Search Results (724)

Camellia azalea is an endemic species within the genus Camellia that exhibits the trait of summer flowering, which is of significant ornamental and research value. Nevertheless, research on the regulatory mechanisms of flower formation in C. azalea is still limited, so in this study, transcriptome sequencing and analysis of endogenous hormone contents were conducted at three distinct growth stages: floral induction, floral organ maturation, and anthesis. Illumina sequencing yielded a total of 20,643 high-quality unigenes. Comparative analyses of representative samples from the three growth stages identified 6681, 1925, and 8400 differentially expressed genes (DEGs), respectively. These DEGs were further analyzed for functional enrichment using the GO and KEGG databases. Additionally, core genes from each flowering pathway underwent expression pattern analysis and network diagram construction. This revealed that the flower development process in C. azalea is linked to the specific expression of the genes involved in the photoperiod, temperature, and autonomous pathways and is subject to comprehensive regulation by multiple pathways. Further analysis of the dynamic trends of five endogenous hormone contents and plant hormone signal transduction genes revealed significant differences in the requirements of endogenous hormones, such as gibberellins and indoleacetic acid, by C. azalea at distinct growth stages. Additionally, the majority of genes on the phytohormone signal transduction pathway demonstrated a high correlation with the changes in the contents of each hormone. The present study integrates physiological and molecular approaches to identify key genes and metabolic pathways that regulate the summer flowering of C. azalea, thereby laying a theoretical foundation for further investigations into its flowering mechanism and related functional genes. Full article

Plant secondary metabolites regulate plant growth and serve as valuable pharmaceutical resources. Napier grass (Pennisetum purpureum Schumach.), a Poaceae species, shows potential as a functional food. In this study, we employed high-resolution mass spectrometry combined with a data-independent acquisition (DIA) strategy for the untargeted detection of anthocyanins, a group of secondary metabolites, in napier grass. Clear MS² fragmentation patterns were observed for anthocyanins, characterized by diagnostic aglycone signals and sequential losses of hexosyl (C₆H₁₀O₅), deoxyhexosyl (C₆H₁₀O₄), pentosyl (C₅H₈O₄), and p-coumaroyl groups (C₉H₈O₃). Based on matching with authentic standards and an in-house database, ten anthocyanins were identified, seven of which were newly reported in napier grass. In a single-laboratory validation analysis, both absolute and semi-quantitative results reliably reflected the specific distribution of metabolites across different cultivars and plant organs. The purple cultivar (TS5) exhibited the highest anthocyanin content, with the cyanidin 3-O-glucoside content reaching 5.0 ± 0.5 mg/g, whereas the green cultivar (TS2), despite its less pigmented appearance, contained substantial amounts of malvidin 3-O-arabinoside (0.7 ± <0.1 mg/g). Flavonoid profiling revealed that monoglycosylated anthocyanins were the dominant forms in floral tissues. These findings shed light on napier grass metabolism and support future Poaceae breeding and functional food development. Full article

Accurate counting of cucumber flowers using intelligent algorithms to monitor their sex ratio is essential for intelligent facility agriculture management. However, complex greenhouse environments impose higher demands on the precision and efficiency of counting algorithms. This study proposes a dual-area counting algorithm based on an improved YOLOv8n-Track (YOLOv8n-T) and ByteTrack cascaded framework. This method accomplishes the cucumber flower counting task by detecting flower targets, tracking them frame-by-frame, and validating the count through dual-area counting. The YOLOv8n-T incorporates a Coordinate Attention (CA) mechanism and lightweight modules while optimizing the loss function, thereby improving floral feature extraction capabilities and reducing computational complexity. By integrating the ByteTrack tracking algorithm with a dual-area counting strategy, the robustness of flower counting in dynamic environments is strengthened. Experimental results show that the improved YOLOv8n-T achieves mAP and F1 scores of 86.9% and 82.1%, surpassing YOLOv8n by 3% and 2.6%, respectively, with a 0.3 G reduction in model parameters. The integrated framework achieves a detection accuracy of 82.4% for cucumber flower counting. This research provides a new method for monitoring cucumber flower sex ratios in facility agriculture, promoting the development of intelligent agricultural management. Full article

