Genomic Approaches to Neuronal Diversity and Plasticity
Genomic Approaches to Neuronal Diversity and Plasticity
批准号:
7482815
负责人:
JINGYUE JU
金额:
$15.7万
依托单位国家:
美国
项目类别:
财政年份:
2003
资助国家:
美国
项目状态:
已结题
起止时间:
2003-09-05 至 2008-07-31
关键词:
Afferent NeuronsAplysiaAreaArtsAxonBase SequenceBehaviorBiochemistryBioinformaticsBiologicalBlood capillariesBrainCellsChemistryChromosome PairingCitiesColorComplementary DNACultured CellsCustomCytoplasmDNADNA FingerprintingDNA SequenceDendritesDetectionDevelopmentElementsEnergy TransferEngineeringEquipment and supply inventoriesError SourcesEukaryotic CellExperimental ModelsExpression LibraryFMRFamideFaceFacility Construction Funding CategoryFirst NameFloridaFluorescenceFunctional ImagingGene ExpressionGene Expression ProfilingGenerationsGenesGeneticGenomicsGrowthHumanHuman ResourcesIllinoisImageImaging technologyIndividualInformation SystemsInstructionInterneuronsInvertebratesLabelLast NameLearningLifeLocalizedMagnetismMeasurementMeasuresMemoryMessenger RNAModelingMolecularMolecular ProfilingMonitorMotor NeuronsNamesNanoarray Analytical DeviceNanotechnologyNervous system structureNeuritesNeuronal PlasticityNeuronsNeurophysiology - biologic functionNeurosciencesNew YorkNucleic AcidsNumbersOligonucleotidesOpticsOrganismPatternPerformancePhenotypePhotochemistryPolymerasePolymerase Chain ReactionPostdoctoral FellowPresynaptic TerminalsPrincipal InvestigatorPrintingProcessProtocols documentationPuerto RicoRNAReactionResearchResearch PersonnelResearch Project GrantsResolutionRoleSamplingSchemeScientistSenior ScientistSensorySensory ProcessSerotoninSignal TransductionStudentsSynapsesSynthesis ChemistrySystemTechnologyTestingTimeTranscriptTransport ProcessUniversitiesbasecapillarycell typecombinatorialdensitydesignexperimental analysisfunctional genomicsimprovedinnovationlithographynanolitrenanoparticlenanosciencenetwork modelsneuronal cell bodyneuronal growthnucleotide analogoptical imagingprofessorprogramsresearch and developmentresponseserial analysis of gene expressionsynaptogenesistooltwo-dimensional
中文摘要
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英文摘要
The objectives of the proposed research are the development of new genomic technologies for massively parallel DNA sequencing and large-scale gene expression analysis from single living nerve cells, and application of these technologies to study neural functions. The research teams from Columbia University and the University of Florida will closely interact to develop three innovative genomic technologies:(i) Massively Parallel DNA sequencing Chip System for sequencing SAGE library from neurons; (ii) Nanoscopic DNA Arrays for global gene expression profiling at the level of individual cells and subcellular compartments, and (iii) Real-time monitoring of multiple mRNA species in living neurons and defined cellular microdomains with high spatial resolution and fast temporal resolution. Each of these technologies will be rigorously tested and validated using a model memory-forming network of Aplysia. The technologies will then be implemented to explore three fundamental brain mechanisms: (1) the molecular basis of neuronal identity, (2) the molecular signals controlling the formation of the precise pattern of interconnections, which underlie behavior and, (3) the molecular basis of synapse-specific neuronal plasticity and neuronal growth. Using identified neurons in networks of Aplysia as experimental models we will study the role of asymmetric mRNA distribution in integrative functions and phenotypes of eukaryotic cells. We will use a hierarchical design to achieve structural resolution of single-cell profiling in a descending fashion, where a parallel genomic and functional analysis within the same memory-forming networks will be performed in the scheme: single neuron to single axon to single synapse. The gene expression profiling will be correlated with functional imaging at functionally characterized neurons and synaptic terminals in a simple network during the memory consolidation. The combined approach based on genomics, photochemistry, nanoscience and engineering, biochemistry, and neuroscience will be used to understand how neurons and synapses operate in the context of learning and memory. The technologies developed and the biological discoveries made in the project will have broad impact and applications to study how genes regulate cellular and organism behavior on the scale from simpler nervous systems in invertebrates to the human brain.
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DOI:
10.1002/jez.b.21383
发表时间:
2011-03-15
期刊:
JOURNAL OF EXPERIMENTAL ZOOLOGY PART B-MOLECULAR AND DEVELOPMENTAL EVOLUTION
影响因子:
2.2
作者:
[Heyland, Andreas, Vue, Zer, Voolstra, Christian R., Medina, Monica, Moroz, Leonid L.]
通讯作者:
Moroz, Leonid L.
Two-photon excitation induced fluorescence of a trifluorophore-labeled DNA.
双光子激发诱导三荧光团标记 DNA 发出荧光。
DOI:
10.1562/2004-09-27-ra-329
发表时间:
2005
期刊:
Photochemistry and photobiology.
