Environmental and Experimental Botany

Proline metabolism influences metabolic and signaling pathway in regulating plant stress responses. This study aimed to characterize the physiological significance of glutamate (Glu)-mediated proline metabolism in the drought stress responses, focusing on the hormonal regulatory pathway. The responses of cytosolic Ca2+ signaling, proline metabolism and redox components to the exogenous application of Glu in well-watered or drought-stressed plants were interpreted in relation to endogenous hormone status and their signaling genes. Drought-enhanced abscisic acid (ABA) were concomitant with ROS and proline accumulation, accompanied by decreased NAD(P)H/NAD(P)+ and GSH/GSSG ratios. Exogenous Glu-feeding under drought resulted in an increase of salicylic acid (SA) with an antagonistic decrease of ABA. Glu-enhanced SA coincided with the highest expression of SA synthesis related gene ICS1 and Ca2+-dependent protein kinase CPK5. SA-enhanced CPK5 expression was closely associated with further enhancement of proline synthesis-related genes (P5CS1, P5CS2, and P5CR) expression. The Glu-activated proline synthesis was responsible for the reset of reducing potential with enhanced expression of redox regulating genes TRXh5 and GRXC9 in a SA-mediated NPR1- and/or PR1-dependent manner. These results clearly indicate that Glu-activated interplay between SA- and CPK5-signaling and Glu-enhanced proline synthesis are crucial in the amelioration of drought stress in B. napus.\n\nHighlightO_LIDrought-induced oxidative stress and symptom are developed by ABA-dependent manner\nC_LIO_LIGlu-application increases endogenous SA level with an antagonistic decrease of ABA\nC_LIO_LIDrought-induced proline accumulation was further enhanced by exogenous Glu-application\nC_LIO_LIGlu-enhanced proline synthesis accompanied with SA-mediated regulatory pathway\nC_LIO_LIGlu-enhanced SA-modulated proline metabolism is an integrated process of redox control\nC_LI

Indole-3-acetic acid (IAA) plays a critical role as a plant hormone in regulating the growth and development of the root system in plants, particularly in enhancing their ability to withstand abiotic stress. In this study, we found that overexpression of OsAAI1 promoted the growth of rice root system. The length of primary root, the number of lateral roots, the density of lateral roots, and the number of adventitious roots of overexpression of OsAAI1 (OE19) were significantly better than those of the wild type (ZH11) and the mutant line (osaai1), and the IAA content of OE19 was significantly higher than those of ZH11 and osaai1. We also found that exogenous application of IAA could compensate for the root growth defect caused by the osaai1 mutation. OE19 had the highest number and widest distribution of total roots under the water-cut drought treatment, and exogenous application of IAA attenuated the growth inhibitory effect of drought stress on osaai1. Our study also revealed that OsAAI1 interacts with the MADS-box family transcription factor OsMASD25. Additionally, the application of IAA helped alleviate the growth inhibitory effects of drought stress on osmads25.Importantly, OsMADS25 interaction with OsAAI1 was found to enhance the transcriptional expression of its downstream target genes LAX1 and OsBAG4, which are crucial genes in rices response to drought stress. These findings suggest that OsAAI1 and OsMADS25 are crucial in rices drought acclimation process by regulating downstream gene expression and influencing the IAA signaling pathway. Author summaryThe root system is a crucial organ for crop plants as it facilitates the absorption of water and nutrients, contributing to their drought resistance. Indole-3-acetic acid (IAA) plays a pivotal role in the growth of various types of roots in plants. Under drought stress conditions, changes in IAA levels and transport can impact the morphology of plant roots. This research illustrates that OsAAI1 positively influences rice root development and enhances the plants response to drought stress through the auxin signaling pathway. The study reveals a physical interaction between OsAAI1 and the transcription factor OsMADS25. This interaction boosts the expression of the auxin synthesis gene OsYUC4 and suppresses the auxin inhibitory factor OsIAA14, thereby promoting the auxin signaling pathway, stimulating rice root growth, and enhancing the plants ability to withstand drought. Furthermore, the interaction between OsAAI1 and OsMADS25 has been found to also positively affect the expression of the genes LAX1 and OsBAG4, which is associated with activated drought resistance in rice plants.

