Volatile organic compounds(VOCs)are the main chemical compounds that determine the characteristic aroma and flavor of fruit.In this study,we identified a total of 97 VOCs,including 5C6 compounds,12 aldehydes,4 alcohol...Volatile organic compounds(VOCs)are the main chemical compounds that determine the characteristic aroma and flavor of fruit.In this study,we identified a total of 97 VOCs,including 5C6 compounds,12 aldehydes,4 alcohols,10 esters,13 lactones,18 terpenes,8 norisoprenoids,8 ketones,3 hydrocarbons,8 phenylalanine derivates,and 8 other compounds,in 60 peach cultivars using headspace solid-phase microextraction(HS-SPME)combined with gas chromatography-mass spectrophotometry(GC-MS).A wide range of VOCs were detected in these germplasm resources with respect to both quantity and concentration.Correlation analysis with different physiological traits demonstrated that the genetic background exerts a significant influence on the composition and content of VOCs among peach cultivars.For example,the content of norisoprenoid was significantly lower in yellow-fleshed peach than in white-fleshed peach,and lactones were almost undetectable in stony hard peach.Among the 97 VOCs,26 exhibited odor activity values(OAVs)exceeding 1,suggesting that these compounds act as key odorants in the peach VOC composition.Moreover,six structural genes associated with the synthesis of γ-decalactone and(Z)-3-hexenyl acetate and five genes linked to aldehyde and 1-octen-3-one biosynthesis were identified through weighted gene co-expression network analysis(WGCNA).Additionally,15 transcription factors(TFs)were identified as potentially regulating VOC synthesis.Overall,these data provide insight into the factors contributing to the differences in aroma qualities among peach cultivars,which can help to promote the development of peach breeding.展开更多
Cytoplasmic male sterility(CMS)is a widespread phenomenon in crops and is beneficial for commercial hybrid breeding.Although CMS systems in Brassica species are extensively utilized,they are derived from relatively li...Cytoplasmic male sterility(CMS)is a widespread phenomenon in crops and is beneficial for commercial hybrid breeding.Although CMS systems in Brassica species are extensively utilized,they are derived from relatively limited sources,and the underlying molecular mechanisms are not well understood.In this study,a novel CMS line,named Neau,was identified through distant hybridization between Matthiola incana and Brassica rapa.Neau CMS exhibits agronomic traits similar to its maintainer line of Chinese cabbage and displays sterility at the tetrad stage.The mitochondrial genomes of Neau CMS and its maintainer line were assembled to 359596 bp and 219771 bp,respectively,encoding 99 and 66 unknown open reading frames(orfs).Six orfs were identified as specific to Neau CMS with sequence alignments,with orf154 and two copies of orf138 identified as candidate genes based on their transmembrane structures and their ability to encode toxic proteins that inhibited Escherichia coli cell growth.The expression of orf154 was induced during the tetrad stage by quantitative real-time polymerase chain reaction(qRT-PCR),whereas orf138a showed higher expression at the microspore mononuclear stage in Neau CMS.Transcriptome analysis revealed reduced expressions of most pollen development-related genes,as well as genes involved in peroxidase/oxidative stress responses and the electron transfer chain in Neau CMS.Additionally,Neau CMS exhibited increased levels of O2.-,H2O2,and malondialdehyde(MDA),alongside reduced activities of SOD,CAT,and POD.Both ATP content and ATPase activity were down-regulated in Neau CMS.Overexpression of orf138 and orf154 in Arabidopsis thaliana resulted in reductions in pollen quantity,viability,and seed production.These findings suggest that orf138 and orf154 are key candidate genes responsible for the sterility observed in Neau CMS in Chinese cabbage.展开更多
Anthocyanins are vital secondary metabolites contributing to fruit pigmentation and antioxidative properties.While light is a well-known regulator of anthocyanin biosynthesis,the molecular basis of light-independent a...Anthocyanins are vital secondary metabolites contributing to fruit pigmentation and antioxidative properties.While light is a well-known regulator of anthocyanin biosynthesis,the molecular basis of light-independent anthocyanin accumulation remains underexplored.In this study,integrated analysis of metabolome and transcriptome showed that the anthocyanin content in blueberry(Vaccinium corymbosum‘Bluetta’)fruit was slightly decreased by light-impermeable bagging treatment,while anthocyanin biosynthetic genes were transcriptionally inhibited to different levels,suggesting a slight influence of the bagging treatment on anthocyanin accumulation.Further observation showed that fruit bagging did not alter ethylene production but decreased ABA content.Noticeably,two VcMYBA/MYB1s were not transcriptionally altered by the light-impermeable bagging treatment.Consistently,histochemical GUS analysis and pharmacological manipulation suggested light-independent and ethylene-inducible expression of VcMYBA/MYB1.Moreover,WGCNA analysis revealed 3759 genes positively associated with MYBA/MYB1 such as ethylene-associated genes,etc.Additionally,VcbZIP55s and VcCOP1s were activated and inactivated by the bagging treatment,respectively.These findings provided a framework of light-independent anthocyanin biosynthesis in blueberry fruit.展开更多
The evolutionary development of adventitious roots(ARs)in plants enhances their capacity to adapt to various stress conditions.A thorough analysis of the influencing factors in their morphological construction holds s...The evolutionary development of adventitious roots(ARs)in plants enhances their capacity to adapt to various stress conditions.A thorough analysis of the influencing factors in their morphological construction holds significant theoretical value and practical guidance for overcoming rooting obstacles in cuttings,as well as for cultivating superior varieties characterized by broad adaptability and stress resistance.In this study,we investigated the molecular mechanisms underlying the development of ARs in tomato(Solanum lycopersicum)by performing transcriptome sequencing(RNA-seq).We analyzed the transcription profiles of relevant genes in the"Y962"strain,which exhibits spontaneous AR formation,and the"W961"strain,which does not form ARs.Our findings indicate that the AR induction stage represents an active phase of development,during which we identified 1,676 overlapping genes across the three comparison groups,highlighting the most differentially expressed genes.Functional enrichment analysis showed that they were most closely related to response to auxin,and were also dependent on the crosstalk between other hormones and carbohydrates.Furthermore,through the measurement of endogenous auxin levels and the induction tests with exogenous auxin,it was established that the formation of ARs is closely linked to the accumulation and transport of auxin.Notably,the auxin efflux SIPIN3,which was enriched in the auxin response pathway,exhibited significantly high expression during the induction phase of ARs.The slpin3 mutant,generated using the CRISPR/Cas9 editing system,exhibited a significant reduction in the number of ARs,highlighting the close relationship between polar transport regulated by SIPIN3 and auxin-induced AR formation.In summary,this study not only enriches the developmental network of AR formation in tomatoes with a wealth of data but also elucidates the potential mechanisms for promoting AR development by targeting SIPIN3.展开更多
For red pear,the anthocyanin content is a crucial factor determining the fruit skin color,which affects consumer preferences.Low overnight temperatures promote anthocyanin accumulation,but the molecular mechanism resp...For red pear,the anthocyanin content is a crucial factor determining the fruit skin color,which affects consumer preferences.Low overnight temperatures promote anthocyanin accumulation,but the molecular mechanism responsible is unclear.In this study,‘Hongzaosu’pear(Pyrus pyrifolia×Pyrus communis)fruit were treated with a low nighttime temperature(LNT,16℃)or a warm nighttime temperature(WNT,26℃),with sampling conducted within two diurnal cycles.The results showed that LNT promoted anthocyanin accumulation in the fruit skin.The structural anthocyanin biosynthetic genes PpCHS,PpF3H,and PpUFGT exhibited a rhythmic increase in expression at night under LNT.To examine the underlying mechanism,RNA sequencing was conducted using pear calli exposed to LNT and WNT for different durations(24,48,72,or 96 h).Transcriptome analysis revealed 285 differentially expressed genes(DEGs)common to all pairwise comparisons of LNT-and WNT-treated calli of‘Clapp's Favorite’(P.communis)at the sampling time points.KEGG pathway and gene ontology enrichment analyses indicated that the common DEGs were enriched in secondary metabolic processes and phenylpropanoid metabolic processes,which are associated with anthocyanin biosynthesis.The transcription factor PpCDF5,which was responsive to LNT,was selected for further study.Dual-luciferase assays showed that PpCDF5 activated the transcription of anthocyanin biosynthetic genes PpMYB10,PpCHS,PpF3H,PpDFR,PpANS,and PpUFGT.The yeast one-hybrid and EMSA assays demonstrated that PpCDF5 directly binds to the PpF3H promoter,which contains an AAAG motif.Overexpression of PpCDF5 in pear calli and transient overexpression in pear fruit both increased anthocyanin accumulation.The results indicate that PpCDF5 is involved in LNT-induced anthocyanin biosynthesis in pear fruit and provide insights into the molecular regulation of commercial fruit coloration.展开更多
