Die and let live: leaf senescence contributes to plant survival under drought stress

2004 ◽  
Vol 31 (3) ◽  
pp. 203 ◽  
Author(s):  
Sergi Munné-Bosch ◽  
Leonor Alegre

Leaf senescence is a highly regulated physiological process that leads to leaf death and is, as such, the last developmental stage of the leaf. Plant aging and environmental stresses may induce the process of senescence. Here we will focus on the role of leaf senescence in field-grown plants as a response to adverse climatic conditions and, more specifically, on how it contributes to plant survival under drought stress. Drought induces several responses in plants including leaf senescence, which plays a major role in the survival of several species. Drought-induced leaf senescence contributes to nutrient remobilisation during stress, thus allowing the rest of the plant (i.e. the youngest leaves, fruits or flowers) to benefit from the nutrients accumulated during the life span of the leaf. In addition, drought-induced leaf senescence, especially when accompanied by leaf abscission, avoids large losses through transpiration, thus contributing to the maintenance of a favourable water balance of the whole plant. Drought-induced leaf senescence occurs gradually and is characterised by specific macroscopic, cellular, biochemical and molecular changes. Leaf yellowing (i.e. chlorophyll degradation) and specific changes in cell ultrastructure (e.g. chromatin condensation, thylakoid swelling, plastoglobuli accumulation), metabolism (e.g.�protein degradation, lipid peroxidation) and gene expression occur during leaf senescence in drought-stressed plants. Cytokinins and ABA have been shown to be involved in the regulation of drought-induced leaf senescence, although the possible role of other plant hormones should not be excluded. Reactive oxygen species, whose concentrations increase during drought-induced leaf senescence, are also known to be regulators of this process. The complex mechanisms of regulation of leaf senescence in drought-stressed plants are discussed, and attention is drawn to those aspects that still require investigation.

Author(s):  
Alice Gauthey ◽  
Jennifer Peters ◽  
Rosana López ◽  
Madeline Carins Murphy ◽  
Celia M. Rodriguez-Dominguez ◽  
...  

The mechanisms by which woody plants recover xylem hydraulic capacity after drought stress are not well understood, particularly with regard to the role of embolism refilling. We evaluated the recovery of xylem hydraulic capacity in young Eucalyptus saligna plants exposed to cycles of drought stress and rewatering. Plants were exposed to moderate and severe drought stress treatments, with recovery monitored at time intervals from 24 hrs to 6 months after rewatering. The percentage loss of xylem vessels due to embolism (PLV) was quantified at each time point using micro-computed tomography with stem water potential (Ψx) and whole plant transpiration (Eplant) measured prior to scans. Plants exposed to severe drought stress suffered high levels of embolism (47.38 ± 10.97 % PLV) and almost complete canopy loss. No evidence of embolism refilling was observed at 24 hrs, one week, or three weeks after rewatering despite rapid recovery in Ψx. Recovery of hydraulic capacity was achieved over a 6-month period by growth of new xylem tissue, with canopy leaf area and Eplant recovering over the same period. These findings indicate that E. saligna recovers slowly from severe drought stress, with potential for embolism to persist in the xylem for many months after rainfall.


2022 ◽  
Vol 27 (1) ◽  
Author(s):  
Ulrike Zentgraf ◽  
Ana Gabriela Andrade-Galan ◽  
Stefan Bieker

AbstractLeaf senescence is an integral part of plant development and is driven by endogenous cues such as leaf or plant age. Developmental senescence aims to maximize the usage of carbon, nitrogen and mineral resources for growth and/or for the sake of the next generation. This requires efficient reallocation of the resources out of the senescing tissue into developing parts of the plant such as new leaves, fruits and seeds. However, premature senescence can be induced by severe and long-lasting biotic or abiotic stress conditions. It serves as an exit strategy to guarantee offspring in an unfavorable environment but is often combined with a trade-off in seed number and quality. In order to coordinate the very complex process of developmental senescence with environmental signals, highly organized networks and regulatory cues have to be in place. Reactive oxygen species, especially hydrogen peroxide (H2O2), are involved in senescence as well as in stress signaling. Here, we want to summarize the role of H2O2 as a signaling molecule in leaf senescence and shed more light on how specificity in signaling might be achieved. Altered hydrogen peroxide contents in specific compartments revealed a differential impact of H2O2 produced in different compartments. Arabidopsis lines with lower H2O2 levels in chloroplasts and cytoplasm point to the possibility that not the actual contents but the ratio between the two different compartments is sensed by the plant cells.