The floral transition in Chinese cabbage (Brassica rapa ssp. pekinensis) is governed by a complex interplay of gene expression and hormonal regulation. Temporal transcriptome profiling was conducted across three developmental stages: pre-bolting (PBS), bolting (BS), and flowering stages (FS), to investigate the underlying molecular mechanisms. A total of 7092 differentially expressed genes (DEGs) were identified, exhibiting distinct expression trajectories during the transition. Moreover, functional enrichment analyses revealed strong associations with plant hormone signaling, MAPK pathways, and developmental regulation processes. Key flowering-related genes, such as BrFLM, BrAP2, BrFD, BrFT, and BrSOC1s displayed antagonistic expression patterns. Hormonal pathways involving auxin, ABA, ET, BR, GA, JA, CK, and SA showed stage-dependent modulation. Further, orphan genes (OGs), especially EARLY FLOWERING 1 (EF1), showed significant upregulation during the transition, which exhibited 1.84-fold and 1.93-fold increases at BS and FS compared to PBS, respectively (p < 0.05). Functional validation through EF1 overexpression (EF1OE) in Arabidopsis consistently promoted early flowering. The expression levels of AtFT and AtSOC1 were significantly upregulated in EF1OE lines compared to wild-type (WT) plants. The findings contribute to understanding the coordinated genetic and hormonal events driving floral development in Chinese cabbage, suggesting EF1 as a candidate for bolting resistance breeding. This work also expands the existing regulatory framework through the successful integration of OGs into the complex floral induction system of Brassica crops. Full article

Climate change can severely impact plant-pollinator interactions and have serious effects on ecosystem services such as pollination. This study was carried out in 2023 and 2024, and it examined the effects of drought on flowering and nectar production in one cultivar of white mustard (Brassica alba cv. Palma), an important entomophilous crop of the temperate zone with several attributes that make it promising for sustainable agricultural practices. Drought-stressed plants delayed the flowering time, shortened the flowering duration, and developed significantly fewer flowers. Nectar production in white mustard depends on soil moisture levels and short-term changes in meteorological conditions (e.g., air humidity, air temperature). At reduced soil moisture, the total sugar yield per plant decreased by 60%, compared to control plants, resulting in lower availability of caloric food resources, which should be considered when developing strategies supporting pollinators. Changes in floral traits resulted in differences in the frequency of insect visits, which may exert a negative impact on white mustard pollination under drought stress and may have indirect consequences for seed yield resulting from increased drought intensity associated with climate change. The results provide important data for the management of the white mustard crop and indicate the need for broader evaluation of cultivars to promote drought-resistant B. alba cultivars. Full article

Floral pigmentation contributes directly to reproductive strategies and fitness by shaping pollinator behaviour, and its regulation therefore represents a critical aspect of flower development. Additionally, it is a major determinant of aesthetic and economic value in the ornamental plant industry. This review explores the genetic, biochemical, and ecological bases of floral colour change, focusing on the biosynthesis and regulation of the three major classes of plant pigments: carotenoids, flavonoids (particularly anthocyanins), and betalains. These pigments, derived from primary metabolism through distinct biosynthetic pathways, define the spatial and temporal variability of floral colouration. We discuss the molecular mechanisms underlying flower colour change from opening to senescence, highlighting pigment biosynthesis and degradation, pH shifts, metal complexation, and co-pigmentation. Additionally, we address the regulatory networks, including transcription factors (MYB, bHLH, and WDR) and post-transcriptional control, that influence pigment production. Finally, we provide a comprehensive survey of angiosperm species exhibiting dynamic petal colour changes, emphasizing how these mechanisms are regulated. Full article

The singular biodiversity of the Brazilian Caatinga inspires innovative solutions in food science. In this study, we evaluated the prebiotic potential of honeys produced by Apis mellifera in the Pajeú hinterland, Pernambuco, Brazil (Caatinga Biome), with different floral origins: Mastic (Aroeira), Mesquite (Algaroba), and mixed flowers. These were used to formulate synbiotic and alcoholic beverages fermented by Saccharomyces boulardii CNCM I-745. Static and dynamic simulations of the human gastrointestinal tract (GIT) were used, as well as physicochemical, rheological, and microbiological analyses. The results revealed that honey positively influences the viability and resilience of probiotic yeast, especially honey with a predominance of Algaroba, which promoted the highest survival rate (>89%) even after 28 days of refrigeration and in dynamic in vitro simulation of the GIT (more realistic to human physio-anatomical conditions). The phenolic composition of the honeys showed a correlation with this tolerance. The use of complementary methodologies, such as flow cytometry, validated the findings and highlighted the functional value of these natural matrices, revealing an even greater longevity potential compared to conventional microbiological methodology. The data reinforces the potential of the Caatinga as a source of bioactive and sustainable compounds, proposing honey as a promising non-dairy synbiotic vehicle. This work contributes to the appreciation of the biome and the development of functional food products with a positive social, economic, and ecological impact. Full article

