SUMO conjugation in cell biology and Development
细胞生物学和发育中的相扑结合
基本信息
- 批准号:7569505
- 负责人:
- 金额:$ 23.89万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2001
- 资助国家:美国
- 起止时间:2001-09-15 至 2010-11-30
- 项目状态:已结题
- 来源:
- 关键词:AffinityAnimal ModelBiochemicalBiogenesisBiologicalBiological PhenomenaBiological ProcessCell NucleusCellsCellular biologyChromatin StructureComplexDatabasesDevelopmentDisease modelDrosophila genusDrosophila melanogasterEmbryoEmbryonic DevelopmentEmbryonic Pattern SpecificationEnzymesEpigenetic ProcessGenesGeneticGenotypeGoalsHomeobox GenesHuntington DiseaseInheritance PatternsJUN geneMalignant NeoplasmsMass Spectrum AnalysisMediatingNatural ImmunityNerve DegenerationNeurodegenerative DisordersOncogene ProteinsOrganismPathway interactionsPattern FormationPlayPolycombPost-Translational Protein ProcessingProcessProtein p53ProteinsProteomicsRegulationRepressionResearchRoleSAM DomainSpecificityStagingStructureSumoylation PathwaySystemTechniquesTestingTranscriptional RegulationTransgenesTumor Suppressor ProteinsUbiquitin Like ProteinsWingbiological adaptation to stressfitnessflexibilityflygenetic regulatory proteinhuman Huntingtin proteinhuman diseaseprotein foldingresearch study
项目摘要
DESCRIPTION (provided by applicant): Project Summary: SUMO is a ubiquitin-like protein that is reversibly conjugated to a wide variety of target proteins, thereby serving as a flexible switch to control protein subcellular localization and biochemical activity. SUMO conjugation ("sumoylation") plays central roles in many crucial biological processes including epigenetic inheritance and pattern formation. The long-term goal of this research is to illuminate the connections between sumoylation and these biological phenomena using the easily manipulated model organism Drosophila melanogaster. The specific aims are: 1. To determine the role of SUMO in Polycomb Group (PcG) function. PcG factors play essential roles in maintaining the silent epigenetic state of genes that regulate development. Two PcG factors, Ph and Scm, appear to be regulatory targets of sumoylation. Genetic, cell biological, and biochemical approaches will be employed to make mechanistic connections between the sumoylation of these proteins and transcriptional silencing. 2. To carry out a system wide analysis of the effects of genotype and developmental stage on the spectrum of SUMO-conjugated proteins. The pleiotropic roles of SUMO suggest the existence of many unidentified SUMO conjugation targets. Proteomic techniques will be used to characterize the spectrum of SUMO conjugated proteins in the intact organism as a function of genotype and developmental stage. The creation of a multi-dimensional database of SUMO-conjugated proteins will allow us to test hypotheses about how SUMO conjugating and deconjugating enzymes determine the specificity of conjugation, and about the role of SUMO in such processes as protein biogenesis, epigenetic transcriptional control, and embryogenesis. Relevance: The sumoylation pathway has been implicated in both neurodegenerative disorders and cancer. For example, sumoylation of Huntingtin, the pathogenic protein in Huntington's disease, exacerbates neurodegeneration in a Drosophila model of this disease. Furthermore, the sumoylation of numerous oncoproteins (c-jun, elk-1, and TEL) and tumor suppressor proteins (p53, RB, and PML) modulates their function. Consequently, the research proposed here will advance our understanding of human disease.
描述(由申请人提供):项目摘要:相扑是一种泛素样蛋白,可与多种目标蛋白可逆结合,从而成为控制蛋白质亚细胞定位和生化活性的灵活开关。相扑接合(“相扑”)在包括表观遗传和模式形成在内的许多重要的生物学过程中起着核心作用。这项研究的长期目标是使用易于操纵的模式生物黑腹果蝇来阐明苏莫化和这些生物现象之间的联系。具体目的是:1.确定相扑在PcG功能中的作用。PCG因子在维持调节发育的基因的沉默表观遗传状态方面发挥着至关重要的作用。Ph和SCm这两个PcG因子似乎是苏木糖基化的调节靶点。遗传、细胞生物学和生化方法将被用来在这些蛋白质的总甲基化和转录沉默之间建立机械性的联系。2.系统分析不同基因和发育阶段对SUMO结合蛋白谱的影响。相扑的多效性表明,存在许多未知的相扑共轭靶标。蛋白质组学技术将被用来表征完整生物体中相扑结合蛋白的光谱,作为基因和发育阶段的函数。相扑结合蛋白多维数据库的建立将使我们能够检验相扑结合和去结合酶如何决定接合的特异性,以及相扑在蛋白质生物发生、表观遗传转录控制和胚胎发生等过程中的作用。相关性:苏莫化途径与神经退行性疾病和癌症都有关联。例如,亨廷顿病的致病蛋白亨廷顿蛋白的苏莫化会加剧这种疾病的果蝇模型的神经退化。此外,许多癌蛋白(c-jun、elk-1和tel)和肿瘤抑制蛋白(p53、Rb和PML)的总和作用调节它们的功能。因此,这里提出的研究将促进我们对人类疾病的理解。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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ALBERT J COUREY其他文献
ALBERT J COUREY的其他文献
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{{ truncateString('ALBERT J COUREY', 18)}}的其他基金
Repressor/co-repressor oligomerization and development
阻遏物/共阻遏物寡聚化和发育
- 批准号:
7988997 - 财政年份:2009
- 资助金额:
$ 23.89万 - 项目类别:
Smt3 conjugation in cell biology and development
细胞生物学和发育中的 Smt3 缀合
- 批准号:
6360273 - 财政年份:2001
- 资助金额:
$ 23.89万 - 项目类别:
SUMO conjugation in cell biology and Development
细胞生物学和发育中的相扑结合
- 批准号:
7196827 - 财政年份:2001
- 资助金额:
$ 23.89万 - 项目类别:
Smt3-conjugation in cell biology and development
细胞生物学和发育中的 Smt3 缀合
- 批准号:
6657425 - 财政年份:2001
- 资助金额:
$ 23.89万 - 项目类别:
Smt3-conjugation in cell biology and development
细胞生物学和发育中的 Smt3 缀合
- 批准号:
6796751 - 财政年份:2001
- 资助金额:
$ 23.89万 - 项目类别:
Smt3-conjugation in cell biology and development
细胞生物学和发育中的 Smt3 缀合
- 批准号:
6526176 - 财政年份:2001
- 资助金额:
$ 23.89万 - 项目类别:
DORSOVENTRAL PATTERNING THROUGH TRANSCRIPTIONAL CONTROL
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- 批准号:
6386002 - 财政年份:1990
- 资助金额:
$ 23.89万 - 项目类别:
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- 批准号:
6519399 - 财政年份:1990
- 资助金额:
$ 23.89万 - 项目类别:
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调节发育的启动子的生化分析
- 批准号:
2182551 - 财政年份:1990
- 资助金额:
$ 23.89万 - 项目类别:
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