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Quantitative Insight into Gene Cooperation

Quantitative Insight into Gene Cooperation
基因合作的定量洞察
批准号:
7492428
负责人:
ANDREI Y YAKOVLEV
金额:
$10.21万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2005
资助国家:
美国
项目状态:
已结题
起止时间:
2005-04-01 至 2009-03-31
关键词:
AccountingAcuteAcute Lymphocytic LeukemiaAcute Myelocytic LeukemiaAddressAdverse effectsAffectAgarAlgorithmsAllyB-Cell Acute Lymphoblastic LeukemiaB-LymphocytesBacteriophage lambdaBase PairingBehaviorBindingBiochemicalBioinformaticsBiologicalBiological AssayBiological FactorsBiological ModelsBiological ProcessBleomycinBooksCXCL2 geneCalculiCalibrationCandidate Disease GeneCategoriesCell CycleCell Cycle ProgressionCell DeathCell ProliferationCell SurvivalCell physiologyCellsCharacteristicsChronic Lymphocytic LeukemiaClassClassificationCodeCollectionColonColon CarcinomaColorectal CancerComplementary DNAComplexComputational BiologyComputer SimulationComputer softwareComputersConditionCore FacilityCystatin ADNADNA Microarray ChipDNA Microarray formatDataData AnalysesData CollectionData SetDatabasesDependenceDependencyDevelopmentDimensionsDisease regressionDisruptionDominant-Negative MutationDropsDrug Delivery SystemsDrug resistanceEducational workshopElementsEnd PointEngineeringEnsureEntropyEpithelial CellsEquationEquilibriumEscherichia coliExperimental DesignsExpressed Sequence TagsFacility Construction Funding CategoryFamilyFrequenciesFutureGene ClusterGene CombinationsGene ComponentsGene ExpressionGene FamilyGene TargetingGenesGeneticGenetic ProgrammingGeneticinGenomeGenus ColaGlutamate-Ammonia LigaseGlutathione S-TransferaseGraphHeelHourHousingHumanImmunoglobulinsIndividualInduced MutationInformaticsInterferonsInterleukin-8JointsJournalsKineticsKnowledgeLaboratoriesLawsLeadLeftLengthLeukocyte ElastaseLigandsLigaseLikelihood FunctionsLocationLogicLymphoblastic LeukemiaMammalian CellMasksMeasurementMeasuresMediatingMedicineMetabolic PathwayMethodological StudiesMethodologyMethodsMetricMicroarray AnalysisMicrofluidicsModelingModificationMolecularMolecular ProfilingMonitorMusMutateMutationNamesNatureNeomycin resistance geneNoiseNormal CellNumbersOncogenesOncogenicOne-Step dentin bonding systemOutcomeOutputPaperPathway interactionsPatternPersonal SatisfactionPharmaceutical PreparationsPhenotypePhysical condensationPlant RootsPlayPolymerase Chain ReactionPongidaePopulationPopulation BiologyPreparationProbabilityProceduresProcessProliferatingPropertyProtein OverexpressionProteinsPublicationsPuromycinPurposeQiRNA InterferenceRNAi vectorRangeRateReactionRecommendationRegulator GenesRelative (related person)ReportingReproducibilityResearchResearch PersonnelResortRetroviral VectorRetroviridaeReverse TranscriptionRoleRunningSample SizeSamplingSampling StudiesSchemeScoreScoring MethodSelection BiasSerumSignal TransductionSignaling MoleculeSignificance LevelSiliconSimulateSorting - Cell MovementSpecificitySpeedStagingStandards of Weights and MeasuresStatistical MethodsStatistical ModelsStatistically SignificantStressStructureSumSupporting CellSuspension substanceSuspensionsSystemT-Cell LeukemiaT-LymphocyteTP53 geneTailTechniquesTechnologyTestingTimeTissue-Specific Gene ExpressionTissuesTrainingTransducersTranslatingTreesUncertaintyValidationVariantVesnarinoneWeekWeightWorkZeocinabstractingadipsinanalogangiogenesisbasebiocomputingcancer cellcell motilitycomputer based statistical methodsconceptcostdesignexpression vectorfallsfunctional genomicsgene interactiongenetic manipulationgenetic pedigreegenome-wide analysishygromycin Aimprovedin vivoinsightinterestknock-downknowledge baseleukemialymphotoxin betamodels and simulationmouse genomemutantnetwork modelsneutrophilnovelpancreatic elastase IIpost gamma-globulinsprogramsprototypereceptorreconstructionresearch studyresponsesimulationsizesoftware developmentstatisticssymposiumtherapeutic targettooltraffickingtranscription factorvectoryoung adult

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英文摘要
DESCRIPTION (provided by applicant): The objectives of the proposed research are to provide novel methods for the analysis of the complex interactions between gene products at the level of gene expression. A great deal of research demonstrates that the outcome of exposure of a cell to two different signals is not predictable from the response to each signal on its own. This general principle holds true for the cooperative effects of exogenous signaling molecules as well as the effects of gene expression and mutation. Detailed analysis of the mechanisms by which the consequences of such interactions are created requires novel approaches to the dissection of gene regulatory networks. As the most detailed analysis of interactions between different regulatory pathways has been carried out in regard to the consequences of expression of cooperating oncogenes, this area is especially promising for the application of newly developed analytical tools. The proposed methodology includes the following components: (1) Multivariate search for a set of differentially expressed genes allowing for multidimensional characteristics of gene expression data, (2) Identification of a subset of candidate genes that participate in the cooperative response of a cell to multiple mutations, and (3) Reconstruction of a gene signaling network that underlies the cooperative effect of multiple mutations on a specific cell function, thereby providing the necessary information on causal relationships between cooperating genes. By combining methods of computational biology, multivariate statistics, and experimental studies it is possible to greatly enhance the ability to understand complex mechanisms of cell responses to multiple gene perturbations. While the main objective is to develop a general methodology that will be widely applicable in various experimental settings, biological experiments will be conducted to study the effects of two oncogenic mutations on such fundamental cell functions as survival and proliferation. This experimental program may have additional benefits such as pinpointing drug targets within a particular circuit supporting cell proliferation and/or survival.
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Quantitative Insight into Gene Cooperation
  • 批准号:
    7214135
  • 项目类别:
  • 资助金额:
    $30.03万
  • 财政年份:
    2005
  • 负责人:
    ANDREI Y YAKOVLEV
  • 依托单位:
Quantitative Insight into Gene Cooperation
  • 批准号:
    6985626
  • 项目类别:
  • 资助金额:
    $30.89万
  • 财政年份:
    2005
  • 负责人:
    ANDREI Y YAKOVLEV
  • 依托单位:
Quantitative Insight into Gene Cooperation
  • 批准号:
    7035783
  • 项目类别:
  • 资助金额:
    $30.54万
  • 财政年份:
    2005
  • 负责人:
    ANDREI Y YAKOVLEV
  • 依托单位:
STOCHASTIC MODELING OF MULTI TYPE CELL SYSTEMS
  • 批准号:
    6615577
  • 项目类别:
  • 资助金额:
    $41.07万
  • 财政年份:
    2001
  • 负责人:
    ANDREI Y YAKOVLEV
  • 依托单位:
海外基金