Real-time visualization of neural stem cell transcriptome
Real-time visualization of neural stem cell transcriptome
批准号:
8413889
负责人:
Weihong Guo
金额:
$23.55万
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-09-30 至 2014-08-31
关键词:
AddressBar CodesBiological AssayBiological ModelsBiologyBirth OrderBrainBrain NeoplasmsCell LineageCellsClone CellsCodeColorComplexComputational algorithmComputer AnalysisDataDetectionDevelopmentDiagnostic Neoplasm StagingDrosophila genusExcisionGene ExpressionGene Expression ProfileGene Expression RegulationGenerationsGenesGeneticGenetic TranscriptionHealthHumanImageImage AnalysisImageryIn Situ HybridizationIn VitroInjuryInterventionKnock-outKnowledgeLabelLinkMalignant NeoplasmsMethodsModelingMolecularMolecular ProfilingNeoplasm MetastasisNerve TissueNervous system structureNeuronsNoiseOrganismOutcomePatternPopulationPropertyProteinsProtocols documentationRNA InterferenceRegenerative MedicineRegulationResolutionSignal PathwaySourceStagingStem Cell ResearchStem cellsStrokeStudy modelsTechniquesTestingTherapeutic UsesTimeTissuesTranscriptanticancer researchcell typecombinatorialexpectationfascinatehigh throughput technologyhuman diseasein vivomutantnerve stem cellrepairedself-renewalstem cell differentiationstem cell populationtime usetissue repairtooltranscription factortumor
中文摘要
点击翻译按钮获取中文摘要
英文摘要
DESCRIPTION (provided by applicant): Neural stem cells (NSC) have a fascinating biology of precise transition of cellular states from dormant to proliferative to differentiating, which most recently begun to be understood at the cellular and molecular levels. Despite successful identification of genes linked to each of those cellular steps, a comprehensive and multi-dimensional picture on how those genes are regulated in real-time throughout the differentiation stages of NSC is sorely lacking. This multi- disciplinary proposal will combine for the first time the use of two powerful methods to directly assess the transcriptional state of key genes involved in NSC regulation in vivo, at a single cell resolution. The first technique, Multiplex in situ hybridization, co-developed by one of the PIs, allows direct visualization of transcriptional activity of several genes with single cell resolution. The second technique, known as G-Trace, will be used to generate cellular clones labeled with fluorescent proteins that distinctively mark cell lineages according to their temporal generation. In Aim 1, the combination of these two methods in the Drosophila larval brain will be used to create profiles of normal wild type expression of several genes involved in NSC regulation simultaneously. Further computational image analysis tools will be developed to segment images and reduce noise. We will test the application of a spectral bar coding system as a proof-of-principle to expand the detection of hundreds of active genes analyzed at a time. In Aim 2, brain tumors will be induced by knocking-out key transcription factors to track global alterations in gene expression within labeled clones. The expectation is that these combined methods will reveal key properties of the differentiation progression of NSC into several specific neuronal lineages, with far-reaching implications to a better manipulation of stem cells in general and in other organisms, including humans.
PUBLIC HEALTH RELEVANCE: Our studies will increase knowledge on stem cell regulation and has the potential to impact the fields of regenerative medicine and stem cell cancer research. A better understanding of global gene regulation at the single-cell level is expected to enhance methods employed in a number of applications, such as in vitro neural stem cell differentiation to repair tissue after damage and development of probes for detecting early stages of cancer.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Real-time visualization of neural stem cell transcriptome
-
批准号:8548338
-
项目类别:
-
资助金额:$19.04万
-
财政年份:2012
-
负责人:Weihong Guo
-
依托单位:
海外基金