Red-fleshed fruits are valued for their vibrant color and high anthocyanin content.Pre-harvest fruit bagging enhances fruit peel pigmentation,but its effect on flesh coloration remains poorly characterized.This study ...Red-fleshed fruits are valued for their vibrant color and high anthocyanin content.Pre-harvest fruit bagging enhances fruit peel pigmentation,but its effect on flesh coloration remains poorly characterized.This study revealed that removing bags from‘Gengcunyangtao’red-fleshed peach fruits triggers the rapid and uniform accumulation of anthocyanins in the flesh,resulting in anthocyanin levels that exceed those in unbagged fruits.The exposure to light after bag removal triggered significant increases in anthocyanin levels within 24 h.This was accompanied by the rapid upregulation of light-responsive and flavonoid biosynthetic gene expression levels within 6 h.A metabolomic analysis indicated that anthocyanin precursors,especially p-coumaric acid,accumulated before bag removal,thereby increasing substrate availability for rapid anthocyanin synthesis.On the basis of a weighted gene co-expression network analysis,MYB transcription factors,anthocyanin transporters,glutathione S-transferase,and multidrug and toxic compound extrusion(MATE)were identified as key regulators that coordinate precursor storage along with light-induced transcriptional activation.Notably,PpMYB4 binds to the promoter of PpGSTF14 and activates its expression,thereby promoting anthocyanin accumulation.The study findings elucidated the temporal coordination of metabolic priming and light-responsive transcriptional regulation driving rapid anthocyanin biosynthesis,with possible implications for improving peach fruit flesh coloration.展开更多
Alcoholic liver injury(ALI)has emerged as a significant public health concern,necessitating the urgent identification of medicinal-food resources for its prevention and treatment.As a natural medicinal food resource,C...Alcoholic liver injury(ALI)has emerged as a significant public health concern,necessitating the urgent identification of medicinal-food resources for its prevention and treatment.As a natural medicinal food resource,Chenpi(CHE)is rich in various flavonoid bioactive compounds and exhibits potential antioxidant,anti-inflammatory,and hepatoprotective effects.However,the effect and mechanism of CHE in preventing and improving ALI are not yet known.This study sought to elucidate CHE's hepatoprotective mechanisms in ALI from the biochemical markers,microbiome and transcriptome perspectives.Results showed that CHE ameliorated ALI by improving oxidative stress,inflammatory cytokines and liver function.16S r RNA analysis revealed that CHE alleviated ALI pathological progression primarily by restoring gut microbiota composition.Transcriptomic analysis showed that CHE improved ALI mainly related to MAPK signaling pathway.Pearson correlation analysis revealed that Candidatus_Saccharimonas,Turicibacter,and Clostridium_sensu_stricto_1 play key roles in the process by which CHE ameliorates alcohol-induced inflammation and pathological angiogenesis.These findings revealed that CHE has the potential to be used as a functional food to prevent or improve ALI.展开更多
This study examined the potential response mechanisms of Ligilactobacillus salivarius AR612 to glucose stress through whole-genome and comparative transcriptome analysis.We obtained the basic genome information of L.s...This study examined the potential response mechanisms of Ligilactobacillus salivarius AR612 to glucose stress through whole-genome and comparative transcriptome analysis.We obtained the basic genome information of L.salivarius AR612.The full genome length of L.salivarius AR612 was 1970245 bp,with a GC content of 33.01%and 1894 coding genes.Moreover,we identified many genes associated with genetic adaptations to various stress factors,including temperature,p H,osmotic pressure,bile salts,and oxidative stress.Physiological analysis revealed that the growth and morphology of AR612 changed significantly under glucose stress,with a decrease in the maximum growth and irregular cell morphology.Furthermore,a comparison of transcriptome data indicated that glucose stress induced changes in the number of differential genes.Moreover,AR612 could respond to extracellular glucose stress by changing the expression of genes related to cell morphology,carbohydrate metabolism,amino acid metabolism,fatty acid synthesis,and nucleotide metabolism.This study provides valuable theoretical insights for future research on the adaptation of L.salivarius AR612 to nutritional stress and its application in industrial processes.展开更多
Glucose homeostasis is a fundamental physiological process in both vertebrates and invertebrates,yet its regulatory mechanisms in molluscs remain largely unexplored.This study investigates temporal hemolymph glucose d...Glucose homeostasis is a fundamental physiological process in both vertebrates and invertebrates,yet its regulatory mechanisms in molluscs remain largely unexplored.This study investigates temporal hemolymph glucose dynamics and associated molecular responses in the Pacific oyster Crassostrea gigas.Annual monitoring revealed significant seasonal variation in hemolymph glucose concentrations,with post-spawning oysters exhibiting the lowest levels.A glucose injection experiment demonstrated rapid uptake kinetics,followed by a return to baseline,suggesting the presence of efficient metabolic regulation.Transcriptomic analysis on hepatopancreas tissue identified cgHK2-2 as the dominant hexokinase isoform induced by hyperglycemia,while other HK genes(cgHK2 and cgHK2-like)showed tissue-specific but non-inducible expression profiles in the investigated tissue.Furthermore,upregulation of cgPPP1R3B and cgPCSK1 indicate possibly conserved glycogen metabolism and insulinlike signaling pathways.Phylogenetic analysis revealed divergent evolutionary trajectories of hexokinase in protostomes versus chordates,with oysters lacking a clear glucokinase orthologue.These findings highlight key molecular players in oyster glucose metabolism and suggest both conserved and lineagespecific regulatory strategies.展开更多
Background Subclinical mastitis(SCM)is a major constraint in dairy production and is driven by complex host–pathogen interactions.Although transcriptional responses associated with SCM have been widely investigated,t...Background Subclinical mastitis(SCM)is a major constraint in dairy production and is driven by complex host–pathogen interactions.Although transcriptional responses associated with SCM have been widely investigated,the epigenetic mechanisms that stably regulate these programs remain less well characterized,particularly in crossbred cattle populations.This study aimed to characterize DNA methylation-based regulatory networks by integrating whole-genome methylation and transcriptome data from milk somatic cells of Vrindavani(Bos taurus×Bos indicus)cattle.Whole-genome methylation(n=6)and corresponding transcriptome profiling(n=6)were performed on milk somatic cells from SCM-affected and healthy control cows.Results Differential methylation analysis(q-value<0.05)identified 62,940 differentially methylated cytosines(DMCs),7,706 differentially methylated regions(DMRs),and 6,203 differentially methylated genes(DMGs),with a predominant bias toward hypomethylation in SCM.Integrative analysis using stringent thresholds for both methylation(≥10%)and expression change(|log2 fold change|≥1;P of GMM<0.001)identified 1,407 differentially methylated and expressed genes(DMEGs).Functional enrichment analysis revealed 47 KEGG pathways and 30 Gene Ontology biological process terms(FDR<0.05),primarily associated with immune signaling and inflammatory responses.In contrast,a subset of DMEGs showed methylationassociated repression of lactation-and metabolism-related genes.Selected genes were experimentally validated by qPCR,including upregulation of the inflammatory mediator S100A8 and downregulation of CSN3(κ-casein),a key milk protein gene.Conclusions These findings provide an integrated view of the DNA methylation and transcriptional landscape of SCM in milk somatic cells and demonstrate that epigenetic remodeling is associated with coordinated activation of immune pathways alongside repression of lactation-associated functions.The results contribute to understanding the molecular basis of subclinical mastitis and may inform future efforts toward biomarker development and epigenetically informed strategies for improving disease resilience in dairy cattle.展开更多
