New methods for discovery and study of microRNAs and other small noncoding RNAs
New methods for discovery and study of microRNAs and other small noncoding RNAs
批准号:
7603033
负责人:
Travis John Antes
金额:
$46.93万
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-05-01 至 2011-03-31
关键词:
BioinformaticsBiologicalBiological SciencesBiopsyBlast CellBlood CellsCell CycleCell LineCell ProliferationCellsCharacteristicsClinicalClinical ResearchCloningCollectionComplementary DNACustomDatabasesDevelopmentDiagnosticDisciplineDiseaseEducational process of instructingEmbryoEnzymesExcisionFamilyFigs - dietaryFingerprintFormalinFunctional RNAGenbankGene ExpressionGenerationsGenesGoalsHistocompatibility TestingHumanIndustryKnowledgeLabelLaboratoriesLasersLeftLibrariesMalignant NeoplasmsMethodologyMethodsMicroRNAsMoldsMolecularMolecular BiologyMolecular Biology TechniquesMolecular ProfilingNormal tissue morphologyNorthern BlottingNucleotidesNylonsOligonucleotidesOutputParaffin EmbeddingPatientsPatternPhasePhase I Clinical TrialsPhenotypePost-Transcriptional RegulationProcessProteinsProtocols documentationPublic HealthRNARNA amplificationRaceRadioReportingResearchResearch DesignResearch MethodologyResearch PersonnelReverse Transcriptase Polymerase Chain ReactionReverse TranscriptionRibonuclease IIIRibonucleotidesRibosomal RNASamplingScientistSequence HomologsSerumServicesSmall Business Innovation Research GrantSmall RNASorting - Cell MovementSourceStructureStudy SectionSystemTechniquesTechnologyTimeTissue MicroarrayTissue SampleTissuesTrainingTranscriptTumor-DerivedUntranslated RNAValidationVirus DiseasesWorkadult stem cellbasebiological adaptation to stresscDNA Librarycommercializationdensitydesignexperiencegel electrophoresishuman tissueimprovedinorganic phosphatelaser capture microdissectionmembernext generationnovelnovel strategiesnucleasetooltumorigenesis
中文摘要
描述(由申请人提供):1993年小调控RNA分子的发现告诉我们,分子生物学的中心法则比最初认为的要复杂得多。与其简单地充当构建蛋白质的中间信使,似乎特化的RNA分子可以通过转录后调节微妙地塑造细胞表型。随后的研究表明,miRNA分子参与了关键的调控网络,如分化、应激反应和肿瘤发生。从分子生物学的角度来看,这些非常小的(大约17-26个核苷酸)分子难以操作,被称为microRNAs (miRNAs)。本文讨论的工作将开发和商业化一种独特的分子生物学技术,大大简化了microrna的鉴定和定量。该方法利用了mirna由RNaseIII酶处理的事实,这些酶在其切割产物上留下特征指纹,可以用适当的分子诱饵恢复。报告了先前一期研究的结果,其中获得了原理证明和初步结果。第二阶段的提案概述了实验方法,将改进技术,扩大产品组合,并设计产品,将技术直接带给缺乏任何先前miRNA经验的实验科学家。这项研究工作将通过提供下一代miRNA发现费用的研究来影响公众健康。目前,学术界和工业界实验室都在努力发现mirna及其特定功能。这项研究为我们加深对发育、细胞增殖、分化、细胞周期和疾病(如癌症和病毒感染)的理解提供了一个巨大的机会。根据该SBIR开发的产品将使广泛的生命科学研究人员能够发现miRNA。
英文摘要
DESCRIPTION (provided by applicant): The 1993 discovery of small regulatory RNA molecules has taught us that the central dogma of molecular biology is much more complicated that originally thought. Rather than simply acting as a middle messenger in the quest to build proteins, it seemed that specialized RNA molecules could subtly mold a cellular phenotype through post- transcriptional regulation. Subsequent research has revealed that miRNA molecules are involved in critical regulatory networks such as differentiation, stress response, and oncogenesis. Known as microRNAs (miRNAs), these very small (approximately 17-26 nucleotides) molecules are difficult to manipulate from a molecular biology perspective. The work discussed herein will develop and commercialize a unique molecular biology technique that significantly simplifies the identification and quantitation of microRNAs. The method takes advantage of the fact that miRNAs are processed by RNaseIII enzymes, which leave a characteristic fingerprint on their cleavage products that can be recovered with the appropriate molecular }bait}. Results of a previous Phase I study are reported, in which proof of principle and initial results were obtained. The Phase II proposal outlines the experimental methodology that will refine the techniques, expand the portfolio, and design products that will bring the technology directly to bench scientists that lack any prior miRNA experience. This research effort will impact public health by providing researches with a next generation miRNA discovery tolls. Currently, there is a substantial effort in academic and industry laboratories to discovery miRNAs, as well as their specific functions. This research represents a tremendous opportunity to enhance our understanding of development, cell proliferation, differentiation, cell cycle, and disease (e.g., cancer and viral infections). The products developed under this SBIR will enable a broad class of life science researchers in miRNA discovery.
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会议论文
Permanent Knockdown of MicroRNAs using a Lentiviral-based Anti-miR System
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批准号:7537321
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项目类别:
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资助金额:$14.91万
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财政年份:2008
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负责人:Travis John Antes
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依托单位:
New methods for discovery and study of microRNAs and other small noncoding RNAs
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批准号:7480152
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项目类别:
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资助金额:$50.36万
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财政年份:2006
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负责人:Travis John Antes
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依托单位:
海外基金