Plants are key to the functionality of many ecosystem processes. The duration and intensity of water stress are anticipated to increase in the future; however, an elucidation of the responses of plants to water stress remains incomplete. For this study, we present a global meta-analysis derived from 1301 paired observations from 84 studies to evaluate the response patterns and mechanisms of plants to water stress. The results revealed that while water stress inhibited plant growth and photosynthesis, reactive oxygen species (ROS), plasma membrane permeability, enzymatic antioxidants, and non-enzymatic antioxidants increased. These responses generally increased with the intensity of water stress but were mitigated with experimental duration. Our findings suggested that the overproduction of ROS was the primary mechanism of plants in response to water stress and that plants tend to acclimate to water stress over time to some extent. Our synthesis provides a framework for understanding the responses and mechanisms of plants under drought conditions. One senence summaryThe overproduction of ROS was the primary mechanism of plants in response to water stress and that plants tend to acclimate to water stress over time to some extent.

Plants possess a diversity of Reactive Oxygen Species (ROS)-processing enzymes involved in sensing and controlling ROS levels under basal and stressful conditions. There is little information on the transcriptional regulators that control the expression of these ROS-processing enzymes, particularly at the onset of the defense response to abiotic stress. Filling this gap, this paper reports a critical role for Arabidopsis TGA class II factors (TGA2, TGA5, and TGA6) in the tolerance response to UV-B light and photooxidative stress, by activating the expression of genes with antioxidative roles. We identified two clusters of genes responsive to UV-B and activated by TGA2/5/6 were identified using RNAseq and clustering analysis. The GSTU gene family, which encodes glutathione transferase enzymes from the Tau subclass, was overrepresented in these clusters. We corroborated the TGA2-mediated activation in response to UV-B for three model genes (GSTU7, GSTU8, and GSTU25) using RT-qPCR and ChIP analyses. Interestingly, using tga256 mutant and TGA2- and GSTU7-complemented mutant plants, we demonstrated that TGA2-mediated induction of GSTU genes is essential to control ROS levels and oxidative damage after UV-B and MeV treatments. This evidence positions TGA class II factors, particularly TGA2, as a key players in the redox signaling network of Arabidopsis plants. HighlightArabidopsis TGA2 transcription factor is part of the redox-signaling network controlling ROS levels and oxidative damage in tolerance response to UV-B and photooxidative stress, via activation of antioxidant GSTU genes.

Nitrogen (N) and phosphorus (P) are two essential plant macronutrients that can limit plant growth by different mechanisms. We aimed to shed light on how soybean respond to low nitrogen (LN), low phosphorus (LP) and their combined deficiency (LNP). Generally, these conditions triggered changes in gene expression of the same processes, including cell wall organization, defense response, response to oxidative stress, and photosynthesis, however, response was different in each condition. A typical primary response to LN and LP was detected also in soybean, i.e., the enhanced uptake of N and P, respectively, by upregulation of genes for the corresponding transporters. The regulation of genes involved in cell wall organization showed that in LP roots tended to produce more casparian strip, in LN more secondary wall biosynthesis occurred, and in LNP reduction in expression of genes involved in secondary wall production accompanied by cell wall loosening was observed. Flavonoid biosynthesis also showed distinct pattern of regulation in different conditions: more anthocyanin production in LP, and more isoflavonoid production in LN and LNP, which we confirmed also on the metabolite level. Interestingly, in soybean the nutrient deficiencies reduced defense response by lowering expression of genes involved in defense response, suggesting a role of N and P nutrition in plant disease resistance. In conclusion, we provide detailed information on how LN, LP, and LNP affect different processes in soybean roots on the molecular and physiological levels.