Previous studies have demonstrated that the immunoglobulin G(IgG)N-glycome and transcriptome are potential biochemical signatures of chronological and biological ages,and several aging clocks have been developed.By in...Previous studies have demonstrated that the immunoglobulin G(IgG)N-glycome and transcriptome are potential biochemical signatures of chronological and biological ages,and several aging clocks have been developed.By integrating the IgG N-glycome and transcriptome,we propose a novel aging clock,gtAge.We developed a deep reinforcement learning-based multiomics integration method called AlphaSnake.The results showed that AlphaSnake achieved a predicted coefficient of determination(R2)value of0.853,outperforming the concatenation-based integration method(R2=0.820)The gtAge estimated by AlphaSnake explained up to 85.3%of the variance in chronological age,which was higher than that in age predicted from IgG N-glycome solely(gAge;R2=0.290)and age predicted from transcriptome solely(tAge;R2=0.812).We also found that the delta age-the difference between the predicted age and chronological age-was associated with several age-related phenotypes.Both delta gtAge and tAge were negatively associated with high-density lipoprotein(p=0.02 and p=0.022,respectively),whereas delta gAge was positively correlated with cholesterol(p=0.006),triglyceride(p=0.002),fasting plasma glucose(p=0.014),low-density lipoprotein(p=0.006),and glycated hemoglobin(p=0.039).These findings suggest that gtAge,tAge,and gAge are potential biomarkers for biological age.展开更多
While sex-biased gene expression and its evolutionary dynamics across taxa have been extensively investigated,systematic separate characterization of the evolutionary patterns in transcriptome divergence between male ...While sex-biased gene expression and its evolutionary dynamics across taxa have been extensively investigated,systematic separate characterization of the evolutionary patterns in transcriptome divergence between male and female lineages remains underexplored.Here,we analyze a comprehensive RNA-seq data set from the house mouse complex,spanning multiple organs across subspecies and species,to delineate the evolutionary trajectories of gene expression in males and females in intra-and inter-species contrasts.For both sexes,we find specific gene expression divergence patterns across the surveyed organs,with a particularly high divergence rate at early evolutionary stages of separation.Comparative analysis between sexes demonstrates male reproductive organs,particularly the testis,displaying accelerated evolutionary rates of expression divergence.Strikingly,testicular long non-coding RNA genes show the most pronounced acceleration,with differences emerging already after a few thousand years of population separation.In contrast,somatic organs and female reproductive auxiliary tissues show no major sex-specific evolutionary dynamics.Genes with sex-biased expression substantially contribute to differentially expressed genes across evolutionary transitions,though without predominant directional bias toward either sex.Notably,these differentially expressed genes display significant over-representation on autosomes.A general functional divergence process is found between male and female transcriptomes across organs mainly driven by sex-specific differentially expressed genes.Collectively,our findings establish a new evolutionary framework for sex-specific expression divergence and provide novel insights into the role of reproductive constraints in shaping transcriptome evolution in mammals.展开更多
Atmospheric carbon dioxide(CO2)levels are escalating at an unprecedented rate,leading to the phenomenon of ocean acidification(OA).Parental exposure to acidification has the potential to enhance offspring resilienc...Atmospheric carbon dioxide(CO2)levels are escalating at an unprecedented rate,leading to the phenomenon of ocean acidification(OA).Parental exposure to acidification has the potential to enhance offspring resilience through cross-generation plasticity.In this study,we analyzed larval growth and transcriptomic profiles in the Pacific oyster,Crassostrea gigas,a species of significant ecological relevance,under both control and elevated CO2conditions experienced by their parental generation.Our findings indicate that the oyster populations exposed to OA exhibited a higher incidence of abnormalities during the D-shaped larval stage,followed by accelerated growth at the eyed stage.Through a comparative transcriptomic investigation of eyed larvae(25 d after fertilization),we observed that parental exposure to OA substantially influenced the gene expression in the offspring.Genes associated with lipid catabolism and shell formation were notably upregulated in oysters with parental OA exposure,potentially playing a role in cross-generational conditioning and conferring resilience to OA stressors.These results underscore the profound impact of OA on oyster larval development via cross-generational mechanisms and shed light on the molecular underpinnings of cross-generation plasticity.展开更多
The Japanese eel(Anguilla japonica)is a catadromous migratory fish with a high economic value.The gonads of captive eels do not mature naturally.Under artificial maturation,the hypothalamic-pituitary-gonadal(HPG)axis ...The Japanese eel(Anguilla japonica)is a catadromous migratory fish with a high economic value.The gonads of captive eels do not mature naturally.Under artificial maturation,the hypothalamic-pituitary-gonadal(HPG)axis is activated,and the maturation coefficient of the gonads increased significantly.Prior research investigations into Japanese eel breeding have primarily focused on elucidating the mechanisms underlying gonadal development.However,the problems plaguing the artificial breeding of Japanese eels have remained unsolved.Additionally,the insights into the molecular mechanisms within the pituitary,which acts as an upstream regulatory hub,and its impact on ovarian development are limited.To address these,the pre-matured pituitary(PP)and artificially matured pituitary(AP)tissues from female Japanese eels were subjected to transcriptomics using a method combining PacBio Iso-seq with Illumina RNA-Seq.PacBio sequencing produced 19576 filtered consensus sequences from PP and 39828 from AP.Then,we predicted gene regulatory elements such as alternative polyadenylation,transcription factors,and long noncoding RNAs.A total of 3016 differentially expressed genes(DEGs)were identified based on the Illumina RNA-seq data.Further gene ontology and Kyoto Encyclopedia of Genes and Genomes enrichment analyses were performed.Several DEGs that were upregulated in the pituitary were identified.These genes,including nr5a2,pgr,greb1,smad4,bmp5,ar,lhb,adcy5,and tgfbr3,most likely regulate downstream gonadal development via the pituitary.In conclusion,this study obtained the differential expression and full-length transcriptomes of the pituitary in the pre-matured and artificially matured female Japanese eel.These results offer substantial evidence for developing more efficient sex hormones during the captive breeding of eels,while also furnishing a scientific basis for the conservation of eel resources.展开更多
Light is one of the important environmental factors on life activities of aquatic animals.Eyestalks are a multifunctional organ of crustaceans that conducts light signals,produces neurohormones,and regulates growth.Ho...Light is one of the important environmental factors on life activities of aquatic animals.Eyestalks are a multifunctional organ of crustaceans that conducts light signals,produces neurohormones,and regulates growth.However,the mechanism of growth regulation by light intensity remains poorly studied.We evaluated the growth performance of ridgetail white prawn(Exopalaemon carinicauda)under different light intensities(0,100,200,and 400 lx),and determined the regulatory mechanism of growth in response to light intensity through transcriptome analysis of eyestalks.Results show that light intensity at 100 lx significantly improved growth performance in growth rate,specific growth rate,and biomass increase rate,while 0-lx and 400-lx conditions inhibited the growth.A total of 931 DEGs were identified between the 100-lx and 0-lx groups,of which 411 were upregulated and 520 were downregulated.In addition,456 DEGs were identified between groups of 100-lx and 400-lx,including 155 upregulated DEGs and 301 downregulated DEGs.The light intensity at 100 lx significantly improved the growth performance by upregulating the oxidative phosphorylation,Toll and Imd signaling pathway,and ribosome pathway,and downregulating the tyrosine metabolism,phagosome,lysosome,autophagy,and Hippo signaling pathway,whereas 0 lx and 400 lx inhibited growth in the opposite patterns.In total,eight growth-regulation-related candidate genes,i.e.,hemocyanin,NADH dehydrogenase,cytochrome c oxidase,ATP synthase,cathepsin L,phenoloxidase activating factor,CLIP domain-containing serine protease,and 40S/60S ribosomal protein were identified.The optimal light intensity for improved growth of E.carinicauda was about 100 lx when reared indoor.These data shall provide key information for further understanding of the regulatory mechanism of light intensity on the growth performance of this species.展开更多
Multiple sclerosis(MS)is a chronic disorder of the central nervous system characterized by multifocal lesions where inflammation,demyelination,and neurodegeneration occur(Jakimovski et al.,2024).MS diagnosis primarily...Multiple sclerosis(MS)is a chronic disorder of the central nervous system characterized by multifocal lesions where inflammation,demyelination,and neurodegeneration occur(Jakimovski et al.,2024).MS diagnosis primarily relies on the demonstration of dissemination in time and space of the lesions based on clinical,magnetic resonance imaging(MRI),and cerebrospinal fluid assessments(Jakimovski et al.,2024).展开更多