Quinoa (Chenopodium quinoa Willd) is a tetraploid crop that has provided vital subsistence, nutrition, and medicine for Andean indigenous cultures. In recent years, quinoa has gained global importance all over the world. However, variations in fertility have been frequently observed during the flower development of quinoa, severely affecting quinoa production. To comprehend the fundamental causes of fertility variation in quinoa, this research examined hormonal metabolism and gene expression across three ecotypes: normal fertility (F), absent stamens (S1), and abnormal stamens (S3). S1 and S3 presented absent and abnormal stamens, respectively, compared with F. Phytohormone profiling yielded 60 metabolites and revealed the clear separation between different ecotypes at different developmental stages according to principal component analysis (PCA). The results of transcriptomics showed more DEGs (differentially expressed genes) identified between F and S1 ecotypes (8002 and 10,716 for earlier and later stages, respectively) than F vs. S3 (4500 and 9882 for earlier and later stages, respectively) and S1 vs. S3 (4203 and 5052 for earlier and later stages, respectively). Zeatin biosynthesis and hormone signal transduction pathways were enriched among 19 KEGG (Kyoto Encyclopedia of Genes and Genomes) terms, indicating their potential roles in quinoa flower fertility regulation. The correlation-based network presented the associations between selected hormones and genes, possibly regulating fertile ecotypes. Furthermore, we explored the expression of flower development-related genes in three ecotypes using RT-PCR, showing the higher expressions of AP1, AP3, and FLS in sterile ecotypes than fertile ecotypes at both stages. These findings reveal new insights into the hormonal and genetic regulations of floral fertility in quinoa, which may have consequences for developing high-yielding cultivars. Full article

Bract coloration in ornamental plants is a complex trait governed by diverse pigments (chlorophylls, anthocyanins, betalains, and carotenoids), their biosynthetic pathways, and regulatory networks. While previous research has primarily focused on floral pigmentation, studies on bract coloration—particularly in species where bracts serve as the primary ornamental feature—have received less attention until recent advances. This review synthesizes current understanding of bract color diversity, pigment biochemistry, and molecular regulation in key species including Bougainvillea, Euphorbia pulcherrima, Anthurium andraeanum, Curcuma alismatifolia, and Zantedeschia hybrida. Anthocyanins predominantly contribute to red-to-purple hues, while betalains generate red, purple, or yellow coloration through differential accumulation of betacyanins and betaxanthins. Developmental color transitions are mediated by chlorophyll degradation and carotenoid dynamics. The spatiotemporal regulation of pigment accumulation involves coordinated interactions between key structural genes (CHS, DFR, ANS for anthocyanins; DODA, CYP76AD1 for betalains), transcription factors (MYB, bHLH, WRKY), and plant growth regulators (BAP, GA, MeJA). Despite these advances, significant knowledge gaps remain in genetic inheritance patterns, epigenetic regulation, cross-pigment pathway crosstalk, and environmental modulation. Future research directions should integrate multi-omics approaches, wild germplasm resources, and gene-editing technologies to develop novel breeding strategies for bract color improvement. Full article

