Functional Determinants of Chromosome Segregation
Functional Determinants of Chromosome Segregation
批准号:
8235734
负责人:
Philip A. Hieter
金额:
$22.41万
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-03-01 至 2012-12-31
关键词:
AllelesAnimal ModelApplications GrantsApplied GeneticsBiochemicalBiologyCandidate Disease GeneCatalogingCatalogsCell physiologyCellsChromosomal InstabilityChromosome SegregationChromosomesComplexDNA DamageDefectDrug Delivery SystemsEssential GenesEventExhibitsGenesGeneticGenomeGenomic InstabilityGoalsHumanKnowledgeLengthMalignant NeoplasmsMammalian CellMammalsMetabolismMethodologyMethodsMitotic ChromosomeModelingMolecularMutateMutationOrganismPathway interactionsPhenotypePredispositionPrincipal InvestigatorProcessRNARNA InterferenceRNA ProcessingRNA SplicingResourcesRoleSaccharomycetalesScreening procedureSignal TransductionSomatic MutationTelomere ShorteningTestingTherapeuticWorkYeastsabstractingbasecancer cellcancer initiationcancer therapychromatin immunoprecipitationinsightmRNA Cleavage and Polyadenylation Factorsmutantprogramsprotein complexresearch studyresponsetelomeretransmission processtumortumor progressiontumorigenesisyeast genetics
中文摘要
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英文摘要
DESCRIPTION (provided by applicant):
PROJECT SUMMARY/ABSTRACT Mutations that cause chromosome instability (CIN) are considered important predisposing events that contribute to the initiation and/or progression of cancer. Our approach is to develop and apply genetic and biochemical methodologies to obtain an understanding of molecular components required for chromosome transmission, with the overarching goal of relating our work in yeast to human cancer. The specific aims are: 1. To characterize essential CIN genes/pathways: shortened telomere CIN genes and the ASTRA complex. We will dissect the function of the ASTRA complex and its role in telomere biology and TORC1 signaling. 2. To characterize the roles of DNA damage and RNA processing in genome integrity. Five subunits of the mRNA cleavage and polyadenylation factor (CPF) exhibit CIN and high rates of spontaneous Rad52-foci while splicing factors show wild-type levels of damage. We will characterize the mechanism by which the CPF complex and other RNA processing factors cause DNA damage and/or CIN. 3. To validate candidate somatic mutations in CIN genes involved in telomere biology and RNA metabolism, and assess sensitization of cells to knockdown of candidate synthetic lethal partners. We will evaluate methods in yeast to determine whether specific mis-sense somatic mutations found in tumors are "functional" and test synthetic lethal interactions predicted from yeast genetic interaction networks for evolutionary conservation in cultured mammalian cells. Further elucidation of the genetic basis of CIN in yeast will provide a mechanistic basis for understanding this process in human cells, and will provide candidate genes for those CIN genes mutated in cancer. Therefore, knowledge gained from this work will provide insight into tumorigensis. PHS 398/2590 (Rev. 06/09) Page Continuation Format Page
PUBLIC HEALTH RELEVANCE:
Program Director/Principal Investigator (Last, First, Middle): Hieter, Philip A. PROJECT NARRATIVE We will be further defining the functions and mutational spectrum of genes that cause chromosome instability (CIN) in cancer using yeast as a model. By definition, mutations that cause CIN in cancer cells produce "sub- lethal" deficiencies in an essential cellular process (chromosome segregation) and therefore may represent a major untapped resource that could be exploited for therapeutic benefit in the treatment of cancer. PHS 398/2590 (Rev. 06/09) Page Continuation Format Page
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Functional Determinants of Chromosome Segregation
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批准号:8594232
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项目类别:
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资助金额:$21.74万
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财政年份:2012
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负责人:Philip A. Hieter
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依托单位:
Functional Determinants of Chromosome Segregation
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批准号:8784057
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项目类别:
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资助金额:$22.41万
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财政年份:2012
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负责人:Philip A. Hieter
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依托单位:
Functional Determinants of Chromosome Segregation
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批准号:8434750
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项目类别:
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资助金额:$21.07万
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财政年份:2012
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负责人:Philip A. Hieter
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依托单位:
CHARACTERIZATION OF ESSENTIAL PROTEINS INVOLVED IN CHROMOSOME SEGREGATION
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批准号:7957797
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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:Philip A. Hieter
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依托单位:
CHARACTERIZATION OF THE PHYSICAL AND GENETIC INTERACTIONS OF CTF4
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批准号:7723758
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项目类别:
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资助金额:$0.73万
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财政年份:2008
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负责人:Philip A. Hieter
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依托单位:
CHARACTERIZATION OF ESSENTIAL PROTEINS INVOLVED IN CHROMOSOME SEGREGATION
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批准号:7723753
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项目类别:
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资助金额:$0.67万
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财政年份:2008