BACKGROUND Glycolipid metabolic disorder includes a series of chronic diseases that are closely associated with disturbances in both glucose and lipid metabolism.Jiangtang Tiaozhi formula(JTTZF)demonstrating significa...BACKGROUND Glycolipid metabolic disorder includes a series of chronic diseases that are closely associated with disturbances in both glucose and lipid metabolism.Jiangtang Tiaozhi formula(JTTZF)demonstrating significant hypoglycemic,lipidmodifying,and anti-inflammatory effects.However,the specific molecular mechanisms underlying JTTZF’s hepatoprotective effects and its ability to ameliorate glycolipid metabolic disorder remain largely unexplored.AIM To investigate how JTTZF improves glycolipid metabolic disorder using hepatic transcriptome and metabolome analyses.METHODS To induce glycolipid metabolic disorder,male C57BL/6J mice were fed a high-fat diet(HFD)for 12 weeks,after which they received an 8-week administration of JTTZF.Liver tissues were analyzed using transcriptomics and metabolomics.Real-time quantitative polymerase chain reaction validated key gene expression.RESULTS Metabolomics data revealed that JTTZF significantly regulated HFD-induced alterations in glycolipid metabolism,with notable changes in pathways such as the pentose phosphate pathway,steroid hormone biosynthesis,and purine metabolism.Transcriptomics profiles indicated that JTTZF exerted regulatory effects on lipid and glucose metabolism,primarily through pathways including peroxisome proliferators-activated receptor signaling,drug metabolism other enzymes,and regulation of lipolysis in adipocytes.Real-time quantitative polymerase chain reaction confirmed that JTTZF modulated pivotal genes associated with fatty acid synthesis,lipolysis,insulin resistance,energy metabolism,and inflammation.These findings suggest that JTTZF may act through multiple pathways to improve glycolipid metabolic disorder.CONCLUSION JTTZF can ameliorate the glycolipid metabolic disorder induced by HFD-diet by regulating lipid metabolism and improving insulin tolerance.展开更多
●AIM:To investigate the transcriptional profiling of ocular surface ectoderm(OSE)derived from human embryonic stem cells(hESC),and identified CACNG6 and AQP3 as the surface markers of OSE.●METHODS:hESCs were differe...●AIM:To investigate the transcriptional profiling of ocular surface ectoderm(OSE)derived from human embryonic stem cells(hESC),and identified CACNG6 and AQP3 as the surface markers of OSE.●METHODS:hESCs were differentiated into OSE,neuroectoderm(NE),surface ectoderm(SE),and other surface ectoderm(OE)cells in vitro.RNA-seq was performed to analyze transcriptomic profiling of hESC-derived OSE,NE,OE,and SE.The differential expressed genes(DEGs)were identified,and Gene Ontology(GO),Kyoto Encyclopedia of Genes and Genomes(KEGG)databases,and protein-protein interaction(PPI)network analyses were performed to screen the signals and hub genes associated to OSE commitment.Also,the highly expressed transcription factors(TFs)and membrane proteins(MPs)in OSE cells were identified.●RESULTS:Transcriptome analysis revealed that OSE development is dually regulated by signals associated with both SE and NE development.The signaling pathways such as Hippo,encoding extracellular matrix(ECM)-receptor interaction,and transforming growth factor-β(TGF-β)might delineate the surface ectodermal phenotype of OSE,with FN1,COL1A1,and TGFB1 identified as hub genes.Additionally,pathways such as axon guidance,might elucidate the influence of NE in OSE commitment,and with PAX6,LHX2,FOXG1,SOX2,MSI1,and DCLK1 recognized as the hub genes.Genes implicated in retinoic acid(RA)synthesis(ALDH1A1,ALDH1A3,and RDH10)exhibited high expression in OSE,indicating the significant role of the RA signaling pathway in OSE development.Furthermore,OSEspecific transcription factors and surface markers(CACNG6 and AQP3)were identified.●CONCLUSION:This study reveals the transcriptome profiling of OSE,which could provide insights into the characteristics of OSE and the underlying molecular mechanisms involved in its derivation.展开更多
Jiangtang Tiaozhi formula(JTTZF)has been widely used in the management of glycolipid metabolic disorders,yet its underlying molecular mechanisms remain incompletely understood.Tian et al recently published a study in ...Jiangtang Tiaozhi formula(JTTZF)has been widely used in the management of glycolipid metabolic disorders,yet its underlying molecular mechanisms remain incompletely understood.Tian et al recently published a study in the World Journal of Diabetes,which reported a comprehensive hepatic transcriptomic and metabolomic analysis that provides important insights into the regulatory effects of JTTZF on glucose and lipid homeostasis.This multi-omics strategy offers a valuable systems-level perspective on the pharmacological actions of this traditional Chinese medicine formulation.In this commentary,we highlight the strengths of the study and discuss several aspects that warrant further investigation to enhance mechanistic depth and translational relevance.These include dose-response relationships,cellular heterogeneity,causal validation of key pathways,identification of active constituents,and long-term safety evaluation.We also emphasize the potential role of host-related factors,such as immune regulation and gut microbiota-associated metabolic interactions,in influencing therapeutic responsiveness.展开更多
Rapeseed(Brassica napus L.)is a major oil crop worldwide that is vigorously promoted for cultivation in China.Boron(B)is an essential micronutrient for plant growth and development.However,the agricultural soils in ra...Rapeseed(Brassica napus L.)is a major oil crop worldwide that is vigorously promoted for cultivation in China.Boron(B)is an essential micronutrient for plant growth and development.However,the agricultural soils in rapeseed planting areas often show either B deficiency or severe B deficiency.Increasing the resistance to B deficiency is a pivotal goal in the breeding of rapeseed,yet the genetic basis for variations in B efficiency-related traits remains unclear.In this study,a natural population with 391 rapeseed accessions and a nutrient solution system were used to investigate B efficiency-related traits,including relative root length(RRL),shoot dry weight(SDW),root dry weight(RDW),and B efficiency coefficient(BEC),all of which exhibited extensive phenotypic variations under B deficiency.Through a genome-wide association study(GWAS)of B efficiency-related traits using high-density SNP markers obtained from whole-genome resequencing,106 significantly associated SNPs were identified by employing both the general linear model and the mixed linear model.Among these SNP loci,two prominent SNP clusters were detected on chrA03:14,087,835-14,764,672 and chrC03:20,110,319-22,135,492at low B levels across three repeated experiments of multiple traits.Integrating those results with a transcriptome analysis,four genes exhibiting higher differentially expressed fold-change along with favorable haplotypes within the promoter or coding region,BnaA03g29020D,BnaA03g29440D,BnaC03g33010D,and BnaC03g34490D,were identified as candidate genes that could potentially be involved in efficient B utilization,and their favorable haplotypes were found to improve seedling growth and productivity under B deficiency.Considering the lack of B mineral resources in China,the rapid and accurate identification of more B-efficient alleles and studying the genetic mechanism underlying crop responses to B deficiency have important theoretical and practical significance for cultivating B-efficient varieties and maintaining green,sustainable agriculture.展开更多
基金supported by Central Public-interest Scientific Institution Basal Research Fund(Grant NO.1610192023303)Collaborative Research Project of the Shennong Laboratory(SN02-2024-01)+1 种基金Special Fund of Henan Province for Agro-Scientific Research in the Public Interest(Grant NO.201300110500)Agricultural Science and Technology Innovation Program(ASTIP)(CAAS-ASTIP-2025-ZFRI)。
摘要Volatile organic compounds(VOCs)are the main chemical compounds that determine the characteristic aroma and flavor of fruit.In this study,we identified a total of 97 VOCs,including 5C6 compounds,12 aldehydes,4 alcohols,10 esters,13 lactones,18 terpenes,8 norisoprenoids,8 ketones,3 hydrocarbons,8 phenylalanine derivates,and 8 other compounds,in 60 peach cultivars using headspace solid-phase microextraction(HS-SPME)combined with gas chromatography-mass spectrophotometry(GC-MS).A wide range of VOCs were detected in these germplasm resources with respect to both quantity and concentration.Correlation analysis with different physiological traits demonstrated that the genetic background exerts a significant influence on the composition and content of VOCs among peach cultivars.For example,the content of norisoprenoid was significantly lower in yellow-fleshed peach than in white-fleshed peach,and lactones were almost undetectable in stony hard peach.Among the 97 VOCs,26 exhibited odor activity values(OAVs)exceeding 1,suggesting that these compounds act as key odorants in the peach VOC composition.Moreover,six structural genes associated with the synthesis of γ-decalactone and(Z)-3-hexenyl acetate and five genes linked to aldehyde and 1-octen-3-one biosynthesis were identified through weighted gene co-expression network analysis(WGCNA).Additionally,15 transcription factors(TFs)were identified as potentially regulating VOC synthesis.Overall,these data provide insight into the factors contributing to the differences in aroma qualities among peach cultivars,which can help to promote the development of peach breeding.
