Background: RAB Guanine Nucleotide Dissociation Inhibitors (RAB GDIs) are important vesicle transport regulators in eukaryotes, participating in the functional cycle of RAB GTPases by stabilizing their non-active GDP-conformation. Aims: We address the importance of the three Arabidopsis thaliana RAB GDI paralogs by genetic and developmental analyses and put these results into the seed plants evolution context. Methods: We use methods of genetics, microscopy, and phylogenetics. Results: Our genetic analyses of Arabidopsis T-DNA insertional mutants confirm recent CRISPR alleles data indicating lethality of double gdi1 gdi2 mutants, and our microscopic data point to embryo development arrest in double mutant seeds. We also confirm the involvement of GDI2 and GDI3 in pollen tube growth. Moreover, our data show that GDI1 also contributes to proper pollen function. Our phylogenetic analysis reveals independent diversification of RAB GDIs in Gymnosperms and Angiosperms, with early specialization of an Angiosperm reproduction- and gametophyte-related clade. Conclusions: In Arabidopsis, RAB GDI1 and 2 are important for the vegetative growth while RAB GDI2 and 3 are vital for reproduction. Evolution of the RAB GDI family reflects the evolution of seed plants.

A plasmid and two isocaudamer systems, namely, NotI/Bsp120I and SpeI/XbaI/NheI, were used to construct a new type of multi-gene plant transformation vector system. This system included a transformation vector containing the restriction enzyme cutting sites Bsp120I and XbaI as well as a cloning vector containing the restriction enzyme cutting sites NotI, Bsp120I, SpeI, and NheI. The open reading frame of the new target genes was connected to the transformation vector. The original restriction enzyme cutting site disappeared after connecting to the isocaudamer. The plant transformation vector p096871, which contained Bacillus thuringiensis (Bt) genes Cry1Ac and Cry3A as well as p09X6, which contained mtlD, strD, betA, nhaA, and ostAB, were constructed using this vector system. Resistant plants were obtained after tobacco was transformed by two vectors via the Agrobacterium-mediated method. Detection by PCR revealed that all exogenous genes were inserted into the genome of tobacco. Real-time fluorescence quantification PCR, reverse transcription PCR, and ELISA detections were performed on five transgenic lines transformed by two Bt genes. Cry1Ac and Cry3A were inserted into the genome with a single copy to transcribe and express Bt toxins. The proposed vector system reduced the number of operational procedures and minimized the difficulty of the experiment.

Background: Stem base rot disease poses a serious threat to the Cyclocodon lancifolius industry, yet its causal agent remains unidentified. Aims: In this study, we aimed to identify the pathogenic fungi responsible for this disease and to screen for effective biocontrol strains against the causal agent. Methods: We isolated and identified the fungal pathogen from the stem base of diseased plants and confirmed its pathogenicity by fulfilling Koch's postulates. Multilocus sequence analysis identified the pathogen as Stemphylium lycopersici. Results: An antagonistic strain, Bacillus subtilis YHYS1, exhibited significant inhibition (51.8%) of S. lycopersici growth in a plate confrontation assay. Volatile compound analysis further confirmed the fungistatic potential of YHYS1. These findings highlight the promise of YHYS1 as an eco-friendly alternative to chemical fungicides for controlling stem base rot disease in C. lancifolius caused by S. lycopersici. Conclusions: Our characterization of this novel disease in C. lancifolius has elucidated the pathogenic features of Stemphylium species, an essential yet understudied group of plant pathogens. These findings provide valuable references for the diagnosis and control of diseases affecting C. lancifolius.

