Search Results (606)

Phyllanthus emblica L. is a nutraceutically important medicinal plant; however, the relationship between genetic variation and bioactive potential remains poorly understood. This study integrates genome-wide SNP analysis, phytochemical profiling, and functional bioassays to investigate cross-scale differentiation among fourteen cultivars. Genotyping-by-sequencing (GBS) identified 5644 high-quality SNPs from an initial dataset of 9018 SNPs, revealing moderate but structured genomic divergence (0.0275–0.0845). Phytochemical analysis of five commercial cultivars demonstrated significant variation (p < 0.05) in total phenolic content (6.58–15.53 mg GAE/gDW) and tannin content (284.52–333.81 mg TAE/gDW). Functional assays revealed strong anti-obesity potential, with crude extracts exhibiting superior α-glucosidase inhibition (up to 98.75%), while tannin-enriched extracts showed enhanced pancreatic lipase inhibition (up to 46.26%). Importantly, enzyme inhibition did not correlate directly with total phenolic or tannin content, indicating compound-specific bioactivity. LC-MS/QTOF analysis identified flavonoids (e.g., quercetin and kaempferol), phenolic acids, and other candidate metabolites potentially associated with enzyme inhibitory activity. These findings demonstrate a non-proportional association among genomic variation, metabolite composition, and functional bioactivity, suggesting that bioactivity may be influenced more strongly by compound-specific metabolite composition than by genome-wide similarity alone. Full article

Background: Although emerging evidence indicates that major depressive disorder (MDD) raises the risk of developing ovarian cancer (OC) and worsens survival, the biological mechanisms underlying this relationship remain unclear. This study explores the MDD-OC association using single-cell transcriptomics and genetic approaches. Methods: Using single-cell RNA-seq profiles of peripheral blood from MDD and OC patients, we compared shifts in immune cell subsets and selected the consistently expanded CD8⁺ effector memory (CD8_EM) T cells population for follow-up, validated using flow cytometry. We integrated expression quantitative trait loci (eQTL) data from CD8_EM T cell-specific genes with OC genome-wide association study (GWAS) summary statistics through two-sample Mendelian randomization (MR). In vitro experiments were additionally conducted to assess CLSTN3’s role in OC cell proliferation. Results: Among the 554 differentially expressed genes (DEGs) identified in CD8_EM T cells, MR showed a nominal association between CLSTN3 and ovarian cancer risk (OR 1.21, 95% CI 1.03–1.43), though this did not withstand correction for multiple comparisons. Colocalization analysis confirmed that CLSTN3 expression, regulated by the genetic variant rs3759416, shares a causal variant with the OC GWAS signal (PPH4 = 99.99%). Functionally, siRNA-mediated CLSTN3 silencing in HOC7 cells significantly reduced cell viability (CCK-8 assay). Conclusions: By focusing on CD8_EM T cells shared by MDD and ovarian cancer, we identified CLSTN3 as a candidate molecule through nominated by the convergence of genetic, transcriptomic, and functional evidence. These findings provide preliminary insights into the connection between depression and OC, though further validation is warranted. Full article

Background/Objectives: Tree peony (Paeonia suffruticosa) has a short flowering period, and its regulatory mechanisms remain poorly understood. These limitations have severely constrained its industrial development. Expansins (EXPs) are key proteins that mediate cell wall loosening associated with petal expansion, yet they remain uncharacterized in tree peony. Methods: This study utilized gene family identification, key gene screening and functional research, as well as regulatory network analysis to reveal the role of the EXP family in the regulation of flower opening. Results: This study presents the first genome-wide identification of 36 PsEXP genes in tree peony, classifying them into four evolutionarily conserved subfamilies (PsEXPA, PsEXPB, PsEXLA, and PsEXLB). Promoter analysis revealed that 28 out of 36 PsEXP promoters contain gibberellin (GA)-responsive elements. Exogenous GA₃ treatment significantly promoted flower opening and upregulated eight PsEXPs, with PsEXPA4-1 showing the highest expression level and promoter GA-responsive element abundance. Subcellular localization confirmed that PsEXPA4-1 was targeted to the cell wall. Overexpression of PsEXPA4-1 in Arabidopsis led to early flowering and enlarged petals, indicating that PsEXPA4-1 had the potential to promote cell expansion, consistent with its proposed role in tree peony flower opening. Mechanistically, we identified a bHLH transcription factor, PsbHLH25, whose expression was induced by GA. Y1H and dual-luciferase assays indicated that PsbHLH25 can bind to the PsEXPA4-1 promoter. Conclusions: This study systematically characterized the EXP gene family in tree peony, revealed PsEXPA4-1 as a key effector downstream of GA promoting flower opening, and discovered PsbHLH25 as a transcriptional activator linking GA signaling to PsEXPA4-1. These findings provided important insights into GA-mediated floral opening and genetic resources for understanding the molecular mechanisms and enabling precise flowering time regulation in tree peony. Full article