影响因子:
--
作者:
[Jockusch,Steffen, Li,Zengmin, Ju,Jingyue, Turro,NicholasJ]
通讯作者:
Turro,NicholasJ
DOI:
10.1016/j.tet.2006.08.109
发表时间:
2007-04
期刊:
Tetrahedron
影响因子:
2.1
作者:
[A. Martí;Xiaoxu Li;S. Jockusch;Nathan Stevens;Zengmin Li;B. Raveendra;S. Kalachikov;I. Morozova;J. Russo;D. Akins;J. Ju;N. Turro]
通讯作者:
A. Martí;Xiaoxu Li;S. Jockusch;Nathan Stevens;Zengmin Li;B. Raveendra;S. Kalachikov;I. Morozova;J. Russo;D. Akins;J. Ju;N. Turro
Molecular engineering approaches for DNA sequencing and analysis.
DNA 测序和分析的分子工程方法。
DOI:
10.1586/14737159.5.5.797
发表时间:
2005
期刊:
Expert review of molecular diagnostics
影响因子:
5.1
作者:
[Bai,Xiaopeng, Edwards,John, Ju,Jingyue]
通讯作者:
Ju,Jingyue
DOI:
10.1021/jo048053c
发表时间:
2005-03
期刊:
The Journal of organic chemistry
影响因子:
--
作者:
[Joanne Dyer;S. Jockusch;V. Balšánek;D. Sames;N. Turro]
通讯作者:
Joanne Dyer;S. Jockusch;V. Balšánek;D. Sames;N. Turro
共 12 条
Discovery and Optimization of Inhibitors of SARS-CoV-2 Polymerase and Exonuclease
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批准号:10513924
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项目类别:
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资助金额:$815.25万
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财政年份:2022
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负责人:JINGYUE JU
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依托单位:
Genomic Approaches to Deciphering Memory Circuits
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批准号:8703796
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资助金额:$39.69万
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财政年份:2012
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负责人:JINGYUE JU
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Genomic Approaches to Deciphering Memory Circuits
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批准号:8542899
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项目类别:
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资助金额:$38.14万
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财政年份:2012
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负责人:JINGYUE JU
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依托单位:
Genomic Approaches to Deciphering Memory Circuits
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批准号:8895802
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项目类别:
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资助金额:$39.69万
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财政年份:2012
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负责人:JINGYUE JU
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依托单位:
Genomic Approaches to Deciphering Memory Circuits
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批准号:8439403
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项目类别:
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资助金额:$42.73万
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财政年份:2012
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负责人:JINGYUE JU
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依托单位:
Genomic Approaches to Deciphering Memory Circuits
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批准号:9128063
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项目类别:
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资助金额:$39.69万
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财政年份:2012
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负责人:JINGYUE JU
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Single Molecule DNA Sequencing by Fluorescent Nucleotide Reversible Terminators
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批准号:8091384
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项目类别:
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资助金额:$55.81万
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财政年份:2009
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负责人:JINGYUE JU
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依托单位:
Single Molecule DNA Sequencing by Fluorescent Nucleotide Reversible Terminators
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批准号:7714932
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项目类别:
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资助金额:$63.67万
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财政年份:2009
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负责人:JINGYUE JU
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依托单位:
An Integrated System for DNA Sequencing by Synthesis
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批准号:7923565
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项目类别:
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资助金额:$40.48万
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财政年份:2009
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负责人:JINGYUE JU
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依托单位:
Single Molecule DNA Sequencing by Fluorescent Nucleotide Reversible Terminators
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批准号:7923389
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项目类别:
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资助金额:$64.63万
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财政年份:2009
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Molecular Engineering Approach to Study Long Term Synaptic Plasticity
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批准号:7561660
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项目类别:
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资助金额:$56.46万
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财政年份:2008
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负责人:JINGYUE JU
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依托单位:
Molecular Engineering Approach to Study Long Term Synaptic Plasticity
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批准号:7770781
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负责人:JINGYUE JU
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依托单位:
DNA Sequencing with Reversible dNTP and Cleavable Fluorescent ddNTPTerminators
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资助金额:$47.29万
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财政年份:2008
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负责人:JINGYUE JU
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依托单位:
Molecular Engineering Approach to Study Long Term Synaptic Plasticity
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财政年份:2008
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DNA Sequencing with Reversible dNTP and Cleavable Fluorescent ddNTPTerminators
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项目类别:
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资助金额:$47.29万
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财政年份:2008
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负责人:JINGYUE JU
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依托单位:
Molecular Engineering Approach to Study Long Term Synaptic Plasticity
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批准号:8014902
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项目类别:
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资助金额:$55.7万
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财政年份:2008
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负责人:JINGYUE JU
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3'-O-Modified Nucleotide Reversible Terminators for Pyrosequencing
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项目类别:
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资助金额:$32.2万
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负责人:JINGYUE JU
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依托单位:
3'-O-Modified Nucleotide Reversible Terminators for Pyrosequencing
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财政年份:2007
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负责人:JINGYUE JU
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依托单位:
Modulating Nucleotide Size in DNA for Detection by Nanopore
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批准号:6961023
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项目类别:
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资助金额:$32.2万
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财政年份:2005
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负责人:JINGYUE JU
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Modulating Nucleotide Size in DNA for Detection by Nanopore
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财政年份:2005
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依托单位:
海外基金