Vacuole membrane proteins play a critical role in the regulation of plant physiological processes including normal growth and development, and responses to stresses. The killing me slowly 1 (KMS1) gene that encodes a soluble N-ethylmaleimide-sensitive fusion attachment receptor (SNARE) domain-containing vacuole membrane protein was first reported in Arabidopsis. Currently, the function of KMS1 in other plants under stress is poorly understood. In this study, we report cloning, expression, and characterization of a novel KMS1 gene in alfalfa (Medicago sativa L.), designated MsKMS1 (GenBank accession No. JX467688). The full-length cDNA of MsKMS1 was 1 396 bp and contained a complete open reading frame of 1 257 bp, which encoded a putative protein of 418 amino acids. The BLASTp analysis showed that MsKMS1 shared high amino acid sequence similarities with KMS1 from other plants such as Medicago truncatula (99 %), Cicer arietinum (89 %), Glycine max (77 %), Prunus mume (76 %), Ricinus communis (72 %), Populus euphratica (72 %), Theobroma cacao (72 %), and Arabidopsis thaliana (67 %). Transient transformation of onion (Allium cepa) bulb scale epidermal cells by biolistic bombardment showed that MsKMS1 was localized to the plasma membrane. Quantitative real-time PCR revealed that MsKMS1 expression was upregulated under different abiotic stresses (200 mM NaCl, 20 % (m/v) polyethylene glycol 6000] and 10 mg dm^-3 abscisic acid. Transgenic tobacco plants were obtained via Agrobacterium-mediated transformation and treated with 200 mM NaCl. Reverse-transcription PCR data showed that MsKMS1 was successfully transcribed and expressed in the leaves of transgenic plants. The MsKMS1-overexpressors showed a lower malondialdehyde content and maintained a higher relative water content and proline content compared with non-transgenic controls under salt stress. These results indicate that the introduction of the MsKMS1 gene could improve salt stress resistance in tobacco plants. This study reveals the role of MsKMS1 in the regulation of plant responses to abiotic stress and provides evidence for further functional studies of the KMS1 family in alfalfa.

Crop plants are regularly exposed to an array of abiotic and biotic stresses, among them drought stress is a major environmental factor that shows adverse effects on plant growth and productivity. Because of this these factors are considered as hazardous for crop production. Drought stress elicits a plethora of responses in plants resulting in strict amendments in physiological, biochemical, and molecular processes. Photosynthesis is the most fundamental physiological process affected by drought due to a reduction in the CO₂ assimilation rate and disruption of primary photosynthetic reactions and pigments. Drought also expedites the generation of reactive oxygen species (ROS), triggering a cascade of antioxidative defense mechanisms, and affects many other metabolic processes as well as affecting gene expression. Details of the drought stress-induced changes, particularly in crop plants, are discussed in this review, with the major points: 1) leaf water potentials and water use efficiency in plants under drought stress; 2) increased production of ROS under drought leading to oxidative stress in plants and the role of ROS as signaling molecules; 3) molecular responses that lead to the enhanced expression of stress-inducible genes; 4) the decrease in photosynthesis leading to the decreased amount of assimilates, growth, and yield; 5) the antioxidant defense mechanisms comprising of enzymatic and non-enzymatic antioxidants and the other protective mechanisms; 6) progress made in identifying the drought stress tolerance mechanisms; 7) the production of transgenic crop plants with enhanced tolerance to drought stress.

Tomato is an economically important vegetable. Tomato chlorosis virus (ToCV) and Tomato yellow leaf curl virus (TYLCV) are two major viruses that cause serious losses to tomato production. The effective method to control these two viruses is to breed antiviral species by genetic engineering techniques. In order to obtain the RNA interference (RNAi) expression vector of tomato, the coat protein (CP) genes of ToCV and TYLCV were selected in this study. The tandem sequences of the two CP genes were obtained using the recombinant PCR technique. Using Gateway cloning technology, the RNAi expression vector pRNAi-ToCV-TY including the two CP genes was constructed by attB×attP and attL×attR recombination reactions. Polymerase chain reaction and sequencing analysis confirmed that the vector was obtained successfully and contained the ToCV and TYLCV CP genes. The RNAi expression vector pRNAi-ToCV-TY was transformed into Agrobacterium strain GV3101. The RNAi vector was then used to transform tomato. The objective fragments were successfully transformed into a tomato by PCR identification. At the fourth-leaf stage, the positive transgenic plants were challenged with ToCV and TYLCV. Out of 15 transgenic plants, 33 % showed early symptoms within 4 weeks post-infection (WPI); 20 % showed delayed symptoms (5 - 7 WPI); and the remaining 47 % were symptomless even after 9 WPI. The untransformed control plants (90 %) showed severe symptoms within 2 - 4 WPI, whereas 10 % delayed symptoms.