Understanding comprehensive mechanisms of the downregulation of photosynthesis induced by accumulation of non-structural carbohydrates (NSCs) is essential for the future food security.x Despite numerous studies, whether NSCs accumulation directly affects steady-state maximum photosynthesis and photosynthetic induction, as well as underlying gene expression profiles, remains unknown so far. We evaluated the relationship between photosynthetic capacity and NSCs accumulation induced by cold-girdling, sucrose feeding, and low nitrogen treatment in Glycine max and Phaseolus vulgaris. In G. max, changes in transcriptome profiles were further investigated focusing on physiological processes of photosynthesis and NSCs accumulation. NSCs accumulation decreased maximum photosynthetic capacity and delayed photosynthetic induction in both species. In G. max, such photosynthetic downregulation was explained by coordinated downregulation of photosynthetic genes involved in Calvin cycle, Rubisco activase, photochemical reactions, and stomatal opening. Furthermore, sink-source imbalance may have triggered a change in the balance of sugar-phosphate translocators in chloroplast membranes, which may have promoted starch accumulation in chloroplasts. Our findings provided an overall picture of the photosynthetic downregulation and NSCs accumulation in G. max, demonstrating that the photosynthetic downregulation is triggered by NSCs accumulation and cannot be explained simply by N deficiency. One Sentence SummaryAccumulation of nonstructural carbohydrates directly induced both downregulation and delayed induction of photosynthesis by coordinated transcriptomic changes in photosynthetic genes in Glycine max.

The formation of cotton fiber strength largely relies on continuous and steady sucrose supply to cellulose synthesis and is greatly impaired by drought. However, the effects of drought on sucrose import into fiber and its involvement in cellulose biosynthesis within fiber remain unclear. To end this, moisture deficiency experiments were conducted using two Gossypium hirsutum cultivars of Dexiamian 1 (drought-tolerant) and Yuzaomian 9110 (drought-sensitive). Fiber strength was significantly decreased under drought. The results of 13C isotope labeling indicated that drought notably reduced sucrose efflux from cottonseed coat to fiber, and this was caused by down-regulation of sucrose transporter genes (GhSWEET10 and GhSWEET15) in the outer cottonseed coat, finally leading to decreased sucrose accumulation in fiber. Further, under drought, the balance of sucrose allocation within fiber was disrupted by increasing the flow of sucrose into {beta}-1,3-glucan synthesis and lignin synthesis but hindering that into cellulose synthesis in both cultivars. Additionally, glycolysis and starch synthesis were specifically enhanced by drought in Yuzaomian 9110, which further reduced the flow of sucrose into cellulose synthesis. Under drought, the cellulose deposition was decreased due to promoted cellulose degrading process in Dexiamian 1 and stunted cellulose synthesis in Yuzaomian 9110. Consequently, reduced cellulose content was measured in drought-stressed fibers for both cultivars. In summary, the inhibited cellulose accumulation caused by drought was mainly due to reduced sucrose translocation from the outer cottonseed coat to fiber, and less sucrose partitioned to cellulose synthesis pathway under the condition of intensified competition for sucrose by different metabolic pathways within fiber, finally degrading the fiber strength. HighlightThis article revealed the path of sucrose flow from cottonseed coat to cotton fiber and sucrose competition patterns within cotton fiber under drought and their relationships with fiber strength loss.

Light wavelengths modulate plant growth, metabolism, and physiology. Amaranthus, a C4 underutilized climate resilient crop with promising nutritional properties remained unexplored in terms of metabolite enrichment under monochromatic light wavelengths of visible spectrum. In current study, two cultivars of Amaranthus tricolor (green and red) were exposed to seven light regimes of photosynthetically active radiation (PAR; 400-700 nm): deep blue, blue, green, amber, red, deep red, far red, and their metabolic responses were captured using Gas Chromatography-Mass Spectrometry. The metabolic analysis revealed wavelength-specific reprogramming in the levels of organic acids, sugars, amino acids, fatty acids as well as phenolics. In both the green and red Amaranthus, branched-chain amino acids and phenylalanine, which are nutritionally essential, were significantly elevated under far-red light. While the phenolics such as caffeic acid and ferulic acid were elevated under green and deep blue light respectively in green Amaranthus, amber light wavelengths enhanced these phenolics in red Amaranthus. The study highlighted cultivar-specific metabolic rewiring triggered by specific wavelengths. Altogether, these findings provides insights into metabolic adaptation and demonstrate the ability of light wavelength to specifically enrich the targeted metabolite of nutritional relevance in Amaranthus. It offers strategies to improve the nutritional value of crops in controlled agriculture systems. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=167 HEIGHT=200 SRC="FIGDIR/small/714947v1_ufig1.gif" ALT="Figure 1"> View larger version (40K): org.highwire.dtl.DTLVardef@1a4477dorg.highwire.dtl.DTLVardef@518550org.highwire.dtl.DTLVardef@7682dorg.highwire.dtl.DTLVardef@4876e2_HPS_FORMAT_FIGEXP M_FIG C_FIG

