Search Results (43)

Polyamines, a class of low-molecular-weight nitrogen-containing bases with high biological activity, are ubiquitous in organisms and play protective roles in plants under stress. Polyamine oxidase (PAO), a typical flavoprotein characterized as a glycoprotein, is a key enzyme in polyamine catabolism that directly mediates polyamine breakdown and maintains intracellular polyamine homeostasis. However, the specific functions of PAOs in cotton fiber development remain largely unclear. In this study, we identified 23 GhPAO genes from the upland cotton (Gossypium hirsutum L.) genome via comprehensive bioinformatics approaches. We systematically analyzed their physicochemical properties, phylogenetic relationships, gene structures, chromosomal locations, conserved motifs, cis-acting elements, and expression patterns. Quantitative real-time PCR (qPCR) analysis confirmed that GhPAO10 and GhPAO21 exhibited the most pronounced transcript accumulation during both fiber development and stress response processes. Further yeast one-hybrid (Y1H) and dual-luciferase reporter assays indicated that the GhPAO21 promoter was directly regulated by the transcription factor GhTGA1. Our findings provide a foundation for elucidating the functional roles of the PAO gene family in upland cotton and underscore potential candidate genes associated with fiber development and stress responses. Full article

As a class of glutathione-dependent oxidoreductases, glutaredoxins (GRXs) play a central role in maintaining cellular redox homeostasis, thereby influencing diverse biological processes including growth, development, and stress adaptation in plants. This study identified 36 GRX genes in Litsea cubeba through whole-genome analysis. Phylogenetic classification placed them into four subfamilies (CC-, CGFS-, CPYC-type, and a species-specific SS branch), consistent with patterns in model plants like Arabidopsis thaliana and Oryza sativa, indicating evolutionary conservation of GRX core motifs. Genomic analyses including chromosomal location, collinearity, and gene structure revealed family evolution features. Expression profiling showed 11 LcGRX genes were flower-specific, with marked differential expression during stamen (M2) and pistil (F2) degeneration, supporting their roles in sexual dimorphism. Functional assays confirmed that floral highly expressed LcGRX12 directly interacts with TGA transcription factor LcTGA10, similar to its Arabidopsis homolog ROXY1. This study reveals the GRX-TGA module’s role in floral organ development in L. cubeba, offering insights into redox-mediated sex differentiation in Lauraceae and providing candidate genes for molecular breeding. Full article

Salvia miltiorrhiza Bunge is a traditional Chinese medicinal plant whose roots are rich in water-soluble phenolic acids. Rosmarinic acid and salvianolic acid B are representative components that confer antibacterial, antioxidant, and cardio-cerebrovascular protective activities. However, these metabolites often accumulate at low and unstable levels in planta, which limits their efficient development and use. This review summarises recent advances in understanding salvianolic acid biosynthesis and its transcriptional regulation in S. miltiorrhiza. Current evidence supports a coordinated pathway composed of the phenylpropanoid route and a tyrosine-derived branch, which converge to generate rosmarinic acid and subsequently more complex derivatives through oxidative coupling reactions. Key findings on transcription factor families that fine-tune pathway flux by regulating core structural genes are synthesised. Representative positive regulators such as SmMYB111, SmMYC2, and SmTGA2 activate key nodes (e.g., PAL, TAT/HPPR, RAS, and CYP98A14) to promote phenolic acid accumulation. Conversely, negative regulators such as SmMYB4 and SmMYB39 repress pathway genes and/or interfere with activator complexes. Major regulatory features include hormone-inducible signalling, cooperative regulation through transcription factor complexes, and emerging post-transcriptional and post-translational controls. Future directions and challenges are discussed, including overcoming regulatory redundancy and strong spatiotemporal specificity of transcriptional control. Integrating spatial and single-cell omics with functional genomics (e.g., genome editing and rational TF stacking) is highlighted as a promising strategy to enable predictive metabolic engineering for the stable, high-yield production of salvianolic acid-type compounds. Full article

