Genomic Measurement of Alternative Splicing by DNA Array
Genomic Measurement of Alternative Splicing by DNA Array
批准号:
7201585
负责人:
Douglas L Black
金额:
$41.62万
依托单位国家:
美国
项目类别:
财政年份:
2004
资助国家:
美国
项目状态:
已结题
起止时间:
2004-04-01 至 2009-03-31
关键词:
Alternative SplicingArchivesAreaCardiacCell physiologyCellsCollaborationsComplexDNADNA Microarray ChipDNA Microarray formatDataData AnalysesDatabasesDetectionDevelopmentDiseaseEventGene ExpressionGene Expression ProfilingGene Expression RegulationGenesGenomeGenomicsGoalsHeartHousingHuman Cell LineKnock-outLabelLearningLiteratureMalignant NeoplasmsMeasurementMeasuresMethodsMicroarray AnalysisMusNervous system structureNeuronal DifferentiationNeuronsOligonucleotide MicroarraysOligonucleotidesPatternPersonal SatisfactionPliabilityPrincipal InvestigatorPrintingProcessProteinsProtocols documentationQuality ControlRNARNA SplicingRegulationRegulator GenesRegulatory PathwayResourcesRoleSeriesSourceSpliced GenesStandards of Weights and MeasuresSystemTechnology TransferTestingTissuesTranscriptTroponin TYeastscardiogenesiscostdesignimprovedpostnatalprogramsrelating to nervous systemresearch studytechnology developmenttool
中文摘要
描述(由申请人提供):选择性剪接是控制哺乳动物基因表达的关键过程,也是蛋白质多样性的主要来源。剪接调节中的错误与包括癌症在内的许多疾病过程有关,但参与这种调节的细胞电路大多是未知的。利用DNA微阵列进行基因表达谱分析,使我们对基因组范围内的基因调控系统的理解取得了重大进展。然而,没有一个常用的微阵列分析系统可以检测剪接的变化,而是提供每个基因的总体转录物丰度的信息。这些方法提供了基因调控的第一层信息,但忽略了剪接模式改变引起的基因产物的许多重要变化。这里提出的项目将使三个小组合作建立一种新型的DNA微阵列,允许并行分析多种备选剪接模式。这次合作的每个实验室在研究剪接方面都有独特的专业知识。我们将设计和生产用于检测和测量小鼠剪接事件的寡核苷酸阵列。这种微阵列方法已经很好地建立了酵母剪接,最近的结果表明它能够在更复杂的人类细胞系和组织中检测替代剪接。这里的建议是将其应用于老鼠的特定调节系统,包括神经系统和心脏。该项目的目标是将剪接调控的研究提升到全基因组水平,全面搜索受特定剪接调控途径影响的基因,并为基因表达谱提供更高的精度。
英文摘要
DESCRIPTION (provided by applicant): Alternative splicing is a key process in the control of mammalian gene expression and a major source of protein diversity. Errors in splicing regulation are implicated in many disease processes including cancer, but the cellular circuitry involved in this regulation is mostly unknown. Gene expression profiling using DNA microarrays has led to major advances in our understanding of gene regulatory systems on a genome wide scale. However, none of the commonly available systems of microarray analysis can detect changes in splicing and instead give information on the overall transcript abundance from each gene. These methods provide information on the first layer of gene regulation but miss many important changes in gene product caused by alterations in splicing pattern. The project proposed here will enable three groups to collaborate on establishing a new type of DNA microarray that allows the parallel analysis of multiple alternative splicing patterns. Each of the labs in this collaboration has unique expertise in the study of splicing. We will design and produce arrays of oligonucleotides that detect and measure splicing events in the mouse. This microarray method is well established for yeast splicing, and recent results demonstrate its ability to detect alternative splicing in more complex human cell lines and tissues. The proposal here is to apply it to specific systems of regulation in the mouse, including the nervous system and the heart. The goals of the project are to move the study of splicing regulation to the level of the whole genome, to comprehensively search for genes subject to specific splicing regulatory pathways, and to provide greater precision to gene expression profiling.
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海外基金