Rhizospheric pH severely impacts plant growth and fitness through a numerous process and has emerged as a major determinant of crop productivity. Despite numerous attempts, the key questions related to plants response against rhizospheric pH remains largely elusive. The present study provides a mechanistic framework for rhizospheric pH-mediated root growth inhibition (RGI). Utilizing various genetic resources combined with pharmacological agents and high-resolution confocal microscopy, the study provides direct evidences for the involvement of jasmonates and auxin in rhizospheric pH-mediated RGI. We show that auxin maxima at root tip is tightly regulated by the rhizospheric pH. In contrast, jasmonates (JAs) abundance inversely correlates with rhizospheric pH. Further, JA mediated regulation of auxin maxima by GRETCHEN HAGEN 3 (GH3) family genes explains the pattern of RGI observed over the entire range of rhizospheric pH. Our findings revealed auxin as the key regulator of RGI during severe pH conditions, while JAs antagonistically regulate auxin response against rhizospheric pH. HighlightThe current study identifies the mechanistic framework of rhizospheric pH mediated root growth inhibition in model plant Arabidopsis through a prominent crosstalk between two phytohormones i.e. auxin and jasmonates.

Submergence induced hypoxic condition is one of the abiotic stresses which negatively affects the plant growth and development, and causes early onset of senescence. Hypoxic conditions ateres the expression of a number of non-coding microRNAs (miRNAs), besides protein-coding genes. However, the molecular function of stress-induced miRNA in submergence induced physiological or developmental changes and recovery remains to be understood. The expression of miR775 is highly induced under hypoxic stress conditions. Here, we show that miR775 is a potential post-transcriptional regulator number of targets, including Galactosyltransferase (GALT9). The expression of miR775 and target GALT9 was significantly induced and reduced respectively at 24 hours of submergence. The overexpression of miR775 (miR775-Oe) confers enhanced recovery from submergence stress and reduced accumulation of ROS, in contrast to wild type and endogenous target mimic of miR775 (MIM775) Arabidopsis plants. We observed a similar recovery phenotype in case of target galt9 mutant plants, indicating the role of miR775-GALT9 module in recovery from submergence. Further, we showed that the expression of SENESCENCE ASSOCIATED GENES (SAGs), such as SAG12, SAG29, and ORE1. was increased in MIM775 and reduced in miR775-Oe and galt9 plants. Thus, our results suggest that miR775-GALT9 module plays a crucial role in the recovery from submergence by modulating the expression of SAGs through differential accumulation of ROS.

Salt tolerant is strongly related to potassium (K+) retention in plant tissues under salt stress conditions. However, it is unclear for different Echinacea species. So, mechanistic basis of four Echinacea species (i.e. Echinacea purpurea, Echinacea angustifolia, Echinacea pallida, and Echinacea sanguinea) to salinity stress tolerance, and K+ retention were assessed in the present study. Non-invasive microelectrode ion flux measuring, DHAR and MDHAR activities, and pharmacological measurements were performed based on the standard methods. Ion flux measurements revealed higher K+ efflux in E. pallida and E. sanguinea species compared to the E. purpurea and E. angustifolia species in the elongation zone. Higher salinity-induced H+ efflux was found in the elongation zone than mature zone. However, E. angustifolia and E. purpurea had more Ca2+ influx compared to E. pallida and E. sanguinea species. Net K+ efflux decreased (> 90%) in the presence of TEA and GdCl3. Increasing of Ca2+ uptake and K+ loss in four Echinacea species roots were found in the presence of 0.3 mM Cu/Ascorbate (Cu/Asc). The significant role of H+-ATPase in H+ efflux was demonstrated by Sodium orthovanadate. Ultimately, the physiological properties of Echinacea species have a critical role in salinity-resistant/sensitive differences. Future scientific understanding of Echinacea species physiognomies may be necessary for better understanding of the plant behavior to salinity stress. One-sentence summaryHigher K+ efflux in E. pallida and E. sanguinea species as a result of NaCl and ROS act as a metabolic switch to save energy for adaptations and repairs in salinity stress conditions.

