Structural Mechanisms Controlling Cell-Cycle Gene Expression
Structural Mechanisms Controlling Cell-Cycle Gene Expression
批准号:
9892880
负责人:
Seth Michael Rubin
金额:
$32.82万
依托单位国家:
美国
项目类别:
财政年份:
2018
资助国家:
美国
项目状态:
已结题
起止时间:
2018-05-01 至 2022-03-31
关键词:
ArchitectureBindingBiochemicalBiological AssayC-terminalCell CycleCell Cycle RegulationCell ProliferationCell divisionChromatinChromatin StructureComplexCrystallizationCyclin-Dependent KinasesDNADNA BindingDNA Binding DomainDataDefectElectron MicroscopyElementsGene ActivationGene ExpressionGene Expression RegulationGenesGenetic TranscriptionHealthHistone CodeHistone H3HistonesLeadLinkMalignant NeoplasmsMediatingMitosisMitoticModelingMolecularNeoplasm MetastasisNormal CellNucleosomesPhosphorylationPositioning AttributeProcessPromoter RegionsProteinsPublishingRepressionResearch Project GrantsResearch Project SummariesShapesStructureSystemTestingTimeTranscription Initiation SiteWorkcancer cellcdc Genescell growthgene repressioninsightneoplastic cellnoveloutcome forecastpromoterprotein complexreconstitutionrecruitsuccesstranscription factortumorigenesis
中文摘要
项目总结
该研究项目旨在确定Dream和Myb-MuvB(MMB)蛋白是如何
复合体调节转录以控制细胞增殖。保守的MuvB
蛋白质复合体通过与细胞周期基因的适时结合抑制或激活细胞周期基因
特异性DNA结合转录因子包括E2F4-p130(DREAM)和Myb
(MMB)。然而,五种蛋白MuvB复合体的生化功能尚不清楚。
我们提出并将测试MuvB如何与染色质相关联的新假设,
DREAM如何通过稳定染色质结构抑制转录,以及Myb如何
通过与MuvB的结合激活基因表达。这些研究将提供
关于细胞周期如何控制的基本新见解,并将揭示
转录因子直接调控基因表达的新机制
通过核小体定位。
英文摘要
Project summary
This research project aims to determine how the DREAM and Myb-MuvB (MMB) protein
complexes regulate transcription to control cell proliferation. The conserved MuvB
protein complex either represses or activates cell-cycle genes by timely association with
specific DNA-binding transcription factors including E2F4-p130 (DREAM) and Myb
(MMB). However, the biochemical function of the five protein MuvB complex is unknown.
We propose and will test novel hypotheses for how MuvB associates with chromatin,
how DREAM inhibits transcription by stabilizing chromatin structure, and how Myb
activates gene expression through its association with MuvB. These studies will provide
fundamental new insights regarding how the cell cycle is controlled and will uncover a
novel mechanism for how transcription factors directly modulate gene expression
through nucleosome positioning.
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