Studying the Role of Ran in Mitosis
Studying the Role of Ran in Mitosis
批准号:
7532372
负责人:
Rebecca W Heald
金额:
$32.68万
依托单位国家:
美国
项目类别:
财政年份:
2003
资助国家:
美国
项目状态:
已结题
起止时间:
2003-07-01 至 2012-06-30
关键词:
AffectAfricanAnisotropyBehaviorBindingBiochemicalBiological AssayBiological ModelsBiosensorCell CycleCell Division ProcessCell ExtractsCell divisionCellsChromatinChromosomesClassClassificationComplexCongenital AbnormalityCytoplasmEukaryotaEukaryotic CellFluorescenceFluorescence Resonance Energy TransferFunctional RNAGeneticGenomeGoalsGuanine Nucleotide Exchange FactorsGuanosine Triphosphate PhosphohydrolasesHela CellsHumanImageIn VitroInterphaseLeadMalignant NeoplasmsMeasurementMediatingMeiosisMetaphaseMicroinjectionsMicrotubule PolymerizationMicrotubulesMitosisMitoticMitotic spindleModelingMolecularMonomeric GTP-Binding ProteinsNatureNucleotidesPathway interactionsPositioning AttributeProcessProteinsRNARanaRegulationResearch ProposalsRibonucleoproteinsRoleRunningShapesSignal TransductionSomatic CellStructureTestingThinkingXenopusXenopus laevisbasecancer therapycell typedaughter cellegghigh throughput screeninghuman diseaseinhibitor/antagonistinsightnovelnovel strategiesnucleocytoplasmic transportreceptorreconstitutionresearch studysensorsizesmall moleculetissue/cell culturetooltransmission process
中文摘要
描述(由申请人提供):细胞分裂过程的核心重要性是将一套完整的染色体准确传递到每个子细胞,这在真核生物中通过有丝分裂纺锤体的功能实现。这项研究的目的是阐明高度保守的GTdR在细胞分裂中的作用。目前的模型表明,RanGTP功能作为一个空间标记,信号的基因组在真核细胞中的位置。在有丝分裂期间,RanGTP被认为通过刺激微管聚合和染色体附近的组织来促进纺锤体组装。这种“局部效应”是由RCC 1的染色体定位引起的,RCC 1是产生RanGTP的鸟嘌呤核苷酸交换因子,RanGTP与转运因子结合,使它们释放纺锤体组装所需的货物。然而,货物的性质,它们的有丝分裂功能和RCC 1-RAN-微管信号级联反应的分子机制仍然知之甚少。本提案中描述的一个主要实验方法利用了从非洲爪蟾卵中制备的复杂细胞提取物,可以使用生物化学和功能测定进行研究。这提供了一个很好的模型系统来表征有丝分裂货物的组分和功能,表征有丝分裂梯度,并开发新的重建测定。我们的目标是:(1)为了阐明Ran调节的货物Rae 1的功能,并研究纺锤体相关RNA,Rae 1存在于需要RNA才能发挥其活性的复合体中。(2)使用荧光传感器可视化和表征提取物和各种细胞类型中RCC 1诱导的整个细胞周期梯度。(3)使用RCC 1包被微珠重建RanGTP梯度和纺锤体组装。(4)利用新开发的Ran通路的小分子抑制剂进一步研究RanGTP在细胞分裂中的功能。在所有的真核生物中,纺锤体的组装和功能对于细胞分裂过程中精确分配遗传信息至关重要,而这一过程中的错误与出生缺陷和癌症有关。有丝分裂Ran途径中因子的鉴定和表征不仅是我们理解有丝分裂和减数分裂纺锤体组装的基础,而且还可能为我们理解人类疾病提供重要的新见解。
英文摘要
DESCRIPTION (provided by applicant): Of central importance to the process of cell division is the accurate transmission of a complete set of chromosomes to each daughter cell, which in eukaryotes is achieved through the function of the mitotic spindle. The goal of this research proposal is to elucidate the role of the highly conserved GTPase Ran in cell division. The current model suggests that RanGTP functions as a spatial marker that signals the position of the genome in eukaryotic cells. During mitosis, RanGTP is thought to promote spindle assembly by stimulating microtubule polymerization and organization in the vicinity of chromosomes. This "local effect" results from the chromosomal localization of RCC1, the guanine nucleotide exchange factor that generates RanGTP, which binds to transport factors causing them to release cargoes required for spindle assembly. However, the nature of the cargoes, their mitotic function and the molecular mechanisms underlying the RCC1-Ran-microtubule signaling cascade are still poorly understood. A major experimental approach described in this proposal takes advantage of complex cellular extracts prepared from eggs of the African frog Xenopus laevis that can be studied using biochemical and functional assays. This provides an excellent model system to characterize the components and function of mitotic cargoes, to characterize mitotic gradients, and to develop novel reconstitution assays. Our aims are: (1) To elucidate the function of a Ran-regulated cargo, Rae1 that exists in a complex requiring RNA for its activity, and investigate spindle-associated RNAs. (2) To use fluorescent sensors to visualize and characterize RCC1-induced gradients throughout the cell cycle in extracts and in a variety of cell types. (3) To reconstitute RanGTP gradients and spindle assembly using RCC1-coated beads. (4) To use a newly developed small molecule inhibitor of the Ran pathway to further dissect the functions of RanGTP during cell division. In all eukaryotes, assembly and function of the spindle apparatus is essential to accurately distribute the genetic information during cell division, and errors in this process are associated with birth defects and cancer. The identification and characterization of factors in the mitotic Ran pathway is not only fundamental to our understanding of mitotic and meiotic spindle assembly, but may also provide important new insight into our understanding of human diseases.