Water deficit impairs growth and survival of plants. Many water stress responses are under control of abscisic acid (ABA) but little is known about growth control under osmotic stress. Based on the previously described growth-promoting activity of the peptide hormone phytosulfokine (PSK), we hypothesized that it may contribute to growth regulation under water stress conditions. To test this hypothesis, we analyzed the Arabidopsis thaliana PSK receptor (PSKR) null mutant pskr1-3 pskr2-1 under mannitol and drought stress. In particular under mild water stress, fresht weight and photosynthetic efficiency were more reduced in pskr1-3 pskr2-1 than in wild type. Hydroponic and grafting experiments showed that PSKR signaling was not required for long-distance signaling from mannitol-stressed roots to shoot but rather for cell growth promotion in the shoot. Unlike wild type, pskr1-3 pskr2-1 shoots did not accumulate ABA in response to mannitol, showed misregulation of ABA synthesis genes and elevated expression of ABI1 and ABI2, repressors of ABA signaling whereas application of ABA partially reversed shoot growth inhibition by mannitol in pskr1-3 pskr2-1. In turn, mannitol and ABA induced expression of PSK3 and PSKR1, and ABA promoted expression of PSK2 and PSK4 revealing feedback regulatory loops between PSKR and osmotic stress signaling. HighlightPhytosulfokine receptor signaling regulates ABA synthesis and signaling genes and promotes ABA accumulation in the shoot of water-stressed plants and maintains leaf growth and photosynthetic efficiency which ensures plant health.

Water deficit, heat stress, and a combination of water deficit and heat stress are highly disruptive to crop yield worldwide. Unfortunately, the frequency and intensity of these conditions is gradually increasing due to climate change. Previous studies of water deficit and heat stress combination were primarily conducted under controlled growth conditions, revealing that the combination of water deficit and heat stress resulted in the activation of unique stress responses and acclimation pathways. However, whether similar responses to stress combination occur in the field remained largely unknown. Here we report on a two-year field study in which the transcriptomic and physiological responses of vegetative and reproductive tissues of soybean (Glycine max) to water deficit, heat treatment and their combination were studied. Our findings reveal that the transcriptomic responses of soybeans grown in the field are different from those grown under controlled growth chamber conditions. These differences were especially noticeable in plants subjected to the heat or water deficit treatments, and less in plants subjected to the stress combination. In addition, we report that differential transpiration between leaves and pods, that was originally discovered in plants grown under controlled growth conditions, occurs in field grown soybeans in response to heat stress, as well as heat stress combined with water deficit. We hope that the transcriptomic datasets generated by our study will contribute to future studies of crop responses to different stresses in the field, as well as highlight the need for more omics studies of plants grown under field conditions.

