Mechanistic study of pioneer factors
Mechanistic study of pioneer factors
批准号:
9219420
负责人:
Lu Bai
金额:
$30.83万
依托单位国家:
美国
项目类别:
财政年份:
2017
资助国家:
美国
项目状态:
已结题
起止时间:
2017-01-01 至 2020-12-31
关键词:
AffectBindingBinding SitesBiologicalBiological AssayCell Differentiation processCellsChromatinChromatin ModelingChromosomesCompetenceComplexDNADataDevelopmentDiseaseDissectionEukaryotic CellFluorescence MicroscopyFunctional disorderFutureGene ActivationGene ExpressionGene Expression RegulationGeneticGenetic TranscriptionGenomeGenomicsGoalsHistonesHumanIn VitroIndividualInvadedKineticsKnowledgeLeadLightLinkLocationMalignant NeoplasmsMeasurementMeasuresMolecularMolecular ChaperonesMutationNucleosomesPathway interactionsPlayPopulationProcessPropertyRegulationRegulator GenesRoleSeriesSiteSurfaceTechniquesTechnologyTestingTimeYeastsbasecancer cellcancer therapyclinical applicationcombatdesignfitnessgene synthesisgenome-widehigh throughput screeninghistone modificationhuman diseasein vivoinnovationinsightinterestmicrochipnext generationnovelnovel therapeuticspreventpromotersingle moleculesingle-molecule FRETsynthetic biologytime usetranscription factor
中文摘要
点击翻译按钮获取中文摘要
英文摘要
Project Summary
In eukaryotic cells, nucleosomes prevent efficient binding of transcription factors and transcription machinery to
their genomic targets. A special group of transcription factors called “pioneer factors” can invade compact
chromosome and remodel nucleosomes near their binding sites, allowing the access of transcription factors
and triggering their transcriptional competency. Pioneer factors play critical roles in gene regulation and cell
differentiation. Mutation or mis-regulation of pioneer factors are associated with developmental diseases and
many types of human cancer.
Despite their essential functions, the mechanism underlying the pioneer activity is unclear. Our long-term goal
is to develop a detailed mechanistic understanding of how pioneer factors access their nucleosomal binding
sites, disrupt histone-DNA contacts, and activate gene expression. To achieve this goal, our overall objective in
this proposal is to quantitatively measure the binding, nucleosome-depleting, and gene regulatory activities of
pioneer factors under a variety of genetic and cellular conditions. We will perform these measurements into
three aims. At the population level, we will determine the steady-state nucleosome-depleting activities among
genome-wide TFs to understand what kind of TFs can serve as pioneers and how their nucleosome-depleting
activities are regulated in vivo (aim 1). At the single cell level, we will evaluate the gene regulatory activities of
pioneer factors and their cell-to-cell variability (aim 2). At the single molecule level, we will directly measure the
kinetics of pioneer factor binding and invasion of the nucleosome substrates in vitro (aim 3). Completion of
these aims is expected to advance the fundamental knowledge of pioneer factors and their role in chromosome
opening and gene regulation. It will also contribute to future dissection of the functional roles of pioneer factors
in cancer cells and the development of novel therapies to combat their dysfunction.
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