth temperature and winter duration on the leaf phenology of Erythronium japonicum were examined in two experiments. Bulbs wintered in the field were cultivated at 10 and 20° C and the bulbs were cultivated at 15° C after chilling treatment at 3° C for 60 and 120 days and without chilling in winter. The plants cultivated at 20° C showed significantly earlier leaf emergence, a more rapid rate of leaf extension and shorter leaf longevity than those cultivated at 10° C. The decrease in the leaf longevity at 20° C resulted from the decreases in the durations of all of the developmental, mature, and senescent phases. The bulbs without chilling treatment did not sprout leaves and those with chilling treatment sprouted leaves. The increase in the length of chilling treatment from 60 to 120 days affected leaf phenology in same manner as the increase in the growth temperature from 10 to 20° C.     

Cytokinin inhibition of leaf senescence

The senescence delaying effect of cytokinin is well known, however, the details behind how this process occurs remain unclear. Efforts to improve understanding of this phenomenon have led to the identification in Arabidopsis of specific cytokinin signaling components through which senescence signal responses are regulated. These include the cytokinin receptor (AHK3), the type-B response regulator (ARR2) and the recently identified cytokinin response factor (CRF6). At the mechanistic end of this process, it was found that increased cell-wall invertase activity which occurs in response to cytokinin is both necessary and sufficient for the inhibition of senescence. Yet, a direct link between the signaling and mechanistic steps of a cytokinin regulated senescence process has yet to be demonstrated. This may be in part because the relationship between senescence and primary metabolism implied by the key role of cell-wall invertase is the subject of two apparently opposing bodies of evidence. Here we briefly summarize and propose a model in which cytokinin mediated changes in sink/source relationships leads to delayed senescence which is consistent with existing evidence both for and against sugars as a trigger for developmental senescence.     

Retardation of soybean leaf senescence and associated effects on seed composition

Soybean leaf senescence, leaf abscission, and pod yellowing were markedly delayed by sprays of 10^–4 M 6-benzylamino-9-(tetrahydropyran-2-yl)purine plus 5×10^–5 M -naphthalene acetic acid. The pods on the sprayed plants turned yellow 5–7 days later than those on the control plants, and the treated leaves remained dark green even when the pods had already desiccated. The antisenescence spray did not change pod numbers, seed numbers, seed size, or the yield. By retarding senescence, seed nitrogen content was increased in both TCA-soluble and TCA-insoluble fractions. Seed total protein, buffer-extractable total protein, and globulin were increased by 26, 28, and 33 mg/g of seed flour, respectively, and albumin was decreased by 6 mg/g. The overall increase in seed protein caused by spray treatment is confined to the globulin portion.     

Trans-translation and protein synthesis inhibitors

Trans-translation is a process found in all bacteria, which contributes to the release of ribosomes that are stalled through a variety of causes, for example when the 3' end of a truncated mRNA lacking a stop codon is reached or at internal clusters of rare codons. Trans-translation requires tmRNA. Trans-translation is not essential for cell viability under laboratory conditions, but recently it has been shown that it can contribute to cell viability in the presence of protein synthesis inhibitors. In this minireview, we consider the connection between trans-translation and antibiotics and the potential of using trans-translation as a therapeutic target.