As sessile organisms, plants are increasingly vulnerable to environmental stresses because of global warming and climate change. Stress-induced reactive oxygen species (ROS) accumulation results in plant cell damages and even cell death. Anthocyanins are important antioxidants that scavenge ROS to maintain ROS homeostasis. However, the mechanism underlying ROS-induced anthocyanin accumulation is unclear. In this study, we determined that in pear the HD-Zip I family member PuHB40 mediates ROS-dependent anthocyanin biosynthesis under high-light stress. Specifically, PuHB40 is a transcription factor that induces PuMYB123-like/PubHLH3 complex for anthocyanin biosynthesis. The transcriptional activation by PuHB40 depends on its phosphorylation level, which is regulated by protein phosphatase 2A (PP2A). High ROS contents maintain the phosphorylation of PuHB40 at a high level, while also enhancing PuHB40-induced PuMYB123-like transcription by decreasing the transcription of PuPP2AA2, ultimately leading to increased anthocyanin biosynthesis. Our study revealed the pathway regulating ROS-induced anthocyanin biosynthesis in pear, further clarifying the mechanism underlying abiotic stress-induced anthocyanin biosynthesis, which may have implications for improving plant stress tolerance. IN A NUTSHELLO_ST_ABSBackgroundC_ST_ABSVarious abiotic stresses, including high-light intensity, promote the accumulation of anthocyanins in plants, while also activating the production of reactive oxygen species (ROS). Anthocyanins can attenuate the negative effects of high-light stress by acting as antioxidants that restrict ROS accumulation. Several reports have shown that ROS can stimulate anthocyanin accumulation, but whether high-light stress-induced anthocyanin accumulation depends on ROS is undetermined. Additionally, the mechanism underlying ROS-dependent anthocyanin biosynthesis remains unclear. QuestionDoes high-light stress-induced anthocyanin biosynthesis depend on ROS? What is the molecular basis of high-light stress-induced anthocyanin biosynthesis? FindingsHigh-light stress-induced anthocyanin biosynthesis in pear seedlings is dependent on ROS accumulation. PuMYB123-like is the key MYB transcription factor for anthocyanin biosynthesis, while PuHB40 activates anthocyanin biosynthesis in response to ROS under high-light stress. Specifically, PuHB40 activates the transcription of PuMYB123-like, with the encoded protein combining with PubHLH3 to form an MBW complex that promotes anthocyanin biosynthesis. The transcriptional activation by PuHB40 depends on its phosphorylation status, which is regulated by protein phosphatase 2A (PP2A). High ROS levels inhibit the transcription of PuPP2AA2, thereby maintaining the phosphorylation of PuHB40, enhancing the transcriptional activation by PuHB40, inducing PuMYB123-like transcription, and ultimately leading to increased anthocyanin biosynthesis. Next stepsOur future research will focus on whether ROS and the MYB123-like- PuHB40-PP2A regulatory module are also involved in the anthocyanin biosynthesis induced by other abiotic and biotic stresses, which will provide insights into biotic stress-induced anthocyanin biosynthesis and form the theoretical basis for improving fruit coloration.

The response of photosynthetic CO2 assimilation to changes of illumination affects plant growth and crop productivity under natural fluctuating light conditions. However, the effects of nitrogen (N) supply on photosynthetic physiology after transition from low to high light are seldom studied. To elucidate this, we measured gas exchange and chlorophyll fluorescence under fluctuating light in tomato (Solanum lycopersicum) seedlings grown with different N conditions. After transition from low to high light, the induction speeds of net CO2 assimilation (AN), stomatal conductance (gs) and mesophyll conductance (gm) delayed with the decline in leaf N content. The times to reach 90% of maximum AN, gs and gm were negatively correlated to leaf N content. This delayed photosynthetic induction in plants grown under low N concentration was mainly caused by the slow induction response of gm rather than that of gs. Furthermore, the photosynthetic induction upon transfer from low to high light was hardly limited by photosynthetic electron flow. These results indicate that decreased leaf N content declines carbon gain under fluctuating light in tomato. Increasing the induction kinetics of gm has the potential to enhance the carbon gain of field crops grown in infertile soil.

Plant growth and stress responses largely depend on the chloroplast retrograde signaling. Stoichiometry of carbon dioxide assimilation and transpiration, efficiency of photosynthesis, and absorbed energy fate in photosystems between photochemistry, fluorescence and heat channels impact on the chloroplast retrograde signaling. Recent studies revealed that 22 kDa photosystem II protein (PsbS) and plant {beta} carbonic anhydrases ({beta}CAs), except their obvious functions, are also involved in regulation of plant stress responses. Obtained results suggest that simultaneous overexpression of {beta}CA1 and/or {beta}CA2 with PsbS genes leads to improved photoprotection, acclimation to variable light conditions, and water use efficiency. However, this was achieved on the costs of lower biomass gain in double and triple (oePsbSoe{beta}CA1 and oePsbSoe{beta}CA1{beta}CA2, respectively) transgenic lines in comparison to Col-0, and npq4-1 mutant. After bicarbonate fertilization we observed significant increase in biomass production in triple transgenic lines compared to oePsbS and npq4-1 plants, but not to Col-0. Transcriptomic analysis revealed that bicarbonate treatment of double and triple transgenic lines specifically induced expression of genes and transcription factors related to hypoxia, freezing, drought, high light, and pathogen attack stress responses, contrary to other genotypes. Interestingly, expression of two of these transcription factors, DREB - CBF2 subfamily (A-1 of ERF/AP2), and BT2 were reduced in oePsbS transgenic line. Our results suggest a novel regulatory role of {beta}CAs and bicarbonate in the regulation of stress responses and plant productivity.