基金funded by National Natural Science Foundation of China(Grant No.32202483)the Foundation for Key Research and Development Program of Heilongjiang Province(Grant No.SC2022ZX02C0202).
摘要Cytoplasmic male sterility(CMS)is a widespread phenomenon in crops and is beneficial for commercial hybrid breeding.Although CMS systems in Brassica species are extensively utilized,they are derived from relatively limited sources,and the underlying molecular mechanisms are not well understood.In this study,a novel CMS line,named Neau,was identified through distant hybridization between Matthiola incana and Brassica rapa.Neau CMS exhibits agronomic traits similar to its maintainer line of Chinese cabbage and displays sterility at the tetrad stage.The mitochondrial genomes of Neau CMS and its maintainer line were assembled to 359596 bp and 219771 bp,respectively,encoding 99 and 66 unknown open reading frames(orfs).Six orfs were identified as specific to Neau CMS with sequence alignments,with orf154 and two copies of orf138 identified as candidate genes based on their transmembrane structures and their ability to encode toxic proteins that inhibited Escherichia coli cell growth.The expression of orf154 was induced during the tetrad stage by quantitative real-time polymerase chain reaction(qRT-PCR),whereas orf138a showed higher expression at the microspore mononuclear stage in Neau CMS.Transcriptome analysis revealed reduced expressions of most pollen development-related genes,as well as genes involved in peroxidase/oxidative stress responses and the electron transfer chain in Neau CMS.Additionally,Neau CMS exhibited increased levels of O2.-,H2O2,and malondialdehyde(MDA),alongside reduced activities of SOD,CAT,and POD.Both ATP content and ATPase activity were down-regulated in Neau CMS.Overexpression of orf138 and orf154 in Arabidopsis thaliana resulted in reductions in pollen quantity,viability,and seed production.These findings suggest that orf138 and orf154 are key candidate genes responsible for the sterility observed in Neau CMS in Chinese cabbage.
基金funded by the National Key R&D Program of China(Grant No.2022YFD1600500)the National Natural Science Foundation of China(Grant No.32272680).
摘要Anthocyanins are vital secondary metabolites contributing to fruit pigmentation and antioxidative properties.While light is a well-known regulator of anthocyanin biosynthesis,the molecular basis of light-independent anthocyanin accumulation remains underexplored.In this study,integrated analysis of metabolome and transcriptome showed that the anthocyanin content in blueberry(Vaccinium corymbosum‘Bluetta’)fruit was slightly decreased by light-impermeable bagging treatment,while anthocyanin biosynthetic genes were transcriptionally inhibited to different levels,suggesting a slight influence of the bagging treatment on anthocyanin accumulation.Further observation showed that fruit bagging did not alter ethylene production but decreased ABA content.Noticeably,two VcMYBA/MYB1s were not transcriptionally altered by the light-impermeable bagging treatment.Consistently,histochemical GUS analysis and pharmacological manipulation suggested light-independent and ethylene-inducible expression of VcMYBA/MYB1.Moreover,WGCNA analysis revealed 3759 genes positively associated with MYBA/MYB1 such as ethylene-associated genes,etc.Additionally,VcbZIP55s and VcCOP1s were activated and inactivated by the bagging treatment,respectively.These findings provided a framework of light-independent anthocyanin biosynthesis in blueberry fruit.
基金supported by the Natural Science Foundation of Heilongjiang Province,China(LH2024C010 and YQ2024C010)the China Agriculture Research System(CARS-23-A11)the Special Project of Key R&D Program in Heilongjiang Province,China(SC2022ZX02C0202-01)。
摘要The evolutionary development of adventitious roots(ARs)in plants enhances their capacity to adapt to various stress conditions.A thorough analysis of the influencing factors in their morphological construction holds significant theoretical value and practical guidance for overcoming rooting obstacles in cuttings,as well as for cultivating superior varieties characterized by broad adaptability and stress resistance.In this study,we investigated the molecular mechanisms underlying the development of ARs in tomato(Solanum lycopersicum)by performing transcriptome sequencing(RNA-seq).We analyzed the transcription profiles of relevant genes in the"Y962"strain,which exhibits spontaneous AR formation,and the"W961"strain,which does not form ARs.Our findings indicate that the AR induction stage represents an active phase of development,during which we identified 1,676 overlapping genes across the three comparison groups,highlighting the most differentially expressed genes.Functional enrichment analysis showed that they were most closely related to response to auxin,and were also dependent on the crosstalk between other hormones and carbohydrates.Furthermore,through the measurement of endogenous auxin levels and the induction tests with exogenous auxin,it was established that the formation of ARs is closely linked to the accumulation and transport of auxin.Notably,the auxin efflux SIPIN3,which was enriched in the auxin response pathway,exhibited significantly high expression during the induction phase of ARs.The slpin3 mutant,generated using the CRISPR/Cas9 editing system,exhibited a significant reduction in the number of ARs,highlighting the close relationship between polar transport regulated by SIPIN3 and auxin-induced AR formation.In summary,this study not only enriches the developmental network of AR formation in tomatoes with a wealth of data but also elucidates the potential mechanisms for promoting AR development by targeting SIPIN3.
基金supported by the National Natural Science Foundation of China(Grant Nos.32072545,32272639 and 32260745)Zhejiang Provincial Natural Science Foundation of China(Grant Nos.LTGN23C150009 and LY22C150003)Zhejiang University Experimental Technology Research Project(Grant No.SYBJS202217).
摘要For red pear,the anthocyanin content is a crucial factor determining the fruit skin color,which affects consumer preferences.Low overnight temperatures promote anthocyanin accumulation,but the molecular mechanism responsible is unclear.In this study,‘Hongzaosu’pear(Pyrus pyrifolia×Pyrus communis)fruit were treated with a low nighttime temperature(LNT,16℃)or a warm nighttime temperature(WNT,26℃),with sampling conducted within two diurnal cycles.The results showed that LNT promoted anthocyanin accumulation in the fruit skin.The structural anthocyanin biosynthetic genes PpCHS,PpF3H,and PpUFGT exhibited a rhythmic increase in expression at night under LNT.To examine the underlying mechanism,RNA sequencing was conducted using pear calli exposed to LNT and WNT for different durations(24,48,72,or 96 h).Transcriptome analysis revealed 285 differentially expressed genes(DEGs)common to all pairwise comparisons of LNT-and WNT-treated calli of‘Clapp's Favorite’(P.communis)at the sampling time points.KEGG pathway and gene ontology enrichment analyses indicated that the common DEGs were enriched in secondary metabolic processes and phenylpropanoid metabolic processes,which are associated with anthocyanin biosynthesis.The transcription factor PpCDF5,which was responsive to LNT,was selected for further study.Dual-luciferase assays showed that PpCDF5 activated the transcription of anthocyanin biosynthetic genes PpMYB10,PpCHS,PpF3H,PpDFR,PpANS,and PpUFGT.The yeast one-hybrid and EMSA assays demonstrated that PpCDF5 directly binds to the PpF3H promoter,which contains an AAAG motif.Overexpression of PpCDF5 in pear calli and transient overexpression in pear fruit both increased anthocyanin accumulation.The results indicate that PpCDF5 is involved in LNT-induced anthocyanin biosynthesis in pear fruit and provide insights into the molecular regulation of commercial fruit coloration.