The NAC transcription factor superfamily is one of the most prominent plant-specific regulatory gene families, extensively participating in multiple metabolic processes that govern plant growth, tissue development and stress adaptation. Masson pine (Pinus massoniana Lamb.) is a native dominant conifer widely cultivated across South China, whose timber resources possess great exploitation potential in pulp manufacturing and the paper industry. In this study, a total of 98 non-redundant NAC family members were mined at the genome-wide level. Functional validation revealed that PmNAC82, a member belonging to the VND evolutionary subgroup, acts as a core regulatory factor controlling wood formation. Subcellular localization tests confirmed PmNAC82 exclusively resides in the cell nucleus. Heterologous genetic transformation in poplar demonstrated that this gene positively regulates the accumulation of lignin and cellulose. Furthermore, through RT-qPCR, yeast one-hybrid assays, and EMSA, we confirmed that PmNAC82 can bind to the promoters of PtrMYB3, PtrMYB21 and PmCesA7. These findings provide a solid foundation for further investigation into the molecular functions of NAC genes in Masson pine as well as their potential application towards molecular breeding strategies aimed at improving wood quality. Full article

Jasmonate ZIM-domain (JAZ) proteins are pivotal repressors in the jasmonate (JA) signaling pathway, yet their specific roles in garlic (Allium sativum) remain largely unexplored. In this study, 28 AsJAZ genes were identified through a genome-wide analysis. The expansion of this family was primarily driven by whole-genome duplication events, with a significant majority (71.43%) of members belonging to a lineage-specific clade, Subfamily E. While AsJAZ proteins harbor conserved TIFY and Jas domains, they exhibit diverse gene structures and subcellular localization patterns. Notably, AsJAZ17 is strictly localized to the nucleus, whereas AsJAZ16 shows a nucleocytoplasmic distribution, suggesting potential functional compartmentalization within the family. Transcriptomic and qRT–PCR analyses revealed that most AsJAZ genes are responsive to heat, salt, and methyl jasmonate (MeJA) treatments. Protein–protein interaction (PPI) modeling and yeast two-hybrid (Y2H) assays confirmed that AsJAZ17 physically interacts with the MYC2 transcription factor, identifying it as a key regulator within the conserved COI1-JAZ-MYC2 signaling module. Functional validation demonstrated that overexpression of AsJAZ17 in Arabidopsis significantly enhances salt tolerance. This improvement is attributed to an optimized growth-defense trade-off and a reinforced antioxidant defense system, as evidenced by the increased activities of superoxide dismutase (SOD), peroxidase (POD), and catalase (CAT), which collectively maintain reactive oxygen species (ROS) homeostasis under stress. These findings provide comprehensive insights into the evolutionary and functional landscape of the garlic JAZ family and identify AsJAZ17 as a promising candidate gene for molecular breeding to improve abiotic stress resilience in Allium crops. Full article

Usutu virus (USUV) is a mosquito-borne flavivirus, widely distributed in Central Europe, where it causes avian outbreaks with large-scale mortality. Although most human infections are asymptomatic or mild, the reports of USUV neurologic infections are increasing, especially among immunocompromised patients. Cross-reactivity in serological and molecular assays is often seen between USUV and the genetically and antigenically related West Nile virus (WNV). Here, we report the first USUV infection in Greece in an asymptomatic blood donor who tested positive in the automated nucleic acid test during screening for WNV, which is endemic in the country. Following the blood donation surveillance plan, a serum sample taken two weeks post-donation was tested for WNV IgM and IgG antibodies. The borderline index of the IgM antibodies, combined with negative result for IgG antibodies, raised the suspicion of molecular cross-reactivity with USUV. Although the USUV-specific PCR in donor’s plasma was negative, its result was positive following amplification of the virus in cell culture, as USUV RNA was detected in the culture supernatant confirming the USUV infection. Whole genome sequence was taken using an Ion Torrent next-generation sequencing platform. Phylogenetic analysis showed that the Greek strain clusters within the USUV Europe 2A genetic lineage. The detection of USUV human infection in Greece prompts for surveillance studies to elucidate its epidemiology and ecology in the country. Full article