Plants have developed adaptive strategies to survive under different abiotic stressors. To identify new components involved in abiotic stress tolerance, we screened unannotated expressed sequence tags (ESTs) and evaluated their cold or drought response in Arabidopsis. We identified a drought response gene (DRG) encoding a 39.5-kDa polypeptide. This protein was expressed specifically in siliques and was induced by drought stress in most tissues. When a DRG-GFP construct was introduced into Arabidopsis protoplasts, GFP signals were detected only in the nucleus. The drg mutant plant was more sensitive to mannitol-induced osmotic stress in agar plates and to drought or freezing stress in soil than the wild-type. Activating the DRG restored the normal sensitivity of drg mutants to abiotic stressors. No differences in drought or freezing tolerance were observed between the wild-type and transgenic plants overexpressing the DRG. When DRG was expressed in a cold-sensitive Escherichia coli strain BX04, the transformed bacteria grew faster than the untransformed BXO4 cells under cold stress. These results demonstrate that DRG is a nuclear protein induced by abiotic stresses and it is required for drought and freezing tolerance in Arabidopsis.

Light and temperature are two essential environmental cues for plants, helping to optimize plant body architecture and physiology. To sense a broad spectrum of sun radiation spanning from UV-B to far-red wavelength, plants are equipped with a sophisticated array of photoreceptors, including phytochromes, cryptochromes, phototropins, Zeitlupes, and UV-B photoreceptor UVR8. On the contrary, since the thermodynamic effects extensively affect the molecular and supramolecular structures, it is difficult to identify the entry point or initial receptor of temperature. Even so, several putative temperature sensors have been proposed, such as calcium ion channels, H2A.Z, and the thermodynamic change of plasma membrane fluidity. Considering that many processes in plant respond to irradiance and temperature, scientists devote to finding out the converge point of these environmental cues. As a typical example, circadian rhythm is such an integration point, which receives the signal input of both irradiance and temperature. The updating evidence shows, as an important photoreceptor, phytochrome B acts as temperature sensors via a thermodynamic active state revision. These findings suggest that the studies on light and temperature receptors in plants should not be separated. Their extensive convergence during signalling provides a new direction for understanding the stimuli perception mechanisms.

Virus-induced gene silencing (VIGS) is a technological process in which the expression of a plant target gene is down-regulated by inoculating a plant with a recombinant virus-based vector carrying part of the coding sequence of the target gene (Baulcombe, 1999a; Burch-Smith et al., 2004). VIGS uses an RNA silencing-based defence mechanism in which double-stranded RNAs (dsRNAs) of viral origin, as templates, are processed into small interfering RNAs by Dicer-like enzymes. The resulting siRNA is incorporated into an RNA-induced silencing complex, which leads to the degradation of the RNA (viral RNA, mRNA) with sequences complementary to the siRNA. Thus, VIGS utilises foreign plant genes/targets harboured by a viral vector to produce dsRNA, a source of siRNAs that triggers RNA-mediated silencing of the corresponding target gene. VIGS has proven to be a powerful and cost-effective method for functional genomics studies in plants (Rössner et al., 2022).

Cellulose is the most abundant polysaccharide produced by plants. In the form of rigid microfibrils surrounding the cells, cellulose constitutes the load-bearing cell wall element that controls cell growth and shape. Cellulose microfibrils are laid down outside the cell by the multimeric plasma membrane-inserted cellulose synthase complexes (CSCs), which move along underlying cortical microtubules (CMTs). In plants, CSCs are shaped as rosettes with six lobes symmetrically arranged in a hexagonal structure. In Arabidopsis, the CSC is composed of at least three functionally non-redundant cellulose synthase (CESA) glycosyltransferases in both primary and secondary cell walls. The number, organization, and interactions of CESA proteins within the CSC have been debated for many years on the basis of numerous lines of evidence provided by electron microscopy, biochemical and genetic approaches, spectroscopic techniques, as well as computational modeling. The Arabidopsis thaliana model was extremely useful in elucidating the molecular composition of CSC and enabled to elucidate the specialized functions of distinct AtCESA isoforms. Several additional, non-CESA proteins involved in cellulose synthesis and its regulation were also identified in Arabidopsis. This review outlines the latest findings on CSC organization, trafficking, and plant-specific proteins directly associated with the complex and interconnecting CESAs with CMTs.