Fluctuating light (FL) and drought stress usually occur concomitantly. However, whether drought stress affects photosynthetic performance under FL remains unknown. Here, we measured gas exchange, chlorophyll fluorescence, and P700 redox state under FL in drought-stressed tomato (Solanum lycopersicum) seedlings. Drought stress significantly affected stomatal opening and mesophyll conductance after transition from low to high light and thus delayed photosynthetic induction under FL. Therefore, drought stress exacerbated the loss of carbon gain under FL. Furthermore, restriction of CO2 fixation under drought stress aggravated the over-reduction of photosystem I (PSI) upon transition from low to high light. The resulting stronger FL-induced PSI photoinhibition significantly supressed linear electron flow and PSI photoprotection. These results indicated that drought stress not only affected gas exchange under FL but also accelerated FL-induced photoinhibition of PSI. Furthermore, drought stress enhanced relative cyclic electron flow in FL, which partially compensated for restricted CO2 fixation and thus favored PSI photoprotection under FL. Therefore, drought stress has large effects on photosynthetic dark and light reactions under FL.

The development and growth of plants are significantly impacted by adverse surroundings, particularly drought conditions. The yield and quality of plants, in particular, are heavily reliant on the presence of favorable growth conditions. Here, we performed comprehensive research to investigate phenotype, physiological characteristics, transcriptomic and metabolomic changes in Nicotiana tabacum (N. tabacum) in responses to drought stress (DS). This work aimed to investigate the detailed responses of N. tabacum to DS under different drought conditions (CK, well-watered; LD, light drought; MD, moderate drought and SD, severe drought). N. tabacum grew normally under CK but was inhibited under LD, MD and SD stress; the relative water content, transpiration rate and protective enzyme activity significantly influenced under DS. In the LD/CK, MD/CK and SD/CK comparison groups, there were 7483, 15558 and 16876 differentially expressed genes (DEGs), respectively, and 410, 485 and 523 differentially accumulated metabolites (DAMs), respectively. The combined analysis of transcriptomic and metabolomic data unveiled the significant involvement of phenylpropanoid biosynthesis in the N. tabacums response to drought stress. These findings characterized the key metabolites and genes in responses to drought stress in N. tabacum, hence offering valuable insights into the underlying mechanisms driving these responses to DS and maintaining plant health under climate change.

To investigate the molecular mechanism underlying increasing leaf area in {gamma}-Aminobutyric acid (GABA) biosynthetic mutants, the first pair of true leaves of GABA biosynthetic mutants was measured. The results showed that the leaf blade area in GABA biosynthetic mutants was larger than that of the wild type to different extents, and the area of the leaf epidermal cells in mutants was larger than that of the wild type. DNA polyploid analysis showed that polyploid cells in GABA biosynthetic mutants were appearing earlier and more abundant than in the wild type. To check the correlation between cell size and endoreplication, the expression of factors involving endocycles, including D-type cyclin gene (CYCD3;1, CYCD3;2, CYCD3;3, and CYCD4;1) and kinase CKDA;1, were analysed by qRT-PCR. The results showed that CKDA;1 in GABA biosynthetic mutants was downregulated, and four types of CYCDs showed different expression patterns in different GABA biosynthetic mutants. Inconsistent with this result, for CCS52A (CELL CYCLE SWITCH 52A) (controlling the endocycle entry) in gad2 and gad1/gad2 mutants, the expression of CCS52A2 was significantly higher than that in the wild type. The expression of SIM (SIAMESE) and SMR (SIAMESE-RELATED), which inhibit kinase activity, were also upregulated compared with the control. To further study the possible potential relationship between GABA metabolism and endoreplication, we analysed the reactive oxygen species (ROS) levels in guard cells using ROS fluorescent probes. ROS levels were significantly higher in GABA biosynthetic mutants than the control. All results indicated that cyclin, the cyclin-dependent kinase, and its inhibitory protein were coordinated to participate in endoreplication control at the transcription level in the leaves of GABA biosynthetic mutant Arabidopsis. Contribution to the field statement{gamma}-Aminobutyric acid (GABA) metabolic pathway plays a dual role in plant development. This research investigated the perturbation of GABA biosynthesis on Arabidopsis leave endoreplication for the first time. In the GABA biosynthetic mutants, many genes, participating in cell division regulation, are coordinately transcriptionally expressed to trigger the onset and maintenance of endoreplication, and this led to the cell expansion and the increase leaf blade area. However, this initiation of endoreplication links with the decrease of endogenous GABA level and the increase Reactive oxygen species (ROS). This may be a compensation mechanism to adapt to abnormal GABA level in plant leaf development. Present evidence provided hypothesized that the normal GABA level in plant leaf development plays a brake to inhibit the immature cell expansion and differentiation, and this negative regulation functions a guarantee mechanism to watchdog the normal leaf development. In all, this contribution provides an updated perspective on the role of GABA in plant development.