The Arabidopsis heme oxygenase 1 (HY1) plays a significant role in the signal transduction of abiotic stimuli and hormonal response. To characterize the HY1 promoter, an approximately 1.8 kb of it (pHY1, -1666 to +132) and its deletion fragments (5D1, -1528 to +132; 5D2, -1109 to +132; 5D3, -688 to +132; 5D4, -169 to +132; 3D1, -1666 to +100; 3D2, -1666 to -1; and 3D3, -1666 to -170), were fused to the β-glucuronidase (GUS) reporter gene and transformed into Arabidopsis. The transgenic plants were subjected to several environmental stimuli (especially to mild salinity, iron deficiency, and mercury exposure). The results show that the region from +1 to +100 in the 5'-untranslated region were essential for HY1 basal promoter activity. The induced GUS activities under NaCl and H₂O₂ treatments were slowed down by the progressive 5' deletion (from -1666 to -688) and correlated with the reduced numbers of myeloblastosis (MYB) binding sites (MBSs; -1542, -1333, -1078, and -177). The MBS-free promoter construct 5D4 (-169 to +132), however, fully lost the inducibility. Therefore, we propose that the MBS elements existing in the HY1 promoter might be crucial for salinity-induced HY1 up-regulation in an H₂O₂-dependent fashion. Moreover, the regions from -169 to -1 and -688 to -169 were presumed as the regulatory regions of HY1 promoter in response to iron deficiency and mercury exposure, respectively.

Background and aims: There appears to be a strong correlation between the rapid proliferation of shrubs in the alpine grassland of the Qinghai-Tibet Plateau and the root exudates of these plants. The dynamics of root exudates during shrub development, however, have been the subject of few investigations. Methods: This work examined Lonicera thibetica, a plant found on the eastern edge of the Qinghai-Tibet Plateau. It focused on the root systems of 5-, 10-, 15-, and 20-year-old L. thibetica plants and how their primary organic acid components changed with the seasons and other circumstances. Results: The findings revealed that the primary components of acid secretion in the roots of L. thibetica were oxalic acid, lactic acid, and tartaric acid; of these, oxalic acid made up over 50% of the total organic acid content. The levels of these organic acids often dropped as shrubs got older, and their seasonal dynamics exhibited a parabolic shift pattern, typically peaking during the robust development stage. According to regression analysis, soil moisture was the primary determinant of the concentration of organic acids produced by alpine shrub roots, suggesting that soil moisture played a crucial role in the secretion process. Conclusions: The physiological dynamics of roots and the mechanisms that regulate them throughout the expansion of alpine shrubs can be better understood thanks to this work.

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.

This study aimed to develop a new vector system to remove selection genes and to introduce two or more genes of interest into plants in order to express them in a coordinated manner. A multigene expression vector was established based on pCamBIA2300 using a selectable marker gene (SMG)-free system based on the combination of the isocaudamer technique and double T-DNA. The vector DT7 containing seven target genes was constructed and introduced into tobacco using Agrobacterium-mediated transformation. Twenty-one of 27 positive transgenic plants contained both T-DNA regions. The co-transformation frequency was 77.8 %. The frequency of unlinked integration of two intact T-DNAs was 22.22 % (6/27). The frequency of removal of SMG from transgenic T1 plants was 19.10 %. These results suggest that this vector system was functional and effective for multigene expression and SMG-free transgenic plant cultivation. At least seven target genes can be co-expressed using this system. Overall, these findings provide a new and highly effective platform for multigene and marker-free transgenic plant production.

Agarwood, the resin part of Aquilaria spp., is valued in medicine, perfumes, and incense. The most important components of agarwood are sesquiterpenes, which are produced only when a healthy tree is wounded. Agarwood sesquiterpene synthase 1 (ASS1) is one of key enzymes responsible for the biosynthesis of sesquiterpenes in Aquilaria sinensis (Lour.) Gilg, and it is a typical wound-inducible synthase. To elucidate its regulatory mechanism at the transcriptional level, a 978-bp sequence upstream of the translation initiation codon ATG of the promoter for ASS1 was cloned. Computational analysis revealed that this promoter contained many known cis-elements including several defense related transcriptional factor-binding boxes. To functionally validate the promoter, a 5' truncated fragment fused with the β-glucuronidase (GUS) reporter gene was used for generating stable transgenic Arabidopsis plants. The spatial and temporal expression patterns of GUS in transgenic Arabidopsis showed that the promoter of ASS1 was induced by mechanical wound and mainly expressed in vascular bundles. Subcellular localization showed that ASS1 localized in the nucleus and plasma membrane. Here, identification of the ASS1 promoter not only lays a foundation for studying its transcriptional regulation, but also provides clues for studying the synthesis mechanism of agarwood sesquiterpenes.

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.

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.

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.

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).

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.

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).

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.

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.

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.

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.

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.

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).

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.

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.

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.