Fusarium oxysporum-induced soft rot severely threatens postharvest pitaya quality and storage life, and while vanillin shows promise in the disease management, its mechanisms for controlling pitaya decay remain incompletely understood. In this study, we systematically investigated the molecular mechanism by which vanillin inhibits soft rot in postharvest pitaya, employing physiological and biochemical characterization, bioinformatics analysis, and molecular biology techniques. Compared with control fruit on 10 d, vanillin treatment significantly reduced disease index and lesion area by 27.12% and 67.43%, respectively. Meanwhile, vanillin treatment delayed the degradation of total soluble solids (TSSs) and titratable acidity (TA) and promoted the accumulation of total phenolics and flavonoids. Additionally, vanillin enhanced the activities of defense-related enzymes, such as catalase (CAT), superoxide dismutase (SOD), phenylalanine ammonia-lyase (PAL), β-1,3-glucanase (GLU), chitinase (CHI), peroxidase (POD) and polyphenol oxidase (PPO), and increased antioxidant capacity, as evidenced by increased DPPH radical scavenging capacity and ascorbic acid content. This resulted in reduced oxidative damage, as indicated by decreased levels of malondialdehyde (MDA), H₂O₂ and O₂^•−. Yeast one-hybrid (Y1H), dual-luciferase reporter (DLR) and subcellular localization revealed that HuTGA1, a nuclear-localized transcriptional activator, specifically bound to the as-1 cis-acting element and activated expression of HuNPR1 and HuNPR5-1. Transient overexpression of HuTGA1 reduced reactive oxygen species (ROS) accumulation and upregulated related genes. These findings suggest that vanillin treatment might enhance pitaya resistance by activating the HuTGA1-HuNPR signaling module, providing insights into the molecular mechanisms underlying vanillin-induced resistance. Full article

Mustard (Brassica juncea), an essential leaf and oil crop in China, exhibits notable yield potential and adaptability, both of which are influenced by the morphology of the leaf margin. Despite its agronomic importance, the genetic regulatory mechanisms governing this trait remain poorly understood, posing a challenge to molecular breeding efforts. In this study, mustard varieties with lobed and non-lobed leaf margins were used to systematically investigate the genetic basis of leaf margin differentiation through BSA-seq, RNA-seq, and bioinformatics analyses. BSA-seq screening identified four LMI1 homologous genes, including BjuOA10G33260, which may fissure the leaf margin by suppressing cytokinin signaling. RNA-seq analysis revealed significant enrichment of ethylene and growth hormone pathways during key stages of leaf development (at 12 days post-sowing). Integrated analysis of BSA-seq and RNA-seq data identified 15 genes involved in leaf morphogenesis, including BjuOB05G34700 (ADF4, an actin depolymerization factor), BjuOA08G35830 (GATA transcription factor 11), BjuOA09G42060 (ERF transcription factor), and BjuOA07G29650 (GATA transcription factor). Notably, BjuOA10G30380 (TGA2) and BjuOA10G34680 (LAX1) may regulate cytoskeletal dynamics and hormonal signaling, contributing to the development of leaf morphology. This study presents the first molecular network regulating the morphogenesis of the leaf edge in mustard, offering a theoretical foundation and valuable genetic resources for breeding new varieties with optimized leaf architecture. Full article

Background: The TGACG-BINDING FACTORS (TGA) gene family, a key subgroup of bZIP transcription factors, mediates plant stress responses and developmental processes by binding to the as-1 cis-element in target gene promoters to regulate transcriptional activation or repression. Despite its functional significance, systematic characterization of TGA genes in cotton (Gossypium spp.) remains insufficient. Methods: In this study, we performed a comprehensive genome-wide identification and phylogenetic analysis of TGA members across 10 Gossypium species and verified the functions of candidate genes using VIGS technology. Results: A total of 74 TGA homologous genes with conserved DOG1 and bZIP domains were identified. Evolutionary analysis revealed that the cotton TGA gene family can be classified into five distinct branches, suggesting functional diversification. Functional prediction analyses indicated these genes in cotton growth regulation and stress adaptation, potentially through hormone-mediated signaling pathways. Expression profiling demonstrated both tissue-specific expression patterns and salt-stress responsiveness in Gossypium hirsutum TGA genes, and GhTGA2 exhibited the most significant up-regulated expression under salt stress. Virus-induced gene silencing (VIGS)-mediated GhTGA2 silencing significantly reduced the salt tolerance in cotton. Conclusions: The TGA gene family is involved in regulating cotton growth, development, and stress responses, and plays a critical role in mediating salt stress tolerance in cotton. Our results provide mechanistic insights into cotton stress adaptation and establish a valuable genetic resource for developing elite salt-tolerant cotton cultivars, with direct implications for sustainable cotton production. Full article