2012 ◽  
Vol 58 (No. 4) ◽  
pp. 181-185 ◽  
Author(s):  
A. Bano ◽  
F. Ullah ◽  
A. Nosheen

The effect of drought stress and abscisic acid (ABA) applied at tillering stage (55 days after sowing) was compared in 2 wheat cultivars differing in drought tolerance. The activities of superoxide dismutase (SOD) and peroxidase (POD) and contents of endogenous ABA in plants were measured at 3 days of drought stress in cv. Chakwal-97 (drought tolerant) and cv. Punjab-96 (drought susceptible). ABA was applied at 10<sup>&ndash;6</sup> mol/L as presowing seed treatment for 18 h. Drought tolerant cultivar has a more efficient mechanism to scavenge reactive oxygen species as shown by a significant increase in the activity of antioxidant enzyme SOD. Under drought stress, ABA significantly increased the activities of SOD and POD, showing a significant decline on rewatering. The relative water content was significantly increased by ABA priming under drought stress in both wheat cultivars. The sensitive cultivar exhibiting lower endogenous ABA content was more responsive to ABA priming. On rewatering, the magnitude of recovery from drought stress was greater in tolerant cultivar. ABA was highly effective in improving grain weight of tolerant cultivar under drought stress. &nbsp;


Antioxidants ◽  
2021 ◽  
Vol 10 (6) ◽  
pp. 833
Author(s):  
Supapohn Yamuangmorn ◽  
Chanakan Prom-u-Thai

Purple rice is recognized as a source of natural anthocyanin compounds among health-conscious consumers who employ rice as their staple food. Anthocyanin is one of the major antioxidant compounds that protect against the reactive oxygen species (ROS) that cause cellular damage in plants and animals, including humans. The physiological role of anthocyanin in plants is not fully understood, but the benefits to human health are apparent against both chronic and non-chronic diseases. This review focuses on anthocyanin synthesis and accumulation in the whole plant of purple rice, from cultivation to the processed end products. The anthocyanin content in purple rice varies due to many factors, including genotype, cultivation, and management as well as post-harvest processing. The cultivation method strongly influences anthocyanin content in rice plants; water conditions, light quantity and quality, and available nutrients in the soil are important factors, while the low stability of anthocyanins means that they can be dramatically degraded under high-temperature conditions. The application of purple rice anthocyanins has been developed in both functional food and other purposes. To maximize the benefits of purple rice to human health, understanding the factors influencing anthocyanin synthesis and accumulation during the entire process from cultivation to product development can be a path for success.


OENO One ◽  
2015 ◽  
Vol 49 (3) ◽  
pp. 165 ◽  
Author(s):  
Magdalena Gamm ◽  
Marie-Claire Héloir ◽  
Marielle Adrian

<p style="text-align: justify;"><strong>Aims</strong>: The effects of trehalose and trehalose-6-phosphate (T6P), among other sugars, were assessed on grapevine stomatal movements.</p><p style="text-align: justify;"><strong>Methods and results</strong>: Epidermal peels were used to assess the effects of sugars. Low concentrations of trehalose and T6P (1 µM) induced an osmotic-independent reduction of the stomatal aperture in light conditions. Furthermore, ABA-induced stomatal closure was reduced by sugar application in association with lower accumulation of reactive oxygen species in guard cells. Similar effects, although weaker, were observed in response to the disaccharides sucrose and maltose, but not in response to the monosaccharides fructose and glucose.</p><p style="text-align: justify;"><strong>Conclusion</strong>: This study clearly highlights the effects of sugars, especially trehalose and T6P, on grapevine stomatal movements.</p><p style="text-align: justify;"><strong>Significance and impact of the study</strong>: This is the first time that such effects are described in grapevine and the results obtained provide new insights about the role of sugars on stomatal regulation at the whole plant level.</p>


2021 ◽  
Vol 12 ◽  
Author(s):  
Veronica Castañeda ◽  
Esther M. González ◽  
Stefanie Wienkoop

During moderate drought stress, plants can adjust by changes in the protein profiles of the different organs. Plants transport and modulate extracellular stimuli local and systemically through commonly induced inter- and intracellular reactions. However, most proteins are frequently considered, cell and organelle specific. Hence, while signaling molecules and peptides can travel systemically throughout the whole plant, it is not clear, whether protein isoforms may exist ubiquitously across organs, and what function those may have during drought regulation. By applying shotgun proteomics, we extracted a core proteome of 92 identical protein isoforms, shared ubiquitously amongst several Medicago truncatula tissues, including roots, phloem sap, petioles, and leaves. We investigated their relative distribution across the different tissues and their response to moderate drought stress. In addition, we functionally compared this plant core stress responsive proteome with the organ-specific proteomes. Our study revealed plant ubiquitous protein isoforms, mainly related to redox homeostasis and signaling and involved in protein interaction networks across the whole plant. Furthermore, about 90% of these identified core protein isoforms were significantly involved in drought stress response, indicating a crucial role of the core stress responsive proteome (CSRP) in the plant organ cross-communication, important for a long-distance stress-responsive network. Besides, the data allowed for a comprehensive characterization of the phloem proteome, revealing new insights into its function. For instance, CSRP protein levels involved in stress and redox are relatively more abundant in the phloem compared to the other tissues already under control conditions. This suggests a major role of the phloem in stress protection and antioxidant activity enabling the plants metabolic maintenance and rapid response upon moderate stress. We anticipate our study to be a starting point for future investigations of the role of the core plant proteome. Under an evolutionary perspective, CSRP would enable communication of different cells with each other and the environment being crucial for coordinated stress response of multicellular organisms.


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