AT-hook motif nuclear-localized (AHL) genes play critical roles in chromatin remodeling and gene transcription regulation, profoundly influencing plant growth, development, and stress responses. While AHL genes have been extensively characterized in multiple plant species, their biological functions in pepper (Capsicum annuum L.) remain largely uncharacterized. In this study, we identified 45 CaAHL genes in the pepper genome through bioinformatics approaches. Comprehensive analyses were conducted to examine their chromosomal distribution, phylogenetic relationships, and the structural and functional features of their encoded proteins. Phylogenetic clustering classified the CaAHL proteins into six distinct subgroups. Transcriptome profiling revealed widespread expression of CaAHL genes across diverse tissues—including roots, stems, leaves, flowers, seeds, pericarp, placenta, and fruits—at various developmental stages. Quantitative real-time PCR further demonstrated that CaAHL1, CaAHL33, and CaAHL23 exhibited consistently high expression throughout flower bud development, whereas CaAHL36 showed preferential upregulation at early bud development stages. Expression profiling under hormone treatments and abiotic stresses indicated that CaAHL36 and CaAHL23 are auxin-inducible but are repressed by ABA, cold, heat, salt, and drought stress. Subcellular localization assays in Nicotiana benthamiana leaf epidermal cells showed that both CaAHL36 and CaAHL23 were predominantly localized in the nucleus, with faint expression also detected in the cytoplasm. Collectively, this study provides foundational insights into the CaAHL gene family, laying the groundwork for future functional investigations of these genes in pepper. Full article

Floral ontogeny in soybean (Glycine max) is governed by multilayered regulatory hierarchies that integrate phytohormonal cues with precisely choreographed gene-expression programs. Yet, the transcriptomic architecture underpinning this continuum remains only partially resolved. Here, we generated a strand-specific, high-depth temporal transcriptome atlas of soybean inflorescences spanning four morphologically defined stadiums (Stadium 0–Stadium 3). We detected transcriptional activity for 60,889 loci; pairwise stadium contrasts revealed 4000–7000 differentially expressed genes, with the most extensive reprogramming coinciding with the onset of anthesis (Stadium 2). Unsupervised clustering delineated ~600 genes peaking at the pre-anthesis phase (Stadium 1), a cohort enriched for transcriptional regulators and floral organ-identity determinants. Stadium-resolved gene-set enrichment and KEGG mapping uncovered dynamic modulation of canonical hormone-signaling pathways—including auxin, cytokinin, gibberellin, abscisic acid, ethylene, jasmonate, and salicylate circuits—reflecting shifting developmental priorities. Forty-five MADS-box transcription factor genes were expressed; notably, JOINTLESS was strongly induced at anthesis, while the root-predominant factor GmNMH7 exhibited unexpected floral expression, implicating a hitherto unappreciated role in reproductive development. Quantitative RT-PCR of representative loci corroborated RNA-seq measurements. This high-resolution atlas refines our understanding of the hormonal and genetic circuitry of soybean floral morphogenesis, furnishing molecular targets for engineering flowering time and inflorescence architecture under fluctuating environmental conditions. Full article

This investigation proposes an effective protocol (cutting) for Paulownia tomentosa production in Tunisia during the 2022–2024 period. The effects of the three interactive parameters: root cutting diameter (L1, 0.5; L2, 0.8; L3, 1.25; and L4, 2 cm), indole-3-butyric acid (IBA) hormone concentrations (C, 0; T1, 0.1%; and T2, 0.3%), and soil type (S1: 50% silt + 50% potting soil, and S2: 43% potting soil + 43% silt + 14% sand), were investigated. The data showed that cutting roots with 0.5 cm dimensions, a cutting treatment with hormone (0.3%), and the S2 soil type corresponded to a growth enhancement in height. These results revealed the broad changes in flowering of P. tomentosa. Also, data revealed that the root cutting diameter had the greatest influence on the biochemical contents of 4-month-old P. tomentosa sprouts. The studied pathway revealed that the auxin precursor IBA contributes toward active auxin [indole-3-acetic acid (IAA)] biosynthesis. Overall, this study found substantial changes in the morphological, biochemical, and floral features of new P. tomentosa sprouts under the interactive factors. To summarize, vegetative propagation of Paulownia, particularly through root cutting, allows for proliferation and plantation development. These findings can be applied to future breeding efforts with Paulownia to improve and protect it as a woody species, forage, and medicinal plant. Full article