N, as plants’ most essential nutrient, profoundly shapes root system architecture (RSA), with LRs being preferentially regulated. This review synthesizes the intricate molecular mechanisms underpinning N sensing, signaling, and its integration into developmental pathways governing LR initiation, primordium formation, emergence, and elongation. We delve deeply into the roles of specific transporters (NRT1.1, nitrate transporter 2.1 (NRT2.1)), transcription factors (Arabidopsis nitrate regulated 1 (ANR1), NLP7, TGACG motif-binding factor (TGA), squamosa promoter-binding protein-like 9 (SPL9)) and intricate hormone signaling networks (auxin, abscisic acid, cytokinins, ethylene) modulated by varying N availability (deficiency, sufficiency, excess) and chemical forms (NO₃⁻, NH₄⁺, organic N). Emphasis is placed on the systemic signaling pathways, including peptide-mediated long-distance communication (CEP—C-terminally encoded peptide receptor 1 (CEPR1)) and the critical role of the shoot in modulating root responses. Furthermore, we explore the emerging significance of carbon–nitrogen (C/N) balance, post-translational modifications (ubiquitination, phosphorylation), epigenetic regulation, and the complex interplay with other nutrients (phosphorus (P), sulfur (S)) and environmental factors in shaping N-dependent LR plasticity. Recent advances utilizing single-cell transcriptomics and advanced imaging reveal unprecedented cellular heterogeneity in LR responses to N. Understanding this sophisticated regulatory network is paramount for developing strategies to enhance nitrogen use efficiency (NUE) in crops. This synthesis underscores how N acts as a master regulator, dynamically rewiring developmental programs through molecular hubs that synchronize nutrient sensing with root morphogenesis—a key adaptive strategy for resource acquisition in heterogeneous soils. Full article

Fruit shape is an important quality and yield trait of pear, and the fruit shape of ‘Laiyang Cili’ presents a spindle shape which seriously affects its commercial value. Calyx excision treatment could change the fruit shape, while the underlying genes and their regulatory mechanism remain poorly understood. In this study, we constructed RNA-seq libraries of pear treated with calyx excision to explore underlying regulatory mechanisms. At the early stage of the calyx excision treatment, the numbers of differentially expressed genes (DEGs) between each comparison group were relatively high and gradually decreased along with fruit development. The expression pattern of the DEGs ranked in the top 30 of the six groups had obvious divergence, and DEGs were mainly distributed in the “after calyx excision treatment (0 days)” (AC0d) and AC2d groups. The DEGs were mainly enriched in plant hormone signal transduction and plant defense response. We identified 17 candidate genes related to fruit shape and tested their expression patterns along with fruit development. Among them, nine candidate genes expression trends were consistent with fragments per kilobase of exon model per million mapped fragment (FPKM) values, including MYB62, outer envelope pore protein 62 (OEP62), auxin response factor 3 (ARF3), auxin-responsive protein 50 (SAUR50), protein phosphatase 2C 51 (PP2C 51), major allergen Pyr c 1 (PYRC1), aquaporin TIP1-3 (TIP1-3), transcription factor TGA4 (TGA4) and auxin-responsive protein 17 (IAA17). And then, weighted gene co-expression network analysis (WGCNA) analysis revealed that the OVATE family protein (OFP) and SUN domain-containing protein (SUN) were divided into the MEblue model, which had a positive correlation with calyx excision treatment, and the expression trend of LOC103960706 (OFP8) appeared cohesive with FPKM values. Pbr014104.1 and Pbr016952.1, which were the ortholog genes of LOC103960706, were further identified from the pear genome, and were found to be highly expressed in pear fruit through RT-PCR analysis. Taken together, the key stage determining the development of fruit shape was in the early stage after calyx excision treatment, and fruit shape regulation and development were co-regulated by multiple genes. Full article

The TGACG motif-binding factor (TGA) family is an important group of basic region/leucine zipper (bZIP) transcription factors in plants, playing crucial roles in plant development and stress responses. This study conducted a comprehensive genome-wide analysis of the TGA transcription factor (TF) family in common wheat (Triticum aestivum L.). A total of 48 wheat TGAs were identified and classified into four subgroups. Collinearity analysis of the TGAs between wheat and other species identified multiple duplicated gene pairs and highlighted the presence of highly conserved TGAs in wheat. Whole-genome and segmental duplications were identified as the primary drivers of TaTGA expansion. Expression pattern analysis indicated that TaTGAs are involved in plant development and responses to abiotic stresses, including drought, heat, and cold treatment. Among these, TaTGA16-2D was significantly upregulated under both drought and heat stresses, showing more than a five-fold increase in expression. Subcellular localization confirmed its nucleus localization. Functional validation through ectopic expression in Arabidopsis demonstrated that transgenic lines overexpressing TaTGA16-2D exhibited significantly improved stress tolerance. Under heat stress, the survival rates of transgenic lines exceeded 34%, compared to less than 18% in wild-type plants. Overall, this study provides valuable insights into the evolution and functional roles of TaTGAs and identifies TaTGA16-2D as a promising candidate to enhance abiotic stress tolerance in wheat via molecular breeding. Full article