基金supported by the Key Scientific and Technological Grant of Zhejiang for Breeding New Agricultural Varieties(Grant No.2021C12066-4)Huzhou Agricultural Science and Technology Innovation Team Project(Grant No.2022HN01).
摘要Red-fleshed fruits are valued for their vibrant color and high anthocyanin content.Pre-harvest fruit bagging enhances fruit peel pigmentation,but its effect on flesh coloration remains poorly characterized.This study revealed that removing bags from‘Gengcunyangtao’red-fleshed peach fruits triggers the rapid and uniform accumulation of anthocyanins in the flesh,resulting in anthocyanin levels that exceed those in unbagged fruits.The exposure to light after bag removal triggered significant increases in anthocyanin levels within 24 h.This was accompanied by the rapid upregulation of light-responsive and flavonoid biosynthetic gene expression levels within 6 h.A metabolomic analysis indicated that anthocyanin precursors,especially p-coumaric acid,accumulated before bag removal,thereby increasing substrate availability for rapid anthocyanin synthesis.On the basis of a weighted gene co-expression network analysis,MYB transcription factors,anthocyanin transporters,glutathione S-transferase,and multidrug and toxic compound extrusion(MATE)were identified as key regulators that coordinate precursor storage along with light-induced transcriptional activation.Notably,PpMYB4 binds to the promoter of PpGSTF14 and activates its expression,thereby promoting anthocyanin accumulation.The study findings elucidated the temporal coordination of metabolic priming and light-responsive transcriptional regulation driving rapid anthocyanin biosynthesis,with possible implications for improving peach fruit flesh coloration.
基金financially supported by the National Natural Science Foundation of China(32201960,32572622,32330084)Yuelushan Laboratory Breeding Program(YLS-2025-ZY04029),Dongting Laboratory Special Funding Project(2025-DTYB-004)National Key Research and Development Program of China(2022YFD2100804)。
摘要Alcoholic liver injury(ALI)has emerged as a significant public health concern,necessitating the urgent identification of medicinal-food resources for its prevention and treatment.As a natural medicinal food resource,Chenpi(CHE)is rich in various flavonoid bioactive compounds and exhibits potential antioxidant,anti-inflammatory,and hepatoprotective effects.However,the effect and mechanism of CHE in preventing and improving ALI are not yet known.This study sought to elucidate CHE's hepatoprotective mechanisms in ALI from the biochemical markers,microbiome and transcriptome perspectives.Results showed that CHE ameliorated ALI by improving oxidative stress,inflammatory cytokines and liver function.16S r RNA analysis revealed that CHE alleviated ALI pathological progression primarily by restoring gut microbiota composition.Transcriptomic analysis showed that CHE improved ALI mainly related to MAPK signaling pathway.Pearson correlation analysis revealed that Candidatus_Saccharimonas,Turicibacter,and Clostridium_sensu_stricto_1 play key roles in the process by which CHE ameliorates alcohol-induced inflammation and pathological angiogenesis.These findings revealed that CHE has the potential to be used as a functional food to prevent or improve ALI.
基金supported by the Natural Science Foundation of China(32272364)the Shanghai Education Committee Scientific Research Innovation Projects,China(2101070007800120)+2 种基金National Science Foundation for Distinguished Young Scholars(32025029)Shanghai Key Project in Synthetic Biology(23HC1400900)the Shanghai Engineering Research Center of 460 Food Microbiology Program(19DZ2281100).
摘要This study examined the potential response mechanisms of Ligilactobacillus salivarius AR612 to glucose stress through whole-genome and comparative transcriptome analysis.We obtained the basic genome information of L.salivarius AR612.The full genome length of L.salivarius AR612 was 1970245 bp,with a GC content of 33.01%and 1894 coding genes.Moreover,we identified many genes associated with genetic adaptations to various stress factors,including temperature,p H,osmotic pressure,bile salts,and oxidative stress.Physiological analysis revealed that the growth and morphology of AR612 changed significantly under glucose stress,with a decrease in the maximum growth and irregular cell morphology.Furthermore,a comparison of transcriptome data indicated that glucose stress induced changes in the number of differential genes.Moreover,AR612 could respond to extracellular glucose stress by changing the expression of genes related to cell morphology,carbohydrate metabolism,amino acid metabolism,fatty acid synthesis,and nucleotide metabolism.This study provides valuable theoretical insights for future research on the adaptation of L.salivarius AR612 to nutritional stress and its application in industrial processes.
基金Supported by the Key Research and Development Program of Shandong(No.2024LZGCQY003)the Taishan Scholars Program(No.tsqn202211250)。
摘要Glucose homeostasis is a fundamental physiological process in both vertebrates and invertebrates,yet its regulatory mechanisms in molluscs remain largely unexplored.This study investigates temporal hemolymph glucose dynamics and associated molecular responses in the Pacific oyster Crassostrea gigas.Annual monitoring revealed significant seasonal variation in hemolymph glucose concentrations,with post-spawning oysters exhibiting the lowest levels.A glucose injection experiment demonstrated rapid uptake kinetics,followed by a return to baseline,suggesting the presence of efficient metabolic regulation.Transcriptomic analysis on hepatopancreas tissue identified cgHK2-2 as the dominant hexokinase isoform induced by hyperglycemia,while other HK genes(cgHK2 and cgHK2-like)showed tissue-specific but non-inducible expression profiles in the investigated tissue.Furthermore,upregulation of cgPPP1R3B and cgPCSK1 indicate possibly conserved glycogen metabolism and insulinlike signaling pathways.Phylogenetic analysis revealed divergent evolutionary trajectories of hexokinase in protostomes versus chordates,with oysters lacking a clear glucokinase orthologue.These findings highlight key molecular players in oyster glucose metabolism and suggest both conserved and lineagespecific regulatory strategies.
基金supported by the Indian Council of Agricultural Research–Centre for Agricultural Bioinformatics(CABin)Scheme。
摘要Background Subclinical mastitis(SCM)is a major constraint in dairy production and is driven by complex host–pathogen interactions.Although transcriptional responses associated with SCM have been widely investigated,the epigenetic mechanisms that stably regulate these programs remain less well characterized,particularly in crossbred cattle populations.This study aimed to characterize DNA methylation-based regulatory networks by integrating whole-genome methylation and transcriptome data from milk somatic cells of Vrindavani(Bos taurus×Bos indicus)cattle.Whole-genome methylation(n=6)and corresponding transcriptome profiling(n=6)were performed on milk somatic cells from SCM-affected and healthy control cows.Results Differential methylation analysis(q-value<0.05)identified 62,940 differentially methylated cytosines(DMCs),7,706 differentially methylated regions(DMRs),and 6,203 differentially methylated genes(DMGs),with a predominant bias toward hypomethylation in SCM.Integrative analysis using stringent thresholds for both methylation(≥10%)and expression change(|log2 fold change|≥1;P of GMM<0.001)identified 1,407 differentially methylated and expressed genes(DMEGs).Functional enrichment analysis revealed 47 KEGG pathways and 30 Gene Ontology biological process terms(FDR<0.05),primarily associated with immune signaling and inflammatory responses.In contrast,a subset of DMEGs showed methylationassociated repression of lactation-and metabolism-related genes.Selected genes were experimentally validated by qPCR,including upregulation of the inflammatory mediator S100A8 and downregulation of CSN3(κ-casein),a key milk protein gene.Conclusions These findings provide an integrated view of the DNA methylation and transcriptional landscape of SCM in milk somatic cells and demonstrate that epigenetic remodeling is associated with coordinated activation of immune pathways alongside repression of lactation-associated functions.The results contribute to understanding the molecular basis of subclinical mastitis and may inform future efforts toward biomarker development and epigenetically informed strategies for improving disease resilience in dairy cattle.