Plant translation elongation factor 1 alpha (EF1A) is both a protein synthesis factor and an important component of plant signal transduction, immune responses, protein trafficking, and apoptosis. However, its role in plant growth and development remains unclear. Herein, a full-length EF1A gene was isolated from banana (Musa acuminata L.) fruit and termed MaEF1A. We found that MaEF1A shared a high sequence identify with respective genes in other plants and the deduced amino acid sequence contained conserved regions of GTP-EFTU, GTP-EFTU-02, and GTP-EFTU-03, as well as two tRNA binding domains and six GTP-binding sites which represent functional domains for protein biosynthesis. MaEF1A protein is mainly localized to the nucleus. MaEF1A was constitutively expressed in different banana organs including developing fruits, and the highest expression was detected in ovary 4 stage. Arabidopsis thaliana L. (ecotype Columbia) was transformed with MaEF1A and four transgenic lines were obtained. Three transgenic lines were selected for further phenotypic analyses. Our findings indicate that overexpressed MaEF1A could greatly enhance plant height, root length, and both rhachis and silique length by promoting cell expansion and elongation. These experiments suggest an important role for MaEF1A in plant growth and development.

In natural environments, the growth and development of plants are frequently impeded by a variety of stresses. These can be categorized into biotic stresses, such as those caused by fungi and bacteria, and abiotic stresses, including factors like low temperature, drought, and salinity (Zhu, 2016). These stresses impact plant photosynthesis, osmotic adjustment, and nutrient uptake, thereby inhibiting plant growth and ultimately resulting in a reduced crop yield and quality. To adapt to the dynamic changes in the environment, plants have evolved a series of complex defense mechanisms that are precisely regulated at the molecular, cellular, biochemical, and physiological levels to respond to various stresses. Among them, transcription factors (TFs) are key regulators that control the majority of stress response genes and signal transduction pathways. They are activated by different pathways of signal transduction and can directly or indirectly combine with cis-acting elements to modulate the transcription efficiency of target genes, which play a crucial role in the regulation of plant response to biotic and abiotic stresses.

Silicon has been widely reported to have a beneficial effect on improving plant tolerance to biotic and abiotic stresses. However, the mechanisms of Si in mediating responses to simultaneous salt and drought stresses are still poorly understood. Glycyrrhiza uralensis Fisch. is classified as a non-Si accumulator and suffered from salt and drought stresses. In this study, we investigated the long-term application of Si on Si content in G. uralensis roots, stems and leaves, leaf anatomy, ultrastructure, chlorophyll (Chl) content, gas exchange characteristics, relative water content, and growth of two-year-old plants under different salt and drought stresses. Silicon application resulted in a higher Si uptake in G. uralensis roots and more Si accumulation in leaves (especially deposition of Si on cell walls), and Si counteracted the adverse effects induced by salt and drought stresses on the leaf anatomy and ultrastructure. In plants treated with Si, a higher chlorophyll content, net photosynthetic rate and relative water content led to a higher growth rate and dry mass under salt and drought stresses compared with corresponding non-Si treated plants.

Worldwide, a relevant surface of arable lands is facing salt stress, and this surface is increasing continuously due to both natural and anthropogenic activities. Nitric oxide (NO) is a small, gaseous molecule with a plethora of physiological roles in plants. In addition to its normal physiological functions, NO protects plants subjected to different environmental cues including salinity. For example, NO mediates photosynthesis and stomatal conductance, stimulates the activity of Na⁺/H⁺ antiport in tonoplast, promotes the biosynthesis of osmolytes, and counteracts overaccumulation of reactive oxygen species in plant cells under salt stress. Exogenous NO is also beneficial for plants subjected to salinity, in which it increases salinity tolerance via growth promotion, reversing oxidative damage, and maintaining ion homeostasis. This review provides a comprehensive picture of the NO-mediated mechanisms in plants, resulting in salinity tolerance with a particular focus on the photosynthetic processes, the antioxidant patterns as well as the cross-talk with other regulatory compounds in plant cells.

