Experimental and structural evolution of hormone receptors
Experimental and structural evolution of hormone receptors
批准号:
7664934
负责人:
Joseph W Thornton
金额:
$27.19万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-08-01 至 2011-07-31
关键词:
AddressAffinityAgonistAnimal ModelAntineoplastic AgentsBehaviorBindingBiologicalBiological AssayBiologyCrystallographyDNA receptorDataDatabasesDevelopmentDrug Delivery SystemsDrug resistanceEngineeringEstrogen ReceptorsEvolutionFamilyGene FamilyGenesGoalsGrowthHormonalHormone ReceptorHormonesHumanImmunityKnowledgeLigandsLightLinkMalignant NeoplasmsMammary NeoplasmsMapsMetabolicMethodsMicrobeModificationMolecularMolecular AnalysisMolecular EvolutionMolecular StructureMutagenesisOrganismPharmacologic SubstancePhylogenetic AnalysisPhysiologyPopulationProcessProliferatingPropertyProteinsRecurrenceResearchSaccharomycesSequence AnalysisSpecificitySteroid ReceptorsStructureStructure-Activity RelationshipSystemTamoxifenTechniquesTestingVariantVertebral columnYeastsbasecopingdesignenzyme substratefitnessgene functiongene synthesisimprovedinsightmalignant breast neoplasmnovelpreventprotein functionprotein structurereceptorreceptor functionreceptor structure functionreconstructionreproductiveresearch studysteroid hormonesteroid hormone receptorthree dimensional structuretranscription factortumortumor progression
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The goal of this research is to elucidate the evolutionary dynamics and structural basis for the evolution of novel functions in a biomedically important gene family, the steroid hormone receptors. We will combine experimental evolution, crystallography, ancestral gene resurrection, and manipulative assays of gene function to analyze how receptors evolve tight molecular partnerships with novel hormonal ligands. The specific aims are:
1. Use an experimental evolution system in engineered yeast to select for human estrogen receptors which, like those in some mammary tumors, evolve to be stimulated by taxmoxifen, a major breast cancer drug. Using a battery of functional assays and evolutionary techniques for reconstructing the evolution of receptor sequences, we will determine the mechanistic basis for the evolution of this new ER-ligand interaction and the dynamics of receptor-ligand coevolution.
2. We will resurrect ancestral steroid receptors (using phylogenetic analysis and gene synthesis) and then evolve these receptors in this same experimental evolution system. Ancestral receptors will be selected to recapitulate the functional shifts in ligand specificity that occurred during real historical evolution over hundreds of millions of years. The mechanistic basis and evolutionary dynamics of this process will be studied in detail.
3. We will express, crystallize, and determine the three-dimensional structures of ancestral receptors, as well as those of several functionally divergent extant steroid receptors. These structures - together with the data on the evolution of new functions from Aims 1 and 2 - will provide a rich database from which to reconstruct the evolution of receptor protein structures. This is expected to reveal the structural mechanisms by which new receptor functions evolve, both in our experimental evolution system and in real historical evolution.
This synthesis of manipulative, hypothesis-testing techniques will provide unprecedented detailed knowledge of the dynamics and mechanisms by which gene function evolves. These data should help resolve long-standing fundamental issues in evolutionary biology, and also improve our understanding of the structure-function relationships that determine steroid receptor function.
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专著(0)
科研奖励(0)
会议论文
Genetic and biophysical causes of historical protein evolution
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批准号:10656347
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项目类别:
-
资助金额:$49.1万
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财政年份:2022
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负责人:Joseph W Thornton
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依托单位:
Genetic and biophysical causes of historical protein evolution
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批准号:10406781
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项目类别:
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资助金额:$43.48万
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财政年份:2022
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负责人:Joseph W Thornton
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依托单位:
Evolution of molecular complexes: genetic, structural, and functional mechanisms for the evolution of oligomers and allostery
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批准号:9766019
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项目类别:
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资助金额:$30.55万
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财政年份:2019
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负责人:Joseph W Thornton
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依托单位:
Evolution of molecular complexes: genetic, structural, and functional mechanisms for the evolution of oligomers and allostery
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批准号:10251124
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项目类别:
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资助金额:$29.91万
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财政年份:2019
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负责人:Joseph W Thornton
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依托单位:
Evolution of molecular complexes: genetic, structural, and functional mechanisms for the evolution of oligomers and allostery
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批准号:10004121
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项目类别:
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资助金额:$29.93万
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财政年份:2019
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负责人:Joseph W Thornton
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依托单位:
Deep characterization of the sequence space and evolutionary trajectories of reconstructed ancestral proteins - Resubmission 01
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批准号:9901582
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项目类别:
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资助金额:$31.92万
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财政年份:2017
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负责人:Joseph W Thornton
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依托单位:
Deep characterization of the sequence space and evolutionary trajectories of reconstructed ancestral proteins - Resubmission 01
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批准号:9311486
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项目类别:
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资助金额:$31.85万
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财政年份:2017
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负责人:Joseph W Thornton
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依托单位:
Experimental and structural evolution of hormone receptors
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批准号:8010260
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项目类别:
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资助金额:$20.94万
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财政年份:2010
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负责人:Joseph W Thornton
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依托单位:
Experimental and structural evolution of hormone receptors
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批准号:7476575
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项目类别:
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资助金额:$27.14万
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财政年份:2007
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负责人:Joseph W Thornton
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依托单位:
Experimental and structural evolution of hormone receptors
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批准号:7903434
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项目类别:
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资助金额:$25.55万
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财政年份:2007
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负责人:Joseph W Thornton
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依托单位:
Experimental and structural evolution of hormone receptors
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批准号:7299563
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项目类别:
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资助金额:$28.29万
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财政年份:2007
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负责人:Joseph W Thornton
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依托单位:
Experimental evolution of ligand-receptor relationships
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批准号:6888308
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项目类别:
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资助金额:$11.18万
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财政年份:2004
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负责人:Joseph W Thornton
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依托单位:
Experimental evolution of ligand-receptor relationships
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批准号:6767434
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项目类别:
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资助金额:$14.15万
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财政年份:2004
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负责人:Joseph W Thornton
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依托单位:
海外基金