课题基金 / 基金详情

Characterization of the Fetal Primate Epigenome and Metabolome Under In Utero

Characterization of the Fetal Primate Epigenome and Metabolome Under In Utero
子宫内胎儿灵长类动物表观基因组和代谢组的表征
批准号:
7428765
负责人:
Kjersti Marie Aagaard
金额:
$230.25万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-09-30 至 2012-08-31
关键词:
5&apos Flanking RegionADP ribosylationAcetylationAcidsAddressAdipose tissueAdolescentAdultAdult ChildrenAffectAge-MonthsAlanine TransaminaseAmino AcidsAnimal FeedAnimal ModelAnimalsAntibodiesAreaArginineArteriesArtsAuthorization documentationAutopsyAwardBackBarker HypothesisBase SequenceBasic ScienceBehavior TherapyBetaineBilateralBindingBiological ProcessBiologyBiomedical ResearchBiopsyBirth RecordsBlast CellBlood specimenBody WeightBromodomainCCAAT-Enhancer-Binding ProteinsCaliberCaloriesCarbonCardiovascular ModelsCategoriesCell LineCell NucleusCellsCharacteristicsChargeChildChildhoodCholineChromatinChromatin StructureChronicCircadian RhythmsClassificationClimateClinicalClinical MedicineCloningComplementComplexConditionConflict (Psychology)ConsumptionControl AnimalCountyCoupledCpG dinucleotideCuriositiesCustomCytoplasmic OrganelleCytosineDEXADNADNA MethylationDNA MethyltransferaseDNA Modification MethylasesDNA biosynthesisDataDatabasesDedicationsDensitometryDepthDesire for foodDetectionDevelopmentDiabetes MellitusDietDisciplineDiseaseDoctor of PhilosophyDyslipidemiasElementsElevationEmbryonic DevelopmentEnd PointEndocrinologyEnrollmentEnsureEnvironmentEnzymesEpidemicEpigenetic ProcessEukaryotaEukaryotic CellEventExposure toFamilyFastingFat-Restricted DietFatty LiverFatty acid glycerol estersFemaleFetal DevelopmentFetal Growth RetardationFetal LiverFetal WeightFetusFigs - dietaryFolateFolic AcidFormaldehydeFundingGPT2 geneGelGene ExpressionGene Expression RegulationGene SilencingGenerationsGenesGeneticGenomeGenomic ImprintingGenomicsGluconeogenesisGlucoseGlucose ClampGlycerolGrowthHDAC1 geneHealthHeat-Shock Proteins 90HepaticHepatic TissueHepatitisHeredityHigher Order Chromatin StructureHistologicHistone AcetylationHistone CodeHistone DeacetylaseHistone H3HistonesHomeostasisHourHousingHumanHyperinsulinismHypermethylationHypothalamic structureIdahoImmunohistochemistryImpairmentIn VitroIndividualInfantInflammationInflammatory ResponseInstitutionInsulinInsulin ResistanceIntergenic SequenceInterventionIntuitionInvestigationJapanese PopulationKidneyKnowledgeLaboratoriesLactationLanguageLeadLeftLeptinLifeLigationLinkLipid PeroxidationLipidsLiquid ChromatographyLiteratureLiverLysineMAP Kinase GeneMAPK14 geneMAPK8 geneMTHFR geneMacacaMaintenanceMalignant NeoplasmsMalnutritionMammalian CellMammalsMapsMartensMeasuresMediatingMedicalMedicineMemoryMentorsMessenger RNAMetabolicMetabolic DiseasesMetabolismMethionineMethodsMethylationMethylenetetrahydrofolate reductase (NADPH)Microarray AnalysisMobile Genetic ElementsModelingModificationMolecularMolecular ChaperonesMolecular ProfilingMono-SMorbidity - disease rateMothersMusMuscleMutationNF-kappa BNatureNeonatalNeurosecretory SystemsNitric Oxide PathwayNonesterified Fatty AcidsNuclear ExtractNucleic Acid Regulatory SequencesNucleosomesNucleotidesNumbersNutrientNutritionalObesityOralOutcomeOutcome StudyOverweightOxidative StressOxidoreductasePaperParentsParticulatePartner in relationshipPathway interactionsPatient currently pregnantPatternPerinatalPerinatal ExposurePeripheralPeroxisome Proliferator-Activated ReceptorsPhenotypePhosphorylationPhysiologicalPlayPolycombPolymerase Chain ReactionPopulationPopulation DatabasePositioning AttributePost-Translational Protein ProcessingPredispositionPregnancyPregnancy IntervalPreparationPrevalencePreventionPrimatesProcessProsencephalonProteinsPublic HealthPurposeRNA InterferenceRateRattusReactionRecontactsRecordsRecruitment ActivityRegulationRelative (related person)ResearchResearch DesignResearch Ethics CommitteesResearch PersonnelResearch Project SummariesResolutionResourcesRetinol dehydrogenaseReverse Transcriptase Polymerase Chain ReactionRiskRisk FactorsRodentRodent ModelRoleRosaRunningRuralSamplingSatiationScanningScienceSeriesSerumSerum MarkersSiteSodium ChlorideSpecificitySpecimenStaining methodStainsStandards of Weights and MeasuresStatistically SignificantStructureSubarachnoid HemorrhageSumSupplementationSystemTailTechniquesTestingTetrahydrofolatesTextTherapeuticThinkingTimeTissue-Specific Gene ExpressionTissuesTracerTrainingTranscription factor genesTransgenesTransgenic OrganismsTranslatingTranslational ResearchTrichostatin ATriglyceridesUbiquitinationUmbilical Cord BloodUniversitiesUreaUrsidae FamilyUtahValproic AcidVariantVertebral columnVery low density lipoproteinVital StatisticsVitamin B 12WeaningWeight GainWestern BlottingWomanWorkWritingX InactivationYeastsZincabstractingbasebisulfiteblood glucose regulationchromatin immunoprecipitationchromatin remodelingcircadian pacemakercofactorcohortcomparativedata modelingdaydemethylationdensitydesigndevelopmental nutritiondietary supplementsepigenomicsexperiencefallsfeedingfetalgene repressionglucose disposalglucose outputglucose tolerancehealth economicshigh throughput technologyhuman FRAP1 proteinhuman GPT2 proteinin uteroin vivoin vivo Modelinhibitor/antagonistinnovationinterestjuvenile animallipid transportmRNA Differential DisplaysmRNA Expressionmalemature animalmetabolomicsmethionine methyl estermethyl groupmigrationnon-alcoholicnon-alcoholic fatty livernonhuman primatenoveloil red Ooxidationparalogous geneperinatal healthpostnatalpreventprogramspromoterresearch studyresponsesensorsham surgerysocialsuccesstime intervaltraittranscription factortransgene expressiontransmission processvery low density lipoprotein triglycerideyoung adult