Over the past few decades, rice (Oryza sativa L.) has remained a fundamental staple crop and a primary nutritional energy source for nearly 3.5 billion people worldwide, particularly in Asia. With the global population projected to reach 9.6 billion by 2050, rice production must significantly increase to meet the escalating food demand. However, salinity stress poses a major abiotic challenge that severely hampers plant growth and productivity. Soil salinization, driven by climate change and rising temperatures, leads to an excessive accumulation of salts in the soil (Sári et al., 2023). This phenomenon disrupts plant physiology through water deficit, cytotoxic effects of Na⁺ and Cl⁻ ion accumulation, and nutrient imbalances (Isayenkov and Maathuis, 2019). In coastal regions, salinity stress is further intensified by seawater intrusion into groundwater reserves (Muhardi et al., 2020), while in arid and semi-arid areas, low rainfall limits salt leaching, resulting in excessive salt accumulation (Karolinoerita and Yusuf, 2020). Exposure to salinity stress induces the overproduction of reactive oxygen species (ROS), a group of highly reactive free radicals that can damage essential cellular components, including DNA, proteins, lipids, and pigments, ultimately impairing plant function (Ghosh et al., 2021). To mitigate these detrimental effects, plants activate various adaptive responses (Huong et al., 2020), including the upregulation of antioxidant enzyme systems (Jan et al., 2019), which play a crucial role in ROS scavenging and oxidative stress alleviation. These responses involve both well-developed enzymatic and non-enzymatic scavenging pathways or detoxification systems to counter the destructive effects of ROS that include the enzymes superoxide dismutase (SOD), catalase (CAT), ascorbate peroxidase (APX), glutathione reductase (GR), and so forth (Hasanuzzaman et al., 2011).

Plants have developed adaptive strategies to cope with environmental stresses, but mechanisms effective under one stress may be counterproductive under others. This study investigates the effect of moderate drought stress pretreatment on the resistance of Brassica napus to Leptosphaeria maculans, the pathogen causing blackleg disease. B. napus plants were exposed to varying durations of drought stress, followed by a 24-h recovery period before inoculation with L. maculans. The results demonstrate a priming effect of the drought pretreatment, with a reduction in necrotic lesions in cotyledons compared to non-stressed controls. The most pronounced effect was observed in plants that underwent a 68-h drought pretreatment, resulting in a 45% reduction in disease symptoms. The transcriptions of 17 genes involved in B. napus defence against pathogen infection and drought stress were monitored. This revealed the involvement of the salicylic acid signaling pathway, indicated by increased expression of PR1 and PR2 marker genes. Additionally, drought stress marker genes were upregulated. These findings provide insight into the mechanisms of plant adaptation to combined biotic and abiotic stresses, which is essential for sustainable agriculture in a changing environment.

We identified a Populus nigra auxin-regulated gene involved in organ size (PnARGOS)-LIKE, encoding one organ size related protein in black poplar. It is homologous to AtARGOS and AtARGOS-LIKE genes of Arabidopsis thaliana. ABRE-like, G-box, GATA and I-box motifs were discovered in the promoter region of the poplar ARGOS-LIKE gene. In wild type aspen (Populus tremula) plants, an ortholog of the PnARGOS-LIKE gene (PtrARGOS-LIKE) was noticeably expressed in actively dividing and expanding young leaves and calli, whereas its mRNA content increased in response to exogenous 6-benzylaminopurine, 1-naphthaleneacetic acid, and 24-epibrassinolide. Expression of the PtrARGOS-LIKE gene was reduced under a salinity treatment. In addition, we generated transgenic tobacco and aspen plants with an up-regulated expression of the PnARGOS-LIKE gene. A constitutive expression of the gene contributed to an increase in size of stems and leaves of the transgenic tobacco plants. In the transgenic aspen, a constitutive expression of the PnARGOS-LIKE gene promoted an increase in the frequency of leaf initiations and in leaf length and area. The size of transgenic tobacco and aspen leaves increased due to the enlargement of individual cells. The results show the significance of the PnARGOS-LIKE gene for control of leaf initiation and organ growth by cell expansion in poplar.

Tomato spotted wilt virus (TSWV; species Orthotospovirus tomatomaculae, family Tospoviridae) (Kuhn et al., 2023), is a negative strand RNA-virus containing envelope structures, which makes it unique among plant viruses (de Haan et al., 1991). TSWV ranks among the most destructive plant viruses worldwide. First described in Australia in 1919, TSWV has since attained a global distribution, infecting over 1 000 plant species across more than 85 families, including key agricultural crops such as tomato (Solanum lycopersicum), pepper (Capsicum annuum), groundnut (Arachis hypogaea), and various ornamentals (Parrella et al., 2003; Pappu et al., 2009). Infected plants typically exhibit chlorotic or necrotic spots, wilting, stunted growth, and in severe cases, complete crop failure, resulting in considerable economic losses, particularly in Solanaceous and Asteraceous crops (Roselló et al., 1996; Latham and Jones, 1998).