Clubroot is a destructive soilborne disease caused by Plasmodiophora brassicae that threatens the production of Chinese cabbage. The molecular mechanisms underlying the resistance of Chinese cabbage to clubroot remains unclear, making the identification and analysis of resistance genes crucial for developing resistant varieties. Comparative transcriptome analysis of roots from the resistant line “JJ S5-1” and the susceptible line “SYY10-1” revealed significant differences in gene expression profiles at various stages after inoculation. Weighted gene coexpression network analysis revealed midnight blue and green modules as substantially associated with disease response, with each showing positive regulatory patterns. Several defense-related genes and transcription factors important for resistance to Plasmodiophora brassicae were identified, including disease resistance proteins, PR1, PBS1, and TGA, and WRKY transcription factors, most of which were upregulated following inoculation. Key genes associated with trait-related expression patterns were analyzed and a working model was proposed to explain the mechanism of clubroot disease resistance to Plasmodiophora brassicae infection in Chinese cabbage. These findings offer a valuable resource for further investigation of the immune response in the resistance of “JJ S5-1” to clubroot disease. Full article

Seed germination is a complex developmental process and a critical stage in plant development. The mechanism of seed germination in Qiongzhuea tumidinoda remains unclear. In this study, the transcriptomic analysis of four germination stages was conducted to reveal the regulatory mechanism. Totals of 2352, 5523, and 4533 differentially expressed genes (DEGs) were identified in S2 vs. S1, S3 vs. S1, and S4 vs. S1, respectively. A total of 998 DEGs were identified during seed germination. Enrichment studies indicated that the DEGs were mainly involved in plant hormone signal transduction and phenylpropanoid biosynthesis pathways. In addition, 131 transcription factors were differentially expressed, of which ERFs and MYBs may play pivotal roles in seed germination. To sum up, TGA4, IAA24, SAUR32, AHK4, and HCT4 may regulate seed germination. Full article

The TGA (TGACG motif-binding factor) transcription factors are integral to root growth and development, and are pivotal in mediating plant responses to abiotic stresses. Nonetheless, their role in the nutrient absorption processes of banana plants has not been extensively investigated. This research conducted a comprehensive analysis of the MaTGA gene family, emphasizing their physicochemical characteristics, phylogenetic relationships, gene duplication events, promoter cis-regulatory elements and protein interaction networks. Furthermore, this study investigated the expression patterns of MaTGA family members under varying nitrogen conditions. A total of 18 MaTGA members were identified within the banana genome, each encoding proteins characterized by the presence of bZIP and DOG domains. These genes exhibited an uneven distribution across eight chromosomes. Phylogenetic analysis further classified the MaTGA family into four distinct subgroups (I–IV), consisting of three, seven, three, and five members, respectively. An analysis of promoter cis-elements indicated that over 50% of the MaTGA gene family members contain hormone-responsive elements associated with abscisic acid (ABRE), ethylene (ERE), and salicylic acid (SARE), in addition to stress-responsive elements related to drought (MBS) and low temperature (LTR). Regarding gene expression, MaTGA7, MaTGA8, and MaTGA15 exhibited significantly elevated expression levels in the leaves and roots relative to other tissues. Under varying nitrogen conditions, 13 members, including MaTGA7 and MaTGA8, demonstrated the highest expression levels under reduced nitrogen (70%) treatment, followed by low nitrogen (20%) conditions, and the lowest expression levels were observed under nitrogen-deficient conditions. These findings imply that MaTGA genes may play crucial roles in enhancing nitrogen use efficiency. Protein interaction predictions suggest that MaTGA7, MaTGA8, and MaTGA15 may interact with nitrogen-related proteins, including Nitrate Transporter 2 (NRT2.1 and NRT2.2), NIN-Like Protein 7 (NLP7), and Nitrate Transporter 1.1 (NPF6.3). In summary, MaTGA7, MaTGA8, and MaTGA15 are likely involved in the processes of nitrogen absorption and utilization in bananas. The present findings establish a basis for subsequent investigations into the functional roles of MaTGA genes in augmenting nutrient use efficiency and mediating responses to abiotic stresses in banana plants. Full article

