R.M. wrote the article and prepared figures; all authors read and approved the final version of the article. [OPEN] Articles can be viewed without a subscription.
Plants grow and reproduce within a highly dynamic environment that can see abrupt changes in conditions, such as light intensity, temperature, humidity, or interactions with biotic agents. Recent studies revealed that plants can respond within seconds to some of these conditions, engaging many different metabolic and molecular networks, as well as rapidly altering their stomatal aperture. Some of these rapid responses were further shown to propagate throughout the entire plant via waves of reactive oxygen species (ROS) and Ca 2+ that are possibly mediated through the plant vascular system. Here, we propose that the integration of these signals is mediated through pulses of gene expression that are coordinated throughout the plant in a systemic manner by the ROS/Ca +2 waves. The Dynamic Environment of PlantsWhile growing within their natural habitat, or in a manmade field environment, plants are subjected to many different changes in their physical and biological surroundings. These can be gradual, such as the slow decrease in soil water content over time during summer, or rapid, such as changes in light intensity occurring as a result of sun flecks during a cloudy day [1-9] (Figure 1, Key Figure). Some of these rapid changes can occur simultaneously, or on the background of other more persistent stress conditions, such as a prolonged drought or a heat wave, essentially representing a state of stress combination [4,5,10]. In addition, due to the placement of the plant within its environment, for example its position within a row of plants or plot in the field, or its position in nature in close proximity to a tree cover, not all parts or tissues of the plant may experience the rapid change in environmental conditions simultaneously [4,11]. Under such conditions, the rapid responses (see Glossary) at the affected tissue could trigger systemic signaling pathways, such as the ROS [12] and calcium waves [13], electric signals [14], and/or hydraulic waves [15]. The occurrence of rapid changes in the physical and/ or biological environment of the plant, coupled with the discovery of rapid systemic signaling pathways activated by many of these conditions [12][13][14][15], and the discovery of rapid transcriptional and metabolic responses to stress [16,17], support a hypothesis that plants evolved sensing and acclimation mechanisms that may function [ 3 9 0 _ T D $ D I F F ] within the seconds to minute timescale and are important for the overall fitness of the plant and its ability to survive rapid changes within its environment (Figure 1). Here, we examine the molecular networks, and physiological and metabolic changes that occur in plants during rapid responses to stress, and propose that the integration of these responses is mediated through pulses of gene expression that are coordinated throughout the plant in a systemic manner by [ 3 9 1 _ T D $ D I F F ] the ROS/Ca +2 waves. HighlightsRecent studies reveal that plants respond within the seconds to minutes time-scale to different biotic and/or abiotic stimuli.The ra...
Climate change-driven extreme weather events, combined with increasing temperatures, harsh soil conditions, low water availability and quality, and the introduction of many manmade pollutants, pose a unique challenge to plants. Although our knowledge of the response of plants to each of these individual conditions is vast, we know very little about how a combination of many of these factors, occurring simultaneously, that is multifactorial stress combination, impacts plants. Seedlings of wild-type and different mutants of Arabidopsis thaliana plants were subjected to a multifactorial stress combination of six different stresses, each applied at a low level, and their survival, physiological and molecular responses determined. Our findings reveal that, while each of the different stresses, applied individually, had a negligible effect on plant growth and survival, the accumulated impact of multifactorial stress combination on plants was detrimental. We further show that the response of plants to multifactorial stress combination is unique and that specific pathways and processes play a critical role in the acclimation of plants to multifactorial stress combination. Taken together our findings reveal that further polluting our environment could result in higher complexities of multifactorial stress combinations that in turn could drive a critical decline in plant growth and survival.