Nitrogen is an essential nutrient for plants. Different nitrate (NO₃^-)/ammonium (NH₄⁺) ratios have different effects on plant growth. However, the underlying mechanism in Toona sinensis remains unclear. Thus, we determined the effects of five different NO₃^-/NH₄⁺ ratios (16/0, 12/4, 8/8, 4/12, and 0/16, denoted T1, T2, T3, T4, and T5, respectively) in nutrient media on T. sinensis seedling growth. When the nitrogen source was NH₄⁺ alone (T5) or NO₃^- alone (T1), the soluble protein content in the leaves was the lowest. Additionally, the activities of key nitrogen assimilation-related enzymes, such as nitrate reductase (NR), glutamate synthase (GOGAT), and glutamine synthetase (GS), were altered by the NO₃^-/NH₄⁺ ratio. Principal component analysis (PCA) revealed that the T2 treatment was optimal for T. sinensis seedling growth. The NO₃^-/NH₄⁺ ratio regulates nitrogen assimilation at the transcription level, as under high NO₃^- conditions, the expressions of NR, GS, and NADH-GOGAT were high, and nitrate transporter (NRT) family members NRT1, NRT1.1, and NRT1.7 played leading roles in nitrogen transport. However, under low NO₃^- conditions, the level of NRT2.7 increased to ensure nutrient absorption. Our results provide a theoretical basis for understanding how different NO₃^-/NH₄⁺ ratios affect T. sinensis growth.

Plants are severely affected by many biotic stresses, which cause a reduction in crop quality and quantity. One of the strategies to manage biotic stresses is the generation of transgenic plant lines that can be used as biosensors. These biosensor plants can trigger an early warning upon any pathogen infection. Two promoters with β-glucuronidase reporter gene fusions were constructed. The first contained the flagellin sensing 2 gene promoter, whereas the second contained synthetic promoter containing four repeats of cis-acting elements from the pathogen-related protein 1 gene and two transcription enhancers from the 35S promoter. Transformed leaves were treated with a phytohormone salicylic acid to mimic the occurrence of biotic stress. Validation of reporter gene expression induced from both constructs in transformed potato leaves displayed an increase upon salicylic acid treatment. The results reflect that both constructs could serve in the production of potato biotic stress biosensors.

Background: Tomato plants exposed to salinity stress may experience dynamic changes in root growth and cell wall (CW) composition and structure. Aims: Here, we determined the CW composition and cation-exchange capacity (CEC) of two tomato cultivars (Daniela, salt-tolerant and Naomi, salt-sensitive) as well as their growth and root characteristics. Methods: Seedlings of the tomato cultivars were exposed to six NaCl plus CaCl₂ concentrations hydroponically, root growth and CW chemical composition were measured. Results: The root growth of Naomi was adversely (P ≤ 0.05) reduced at the elongation zone, but there was little change in the chemical composition of the CW under salinity. A marked reduction occurred in the CW-constituting polysaccharides of Naomi relative to Daniela, whether at the 8.00 dS m^-1 NaCl treatment or its combination with CaCl₂. For both root zones, CW viscosity was better enhanced under NaCl and CaCl₂ combinations, but the contents of uronic acid across the CW constituents increased under sole treatment with CaCl₂ at the mature root zone of Naomi. The root CW CEC increased (P ≤ 0.05) with increases in the ionic concentration of the external solution. Salt concentrations at 8.0 dS m^-1 NaCl or 8.0 dS m^-1 NaCl + CaCl₂ increased (P ≤ 0.05) the CEC of the CW, especially for Daniela. Conclusions: The overall results showed that CaCl₂ could enhance some tolerance in CW polysaccharides of tomato under salinity stress. The salt-tolerant Daniela with higher CW and ionic contents had superior stability in cell structure under salt stress.

This study investigated the impacts of acid rain stress on Akebia trifoliata and the mitigation effects of exogenous curcumin (CUR) using integrated physiological, anatomical, and transcriptomic analyses. Acid rain stress significantly decreased chlorophyll content (total chlorophyll by 64.8%), leaf epidermal thickness (upper and lower epidermis by 58.9 and 35.6%), and starch content (by 63.9%), while increasing oxidative stress markers (MDA by 82.6%; ROS production by 345.8%) and content of osmolytes (proline by 64.4%). A. trifoliata counteracted acid rain stress by enhancing superoxide dismutase (SOD) and catalase (CAT) activities, and by modifying leaf anatomical structure (increased mesophyll tissue thickness). CUR application, particularly at 50 μmol/L (CUR50), effectively alleviated damage by maintaining leaf structural integrity and promoting growth recovery. Transcriptomic analysis revealed 993 differentially expressed genes between CUR50-treated vs. acid rain-stressed plants, primarily enriched in the plant hormone signal transduction and phenylpropanoid biosynthesis pathways. These results demonstrate that CUR mitigates acid rain stress through coordinated physiological adaptations and transcriptional reprogramming of stress-responsive pathways. This study provides a theoretical basis for cultivating A. trifoliata and implementing phytoremediation strategies in acid rain-affected regions.