基金funded by an Australia–China International Collaborative Grant(NHMRC APP1112767-NSFC 81561128020)the European Union’s Horizon 2020 Research and Innovation Program under grant agreement(779238)+2 种基金the Edith Cowan University Higher Degree by Research Scholarship(ECU-HDR 10492768)the Western Australian Future Health Research and Innovation Funds(WANMA/EL2023-24/2 and WANMA/Ideas2024-25/5)the Edith Cowan University Early-Mid Career Researcher Grant Scheme(G1006465)。
摘要Previous studies have demonstrated that the immunoglobulin G(IgG)N-glycome and transcriptome are potential biochemical signatures of chronological and biological ages,and several aging clocks have been developed.By integrating the IgG N-glycome and transcriptome,we propose a novel aging clock,gtAge.We developed a deep reinforcement learning-based multiomics integration method called AlphaSnake.The results showed that AlphaSnake achieved a predicted coefficient of determination(R2)value of0.853,outperforming the concatenation-based integration method(R2=0.820)The gtAge estimated by AlphaSnake explained up to 85.3%of the variance in chronological age,which was higher than that in age predicted from IgG N-glycome solely(gAge;R2=0.290)and age predicted from transcriptome solely(tAge;R2=0.812).We also found that the delta age-the difference between the predicted age and chronological age-was associated with several age-related phenotypes.Both delta gtAge and tAge were negatively associated with high-density lipoprotein(p=0.02 and p=0.022,respectively),whereas delta gAge was positively correlated with cholesterol(p=0.006),triglyceride(p=0.002),fasting plasma glucose(p=0.014),low-density lipoprotein(p=0.006),and glycated hemoglobin(p=0.039).These findings suggest that gtAge,tAge,and gAge are potential biomarkers for biological age.
基金funded through the following grants:the National Natural Science Foundation of China(32370665)the Guangdong Basic and Applied Basic Research Foundation(2024A1515030117)the Innovation Capability Support Plan Project of Shaanxi Province(2024ZCKJXX-038)to Wenyu Zhang。
摘要While sex-biased gene expression and its evolutionary dynamics across taxa have been extensively investigated,systematic separate characterization of the evolutionary patterns in transcriptome divergence between male and female lineages remains underexplored.Here,we analyze a comprehensive RNA-seq data set from the house mouse complex,spanning multiple organs across subspecies and species,to delineate the evolutionary trajectories of gene expression in males and females in intra-and inter-species contrasts.For both sexes,we find specific gene expression divergence patterns across the surveyed organs,with a particularly high divergence rate at early evolutionary stages of separation.Comparative analysis between sexes demonstrates male reproductive organs,particularly the testis,displaying accelerated evolutionary rates of expression divergence.Strikingly,testicular long non-coding RNA genes show the most pronounced acceleration,with differences emerging already after a few thousand years of population separation.In contrast,somatic organs and female reproductive auxiliary tissues show no major sex-specific evolutionary dynamics.Genes with sex-biased expression substantially contribute to differentially expressed genes across evolutionary transitions,though without predominant directional bias toward either sex.Notably,these differentially expressed genes display significant over-representation on autosomes.A general functional divergence process is found between male and female transcriptomes across organs mainly driven by sex-specific differentially expressed genes.Collectively,our findings establish a new evolutionary framework for sex-specific expression divergence and provide novel insights into the role of reproductive constraints in shaping transcriptome evolution in mammals.
基金Supported by the Key Research and Development Program of Shandong(No.2022LZGC015)the National Key R&D Program of China(No.2022YFD2401400)+1 种基金the Taishan Scholars Program,the National Key R&D Program of China(No.2022YFD2400304)the Agricultural Seed Project of Shandong Key R&D Program(No.2024LZGCQY003)。
摘要Atmospheric carbon dioxide(CO2)levels are escalating at an unprecedented rate,leading to the phenomenon of ocean acidification(OA).Parental exposure to acidification has the potential to enhance offspring resilience through cross-generation plasticity.In this study,we analyzed larval growth and transcriptomic profiles in the Pacific oyster,Crassostrea gigas,a species of significant ecological relevance,under both control and elevated CO2conditions experienced by their parental generation.Our findings indicate that the oyster populations exposed to OA exhibited a higher incidence of abnormalities during the D-shaped larval stage,followed by accelerated growth at the eyed stage.Through a comparative transcriptomic investigation of eyed larvae(25 d after fertilization),we observed that parental exposure to OA substantially influenced the gene expression in the offspring.Genes associated with lipid catabolism and shell formation were notably upregulated in oysters with parental OA exposure,potentially playing a role in cross-generational conditioning and conferring resilience to OA stressors.These results underscore the profound impact of OA on oyster larval development via cross-generational mechanisms and shed light on the molecular underpinnings of cross-generation plasticity.
基金funded by the National Key Research and Development Program of China(No.2024 YFD2401003)the Natural Science Foundation of Fujian,China(No.2024J01104)the Scientific Research Foundation of Jimei University(Nos.ZQ2020003 and ZQ2022019).
摘要The Japanese eel(Anguilla japonica)is a catadromous migratory fish with a high economic value.The gonads of captive eels do not mature naturally.Under artificial maturation,the hypothalamic-pituitary-gonadal(HPG)axis is activated,and the maturation coefficient of the gonads increased significantly.Prior research investigations into Japanese eel breeding have primarily focused on elucidating the mechanisms underlying gonadal development.However,the problems plaguing the artificial breeding of Japanese eels have remained unsolved.Additionally,the insights into the molecular mechanisms within the pituitary,which acts as an upstream regulatory hub,and its impact on ovarian development are limited.To address these,the pre-matured pituitary(PP)and artificially matured pituitary(AP)tissues from female Japanese eels were subjected to transcriptomics using a method combining PacBio Iso-seq with Illumina RNA-Seq.PacBio sequencing produced 19576 filtered consensus sequences from PP and 39828 from AP.Then,we predicted gene regulatory elements such as alternative polyadenylation,transcription factors,and long noncoding RNAs.A total of 3016 differentially expressed genes(DEGs)were identified based on the Illumina RNA-seq data.Further gene ontology and Kyoto Encyclopedia of Genes and Genomes enrichment analyses were performed.Several DEGs that were upregulated in the pituitary were identified.These genes,including nr5a2,pgr,greb1,smad4,bmp5,ar,lhb,adcy5,and tgfbr3,most likely regulate downstream gonadal development via the pituitary.In conclusion,this study obtained the differential expression and full-length transcriptomes of the pituitary in the pre-matured and artificially matured female Japanese eel.These results offer substantial evidence for developing more efficient sex hormones during the captive breeding of eels,while also furnishing a scientific basis for the conservation of eel resources.
基金Supported by the China Agricultural Research System(No.CARS-48)。
摘要Light is one of the important environmental factors on life activities of aquatic animals.Eyestalks are a multifunctional organ of crustaceans that conducts light signals,produces neurohormones,and regulates growth.However,the mechanism of growth regulation by light intensity remains poorly studied.We evaluated the growth performance of ridgetail white prawn(Exopalaemon carinicauda)under different light intensities(0,100,200,and 400 lx),and determined the regulatory mechanism of growth in response to light intensity through transcriptome analysis of eyestalks.Results show that light intensity at 100 lx significantly improved growth performance in growth rate,specific growth rate,and biomass increase rate,while 0-lx and 400-lx conditions inhibited the growth.A total of 931 DEGs were identified between the 100-lx and 0-lx groups,of which 411 were upregulated and 520 were downregulated.In addition,456 DEGs were identified between groups of 100-lx and 400-lx,including 155 upregulated DEGs and 301 downregulated DEGs.The light intensity at 100 lx significantly improved the growth performance by upregulating the oxidative phosphorylation,Toll and Imd signaling pathway,and ribosome pathway,and downregulating the tyrosine metabolism,phagosome,lysosome,autophagy,and Hippo signaling pathway,whereas 0 lx and 400 lx inhibited growth in the opposite patterns.In total,eight growth-regulation-related candidate genes,i.e.,hemocyanin,NADH dehydrogenase,cytochrome c oxidase,ATP synthase,cathepsin L,phenoloxidase activating factor,CLIP domain-containing serine protease,and 40S/60S ribosomal protein were identified.The optimal light intensity for improved growth of E.carinicauda was about 100 lx when reared indoor.These data shall provide key information for further understanding of the regulatory mechanism of light intensity on the growth performance of this species.
