Search Results (8,060)

Small signaling peptides play crucial roles in the regulation of legume–rhizobia symbiosis, yet their potential as exogenous biostimulants remains largely unexplored. In this study, we evaluated the effects of foliar application of the synthetic peptides ENOD40 and CEP1 on common bean (Phaseolus vulgaris) under both greenhouse and field conditions. Using a factorial design, we examined gene expression patterns, nodulation parameters, and yield-related traits in response to peptide treatments alone or in combination with Rhizobium. Results showed that ENOD40 and CEP1 significantly enhanced the transcription of key symbiotic signaling genes (PvENOD40, PvSYMRK, PvCCaMK, PvCYCLOPS, PvVAPYRIN) and modulated defense-related genes (PvAOS, PvICS), with the strongest effects observed at concentrations of 10⁻⁷ M and 10⁻⁸ M. In greenhouse assays, peptide-treated plants exhibited increased root and shoot biomass, nodule number, and seed yield. Field trials confirmed these responses, with CEP1 10⁻⁷ M + Rhizobium treatment achieving the highest grain yield (3322 kg ha⁻¹). Our findings provide the first evidence that ENOD40 and CEP1 peptides can function as foliar-applied biostimulants to enhance nodulation efficiency and improve yield in legumes. This approach offers a promising and sustainable strategy to reduce chemical nitrogen inputs and support biological nitrogen fixation in agricultural systems. Full article

Osteoblastogenesis plays a critical role in bone repair. Insulin and insulin-mimetic compounds, such as vanadium (IV) oxide acetylacetonate (VAC), have been reported to enhance bone healing in various models. This study aimed to evaluate the effects of vanadium compounds, VAC and vanadium (IV) oxide sulfate (VOSO₄), on osteoblast proliferation and function. MC3T3-E1 pre-osteoblast cells were treated with insulin, ascorbic acid, and varying concentrations of VAC or VOSO₄, and samples were collected at multiple time points over 21 days. We assessed cell proliferation, functional markers, and gene and protein expression. Our findings demonstrate that both VAC and VOSO₄ stimulate MC3T3-E1 proliferation, increase calcium and proteoglycan deposition, and enhance phosphorylation of Protein Kinase B (Akt) over time. Gene expression analysis revealed that VAC treatment upregulated RUNX2, BGLAP, and TWIST2 at Day 7 compared to controls, with sustained expression patterns observed at Day 10. These results align with existing literature, supporting that VAC and VOSO₄ promote osteoblastogenesis and may serve as effective adjuvants to accelerate bone regeneration during fracture healing. Full article

Seed storage proteins (SSPs) play a pivotal role in determining the development, quality, and nutritional value of rice seeds. In this study, we conducted a transcriptome-based correlation analysis to identify novel transcription factors (TFs) potentially involved in the biosynthesis and accumulation of SSPs. Our analysis revealed nine TFs—OsGATA8, OsMIF1, OsMIF2, OsGZF1, OsbZIP58, OsS1Fa1, OsS1Fa2, OsICE2, and OsMYB24—that exhibit strong co-expression with key SSP genes, including those encoding glutelin and prolamin. Gene expression profiling using quantitative RT-PCR and GUS reporter assays revealed that these TFs are predominantly expressed during seed development, with peak expression observed at 10 days after flowering (DAF). Promoter analysis further demonstrated an enrichment of seed-specific and hormone-responsive cis-regulatory elements, reinforcing the seed-preferential expression patterns of these TFs. Collectively, our findings identify a set of candidate TFs likely involved in SSP regulation and seed maturation, providing a foundation for the genetic enhancement of rice seed quality and nutritional content through targeted breeding and biotechnological approaches. Full article