Involving the natural host-resistance mechanisms to pathogens are essential and one of the most promising approaches in development of first-line defenses against viral plant diseases. Polysaccharides isolated from natural sources are considered the most active resistance inducers. The biological activity of polysaccharides depends on the nature and chemical structure of the constituent components of complex preparations. In this view, the objective of our study was to evaluate the biological activity of complex preparations composed of glycans, rhamnolipids, and thiosulfonates as inducers of natural plant resistance and inhibitors of tobacco mosaic virus (TMV). Complex preparations were obtained using the following components: biogenic glycolipids - rhamnolipids of the Pseudomonas sp. strain PS-17, glycans - Ganoderma adspersum glucan and Candida maltosa mannan, as well as synthetic biocides - thiosulfonates (methylthiosulfanilate). The biological activity of the preparations was investigated in the host-virus model system Nicotiana tabacum L. and TMV. It was shown that preparations at concentrations of 10 and 100 μg mL^-1 were active plant resistance inducers in N. tabacum cv. Immune 580, hypersensitive to TMV. At the same concentrations, complex preparations also reduced infectivity of TMV on Datura metel L. acting as viral infection inhibitors. The inducing activity of the complex preparations is sensitive to well-known transcription inhibitor actinomycin D (10 μg mL^-1). This fact may indicate the important role of RNA synthesis in the activation of plant virus resistance by the studied preparations.

Drought-responsive element binding (DREB) is involved in the regulation of stress-responsive gene expressions in plants through abscisic acid (ABA)-independent pathway. In this study, constitutive expression of oil palm (Elaeis guineensis) EgDREB1 driven by double strength cauliflower mosaic virus 35S promoter in tomato (Solanum lycopersicum) reduced seed number, produced parthenocarpic fruits, changed morphology of leaves, and increased root biomass of transgenic plants. Early flowering and fruiting of the transgenic lines were observed in the culture vessels. EgDREB1 was specifically expressed in the fruits and its expression was not detected in vegetative tissues (leaves and roots). Altered expression of several endogenous tomato genes involved in the biosynthesis of phytohormones including jasmonic acid, ethylene, auxin, cytokinin, gibberellin (GA) and ABA were observed compared to wild type plants. The expression of AP2-like-ethylene transcription factor (LeAP2), allene oxide synthase (LeAOS), allene oxide cyclase (LeAOC), aminocyclopropane-1-carboxylic acid synthase (LeACS), 1-aminocyclopropane-1-carboxylate oxidase 1 (LeACO), auxin responsive factor 8 (LeARF8), auxin/indole-3-acetic acid (LeAux/IAA), cytokinin oxidase/dehydrogenase-like (LeSlCKX1), adenylate isopentenyltransferase (LeSlIPT1), gibberellin 2-oxidase 2 (LeGa2ox2), gibberellin 20-oxidase 4 (LeGa20ox4) and ABA-aldehyde oxidase (LeAAO) were different in fruits with reduced seed number compared to parthenocarphic fruits. These results suggest that their expression has significant effects on fruit development in transgenic tomato. EgDREB1 may mediate the expression of some of these genes as dehydration-responsive element binding (DRE) motif were found in their promoter sequences. These data indicate that the EgDREB1 controls fruit development in trsngenic plants by regulating the expression of hormone-associated genes.

A photoperiod-sensitive soybean [Glycine max (L.) Merr] cv. ZhongDou 24 (ZD24) exhibiting delayed flowering when grown under long-days (LD, a 16-h photoperiod) was used to identify the genetic control of flowering delay. A differential expression profiling technique enabled identification of a gene fragment that was up-regulated under LD. This fragment was homologous to a gene encoding methionine synthase (MS) in soybean and was named GmMS. The RNA content confirmed that GmMS was expressed in roots, stems, and leaves of soybean grown under LD. The highest expression was in stems. Full length GmMS, encoding 763 amino acids, was transferred into tobacco plants. The ectopic expression of GmMS in tobacco resulted in delayed flowering. Other effects included stunting, an increased MS activity and methionine content, a higher content of alcohol-soluble proteins and of chlorophylls, and a lower content of anthocyanins.