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会议论文
Mechanisms of mitosis and size control in Xenopus
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批准号:10589896
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项目类别:
-
资助金额:$87.01万
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财政年份:2016
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负责人:Rebecca W Heald
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依托单位:
Mechanisms of mitosis and size control in Xenopus
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批准号:10378687
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项目类别:
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资助金额:$87.01万
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财政年份:2016
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负责人:Rebecca W Heald
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依托单位:
Mechanisms of mitosis and size control in Xenopus
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批准号:10166491
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项目类别:
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资助金额:$85.85万
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财政年份:2016
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负责人:Rebecca W Heald
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依托单位:
Mechanisms of mitosis and size control in Xenopus
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批准号:9896841
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项目类别:
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资助金额:$81.63万
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财政年份:2016
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负责人:Rebecca W Heald
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依托单位:
Mechanisms of mitosis and size control in Xenopus
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批准号:9071807
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项目类别:
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资助金额:$62.35万
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财政年份:2016
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负责人:Rebecca W Heald
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依托单位:
Mechanisms of Intracellular Scaling
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批准号:8295911
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项目类别:
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资助金额:$46.37万
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财政年份:2012
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负责人:Rebecca W Heald
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依托单位:
Mechanisms of Intracellular Scaling
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批准号:8906883
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项目类别:
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资助金额:$44.57万
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财政年份:2012
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负责人:Rebecca W Heald
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依托单位:
Mechanisms of Intracellular Scaling
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批准号:8704954
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项目类别:
-
资助金额:$44.57万
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财政年份:2012
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负责人:Rebecca W Heald
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依托单位:
Mechanisms of Intracellular Scaling
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批准号:8516062
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项目类别:
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资助金额:$43.01万
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财政年份:2012
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负责人:Rebecca W Heald
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依托单位:
XENOPUS LINKER PROTEINS
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批准号:8365832
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项目类别:
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资助金额:$1.28万
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财政年份:2011
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负责人:Rebecca W Heald
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依托单位:
XENOPUS LINKER PROTEINS
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批准号:8171406
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项目类别:
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资助金额:$0.24万
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财政年份:2010
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负责人:Rebecca W Heald
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依托单位:
XENOPUS LINKER PROTEINS
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批准号:7957778
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项目类别:
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资助金额:$0.33万
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财政年份:2009
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负责人:Rebecca W Heald
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依托单位:
Cell and Molecular Biology: Chromosomes, Cancer and Stem Cells
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批准号:7749869
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项目类别:
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资助金额:$1.0万
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财政年份:2009
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负责人:Rebecca W Heald
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依托单位:
XENOPUS LINKER PROTEINS
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批准号:7723663
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项目类别:
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资助金额:$0.81万
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财政年份:2008
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负责人:Rebecca W Heald
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依托单位:
NIH Director's Pioneer Award
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批准号:7195843
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项目类别:
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资助金额:$76.0万
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财政年份:2006
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负责人:Rebecca W Heald
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依托单位:
NIH Director's Pioneer Award
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批准号:7683893
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项目类别:
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资助金额:$76.0万
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财政年份:2006
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负责人:Rebecca W Heald
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依托单位:
NIH Director's Pioneer Award
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批准号:7913075
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项目类别:
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资助金额:$76.0万
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财政年份:2006
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负责人:Rebecca W Heald
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依托单位:
NIH Director's Pioneer Award
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批准号:7292779
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项目类别:
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资助金额:$76.0万
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财政年份:2006
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负责人:Rebecca W Heald
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依托单位:
COMPLEX MIXTURE MASS SPECTROMETRY OF CHROMOSOME ASSOCIATED PROTEINS
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批准号:7182357
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项目类别:
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资助金额:$0.4万
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财政年份:2005
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负责人:Rebecca W Heald
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依托单位:
IDENTIFICATION OF NOVEL TARGETS FOR CANCER THERAPY BY FUNCTIONAL PROTEOMIC ANA
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批准号:7182385
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项目类别:
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资助金额:$0.4万
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财政年份:2005
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负责人:Rebecca W Heald
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依托单位:
海外基金