Background: Grassland desertification has garnered significant attention as a pressing issue. Among the key pests affecting plateau meadows, the Gynaephora qinghaiensis (Lepidoptera: Lymantriidae) poses a substantial threat in the Qinghai-Tibet Plateau region, highlighting the urgent need for effective, environmentally friendly control strategies. Insect sex pheromones are increasingly employed in pest monitoring and management. Methods: This study aims to identify and analyze genes associated with sex pheromone synthesis in grassland caterpillars through transcriptome sequencing and tissue-specific expression analysis. Results: A total of 139,599 transcripts and 56,403 Unigenes were obtained from the sex pheromone glands transcriptome database. A total of 31 genes related to sex pheromone synthesis were identified, including 1 ACC, 8 DES, 6 AR, 7 FAR, 5 FAS, and 4 ACT genes. The expression levels of these genes varied significantly across different tissues in both male and female caterpillars (p < 0.05). GqinACC1, GqinDES1, GqinDES4, GqinDES8, GqinAR3, GqinFAR6, GqinACT2, and GqinACT3 exhibited significantly higher expression levels in the female gonads compared to other tissues (p < 0.01). Conclusions: We hypothesize that specific genes play specific roles in the pheromone synthesis pathways of pests, Key genes were identified based on expression patterns for subsequent functional studies. The results of this study offer valuable data support for subsequent investigations into the mechanisms underlying sex pheromone synthesis in G. qinghaiensis. Additionally, these findings may identify potential targets for future research on genes associated with pheromone biosynthesis, which could disrupt their chemical communication and contribute to grassland conservation efforts. Full article

The human gut microbiome is a metabolically active and ecologically dynamic consortium that profoundly influences host physiology, in part by modulating epigenetic mechanisms such as DNA and RNA methylation. These modifications regulate gene expression and phenotypic plasticity and are shaped by a combination of environmental factors, such as diet, stress, xenobiotics, and bioactive microbial metabolites. Despite growing evidence linking microbial signals to host epigenetic reprogramming, the underlying molecular pathways remain incompletely understood. This review highlights recent mechanistic discoveries and conceptual advances in understanding microbiome–host epigenome interactions. We discuss evolutionarily conserved pathways through which gut microbiota regulate host methylation patterns, including one-carbon metabolism, polyamine biosynthesis, short-chain fatty acid signaling, and extracellular vesicle-mediated communication. We also examine how host factors such as aging, diet, immune activity, and sociocultural context reciprocally influence microbial composition and function. Beyond basic mechanisms, we outline translational frontiers—including biomarker discovery, live biotherapeutic interventions, fecal microbiota transplantation, and adaptive clinical trial designs—that may enable microbiome-informed approaches to disease prevention and treatment. Advances in high-throughput methylation mapping, artificial intelligence, and single-cell multi-omics are accelerating our ability to model these complex interactions at high resolution. Finally, we emphasize the importance of rigorous standardization and ethical data governance through frameworks such as the FAIR and CARE principles. Deepening our understanding of how the gut microbiome modulates host epigenetic programs offers novel opportunities for precision health strategies and equitable clinical translation. Full article

Background and Objectives: The Drosophila retinal determination network comprises the transcription factor Teashirt (Tsh) and the transcription co-regulator C-terminal Binding Protein (CtBP), both of which are essential for normal adult eye development. Both Tsh and CtBP show a pattern of co-expression in the proliferating cells anterior to the morphogenetic furrow that demarcates the boundary between the anteriorly placed proliferating eye precursor cells and the posteriorly placed differentiating photoreceptor cells in the larval eye-precursor tissue, the eye–antennal disc. The disc ultimately develops into the adult compound eyes, antenna, and other head structures. Both Tsh and CtBP were found to interact genetically during ectopic eye formation in Drosophila, and both were present in molecular complexes purified from gut and cultured cells. However, it remained unknown whether Tsh and CtBP molecules could interact in the eye–antennal discs and elicit an effect on eye development. The present study answers these questions. Methods: 5′ GFP-tagging of the tsh gene in the Drosophila genome and 5′ FLAG-tagging of the ctbp gene were accomplished by the CRISPR-Cas9 and BAC recombineering methods, respectively, to produce GFP-Tsh- and FLAG-CtBP-fused proteins in specific transgenic Drosophila strains. Verification of these proteins’ expression in the larval eye–antennal discs was performed by immunohistological staining and confocal microscopy. Genetic screening was performed to establish functional interaction between Tsh and CtBP during eye development. Scanning Electron Microscopy was performed to image the adult eye structure. Co-immunoprecipitation and GST pulldown assays were performed to show that Tsh and CtBP interact in the cells of the third instar eye–antennal discs. Results: This study reveals that Tsh and CtBP interact genetically and physically in the Drosophila third instar larval eye–antennal disc to regulate adult eye development. This interaction is likely to limit the population of the eye precursor cells in the larval eye disc of Drosophila. Conclusions: The relative abundance of Tsh and CtBP in the third instar larval eye–antennal disc can dictate the outcome of their interaction on the Drosophila eye formation. Full article