Basic leucine zipper (bZIP) transcription factors are widely involved in plant growth, development, environmental adaptation, and secondary metabolism. However, the bZIP gene family in Taxus yunnanensis has not been systematically characterized, and its potential involvement in shading-responsive regulation of paclitaxel biosynthesis remains unclear. In this study, a genome-wide analysis was performed to identify and characterize the bZIP family in T. yunnanensis. Phylogenetic analysis, conserved motif and domain identification, promoter cis-element analysis, chromosomal localization, and expression profiling were conducted to investigate their structural features and regulatory potential. A total of 18 TyubZIP genes were identified and classified into 10 subfamilies. These genes exhibited variation in physicochemical properties but showed conserved structural features and nuclear localization. Promoter analysis revealed abundant light-responsive, hormone-related, and stress-related cis-elements. Expression profiling indicated tissue-specific expression patterns and diverse responses to shading treatment. WGCNA further identified candidate TyubZIP genes potentially associated with paclitaxel biosynthesis. Among them, TyuHY5 was selected for functional analysis. Subcellular localization and transcriptional assays demonstrated that TyuHY5 can bind to the promoter of TyuDBTNBT and positively regulate its activity. These findings provide the first genome-wide characterization of the bZIP family in T. yunnanensis and identify TyuHY5 as a shading-responsive candidate regulator of paclitaxel biosynthesis, providing insights that may inform the genetic improvement and cultivation strategies of Taxus for enhanced paclitaxel production. Full article

Phytophthora infestans is the causal agent of late blight, one of the most destructive diseases of potato and tomato worldwide. Although qPCR-based methods are widely used to estimate pathogen biomass in infected tissues, methods for specifically assessing sporangial proliferation remain limited. In this study, we developed an RT-qPCR-based assay using PITG_13011, which encodes a predicted major facilitator superfamily transporter, as a sporangia-associated molecular marker in P. infestans. Among five candidate genes selected from transcriptomic data, PITG_13011 showed the strongest association with sporangia-associated samples in our validation assays. PITG_13011 transcripts were detectable from cDNA and genomic DNA derived from as few as 100 sporangia, and transcript abundance showed a strong positive correlation with sporangial number under controlled experimental conditions. In detached leaf inoculation assays, PITG_13011 transcript levels were associated with differences in sporangia-associated proliferation during infection. These results indicate that PITG_13011-based RT-qPCR can serve as a complementary molecular approach for estimating sporangia-associated proliferation of P. infestans in laboratory experiments. This method will be useful when sporangial production, rather than total pathogen biomass alone, is the parameter of interest. Full article

Highly pathogenic avian influenza (HPAI) H5N1 viruses of the goose/Guangdong (Gs/GD) lineage have driven a global panzootic since 2020, with clade 2.3.4.4b establishing sustained transmission in wild birds. In South America, early outbreaks were largely associated with the North American-derived B3.2 genotype, which showed limited diversification after its introduction. Here, we report the genomic characterization of eight H5N1 viruses detected in Uruguay during the reemergence of avian influenza in February–March 2026. Complete genomes were obtained from wild birds exhibiting neurological signs, predominantly Coscoroba coscoroba. All viruses belong to clade 2.3.4.4b but exhibit a reassortant genomic constellation distinct from B3.2. The HA, NA, and MP segments retain the Eurasian backbone, whereas internal genes derive from both South American and North American low-pathogenicity avian influenza lineages. PB2 variation distinguishes two closely related viral groups differing in PB2 origin, whereas the remaining genomic segments retain a shared background. Sequence variation in the neuraminidase gene reduced the sensitivity of a widely used N1-specific RT-qPCR assay, highlighting limitations of existing diagnostic tools during viral evolution. These findings confirm the presence of reassortant H5N1 viruses in Uruguay and, together with recent reports from Argentina and Brazil, support an emerging pattern of genomic diversification in southern South America. Full article