These authors contributed equally. SUMMARYSystemic acquired acclimation (SAA) plays a key role in optimizing growth and preventing damage associated with fluctuating or abrupt changes in the plant environment. To be effective, SAA has to occur at a rapid rate and depend on rapid signaling pathways that transmit signals from affected tissues to all parts of the plant. Although recent studies have identified several different rapid systemic signaling pathways that could mediate SAA, very little information is known about the extent of their involvement in mediating transcriptomic responses. Here we reveal that the systemic transcriptomic response of plants to excess light stress is extensive in its context and involves an early (2 min) and transient stage of transcript expression that includes thousands of genes. This early response is dependent on the respiratory burst oxidase homolog D protein, and the function of the reactive oxygen species (ROS) wave. We further identify a core set of transcripts associated with the ROS wave and suggest that some of these transcripts are involved in linking ROS with calcium signaling. Priming of a systemic leaf to become acclimated to a particular stress during SAA involves thousands of transcripts that display a rapid and transient expression pattern driven by the ROS wave.
Summary Iron–sulfur (Fe–S) clusters play an essential role in plants as protein cofactors mediating diverse electron transfer reactions. Because they can react with oxygen to form reactive oxygen species (ROS) and inflict cellular damage, the biogenesis of Fe–S clusters is highly regulated. A recently discovered group of 2Fe–2S proteins, termed NEET proteins, was proposed to coordinate Fe–S, Fe and ROS homeostasis in mammalian cells. Here we report that disrupting the function of AtNEET, the sole member of the NEET protein family in Arabidopsis thaliana, triggers leaf‐associated Fe–S‐ and Fe‐deficiency responses, elevated Fe content in chloroplasts (1.2–1.5‐fold), chlorosis, structural damage to chloroplasts and a high seedling mortality rate. Our findings suggest that disrupting AtNEET function disrupts the transfer of 2Fe–2S clusters from the chloroplastic 2Fe–2S biogenesis pathway to different cytosolic and chloroplastic Fe–S proteins, as well as to the cytosolic Fe–S biogenesis system, and that uncoupling this process triggers leaf‐associated Fe–S‐ and Fe‐deficiency responses that result in Fe over‐accumulation in chloroplasts and enhanced ROS accumulation. We further show that AtNEET transfers its 2Fe–2S clusters to DRE2, a key protein of the cytosolic Fe–S biogenesis system, and propose that the availability of 2Fe–2S clusters in the chloroplast and cytosol is linked to Fe homeostasis in plants.
Reactive oxygen species (ROS) play a key role in the regulation of many biological processes in plants. Nonetheless, they are considered highly reactive and toxic to cells. Owing to their toxicity, as well as their important role in signaling, the level of ROS in cells needs to be tightly regulated. The ROS gene network, encoding a highly redundant arsenal of ROS scavenging mechanisms and an array of enzymes involved in ROS production, regulates ROS metabolism and signaling in plants. In this article, we review the role of the ROS gene network in plants and examine how it evolved. We identify key components of the ROS gene network in organisms that likely originated as early as 4.1-3.5 billion years ago, prior to the great oxidation event that resulted from the rise of cyanobacteria on Earth. This estimate concurs with recent evidence for the appearance of oxygenic photosynthetic organisms on Earth, suggesting that low and/or localized levels of photosynthetically produced oxygen necessitated the emergence of ROS scavenging mechanisms to protect life. Life forms have therefore evolved in the presence of ROS on Earth for at least 3.8-3.6 billion years, highlighting the intimate relationship that exists today between many physiological and developmental processes and ROS.
A combination of drought and heat stress, occurring at the vegetative or reproductive growth phase of many different crops can have a devastating impact on yield. In soybean (Glycine max), a considerable effort has been made to develop genotypes with enhanced yield production under conditions of drought or heat stress. However, how these genotypes perform in terms of growth, physiological responses, and most importantly seed production, under conditions of drought and heat combination is mostly unknown. Here, we studied the impact of water deficit and heat stress combination on the physiology, seed production, and yield per plant of two soybean genotypes, Magellan and Plant Introduction (PI) 548313, that differ in their reproductive responses to heat stress. Our findings reveal that although PI 548313 produced more seeds than Magellan under conditions of heat stress, under conditions of water deficit, and heat stress combination its seed production decreased. Because the number of flowers and pollen germination of PI 548313 remained high under heat or water deficit and heat combination, the reduced seed production exhibited by PI 548313 under the stress combination could be a result of processes that occur at the stigma, ovaries and/or other parts of the flower following pollen germination.
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