De-coding Cis-regulatory information on a Genome-Wide Level with Single Neuron Re
De-coding Cis-regulatory information on a Genome-Wide Level with Single Neuron Re
批准号:
7247113
负责人:
Oliver Hobert
金额:
$34.41万
依托单位国家:
美国
项目类别:
财政年份:
2000
资助国家:
美国
项目状态:
已结题
起止时间:
2000-04-01 至 2010-06-30
关键词:
AffectAnatomyAnimalsApplications GrantsArchitectureAxonBindingBiogenic Amine ReceptorsBiological AssayCaenorhabditis elegansCellsClassCodeCollectionCuesDefectDevelopmentDissectionElementsEnsureF Box DomainFamilyFibroblast Growth Factor ReceptorsFingersFundingGene ExpressionGenesGeneticGenetic ScreeningGenomeGenomicsGrantGreen Fluorescent ProteinsHandednessHodgkin DiseaseHomeoboxHomeobox GenesHomeodomain ProteinsImmunoglobulin DomainIn VitroIndividualIntegral Membrane ProteinInterneuronsLeftLinkLocalizedLogicMaintenanceMicroRNAsMolecularMotorMotor NeuronsNatureNematodaNerveNervous system structureNeuritesNeuronal DifferentiationNeuronsNuclearPhylogenetic AnalysisPlacementPositioning AttributePostdoctoral FellowProcessProgress ReportsProteinsPublicationsRNA-Binding ProteinsRegulatory ElementRegulatory PathwayReporterReporter GenesResearchRoleScienceSignal TransductionSoftware ToolsSynaptic TransmissionSystemTestingTrans-ActivatorsTransgenic AnimalsUnited States National Institutes of HealthWorkbasecell typegene functioninsightinterestmembermutantnovelpostsynapticprogramspromoterprotein expressionreceptorreceptor expressiontranscription factorubiquitin ligase
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Nervous systems are characterized by an astounding degree of cellular diversity, yet our insights into the mechanisms of creating this diversity are limited. The molecular correlate to neuronal diversity are neuron-type specific gene expression programs. Sets of co-expressed genes that characterize an individual cell type are commonly referred to as gene batteries which are defined by their linkage to conserved, common c/s-regulatory elements. The nature of gene batteries for individual neuronal subtypes as well as their linked cis-regulatory elements are poorly described on a genome-wide level. We propose here to systematically decode cis-regulatory information on a genome-wide level and to determine the identity of a single neuron-specific gene expression program.
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