In this study, we investigate two RpoN homologs in Bradyrhizobium sp. DOA9—chromosomal RpoNc and megaplasmid-borne RpoNp—and their roles in free-living conditions and nitrogen fixation. Phylogenetic analysis showed that RpoNc clusters with RpoN proteins from symbiotic nitrogen-fixing strains, whereas RpoNp forms a distinct clade, consistent with a function in stress responses. RpoNc proved essential for free-living conditions: ΔrpoNc mutants displayed severe growth defects that RpoNp could not compensate for. Transcriptomic comparisons between wild type and mutant RpoN identified 541 differentially expressed genes (DEGs) grouped into three clusters: 100 downregulated, 175 upregulated, and 254 moderately downregulated (with a fold change > 2, and a q-value (FDR, padj) < 0.05). Affected pathways involved nitrogen metabolism, motility, and environmental adaptation. RpoNc controlled major nitrogen fixation genes (nif and fix) along with core growth and stress response functions, while RpoNp mainly influenced stress-adaptation pathways. Genome-wide promoter motif analysis predicted 68 putative RpoNc targets, mainly associated with nitrogen fixation and metabolism, compared with only 22 predicted RpoNp targets, indicating a more restricted regulon. Electrophoretic mobility shift assays (EMSAs) further confirmed that both RpoN proteins directly bind σ⁵⁴-dependent promoters identified from transcriptomic data, supporting their regulatory roles under free-living conditions. Two mutants (ΔrpoNc and ΔrpoNp::ΩrpoNc) showed broad transcriptional disruption across nitrogen fixation, metabolism, and stress responses, underscoring complementary regulation. Overall, RpoNc is the dominant regulator of nitrogen fixation and core metabolism during free-living conditions, whereas RpoNp fine-tunes stress responses, revealing new regulatory insights for DOA9 adaptation. These results clarify how RpoN systems optimize survival across fluctuating conditions. Full article

Real-time selective sequencing on nanopore platforms offers a programmable way to enrich target molecules and deplete background DNA during a run. This approach, widely known as adaptive sampling (AS), has been applied across host depletion, metagenomics, targeted loci, plasmid/AMR workflows, and RNA/transcriptomic protocols, but reported performance varies substantially across studies. This review synthesizes current algorithmic and empirical evidence with emphasis on sequencing-relevant outcomes, including absolute informative yield, target-coverage behavior, throughput effects, and run-to-run stability. Across use cases, relative enrichment is frequently observed, but gains in usable genomic output are strongly conditioned by fragment-length distributions, reference quality, decision-loop latency, and rejection-associated penalties in total yield and pore longevity. Evidence from targeted-panel and complex-locus studies further indicates that improved depth concentration can coexist with coverage non-uniformity and context-specific trade-offs relative to wet-lab enrichment. Overall, the literature supports AS as a valuable but condition-dependent strategy whose benefit is greatest when assay design, reference selection, and computational constraints are jointly optimized. Full article

Papain-like cysteine proteases (PLCPs) are central immune hubs frequently targeted by pathogen effectors. Sugarcane smut, caused by Sporisorium scitamineum, threatens global sugarcane yield, yet effector manipulation of host PLCPs remains unclear. Genome-wide analysis of Saccharum spontaneum AP85-441 identified 61 PLCP-encoding genes, which were classified into nine conserved subfamilies. Among these, ScRD21A, a member of the RD21 subfamily, was prioritized for functional characterization. Two Pit2 homologs, SsPit2A and SsPit2B, were identified from S. scitamineum. Yeast two-hybrid, BiFC and pull-down assays demonstrated that both effectors interact with ScRD21A, and that this interaction depends on a conserved LXRR motif within their PID14-like region. In total protein extracts from Nicotiana benthamiana, co-expression of SsPit2A or SsPit2B reduced ScRD21A-associated cysteine protease activity. Transient expression of ScRD21A enhanced flg22-induced ROS production, attenuated Pst DC3000-induced hypersensitive response-associated necrosis, and increased resistance to Botrytis cinerea. Together, these results support a conserved PLCP-targeting strategy in smut fungi and identify the ScRD21A–SsPit2A/B module as a tractable framework for studying effector–protease interactions relevant to sugarcane smut. Full article