In plant breeding, polyploidization is an established technique to obtain superior phenotypic characteristics. In seed propagated agricultural crops, seed treatments with antimitotic agents are often used to obtain chromosome doubling. Here, we developed a method to induce polyploidization in clonally propagated fodder grasses Lolium, Festuca, and the intergeneric hybrid Festulolium. The aim was to obtain specific genotypes at both the diploid and tetraploid levels. We evaluated different types of plant explants, and the effects of the type, concentration, and application mode of three antimitotic agents (oryzalin, colchicine, and trifluralin) on the survival rate and the polyploidization efficiency. The treatment of greenhouse-grown tillers with antimitotics only resulted in mixoploids, while tissue culture propagated plants were successfully polyploidized. A shock pretreatment, using a high concentration of an antimitotic agent during a short period, successfully induced tetraploids in all three genera. Additionally, supplementing the tissue culture medium with a lower dosage of an antimitotic agent during minimal four weeks after the shock pretreatment further promoted polyploidization. By our methods, we were able to generate diploid and tetraploid plants with an identical genomic constitution but different ploidy allowing investigation of the effects of polyploidization on plant physiology and gene regulatory networks.

Circular RNAs (circRNAs) are relatively new members of the RNA world and can contribute to crucial biological functions. CircRNAs have tissue-specific expression profiles depending on cell type and developmental stage. In Sistan region cultivated grapes are seedless but have small berries. The compact clusters are another notable characteristic of these grape cultivars, which negatively impacts their marketability. In this study, we aimed to identify the circRNAs that are active in cluster formation and investigated the effects of gibberellin treatment on their expression. Eight detection tools were used to predict the expressed circRNAs. Reliable circRNAs were used to identify potential functions of differentially expressed circRNAs by gene ontology (GO) analysis and prediction of target microRNAs (miRNAs). Of the 28 157 circRNAs detected, 3 715 were reliable. 900 differently expressed circRNAs were identified in the three developmental stages of the cluster under gibberellin treatment. Among the 503 target miRNAs found, 12 miRNAs were selected based on the number and expression of their circRNA sponges. Of the 29 circRNAs in the circRNAs-miRNAs-mRNAs interaction network, 12 circRNAs are highly conserved. Our results suggest that circRNAs in grape may play a key role in developmental and environmental adaptation in perennial plants.

Opportunities exist to accelerate genetic gain in forage breeding using genome-wide selection approaches. In this study, we evaluated rapid cycle recurrent genomic selection (GS) as a means of improving genetic gain for value of annual forage yield. A small population of tetraploid half-sib families was evaluated for seasonal forage yield over two years, and the maternal parent plants were genotyped and genomic prediction models developed. The GS model for value of annual forage yield had a predictive ability of 0.23. An initial round of among-family selection based on field evaluations and within-family selection using genomic estimated breeding values was performed. This was followed by two further GS cycles. New synthetics were produced after each round of selection and were established in a field trial alongside the starting population. A positive response to selection was observed in new synthetics after two successive rounds of rapid cycle recurrent genomic selection before declining in the third round. The genetic gain for the value of annual forage yield was 2.4% from C₀ SYN-1 to C₁ SYN-1 and 6.4% from C₁ SYN-1 to C₂ SYN-1_. In the case of C₀ to C₁, genetic gain was compounded by among-family selection based on field evaluations. The implementation of rapid cycle recurrent genomic selection offers an opportunity to increase genetic gain; however, the predictive ability is likely to decay rapidly as selection candidates become more distant from the training population.

Roots are important for plant anchoring, water and nutrient absorption, and other physiological processes. Gravity is a primary determinant of the spatial distribution of plant roots in the soil. Therefore, in-depth understanding of the molecular mechanisms and biochemical networks of root responses to gravity has both theoretical and practical significance in guiding the genetic improvement of plants. Gravitropism, the process through which plants sense the direction of gravity and respond by making the roots grow downward and the stem grow upward, has been widely studied in roots. The perception of gravity and the gravitational growth of roots, key steps in root growth and development, are regulated by auxins and other factors. Here, we review the latest progress in the regulation of root gravitropism by hormone signals and environmental factors from a molecular perspective, and look forward to the direction of future research on root gravitropism.