Paclobutrazol (PAC) is a significant inhibitor of gibberellin biosynthesis that profoundly influences grape seed development (GSD) through the modulation of key molecular pathways. Here, we identified 6659 differentially expressed genes (DEGs) in GSD under PAC treatment, with 3601 up-regulated and 3058 down-regulated. An analysis of hormone-associated DEGs revealed that auxin-related genes (16) were the most up-regulated, followed by genes associated with brassinosteroid and ABA. In contrast, cytokinin- and gibberellin-related genes exhibited a suppressive response. PAC treatment also triggered extensive reprogramming of metabolic pathways, including 44 genes involved in starch and sucrose metabolism (24 up-regulated, 20 down-regulated), 101 cell wall-related genes (53 up-regulated, 48 down-regulated), and 110 transcription factors (77 up-regulated, 33 down-regulated). A cis-element analysis of the promoters of 76 hormone-responsive genes identified 14 types of hormone-responsive cis-elements, with ABRE being the most prevalent. Genes responsible for inactivating active hormones, such as ABA-VvPP2CA, IAA-VvGH3.1, and CK-VvARR9-1, were also identified. Concurrently, PAC negatively regulated hormone-active genes, including BR-VvXTH25, SA-VvTGA21-3, and JA-VvTIFY3B, leading to reduced levels of these hormones. PAC modulates GSD by mediating the dynamic balance of multi-hormone accumulations. Furthermore, development-related cis-elements such as the AACA-motif, AAGAA-motif, AC-I, AC-II, O2-site, as-1, CAT-box, CCAAT-box, circadian, GCN4-motif, RY-element, HD-Zip 1, HD-Zip 3, MSA-like, MYB-like sequence, MYB-binding site, and MYB recognition site, were found in key DEGs involved in starch and sucrose metabolism, cell wall remodeling, and epigenetic regulation. This indicates that these pathways are responsive to PAC modulation during GSD. Finally, we developed a comprehensive regulatory network to illustrate the PAC-mediated pathways involved in GSD. This network integrates multi-hormonal signaling, cell wall remodeling, epigenetic regulation, and transcription factors, highlighting PAC’s pivotal role in GSD. Our findings provide new insights into the complex mechanisms underlying PAC’s effects on grapevine development. Full article

Color variation in plant leaves has a significant impact on their photosynthesis and plant growth. Camellia chekiangoleosa yellow-leaf mutants are ideal materials for studying the mechanisms of pigment synthesis and photosynthesis, but their mechanism of leaf variation is not clear. We systematically elucidated the intrinsic causes of leaf yellowing in the new Camellia chekiangoleosa variety ‘Diecui Liuji’ in terms of changes in its cell structure, pigment content, and transcript levels. This study indicates that the incomplete structure of chloroplast-like vesicles, the decrease in blue-green chlorophyll a, and the increase in yellow-green chlorophyll b in yellowing leaves are the direct causes of yellowing-leaf formation. The high expression of genes that catalyze the degradation of chlorophyll a (PAO and RCCR) and its conversion to chlorophyll b (CAO) in yellowing leaves leads to a decrease in the chlorophyll a content, while the low expression of CLH genes is the main reason for the increase in the chlorophyll b content. We also found transcription factors such as ERF, E2F, WRKY, MYB, TPC, TGA, and NFYC may regulate their expression. RT-qPCR assays of 12 DEGs confirm the RNA-seq results. This study will provide a foundation for investigating the transcriptional and regulatory mechanisms of leaf color changes. Full article

Legumes have the capability to form nodules that facilitate symbiotic nitrogen fixation (SNF) with rhizobia. Given the substantial energy consumption during the process of SNF, legumes need to optimize nodule number in response to everchanging environmental scenarios. The TGACG BINDING FACTOR1/4 (TGA1/4) are key players in the basal immune response of plants. In this study, both β-glucuronidase staining and quantitative reverse transcription PCR (qRT-PCR) demonstrated that both GmbZIP4a and GmbZIP4b are inducible upon rhizobial inoculation. To investigate their roles further, we constructed gmbzip4a/b double mutants using CRISPR/Cas9 system. Nodulation assessments revealed that these double mutants displayed a reduction in the number of infection threads, which subsequently resulted in a decreased nodule number. However, the processes associated with nodule development including nodule fresh weight, structural characteristics, and nitrogenase activity, remained unaffected in the double mutants. Subsequent transcriptome analyses revealed that zeatin biosynthesis was downregulated in gmbzip4a/b mutants post rhizobial inoculation. Supporting these findings, genes associated with cytokinin (CTK) signaling pathway were upregulated in Williams 82 (Wm82), but this upregulation was not observed in the double mutants after rhizobial treatment. These results suggest that GmbZIP4a/b positively influences nodule formation by promoting the activation of the CTK signaling pathway during the early stages of nodule formation. Full article