Background: The circadian rhythm regulates important functions in the body, such as metabolism, the cell cycle, DNA repair, and immune balance. Disruption of this rhythm can contribute to the development of cancer. Circadian rhythm genes (CRGs) are attracting attention for their connection to various cancers. However, their roles in LUAD are not yet well understood. Additionally, our knowledge of how they function at both the bulk tissue and single-cell levels is limited. This gap hinders a complete understanding of how CRGs impact the development and outcomes of LUAD. Methods: We selected 554 CRGs from public databases. We then obtained transcriptome data from TCGA and GEO. A total of 101 machine learning algorithm combinations were tested using 10 algorithms and 10-fold cross-validation. The best-performing model was based on Stepwise Cox regression and SuperPC. This model was validated with additional datasets. We also examined the relationships between CRGs, immune features, tumor mutation burden (TMB), and the response to immunotherapy. Drug sensitivity was also assessed. Single-cell data identified the cell types with active CRGs. Next, we performed qRT-PCR and other basic experiments to validate the expression of ARNTL2 in LUAD tissues and cell lines. The results indicated that ARNTL2 may play a key role in lung adenocarcinoma. Results: The CRG-based model clearly distinguished LUAD patients based on their risk. High-risk patients exhibited low immune activity, high TMB, and poor predicted responses to immunotherapy. Single-cell data revealed strong CRG signals in epithelial and fibroblast cells. These cell groups also displayed different communication patterns. Laboratory experiments showed that ARNTL2 was highly expressed in LUAD. It promoted cell growth, movement, and invasion. This suggests that ARNTL2 may play a role in promoting cancer. Conclusions: This study developed a machine learning model based on CRGs. It can predict survival and immune status in LUAD patients. The research also identified ARNTL2 as a key gene that may contribute to cancer progression. These findings highlight the significance of the circadian rhythm in LUAD and provide new perspectives for diagnosis and treatment. Full article

The orbital fat of bighead carp (Hypophthalmichthys nobilis) represents a structural fat deposit located posterior to the eyes and constitutes an important edible component of the head region. Nevertheless, molecular mechanisms governing lipid accumulation during ontogenetic development remain insufficiently characterized. Here, we performed RNA-Seq on orbital fat tissues from 6-month-old (juvenile) and 18-month-old (market-size) bighead carp. A total of 1042 DEGs were identified, with 807 up-regulated and 235 down-regulated in the 6-month-old stage. Functional enrichment revealed key pathways including fatty acid metabolism, PPAR signaling, and glycolysis/gluconeogenesis. qRT-PCR validation confirmed RNA-Seq reliability. Notably, the differential expression patterns of genes such as cpt1a, cpt1b, slc27a1, fads2, and scd suggest their association with an elevated capacity for lipid synthesis in the orbital fat of 18-month-old bighead carp. This study presents the first transcriptome analysis of orbital fat development in a freshwater fish, offering insights into the genetic improvement of head meat quality traits and growth in bighead carp head. Full article

Heat shock protein 90 (HSP90) is an evolutionarily conserved molecular chaperone. Numerous studies have shown that it is widely involved in protein folding, assembly, stabilization, activation, and degradation in response to various biotic and abiotic stresses in many normal cellular processes and under stress conditions. We identified 11 members of the CqHSP90 gene family in the quinoa (Chenopodium quinoa) genome by bioinformatics analysis. Phylogenetic tree analysis showed that quinoa was more closely related to dicotyledonous plants than to monocotyledonous plants. Quinoa is susceptible to high-temperature stress during its growth and development. We analyzed the cis-acting elements of its promoter, and found that nearly 1/3 of the cis-acting elements were stress-responsive, and 2/3 of them had heat-responsive elements. The results of qRT-PCR showed that heat shock at 40 °C could induce a high expression of CqHSP90.1c and CqHSP90.6a. Subcellular localization indicates that they are all membrane proteins. At the same time, both CqHSP90.1c and CqHSP90.6a overexpression lines improved the tolerance of Arabidopsis thaliana under high temperature, indicating that both of them had a positive regulatory effect under heat stress. Results of this study could provide useful information for further study on the biological role of CqHSP90.1c and CqHSP90.6a, and provide theoretical basis for quinoa resistance breeding. Full article

