Mammalian Replication fork stalling
Mammalian Replication fork stalling
批准号:
7994856
负责人:
Ralph Scully
金额:
$18.35万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-12-01 至 2012-11-30
关键词:
AddressAreaBLM geneBRCA1 geneBRCA2 geneBloom SyndromeCell CycleChromosomal BreaksChromosome BreakageChromosomesControlled StudyDNADNA DamageDNA Restriction EnzymesDNA biosynthesisDNA-Directed DNA PolymeraseDaughterDouble Strand Break RepairEndonuclease IEngineeringEnzymesEventFanconi&aposs AnemiaG2 PhaseGenesGenetic RecombinationGenomic InstabilityGoalsHealthHereditary Breast and Ovarian Cancer SyndromeHumanInheritedIonizing radiationLesionLifeMalignant NeoplasmsMammalian CellMeasuresModelingNBS1 geneNonhomologous DNA End JoiningPathway interactionsPredispositionPremature aging syndromeProcessProteinsReporterS PhaseSignal TransductionSingle-Stranded DNASister ChromatidSiteSourceSusceptibility GeneSystemTestingTumor Suppressor ProteinsWorkendodeoxyribonuclease SceIhomologous recombinationinnovationinterestmutantnovelnovel strategiespreventrepairedresponsetool
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The aim of this proposal is to develop novel tools for studying the relationship between stalled or broken replication forks and sister chromatid recombination in mammalian cells. Although current models propose that recombination at sites of stalled DNA synthesis is critical for preventing genomic instability and cancer, the ability to model this process in mammalian cells is severely limited, due to the absence of recombination reporters that can accurately model this process in a quantitative and mechanistic fashion. Work proposed herein will provide such tools, by combining "state-of-the-art" mammalian reporters of homologous recombination and sister chromatid recombination with novel strategies to cause site-specific replication fork stalling. This work will provide a much needed new tool to study this area of critical importance for human cancer predisposition. Our specific aims are: 1. Adapt a known replication fork barrier for the induction of site-specific HR in mammalian cells. 2. Study HR and SCR at a replication fork barrier in mammalian cells. 3. Develop "nickase" mutants of I-SceI to stimulate HR and SCR at a chromosomal I-SceI site in mammalian cells.
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会议论文
Stalled replication fork repair in cancer predisposition and cancertherapy
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批准号:10517824
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资助金额:$102.2万
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财政年份:2022
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负责人:Ralph Scully
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Stalled replication fork repair in cancer predisposition and cancertherapy
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批准号:10681456
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批准号:10317904
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The DNA damage response of fast-cycling erythroblasts
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资助金额:$58.12万
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财政年份:2021
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依托单位:
The DNA damage response of fast-cycling erythroblasts
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批准号:10674034
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资助金额:$58.12万
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财政年份:2021
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依托单位:
Regulation of stalled fork repair in mammalian cells
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批准号:10434669
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项目类别:
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资助金额:$35.0万
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财政年份:2019
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负责人:Ralph Scully
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依托单位:
Regulation of stalled fork repair in mammalian cells
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批准号:10187598
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资助金额:$35.0万
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Regulation of stalled fork repair in mammalian cells
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批准号:10006891
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资助金额:$35.0万
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财政年份:2019
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依托单位:
FANCM in repair of stalled replication forks
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批准号:9363243
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财政年份:2017
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依托单位:
FANCM in repair of stalled replication forks
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批准号:9924478
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项目类别:
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资助金额:$39.57万
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财政年份:2017
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负责人:Ralph Scully
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依托单位:
A mouse model for studying homologous recombination fidelity during aging
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批准号:8989960
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项目类别:
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资助金额:$21.75万
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财政年份:2015
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依托单位:
Analysis of recombination in vivo
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批准号:8100517
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项目类别:
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资助金额:$18.35万
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财政年份:2010
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负责人:Ralph Scully
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依托单位:
Analysis of recombination in vivo
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批准号:7991129
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资助金额:$22.69万
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财政年份:2010
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依托单位:
Targeting non-homologous end joining in cancer therapy
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批准号:7825831
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项目类别:
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资助金额:$50.26万
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财政年份:2009
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依托单位:
Targeting non-homologous end joining in cancer therapy
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批准号:7944189
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资助金额:$49.74万
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财政年份:2009
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负责人:Ralph Scully
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依托单位:
Mammalian Replication fork stalling
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批准号:7772718
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项目类别:
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资助金额:$22.65万
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财政年份:2009
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依托单位:
ROLE OF HISTONE H2AX IN DOUBLE STRAND BREAK REPAIR
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The chromatin response in mammalian double strand break repair
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批准号:8720011
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财政年份:2005
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The chromatin response in mammalian double strand break repair
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批准号:8294525
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项目类别:
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资助金额:$32.73万
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财政年份:2005
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依托单位:
ROLE OF HISTONE H2AX IN DOUBLE STRAND BREAK REPAIR
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项目类别:
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资助金额:$29.13万
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财政年份:2005
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