This study aimed to examine the effect of the orientation angle of center facing arms on the elongation and strength of 3D-printed textiles with two different re-entrant cellular auxetic structures. An experimental research design, consisting of 6 (auxetic-structure textiles) × 3 (repetition), was employed. Star-shaped re-entrant auxetic structures (star re-entrant) with orientation angles of 25°, 30°, and 35° and floral-based star-shaped re-entrant auxetic structures (floral re-entrant) with orientation angles of 55°, 60°, and 65° were developed using the fused deposition modeling 3D-printing method through identifying commonly used auxetic structures in the 3D-printed textiles’ development. A statistically significant relationship was found between load and elongation of both star re-entrant and floral re-entrant. The findings indicated that 3D-printed textiles with both star re-entrant and floral re-entrant structures exhibited an enhanced elongation with the increase in orientation angle, making the textile products more flexible and potentially providing better wear comfort. However, the strength of both star re-entrant and floral re-entrant textiles was not significantly affected by the orientation angle of center facing arms. The findings demonstrated the potential to enhance the elongation of 3D-printed auxetic-structure textiles without compromising their strength for ensuing comfort by adjusting the orientation angle of center facing arms. Full article

The phosphatidylethanolamine-binding protein (PEBP) gene family, known for its pivotal role in controlling floral transition, regulates flowering time, and, thus, shapes the continuous-flowering trait in ornamental plants. In this study, we conducted the first genome-wide identification and bioinformatics analysis of the PEBP gene family in Begonia semperflorens ‘Super Olympia’, a variety that exhibits year-round flowering. Via phylogenetic analysis, a total of 10 BsPEBP genes were identified and categorized into four subfamilies: the FT-like (two members), TFL1-like (three members), PEBP-like (three members), and MFT-like (two members) subfamilies. Gene structure analysis revealed highly conserved motif compositions among family members, and protein tertiary structure prediction indicated the dominance of random coils in their structures. Promoter cis-acting element analysis revealed light-responsive, hormone-responsive (ABA, GA, and JA), and abiotic stress-responsive elements in the BsPEBP genes, suggesting their potential integration into multiple regulatory pathways. The tissue-specific expression profiles revealed that BsPEBP6 was significantly upregulated in floral organs, whereas TFL1-like subfamily members were predominantly expressed in vegetative tissues. These findings imply that the FT-like and TFL1-like genes antagonistically regulate the continuous-flowering trait of B. semperflorens ‘Super Olympia’ through their respective roles in promoting and repressing flowering. Our findings provide a preliminary theoretical foundation for elucidating the molecular mechanisms by which the PEBP gene family regulates flowering time in ornamental plants and offer valuable insights for developing breeding strategies aimed at flowering time modulation. Full article

Unlike other orchids in the Orchidaceae family, Cymbidium goeringii presents significant challenges for in vitro flowering. In this study, through the screening of different basal media, hormone combinations, and other conditions, we developed efficient rhizome regeneration (micropropagation) and in vitro flowering induction systems from protocorm explants of C. goeringii hybrids. To obtain protocorm explants, seeds were pretreated with either NaOH or NaOCl. Our results indicated that NaOH pretreatment enhanced seed germination more effectively than NaOCl, and Knudson C medium proved more suitable for protocorm induction. The resulting protocorms were then used as primary explants for efficient rhizome micropropagation. An orthogonal design identified the optimal combination for rhizome proliferation: 9.0 mg/L 6-BA, 9.0 mg/L NAA, 3.0 mg/L IBA, and 0.1 g/L activated charcoal (Treatment 9), which achieved a proliferation rate of 35.17%. For rhizome differentiation, MS medium supplemented with 10 mg/L 6-BA, 0.1 mg/L NAA, and 0.1 mg/L AgNO₃ (Treatment 6) achieved a 100% differentiation rate and produced 3.93 buds per explant. Building on this optimized micropropagation system, in vitro flowering was induced directly from rhizomes. The most effective medium was MS (1/3N, 3P) supplemented with 9.0 mg/L 6-BA, 0.1 mg/L NAA, and 0.1–0.3 mg/L TDZ (Treatment 6), resulting in a 36% flower bud induction rate and a 16% normal flower bud formation rate. Orthogonal analysis and ANOVA confirmed that 6-BA was the most significant factor influencing floral transition, with the low-nitrogen and high-phosphorus MS (1/3N, 3P) medium also being a key contributor. Consequently, our study has established an efficient rhizome micropropagation system that enables in vitro flowering induction in C. goeringii hybrids within just six months. This represents a substantial 60–80% reduction in the flowering time (from 6–7 years to 1–2 years), compared to the traditional 6–7-year cultivation period. Future work will focus on ex vitro acclimatization, detailed floral-trait validation, and hormone-regime refinement for fast-tracking breeding programs. Full article