Brain circuit mapping using light inducible recombinase systems
Brain circuit mapping using light inducible recombinase systems
批准号:
9380757
负责人:
Ali Haydar Cetin
金额:
$108.03万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2017
资助国家:
美国
项目状态:
已结题
起止时间:
2017-08-01 至 2019-10-31
关键词:
AdultAnatomyAnimalsArchitectureBehaviorBrainBrain DiseasesCapsidCellsCharacteristicsCoupledDHFR geneDNADNA Modification ProcessDataDevelopmentDimerizationEnzymesFLP recombinaseFoundationsFunctional ImagingGene ExpressionGenerationsGenesGeneticGenetic IdentityGenetic RecombinationGenomicsGlycoproteinsIn VitroIndividualKnowledgeLabelLightLinkLocationMapsMethodsModificationMolecularMorphologyMusNervous system structureNeuronsPatternPharmaceutical PreparationsPhysiologicalPhysiologyPropertyProteinsRabiesRabies virusRecombinant adeno-associated virus (rAAV)ReporterResolutionRoleSiteSpecificitySynapsesSystemTamoxifenTestingTransgenic MiceTransgenic OrganismsTrimethoprimVariantViralViral VectorVirusVisual Cortexbasecalcium indicatorcell typedimerenzyme activityexperimental studyimprovedin vivointerestintersectionalitynovelrecombinasereconstructionrelating to nervous systemspatiotemporaltemporal measurementtooltwo-photonvalidation studies
中文摘要
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英文摘要
Project Summary
Mammalian brain is composed of vast numbers of intricately interconnected neurons with various
molecular, anatomical and physiological identities. To understand the roles of these individual building
blocks of the brain, it will be critical to develop spatio-temporally precise tools that will allow neuronal
subtype specific single cell level analysis. In this project, we propose to develop molecular tools that will
allow high throughput single cell genomic modifications and apply them in order to functionally and
morphologically characterize cell type specific circuits within the mammalian brain. To achieve this, our
approach will be to use light to trigger site-specific DNA modification enzymes. The site-specific DNA
recombinases have been extremely useful tools for dissecting the functional and genetic components of
the nervous system due to their ability to precisely modify individual genes within cells. However, they
lack the ability to be regulated with high spatiotemporal accuracies to precisely target individual cells.
We modified two of these enzymes -Cre and Dre- by combining them with a fungal-based light
inducible protein in such a way that upon light induction the activity of the enzymes can be triggered.
We propose to further apply the same strategy to the Flp recombinase in order to enrich the
intersectional approach. We will then use these recombinases to generate Cre dependent mouse lines
so that we can restrict the light inducible recombination to further subtypes of neurons either alone or in
combination with existing Cre driver lines. Using these lines we will perform light induced focal
recombination in order to perform sparse cell type specific genomic recombination of fluorescent
reporters to fully reconstruct individual neuron subtypes in axonal and dendritic detail. Furthermore we
will combine this approach with 2-photon excitation to perform single cell rabies tracing experiments.
Our results will set the foundation for extremely detailed analysis of neuron type specific functional and
anatomical circuits that will make it possible to link genetic identity, morphology, connectivity and
function.
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