Plant respiratory burst oxidase homolog (Rboh) genes are integral to the production of reactive oxygen species (ROS) and the regulation of stress responses. Here, bioinformatic techniques were employed to identify eight PgRboh genes (PgRbohA–H) in the genome of pomegranate (Punica granatum L.) and conduct a systematic analysis of this family. The findings showed that all PgRbohs proteins possess characteristic NADPH oxidase domains and are predicted to be localized on the cell membrane. Experimental verification confirmed the membrane localization of PgRbohD and PgRbohE proteins. Phylogenetic analysis categorized the PgRbohs proteins into six distinct groups, suggesting potential functional divergence among these groups. Promoter analysis revealed a significant presence of cis-acting elements responsive to low-temperature and methyl jasmonate (MeJA). The expression of PgRboh genes was found to be tissue-specific. Additionally, real-time PCR (RT-qPCR) was used to analyze expression patterns in response to low-temperature stress that involves multiple PgRboh genes in the cold response process. Overall, our results lay an important foundation for subsequent studies on the cold resistance function of pomegranate Rboh genes and provides new ideas for the breeding of new cold-resistant pomegranate varieties. Full article

Trichome birefringence-like proteins function as polysaccharide O-acetyltransferases that catalyze the O-acetylation of cell wall polysaccharides and play widespread roles in regulating plant growth and stress responses. However, no TBL genes have been functionally characterized in maize, and their biological properties remain largely unexplored. Through bioinformatic analysis, we identified 74 maize TBL genes (designated ZmTBL1–ZmTBL74) among the maize genome. Comprehensive analyses of their phylogenetic relationships, basic physicochemical and sequence characteristics, putative upstream regulatory transcription factors and expression patterns were conducted. Expression profiling and qPCR analyses revealed that ZmTBLs respond widely to abiotic stresses, including heat and cold. Association analyses demonstrated that sequence variations in ZmTBL57 and ZmTBL69 correlate with maize agronomic traits. These findings elucidate the molecular characteristics and evolutionary history of maize TBL genes and underscore their roles in abiotic stress responses. In summary, the foundation established by this work will facilitate further functional characterization of TBL genes in maize. Full article

Background/Objective: Orthodontic mini-implants (MI) create new niches that may alter the oral microbiota and modulate host immune responses. While clinical inflammation is not always evident, microbial and molecular changes may precede visible signs of peri-implant infection. This study investigated microbial shifts and inflammatory responses following MI placement, with a focus on Saccharibacteria, nitrate-reducing bacteria (NRB), and periodontopathogens. Methods: Saliva and peri mini-implant crevicular fluid (PMICF) samples were collected from eight orthodontic patients at baseline (T0), one week (T1), and one month (T2) after mini-implant placement. DNA was extracted from each saliva and PMICF sample and pooled across the eight patients for each time point. The pooled DNA were then subjected to 16S rRNA gene sequencing using the Oxford Nanopore MinION platform. Statistical analysis was performed to determine shifts in bacterial abundance, diversity, and co-occurrence patterns across the different sample types (saliva vs. PMICF) and time points. Results: Alpha diversity decreased in PMICF at T2, while it remained stable in saliva samples. Periodontopathogens (Porphyromonas gingivalis, Treponema denticola, Fusobacterium nucleatum) increased in PMICF at T2, while NRB and Saccharibacteria, along with a representative host bacterium (Schaalia odontolytica), remained relatively stable. Co-occurrence analysis showed antagonistic relationships between Saccahribacteria/NRB and periodontopathogens. IL-6 significantly decreased from T1 to T2, while CRP showed a non-significant downward trend. The expression of nitrate reductase genes narG and napA remained stable across time intervals. Conclusions: Despite no clinical inflammation, MI placement led to localized microbial shift and mild inflammatory responses. NRB and Saccharibacteria’s stability and antagonistic relationship to periodontopathogens may indicate that they could be involved in maintaining microbial homeostasis. These findings highlight possible early biomarkers and ecological strategies to support oral health in MI patients. Full article