Since 1960, the positive effects of rare earth elements (REE) on crop physiology have been observed, and support for photosynthesis, biomass accumulation, secondary metabolites, or enzymes has been reported in 40% of studies. A higher content of chlorophylls a and b as well as carotenoids have been found along with an increased efficiency of photosystem II photochemistry and electron transfer rates. An increased activity of a key photosynthetic enzyme was also found in several plants growing in soil with a higher content of REE. An appropriate amount of REE also activates the antioxidant activity of peroxidase, superoxide dismutase, and catalase. These enzymes, together with a higher content of flavonoids and carotenoids, increase the resistance of plants to oxidative stress caused by different abiotic stresses. The positive effect of REE on biomass accumulation was also confirmed, but their affection on mycorrhizal symbiosis remains ambiguous. On the other hand, an excess of REE leads to damage to plants including the chloroplast ultrastructure. Therefore, the positive and negative effects of REE remain controversial, and the mechanisms of effects of REE in plants remain poorly understood. In addition to physiological processes, the absorption, bioavailability, and translocation of REE in plants as well as their possible ecotoxicology and hyperaccumulation are discussed in this review.

Phosphorus is a key limiting factor for plant growth. Several approaches are developed to mitigate the impact of P shortage on plants and to the selection of crops with high P mobilizing capacity from P-deficient soils. In this work, four Medicago truncatula genotypes (A17, TN8.20, TN1.11, and TN6.18) were compared for their efficiency to cope with P limiting conditions using several criteria. Significant differences between genotypes, P deficiency treatments, and the interaction of genotypes with P deficiency treatments were found. P limitation resulted in an important decrease in shoot biomass, P content, P use efficiency, and photosynthetic parameters. A significant variability was found between the four genotypes, with A17 and TN8.20 being the most tolerant genotypes to P deficiency. This was consistent with the better ability of these genotypes to acidify rhizosphere and stimulate the activity of acid phosphatase and its relative gene (MtPAP1). The expression of P transporter genes (MtPT1, MtPT3, and MtPT5) was induced by P deficiency, however, the overexpression of those genes was more pronounced in tolerant genotypes. Overall, our data indicate that A17 and TN8.20 are more efficient in mobilizing P under limiting conditions and could be cultivated in P-deficient soils as forage crops.

This study aimed to evaluate the effect of putrescine priming on the initial growth, chlorophyll fluorescence, primary metabolites accumulation, and antioxidant enzyme activities in two maize hybrids with contrasting drought tolerances. Seeds of Zea mays L. hybrids DKB 390 (drought tolerant) and BRS 1030 (drought sensitive) were primed with putrescine (10 or 100 µM). Paper rolls moistened with distilled water or mannitol (-0.6 MPa) were maintened at 30°C for 7 d. The growth parameters were higher in the DKB hybrid than in the BRS hybrid. Putrescine priming (10 µM) promoted the root growth of BRS at levels similar to those of DKB and improved photochemical and non-photochemical quenching and maximum quantum efficiency of BRS seedlings. Higher levels of reducing sugars were found in DKB seedlings when compared to BRS in both roots and leaves, especially with 100 µM putrescine. Total soluble sugar and starch were lower in the maize roots under water deficit and with 10 µM putrescine for both hybrids. BRS seedlings showed higher starch content in the leaves in the control and 10 µM putrescine treatments. Superoxide dismutase was activated in BRS plants by the priming, especially in the roots, but this effect was not observed for catalase, ascorbate, or guaiacol peroxidase, although the DKB seedlings presented much higher guaiacol peroxidade activity than BRS seedlings in both the roots and shoots. In conclusion, putrescine priming (10 M) improved the morphological and biochemical responses of the drought sensitive maize hybrid BRS.

Lettuce is one of our most important leaf vegetables that can be cultivated safely in organic farming, which is not only pesticide-free, but also aims to maintain and stimulate the presence of naturally occurring beneficial organisms, such as algae, mosses, bacteria, or arbuscular mycorrhiza (AM) fungi. These organisms are all beneficial for soil life and nutrient decomposition. The positive effects of beneficial microorganisms could be enhanced by mulching which is a widely used practice in organic farming. Mulching may also increase soil nutrient substance after decomposition and inhibit weed growth. In our experiment, we sought to determine the effect of different mulching techniques (alfalfa, rye, black foil) on AM root colonisation, leaf chlorophyll (Chl) content, and on peroxidase (POD) activity in Lactuca sativa plants and observe whether there are correlations between these parameters. Results show natural mulching has a positive effect on mycorrhiza fungi root colonisation and therefore lowers the stress in lettuce plant. On the other hand, there was no significant correlation between root colonisation and Chl content. As POD enzymes are directly linked to enzymatic browning, the high colonisation rate of AM may consequently lower post-harvest browning in lettuce.