Temporal, cell type- and locus-specific epigenetic control in transgenic mice
Temporal, cell type- and locus-specific epigenetic control in transgenic mice
批准号:
9064110
负责人:
Bosiljka Tasic
金额:
$46.36万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2013
资助国家:
美国
项目状态:
已结题
起止时间:
2013-09-30 至 2018-05-31
关键词:
AdultAnimalsBindingBiological AssayBiological ModelsBiologyBrainBrain DiseasesCREBBP geneCell MaintenanceCell physiologyCellsCellular MorphologyDNA cassetteDevelopmentDiseaseDoxycyclineEP300 geneES Cell LineEnsureEpigenetic ProcessFutureGene ExpressionGenerationsGenesGeneticGenomeHDAC1 geneHealthHistocompatibility TestingIn VitroKnock-inKnock-in MouseLabelLifeLoxP-flanked alleleMalignant NeoplasmsMental disordersMethodologyModelingModificationMolecularMusNeocortexNeuronsOrganOrganismPhenotypeProteinsReporterResponse ElementsSpecificityTechnologyTestingTetracyclinesTimeTissuesTrans-ActivatorsTranscription CoactivatorTransgenesTransgenic MiceTransgenic OrganismsValidationWithdrawalWorkbasecell typedesigndesign and constructionembryo cellembryonic stem cellepigenetic regulationgenetic approachin vivoinsightinterestknock-downmouse genomenerve stem celloverexpressionpreventprogenitorrecombinase-mediated cassette exchangesmall hairpin RNAtissue culturetooltransgene expression
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Mammalian organs are built of a variety of intermingled cell types, the full extent and diversity of which are unknown. Specification and maintenance of cell identity, from a single cell embryo to any terminally differentiated cell such as an adult neuron, rely heavily on epigenetic mechanisms that act upon the genome to enable or prevent expression of specific sets of genes. In doing so, epigenetic regulation of gene expression enables a single genome to encode a diverse array of cell types in a multicellular organism. Epigenetic modifications ensure that a cell proceeds through a limited set of gene expression possibilities, and once differentiated, that a cell maintains its phenotype throughout its lifetime. As a consequence, disruption of epigenetic modification can result in a variety of diseases, including neurodevelopmental and psychiatric diseases, and cancer. We propose to develop a set of mouse transgenic tools that have the potential to transform the way epigenetic modifications can be studied and understood in this mammalian model system. The new tools will provide regulated expression of epigenetic modifiers in a variety of cell types and their progenitors, while permanently marking these cells or their progeny for examination at any later time point. Moreover, we will develop technology, in which a single locus in the mouse genome can be subjected to epigenetic perturbations in specific cells and at specific times in the animal's life. We will employ these tools to gain understanding of cell-type identity in the cortex as well as the mechanisms responsible for generating and maintaining this identity. Epigenetic regulators have been implicated in a number of brain diseases, and the tools we are developing will facilitate modeling or testing specific hypotheses that relate to perturbations of epigenetic phenomena. The insights gained may also provide guidance for the generation of specific cell types in vitro, and directions for 'repurposing' certain cell types in vivo. Although the focus of ur studies will be on the mouse brain, the versatile and modular design of our tools will enable their
use in studying development, function or disease in any other tissue or cell type. We will ensure easy access to all tools we generate to maximize their impact on understanding various aspects of mammalian biology.
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会议论文
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批准号:10546513
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项目类别:
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依托单位:
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负责人:Bosiljka Tasic
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依托单位:
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资助金额:$117.5万
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负责人:Bosiljka Tasic
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依托单位:
海外基金