Single Cell Studies of Lineage Specific Expression of the Protocadherin Gene Clus
Single Cell Studies of Lineage Specific Expression of the Protocadherin Gene Clus
批准号:
8771637
负责人:
THOMAS P MANIATIS
金额:
$24.0万
依托单位国家:
美国
项目类别:
财政年份:
2014
资助国家:
美国
项目状态:
已结题
起止时间:
2014-07-01 至 2016-06-30
关键词:
AddressAfferent NeuronsAlternative SplicingAutistic DisorderCellsComplementary DNAComplexDataDetectionDevelopmentDrosophila melanogasterExhibitsGene ClusterGene ExpressionGene Expression ProfileGenesGeneticGenetic RecombinationGenetic TranscriptionImmunoglobulinsIn SituIn VitroIndividualLengthMeasuresMediator of activation proteinMethodologyMethodsModelingMolecular ProfilingMood DisordersMusNervous system structureNeuraxisNeuronal DifferentiationNeuronsPatternPolypyrimidine Tract-Binding ProteinProtein IsoformsRNARNA SequencesRNA SplicingRegulationResolutionReverse TranscriptionSensorySourceSpecificityStagingT-Cell ReceptorTechniquesTestingTimeTissuesTranscriptbasecell typegenome-widein vivoinnovationinsightmRNA Precursorneural circuitneurodevelopmentneurogenesisnext generationpromoterpublic health relevancesingle moleculetechnology developmenttranscriptome sequencing
中文摘要
描述(申请人提供):聚集型原钙粘附素(Pcdh)基因似乎是哺乳动物神经系统中单细胞多样性的主要来源。该基因簇的复杂遗传组织表明,单细胞多样性可能是通过体细胞重组产生的,类似于免疫球蛋白和T细胞受体,或者通过一种类似于果蝇Dscam中发现的选择性剪接机制。令人惊讶的是,PcdH异构体的多样性似乎是通过随机的启动子选择和选择性的前mRNA剪接的组合产生的。Pcdh多样性的这个模型主要是基于来自一个神经元亚型的有限数量的数据。本方案的主要目的是开发和应用创新的单细胞表达谱和单分子原位检测方法来检验该模型的有效性和/或通用性,研究Pcdh基因在多种神经细胞类型和发育阶段中表达的复杂性,并确定在神经发生过程中发生Pcdh启动子选择的时间。
英文摘要
DESCRIPTION (provided by applicant): The clustered protocadherin (Pcdh) genes appear to be the primary source of single cell diversity in the mammalian nervous system. The complex genetic organization of this gene cluster suggested that single cell diversity might arise through somatic recombination, akin to that found in Immunoglobulin and T-Cell receptors or through an alternative splicing mechanism similar to that found in Dscam in Drosophila Melanogaster. Surprisingly, Pcdh isoform diversity appears to be generated through a combination of stochastic promoter choice and alternative pre-mRNA splicing. This model for Pcdh diversity is based primarily on a limited amount of data from one neuronal sub-type. The primary objective of the current proposal is to develop and apply innovative single cell expression profiling and single molecule in situ detection methods to examine the validity and/or generality of this model, to study the complexity of Pcdh gene expression in multiple neuronal cell types and developmental stages, and to determine the time during neurogenesis that Pcdh promoter choice occurs.
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海外基金