Control of Cell Cycle Transitions
Control of Cell Cycle Transitions
批准号:
8589592
负责人:
William G Dunphy
金额:
$47.09万
依托单位国家:
美国
项目类别:
财政年份:
1990
资助国家:
美国
项目状态:
已结题
起止时间:
1990-04-01 至 2016-11-30
关键词:
AddressArchitectureAttentionCancer EtiologyCell CycleCell Cycle ArrestCell Cycle ProgressionCell Cycle RegulationCell divisionCellsCheckpoint kinase 1ChromatinChromosomesCollaborationsCyclin-Dependent KinasesDNADNA biosynthesisDNA lesionDefectDockingEnsureEnzymesEukaryotic CellFire - disastersGenetic MaterialsGenomeGenomic DNAGenomic InstabilityGenomicsHealthHumanHuman PathologyInheritedInvestigationKnowledgeLesionLifeMaintenanceMalignant NeoplasmsMediatingMediator of activation proteinModelingMutationNamesPathway interactionsPhosphorylationPlant RootsPlayProcessPropertyProteinsQuality ControlRegulationReplication OriginRoleS PhaseStructureSystemTREX1 geneVertebratesXenopusYeastscombategghelicaseinsightnovelprotein functionpublic health relevanceresearch studyresponserole model
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The division of eukaryotic cells must occur in a highly faithful manner. During the course of the cell cycle, cells must be able to replicate their DNA with great fidelity. Furthermore, when problems arise during replication, cells must impose a checkpoint-mediated arrest of the cell cycle while they attempt to rectify lesions. Recently, we identified a novel protein called Treslin that is essential for DNA replication in vertebrate cells Treslin acts at a critical regulatory juncture in cellular duplication. In particular, Treslin is akey target of the cyclin-dependent kinase (CDK) that promotes the initial firing of replication origins
at the onset of S-phase. Moreover, Treslin also appears to participate in checkpoint regulation. For the studies in this proposal, we will carry out an intensive analysis of Treslin and its functional relationships with other key regulators of S-phase. We will conduct these investigations in both Xenopus egg extracts and human cells. The egg-extract system offers some technical advantages that are not available currently with human cells. Numerous studies have indicated that this Xenopus system offers a valid model for human cells. Overall, we will attempt to reveal how Treslin promotes accurate replication and maintenance of the genome in vertebrates and how cells control the activity of Treslin. In particular, we will analyze the varios domains of Treslin in order to elucidate its functional architecture. We will examine how the collaboration of Treslin with other replication proteins contributes to its function. We will study
further how phosphorylation controls the functional properties of Treslin. Moreover, we will also investigate the role of Treslin in checkpoint responses. Finally, we will attempt to identify new partners of Treslin and elucidate potentially novel functions of this protein. In general, these studies hold the promise to yield valuable insights into how cells maintain genomic integrity throughout their lifetimes. This information would be especially relevant for human health. Derangement of genomic integrity as a consequence of environmental insults or inherited mutations or both can result in various human pathologies, most notably cancer. Thus, a thorough understanding of the root causes for genomic instability will be essential for an informed strategy in combating cancer.
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Role of ATR in Cell Cycle Checkpoints
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批准号:6920654
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项目类别:
-
资助金额:$45.83万
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财政年份:2004
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负责人:William G Dunphy
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依托单位:
Role of ATR in Cell Cycle Checkpoints
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批准号:8325690
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项目类别:
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资助金额:$47.29万
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财政年份:2004
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负责人:William G Dunphy
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依托单位:
Role of ATR in Cell Cycle Checkpoints
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批准号:7727668
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项目类别:
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资助金额:$46.67万
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财政年份:2004
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负责人:William G Dunphy
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依托单位:
Role of ATR in Cell Cycle Checkpoints
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批准号:8130852
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项目类别:
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资助金额:$47.29万
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财政年份:2004
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负责人:William G Dunphy
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依托单位:
Role of ATR in Cell Cycle Checkpoints
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批准号:7448492
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项目类别:
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资助金额:$44.6万
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财政年份:2004
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负责人:William G Dunphy
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依托单位:
Role of ATR in Cell Cycle Checkpoints
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批准号:6769083
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项目类别:
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资助金额:$44.53万
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财政年份:2004
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负责人:William G Dunphy
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依托单位:
Role of ATR in Cell Cycle Checkpoints
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批准号:7111107
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项目类别:
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资助金额:$44.72万
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财政年份:2004
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负责人:William G Dunphy
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依托单位:
Role of ATR in Cell Cycle Checkpoints
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批准号:9198170
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项目类别:
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资助金额:$49.96万
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财政年份:2004
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负责人:William G Dunphy
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依托单位:
BIO-IMAGING ANALYZER
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批准号:2283815
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项目类别:
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资助金额:$18.6万
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财政年份:1993
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负责人:William G Dunphy
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依托单位:
ENZYMOLOGY OF MITOSIS-PROMOTING FACTOR
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批准号:3303109
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项目类别:
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资助金额:$19.51万
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财政年份:1990
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负责人:William G Dunphy
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依托单位:
ENZYMOLOGY OF MITOSIS PROMOTING FACTOR (MPF)
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批准号:6179747
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项目类别:
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资助金额:$23.04万
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财政年份:1990
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负责人:William G Dunphy
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依托单位:
ENZYMOLOGY OF MITOSIS-PROMOTING FACTOR
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批准号:3303106
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项目类别:
-
资助金额:$20.16万
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财政年份:1990
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负责人:William G Dunphy
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依托单位:
Enzymology of Mitosis Promoting Factor (MPF)
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批准号:6682719
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项目类别:
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资助金额:$30.78万
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财政年份:1990
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负责人:William G Dunphy
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依托单位:
Enzymology of Mitosis Promoting Factor (MPF)
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批准号:6976745
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项目类别:
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资助金额:$36.24万
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财政年份:1990
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负责人:William G Dunphy
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依托单位:
Control of Cell Cycle Transitions
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批准号:8434497
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项目类别:
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资助金额:$47.09万
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财政年份:1990
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负责人:William G Dunphy
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依托单位:
Enzymology of Mitosis Promoting Factor (MPF)
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批准号:6829100
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项目类别:
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资助金额:$36.85万
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财政年份:1990
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负责人:William G Dunphy
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依托单位:
Enzymology of Mitosis Promoting Factor (MPF)
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批准号:7740180
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项目类别:
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资助金额:$49.45万
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财政年份:1990
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负责人:William G Dunphy
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依托单位:
ENZYMOLOGY OF MITOSIS PROMOTING FACTOR (MPF)
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批准号:6018797
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项目类别:
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资助金额:$22.46万
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财政年份:1990
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负责人:William G Dunphy
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依托单位:
Enzymology of Mitosis Promoting Factor (MPF)
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批准号:7094895
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项目类别:
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资助金额:$47.07万
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财政年份:1990
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负责人:William G Dunphy
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依托单位:
Control of Cell Cycle Transitions
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批准号:8975776
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项目类别:
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资助金额:$47.09万
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财政年份:1990
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负责人:William G Dunphy
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依托单位:
海外基金