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Project Summary. Obesity causes substantial social, economic and health burdens. The rate of obesity is escalating disproportionately in children (infants to young adults). This rapid increase is unlikely to be due to environment or genetics alone. Accumulating evidence from our laboratory and others suggests that adult metabolic diseases originate in utero, and likely occur through the reprogramming of gene expression via epigenetic changes in chromatin structure (an altered "histone code"). Of interest, we have observed in a rodent transgenerational model of intrauterine growth restriction (IUGR) that a diet supplemented with essential nutrients, yet unaltered in its caloric content, prevents adult metabolic disease and is associated with abrogation of reprogrammed gene expression. However, although such established models in rodents demonstrate that fetal alterations in the histone code are involved in the persistence and conveyance of the altered postnatal phenotype, little is known about the effects of maternal diet and resultant obesity on primate fetal biology. We hypothesized that a high fat diet in non-human primates would induce changes in hepatic chromatin structure resulting in altered expression of fetal genes critical to the development of childhood and adult obesity. Based on our preliminary data, the focus of this proposal is to apply developed high throughput technology (comparative epigenomics and metabolomics) to decipher the primate epigenome and metabolome in the obese maternal environment and then measure the impact of supplementation on the differentially altered epigenome and resultant disease. The novel innovation and significance resides within its potential to provide (1) an expanded understanding of the mechanism through which a maternal high fat diet reprograms primate gene expression and (2) a simple intervention (essential nutrient supplementation with neither diet nor behavioral modification) with tremendous potential impact given the current obesity epidemic and the lack of efficacious therapeutics.
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海外基金