Seed weight is a key agronomic trait determining soybean yield and quality, yet only a few of genes regulating this trait have been functionally characterized to date. In this study, we identified 155 homologous genes in the soybean genome through BLAST searches using 78 functionally validated rice grain weight-related genes as queries. Haplotype analysis prioritized 40 candidate genes exhibiting significant differences in seed weight between haplotypes. To further refine the candidate list, we integrated haplotype frequency analysis, expression–trait association mapping, and tissue-specific expression profiling, ultimately delineating eight key genes. Given the established role of ubiquitination in seed development, we focused on homologs of OsUBP15 and identified three candidate genes, GmUBP5, GmUBP11, and GmUBP33, that exhibited significant haplotype-dependent variation in seed weight. Subcellular localization assays confirmed their nuclear localization. Haplotype frequency analysis revealed that the superior haplotypes of these genes have been preferentially retained during modern breeding and are widely distributed across major soybean-producing regions. Leveraging non-synonymous SNP variants, we developed and validated robust KASP markers that efficiently discriminate germplasm with contrasting seed weight phenotypes. Collectively, our study provides not only high-confidence genetic targets and actionable molecular markers but also insights into pyramiding breeding strategies for improving seed weight in soybean. Full article

Soil salinity limits ginger productivity, but the underlying molecular mechanisms remain largely unclear. The 14-3-3 proteins are conserved regulators in stress signaling. Here, we genome-wide characterized the 14-3-3 family in Zingiber officinale and examined the possible involvement of Zo14-3-3-03 in salt response. A total of 21 Zo14-3-3 genes were identified and classified into four groups with uneven chromosomal distribution. Among them, Zo14-3-3-03 was strongly salt-responsive: transcript levels increased 9.91- to 33.82-fold during 1–7 days of treatment and reached 62.47-fold in leaves at day 14. NaCl treatment elevated GUS expression driven by the Zo14-3-3-03 promoter. Virus-induced gene silencing (VIGS) of Zo14-3-3-03 resulted in silenced plants exhibiting higher malondialdehyde (up to 73.6%), lower antioxidant enzyme activities (SOD, POD, CAT, and APX: 18.9–31.9% reduction), reduced osmolytes (proline, soluble protein, sugars, and ascorbic acid: 23.2–36.2% reduction), excessive reactive oxygen species, and decreased relative water content. Several antioxidant-related genes were significantly downregulated. Protein interaction assays suggested a possible interaction with ZoSOS2, and the expression of SOS2 pathway genes was altered in silenced plants, indicating a potential link to calcium signaling and ion homeostasis. Taken together, these results suggest that Zo14-3-3-03 participates in ginger salt stress response possibly through redox balance, osmotic adjustment, and calcium-mediated pathways which would provide a basis for understanding 14-3-3-mediated stress responses and nominates Zo14-3-3-03 as a candidate requiring deeper validation for salt tolerance improvement in ginger. Nevertheless, due to limited functional validation, its role as a positive regulator and breeding target remains preliminary. Further genetic and mechanistic studies are needed to confirm causality and assess field-level applicability. Full article

A clinical strain of the opportunistic pathogen Serratia rubidaea, a known contaminant of healthcare environments and an emerging cause of invasive infections, is described. The studied isolate, recovered from a nurse’s hand skin swab during routine screening, exhibits a broad profile of antibiotic resistance combined with reduced susceptibility to several disinfectants. Phenotypic susceptibility testing using a tablet-based microdilution and disk diffusion method was employed to determine the minimum inhibitory concentrations (MICs) of antimicrobial agents from different classes, while broth microdilution assays with disinfectants revealed high-level tolerance to widely used agents, including 70% C₂H₅OH, 3% H₂O₂, 0.05% polyhexamethylene guanidine (PHMG) and others. Whole-genome sequencing identified multiple resistance-associated determinants, such as chromosome-encoded class C $\beta$-lactamase (ampC), several efflux systems (sdeXY, macAB, and emrAB) combined with multicopy tolC, and specific transferases (fos and arnT). Shotgun bottom-up HPLC-MS/MS proteomics confirmed baseline expression of these and other stress-tolerance-related proteins under non-inducing conditions. Taken together, these data underscore the importance of surveillance for Serratia spp. in healthcare facilities to detect strains that combine intrinsic or acquired multidrug resistance with robust survival traits such as disinfectant tolerance and biofilm formation. The present study provides a reference-level phenotypic, genomic, and proteomic characterization of a S. rubidaea clinical isolate, contributing to the understanding of the adaptive potential of this resilient opportunistic pathogen in clinical environments. Full article