基金supported by Italian Ministry for Health(RF-2011-02349698,RF-2018-12367731)(to CF).
摘要Multiple sclerosis(MS)is a chronic disorder of the central nervous system characterized by multifocal lesions where inflammation,demyelination,and neurodegeneration occur(Jakimovski et al.,2024).MS diagnosis primarily relies on the demonstration of dissemination in time and space of the lesions based on clinical,magnetic resonance imaging(MRI),and cerebrospinal fluid assessments(Jakimovski et al.,2024).
基金Supported by the National Natural Science Foundation of China,No.82474323CACMS Outstanding Young Scientific and Technological Talents Program,No.ZZ13-YQ-026+2 种基金High Level Chinese Medical Hospital Promotion Project,No.HLCMHPP20230CZ40907Open Project of National Facility for Translational Medicine,No.TMSK-2021-407Qiushi Project of the China Association of Chinese Medicine,No.2024-QNQS-12.
摘要BACKGROUND Glycolipid metabolic disorder includes a series of chronic diseases that are closely associated with disturbances in both glucose and lipid metabolism.Jiangtang Tiaozhi formula(JTTZF)demonstrating significant hypoglycemic,lipidmodifying,and anti-inflammatory effects.However,the specific molecular mechanisms underlying JTTZF’s hepatoprotective effects and its ability to ameliorate glycolipid metabolic disorder remain largely unexplored.AIM To investigate how JTTZF improves glycolipid metabolic disorder using hepatic transcriptome and metabolome analyses.METHODS To induce glycolipid metabolic disorder,male C57BL/6J mice were fed a high-fat diet(HFD)for 12 weeks,after which they received an 8-week administration of JTTZF.Liver tissues were analyzed using transcriptomics and metabolomics.Real-time quantitative polymerase chain reaction validated key gene expression.RESULTS Metabolomics data revealed that JTTZF significantly regulated HFD-induced alterations in glycolipid metabolism,with notable changes in pathways such as the pentose phosphate pathway,steroid hormone biosynthesis,and purine metabolism.Transcriptomics profiles indicated that JTTZF exerted regulatory effects on lipid and glucose metabolism,primarily through pathways including peroxisome proliferators-activated receptor signaling,drug metabolism other enzymes,and regulation of lipolysis in adipocytes.Real-time quantitative polymerase chain reaction confirmed that JTTZF modulated pivotal genes associated with fatty acid synthesis,lipolysis,insulin resistance,energy metabolism,and inflammation.These findings suggest that JTTZF may act through multiple pathways to improve glycolipid metabolic disorder.CONCLUSION JTTZF can ameliorate the glycolipid metabolic disorder induced by HFD-diet by regulating lipid metabolism and improving insulin tolerance.
基金Supported by the National Natural Science Foundation of China(No.82000853)the Natural Science Foundation of Shandong Province(No.ZR2022MH154).
摘要●AIM:To investigate the transcriptional profiling of ocular surface ectoderm(OSE)derived from human embryonic stem cells(hESC),and identified CACNG6 and AQP3 as the surface markers of OSE.●METHODS:hESCs were differentiated into OSE,neuroectoderm(NE),surface ectoderm(SE),and other surface ectoderm(OE)cells in vitro.RNA-seq was performed to analyze transcriptomic profiling of hESC-derived OSE,NE,OE,and SE.The differential expressed genes(DEGs)were identified,and Gene Ontology(GO),Kyoto Encyclopedia of Genes and Genomes(KEGG)databases,and protein-protein interaction(PPI)network analyses were performed to screen the signals and hub genes associated to OSE commitment.Also,the highly expressed transcription factors(TFs)and membrane proteins(MPs)in OSE cells were identified.●RESULTS:Transcriptome analysis revealed that OSE development is dually regulated by signals associated with both SE and NE development.The signaling pathways such as Hippo,encoding extracellular matrix(ECM)-receptor interaction,and transforming growth factor-β(TGF-β)might delineate the surface ectodermal phenotype of OSE,with FN1,COL1A1,and TGFB1 identified as hub genes.Additionally,pathways such as axon guidance,might elucidate the influence of NE in OSE commitment,and with PAX6,LHX2,FOXG1,SOX2,MSI1,and DCLK1 recognized as the hub genes.Genes implicated in retinoic acid(RA)synthesis(ALDH1A1,ALDH1A3,and RDH10)exhibited high expression in OSE,indicating the significant role of the RA signaling pathway in OSE development.Furthermore,OSEspecific transcription factors and surface markers(CACNG6 and AQP3)were identified.●CONCLUSION:This study reveals the transcriptome profiling of OSE,which could provide insights into the characteristics of OSE and the underlying molecular mechanisms involved in its derivation.
摘要Jiangtang Tiaozhi formula(JTTZF)has been widely used in the management of glycolipid metabolic disorders,yet its underlying molecular mechanisms remain incompletely understood.Tian et al recently published a study in the World Journal of Diabetes,which reported a comprehensive hepatic transcriptomic and metabolomic analysis that provides important insights into the regulatory effects of JTTZF on glucose and lipid homeostasis.This multi-omics strategy offers a valuable systems-level perspective on the pharmacological actions of this traditional Chinese medicine formulation.In this commentary,we highlight the strengths of the study and discuss several aspects that warrant further investigation to enhance mechanistic depth and translational relevance.These include dose-response relationships,cellular heterogeneity,causal validation of key pathways,identification of active constituents,and long-term safety evaluation.We also emphasize the potential role of host-related factors,such as immune regulation and gut microbiota-associated metabolic interactions,in influencing therapeutic responsiveness.
基金supported by the National Natural Science Foundation of China(32372805 and 31972483)。
摘要Rapeseed(Brassica napus L.)is a major oil crop worldwide that is vigorously promoted for cultivation in China.Boron(B)is an essential micronutrient for plant growth and development.However,the agricultural soils in rapeseed planting areas often show either B deficiency or severe B deficiency.Increasing the resistance to B deficiency is a pivotal goal in the breeding of rapeseed,yet the genetic basis for variations in B efficiency-related traits remains unclear.In this study,a natural population with 391 rapeseed accessions and a nutrient solution system were used to investigate B efficiency-related traits,including relative root length(RRL),shoot dry weight(SDW),root dry weight(RDW),and B efficiency coefficient(BEC),all of which exhibited extensive phenotypic variations under B deficiency.Through a genome-wide association study(GWAS)of B efficiency-related traits using high-density SNP markers obtained from whole-genome resequencing,106 significantly associated SNPs were identified by employing both the general linear model and the mixed linear model.Among these SNP loci,two prominent SNP clusters were detected on chrA03:14,087,835-14,764,672 and chrC03:20,110,319-22,135,492at low B levels across three repeated experiments of multiple traits.Integrating those results with a transcriptome analysis,four genes exhibiting higher differentially expressed fold-change along with favorable haplotypes within the promoter or coding region,BnaA03g29020D,BnaA03g29440D,BnaC03g33010D,and BnaC03g34490D,were identified as candidate genes that could potentially be involved in efficient B utilization,and their favorable haplotypes were found to improve seedling growth and productivity under B deficiency.Considering the lack of B mineral resources in China,the rapid and accurate identification of more B-efficient alleles and studying the genetic mechanism underlying crop responses to B deficiency have important theoretical and practical significance for cultivating B-efficient varieties and maintaining green,sustainable agriculture.