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负责人:Philip A. Hieter
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依托单位:
IDENTIFICATION OF POTENTIAL NDC10 INTERACTING PROTEINS BY TWO-HYBRID
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批准号:7602236
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项目类别:
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资助金额:$1.04万
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财政年份:2007
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负责人:Philip A. Hieter
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依托单位:
STRUCUTRAL PREDICTION OF THE YEAST KINETOCHORE PROTEIN NDC10
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批准号:7420746
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项目类别:
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资助金额:$0.83万
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财政年份:2006
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负责人:Philip A. Hieter
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依托单位:
FUNCTIONAL DETERMINANTS OF CHROMOSOME SEGREGATION IN YEAST
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批准号:7049162
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项目类别:
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资助金额:$18.84万
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财政年份:2005
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负责人:Philip A. Hieter
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依托单位:
IDENTIFICATION OF PROTEINS INTERACTING WITH MMS22P, RTT101P AND RTT107P
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批准号:7182337
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项目类别:
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资助金额:$0.66万
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财政年份:2005
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负责人:Philip A. Hieter
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依托单位:
GENOMIC Y2H SCREEN OF CTF18, CTF8 AND DCC1
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批准号:7182395
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项目类别:
-
资助金额:$0.66万
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财政年份:2005
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负责人:Philip A. Hieter
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依托单位:
IDENTIFICATION OF APC/C SUBSTRATES
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批准号:6979545
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项目类别:
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资助金额:$2.27万
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财政年份:2004
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负责人:Philip A. Hieter
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依托单位:
RAD61P ROLE IN CHROMOSOME SEGREGATION
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批准号:6979652
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项目类别:
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资助金额:$0.34万
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财政年份:2004
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负责人:Philip A. Hieter
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依托单位:
IDENTIFICATION OF THE RFC (CTF8) COMPLEX
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批准号:6979542
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项目类别:
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资助金额:$0.41万
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财政年份:2004
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负责人:Philip A. Hieter
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依托单位:
IDENTIFICATION OF POTENTIAL NDC10 INTERACTING PROTEINS
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批准号:6979562
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项目类别:
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资助金额:$0.34万
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财政年份:2004
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负责人:Philip A. Hieter
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依托单位:
LOCALIZATION OF SELECTED BUDDING YEAST APC/C SUBUNITS
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批准号:6979568
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项目类别:
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资助金额:$1.02万
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财政年份:2004
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负责人:Philip A. Hieter
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依托单位:
IDENTIFICATION OF APC/C SUBSTRATES
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批准号:6979629
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项目类别:
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资助金额:$0.41万
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财政年份:2004
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负责人:Philip A. Hieter
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依托单位:
FUNCTIONAL DETERMINANTS OF CHROMOSOME SEGREGATION
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批准号:6101792
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项目类别:
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资助金额:$32.18万
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财政年份:1999
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负责人:Philip A. Hieter
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依托单位:
FUNCTIONAL DETERMINANTS OF CHROMOSOME SEGREGATION
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批准号:6268917
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项目类别:
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资助金额:$30.95万
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财政年份:1998
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负责人:Philip A. Hieter
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依托单位:
APPROACHES IN YEAST TO STUDY OF ANEUPLOIDY
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批准号:6108514
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项目类别:
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资助金额:$0.0万
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财政年份:1998
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负责人:Philip A. Hieter
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依托单位:
海外基金