Computational Methods for Unraveling Combinatorial Gene Regulation
Computational Methods for Unraveling Combinatorial Gene Regulation
批准号:
9260006
负责人:
Kai Tan
金额:
$32.61万
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:
2014-06-15 至 2020-03-31
关键词:
AddressArchitectureCellsChIP-seqChromatinCommunicationCommunitiesComputer softwareComputing MethodologiesCuesDataData SetDevelopmentEnhancersEvolutionFutureGene ExpressionGene Expression RegulationGene TargetingGenetic TranscriptionGenomicsGoalsHumanIndividualInvertebratesInvestigationKnowledgeLinkLocationMammalsMapsMechanicsMethodsModelingMolecularMusNoiseOutcomeOutputPatternPerformanceRegulationResearchResearch PersonnelResourcesSeriesSystemTestingThermodynamicsTrainingTranscriptional RegulationTranslatingValidationcell typecombinatorialcomparativecomparative genomicsdata mininggenome-widehuman diseaseinnovationinsightmouse modelnovelopen sourcepredictive modelingpromoterpublic health relevanceresponsesoftware developmenttranscription factor
中文摘要
描述(由申请人提供):多种转录因子组合调控基因表达是调控基因表达的基本机制。尽管这一现象已经研究了几十年,但我们仍然缺乏系统的策略来准确识别增强子上的组合TF相互作用,并模拟它们对靶基因的调控输出,特别是对于哺乳动物物种。如果成功,这项研究将消除该领域的一个瓶颈,并代表着一系列研究的第一步,有望进一步加深我们对基因调控的理解。在我们看来,在这个应用程序中提出的研究是创新的,因为它代表了对现状的新的和实质性的背离。我们将解决该领域研究人员面临的以下三个挑战:1)缺乏识别组合相互作用的策略
英文摘要
DESCRIPTION (provided by applicant): Combinatorial regulation of gene expression by multiple transcription factors (TFs) is a fundamental mechanism for regulating gene expression. Although this phenomenon has been studied for several decades, we still lack a systematic strategy to accurately identify combinatorial TF interactions at enhancers and to model their regulatory output on target gene(s), especially for mammalian species. If successful, the proposed research will remove a bottleneck in the field and represent the first step in a continuum of research that is expected to further our understanding of gene regulation. Research proposed in this application is innovative, in our opinion, because it represents a new and substantive departure from the status quo. We will address the following three challenges facing researchers in the field: 1) lack of strategies to identify combinatorial interactions among
TFs at enhancers; 2) lack of strategies to associate enhancers with their target genes; and 3) limited ability to translate enhancer sequence information to its regulatory output. At the completion of this project, we expect to have developed a set of computational methods that enable genome-scale identification of combinatorial interactions at enhancers and construction of predictive models of combinatorial regulation in mammals. In addition, by applying our methods to large public datasets, we expect to obtain new insights into the evolutionary, spatial, and temporal dynamics of enhancers. The computational methods developed will be implemented as open-source software and made publicly available to the research community.
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