A Functional Census of p53 Cancer and Suppressor Mutants
A Functional Census of p53 Cancer and Suppressor Mutants
批准号:
7426313
负责人:
G. WESLEY HATFIELD
金额:
$33.54万
依托单位国家:
美国
项目类别:
财政年份:
2005
资助国家:
美国
项目状态:
已结题
起止时间:
2005-08-01 至 2010-05-31
关键词:
AffectAmino AcidsAntineoplastic AgentsApoptosisAreaBinding SitesBioinformaticsBiologicalBiological AssayCancerousCatalogingCatalogsCell Cycle ArrestCellsCensusesConsensusDNA BindingDataEngineeringGene TargetingGenomicsGoalsHumanKnowledgeLeadLettersLifeMachine LearningMalignant NeoplasmsMapsMedicalMethodologyMethodsMissense MutationModelingMolecular ConformationMutationNumbersPositioning AttributeProliferatingProtein p53Research PersonnelSignal TransductionSiteSource CodeSpecificityStressSuppressor MutationsSurveysSystems BiologyTP53 geneTechniquesTrainingTumor Suppressor ProteinsValidationVariantWorkYeastsbasecancer therapycomputerized toolsdesignfunctional restorationinterestkillingsmutantprogramsrepairedresearch studysmall moleculetranscription factortumor
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The broad, long-term objectives are (1) demonstrate computational and experimental methods cooperating to achieve a functional census of a large mutation sequence space of great medical importance; (2) contribute to our knowledge of p53 functional rescue mechanisms, and so facilitate the search for a small molecule cancer drug that effects an analogous functional rescue of p53; and (3) elucidate part of the systems biology of cancer by characterizing the spectrum of p53 cancer and suppressor mutants across known downstream p53 DNA binding sites. Mutations to the tumor suppressor protein p53 occur in approximately half of all human cancers, and restoring function to a mutationally defective p53 protein is a long-held medical goal. Biological precedence for rescuing p53 cancer mutations is found in second-site p53 cancer suppressor mutations. The analogous p53 pharmacological rescue would save hundreds of thousands of lives annually. Understanding and predicting p53 rescue is an important step toward that goal.
The specific aims are (1) computationally predict all single suppressor mutations for p53 cancer mutants and validate the results experimentally, (2) optimize the rescue effects of known and putative p53 suppressor regions through two or more coordinated mutation changes, and (3) predict and experimentally validate the DNA binding specificity of p53 cancer and suppressor mutants for known p53 DNA binding sites. Our broad strategy is a coordinated computational and experimental attack. We already have experimental p53 functional assays and computational predictors of p53 activity, developed as part of our Preliminary Studies. Computational predictors will be used to focus experimental work into the highest priority areas. Experimental validation of the predictions will lead to a larger training set for machine learning techniques. The larger training set will lead to even more accurate predictions, thus even more focused experimentation. Thus, the interplay between computation and experiment will become ever more efficient as the project progresses. Variations of this basic strategy apply to each of our Specific Aims, which all rely on closely coordinated experiment and computation.
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Global Regulatory Networks in Escherichia Coli
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批准号:6677631
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财政年份:1998
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财政年份:1998
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财政年份:1998
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依托单位:
BRANCHED CHAIN AMINO ACID BIOSYNTHESIS IN E COLI
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财政年份:1998
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依托单位:
BRANCHED CHAIN AMINO ACID BIOSYNTHESIS IN E COLI
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财政年份:1998
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负责人:G. WESLEY HATFIELD
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依托单位:
CODON PAIRS, CODON CONTEXT AND TRANSLATIONAL EFFICIENCY
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依托单位:
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依托单位:
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财政年份:1993
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依托单位:
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依托单位:
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依托单位:
T RNA MODIFICATION AND GENE EXPRESSION IN MAMMALIAN CELL
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负责人:G. WESLEY HATFIELD
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依托单位:
T RNA MODIFICATION AND GENE EXPRESSION IN MAMMALIAN CELL
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依托单位:
T RNA MODIFICATION AND GENE EXPRESSION IN MAMMALIAN CELL
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依托单位:
海外基金