Low-temperature (LT) stress remains a challenge in rice cultivation and breeding. Despite global warming, cold waves cause damage to rice plants, particularly during pollen development. LTs during early panicle formation worsen pollen formation defects, but the underlying mechanisms remain unclear. We investigated the effects of low temperatures (19.0 °C and 18.5 °C) throughout reproductive growth on the panicle architecture and fertility of 28 japonica rice varieties with different LT tolerances. LT-sensitive varieties like Sasanishiki and conventional LT-tolerant varieties like Hitomebore showed increased spikelet densities on basal branches, whereas extremely LT-tolerant varieties like Tohoku 234 maintained a stable panicle architecture. RNA sequencing of the early panicles revealed LT-induced expression of stress response genes in all varieties. Compared with Hitomebore and Sasanishiki, in Tohoku 234, the expression of genes involved in flowering and sugar metabolism—such as OsGI and OsTOC1—showed stepwise induction with decreasing temperatures, while the expression of genes related to the cell cycle exhibited stepwise suppression. In addition, 24 genes with variety-specific expression patterns were identified. These findings suggested that LTs during the early reproductive stage increased spikelet numbers, along with total anther numbers, which may reduce the pollen formation capacity within each anther in LT-susceptible varieties. This study offers insights into rice’s LT tolerance mechanisms. Full article

Background: The escalating global salinization poses a significant threat to agricultural productivity, necessitating a thorough understanding of plant responses to high salinity. Pea sprouts (Pisum sativum), a nutrient-rich crop increasingly cultivated in salinized regions, serve as an ideal model for such investigations due to their rapid growth cycle and documented sensitivity to ionic stress. Methods: In order to understand the response of pea sprouts in physiological regulation, redox-metabolic adjustments, and transcriptome reprogramming under salt stress, we investigated the effects of high salt concentrations on the ascorbic acid–glutathione cycle, endogenous hormone levels, metabolite profiles, and gene expression patterns in it. Results: Our findings reveal early-phase antioxidant/hormonal adjustments, mid-phase metabolic shifts, and late-phase transcriptomic reprogramming of pea sprouts under salt conditions. In addition, a biphasic response in the ascorbic acid cycle was found, with initial increases in enzyme activities followed by a decline, suggesting a temporary enhancement of antioxidant defenses. Hormonal profiling indicated a significant increase in abscisic acid (ABA) and jasmonic acid (JA), paralleled by a decrease in indole acetic acid (IAA) and dihydrozeatin (DZ), underscoring the role of hormonal regulation in stress adaptation. Metabolomic analysis uncovered salt-induced perturbations in sugars, amino acids, and organic acids, reflecting the metabolic reconfiguration necessary for osmotic adjustment and energy reallocation. Transcriptomic analysis identified 6219 differentially expressed genes (DEGs), with a focus on photosynthesis, hormone signaling, and stress-responsive pathways, providing insights into the molecular underpinnings of salt tolerance. Conclusions: This comprehensive study offers novel insights into the complex mechanisms employed by pea sprouts to combat salinity stress, contributing to the understanding of plant salt tolerance and potentially guiding the development of salt-resistant crop varieties. Full article

MicroRNAs (miRNAs) are short, non-coding RNA molecules that play a crucial role in regulating various biological processes by influencing post-transcriptional gene expression and gene silencing. Background/Objectives: In this study, rabbit embryos were utilised as a model system to investigate potential biomarkers relevant to human embryo development. Seven microRNAs (miRNAs) identified in the embryo culture medium were evaluated as biomarkers by analysing the correlation between their expression levels and the developmental quality of rabbit embryos at days 4 and 6. Methods: We analysed the expression of seven development-specific miRNAs (miR-24-3p, miR-28-3p, miR-103a-3p, miR-181a-5p, miR-191-5p, miR-320a-3p, miR-378a-3p) in 4-day-old and 6-day-old rabbit embryos, along with their culture media. Results: Our findings revealed significant differences in the expression levels of these miRNAs between the 4-day-old and 6-day-old embryos. On the other hand, the expression patterns observed in the culture medium samples showed less variation between the two age groups. Nonetheless, analysis of miRNA expression profiles in the spent culture medium from individually cultured embryos enabled the identification of lower-quality embryos, characterised by smaller size and impaired or delayed development. Conclusions: The detection of these miRNAs in embryo culture medium may serve as a reliable indicator of successful progression to the blastocyst stage. Our experimental results identified specific miRNAs whose expression profiles differ according to embryonic stage and quality, thereby reflecting key developmental milestones. Notably, the detectability of these miRNAs in the medium—without prior RNA isolation—indicates their active secretion into the extracellular environment. By synthesising our findings with the existing literature, we refined a panel of miRNAs essential for the development of implantation-competent embryos in both rabbits and humans. Consequently, we developed a non-invasive assay for predicting implantation and pregnancy outcomes, which may have significant applications in human reproductive medicine. Full article