Hormesis refers to the adaptive mechanism of organisms in response to environmental challenges where a lower dose of a toxic compound induce an improvement in functionality and overall development and a higher dose endangers even the existence of the organism. The recent developments in hormetic studies are of paramount importance in plant research as they help in risk assessment of environmental contaminants, protect the vegetation against pollution, and improve crop productivity. As one of the most toxic contaminants, cadmium is considered to have detrimental effects on the growth and development of plants. However, recent studies have revealed the beneficial effects of cadmium in plants at low levels of exposure however the exact mechanism behind this phenomenon is poorly deciphered. In this study, we have focused on observing the response of tomato seedlings under different concentrations of cadmium. The morphological, biochemical, and histochemical characterization of these seedlings under low cadmium exposure has confirmed their hormetic effects. The differential gene expression by transcriptomic profiling in low cadmium showed that, apart from genes involved in oxidoreductase activity, and signaling, several lncRNAs, also differentially expressed. The lncRNAs are known to regulate gene expression on the chromatin level and post-transcriptional regulation. First time we are reporting the expression of lncRNAs in hormesis as important factor for enhanced growth. In-silico analysis revealed the functions of lncRNAs, involving the prediction of cis-targets, mi-RNA precursors, and their targets. Two miRNAs; sly-MIR396a and sly-MIR1063g were seen to have a direct role in improving the growth of plants treated with low cadmium provided an insight into the molecular mechanisms of their role in cadmium hormesis. These findings provided important understanding of the molecular basis of the hormetic phenomenon which can pave a path for generating crops with improved agronomic characteristics. Graphical abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=149 SRC="FIGDIR/small/663119v1_ufig1.gif" ALT="Figure 1"> View larger version (27K): org.highwire.dtl.DTLVardef@8de5b0org.highwire.dtl.DTLVardef@1e2ad13org.highwire.dtl.DTLVardef@d0f7e2org.highwire.dtl.DTLVardef@14238b3_HPS_FORMAT_FIGEXP M_FIG C_FIG HighlightsO_LILow cadmium exposure on Solanum lycopersicum seedlings showed more promising outcomes in terms of growth and development. C_LIO_LIThe plants exposed to 1{micro}M Cd treatment continued to exhibit superior growth responses despite removing the cadmium from the media after 5 days of treatment. C_LIO_LIThe GO analysis of Differentially Expressed Genes (DEGs) suggested several lncRNAs differentially expressed in 1 {micro}M Cd condition. C_LIO_LIDifferentially expressed LncRNAs Solyc01g006780.4 and Solyc12g019150.1 generated the miRNAs, sly-MIR396a and sly-MIR1063g respectively. C_LIO_LIUpregulation of sly-MIR396a and sly-MIR1063g resulted in the downregulation of GRF12 and NET4B-like proteins respectively leading to increased growth of tomato plants. C_LI