DYNAMICS AND FUNCTION OF G4 DNA
DYNAMICS AND FUNCTION OF G4 DNA
批准号:
7264548
负责人:
Nancy Maizels
金额:
$27.66万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2002
资助国家:
美国
项目状态:
已结题
起止时间:
2002-08-01 至 2009-07-31
关键词:
AffectAmino AcidsBindingBiogenesisCell physiologyCellsCollaborationsDNADNA BindingDevelopmentEnzymesFamilyGenetic PolymorphismGenetic TranscriptionGenomic InstabilityGenomicsGuanineHereditary DiseaseHumanHuman GenomeIn VitroLaboratoriesLifeMaintenanceMalignant NeoplasmsMapsMinisatellite RepeatsMismatch RepairMonitorMutationPathway interactionsPlasmidsRecombinant DNARecruitment ActivityReporterRibosomal DNARibosomal RNASiteSpecific qualifier valueStructureTestingWRN geneYeastsc-Myc Staining Methodc-myc Geneshelicasehuman diseasein vivomutantrepairedresearch studytumor
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): G-rich DNA can form structures stabilized by interactions between guanines, referred to as G4 DNA. These structures have been widely studied in vitro, but until recently had not been shown to form in vivo. My laboratory has very recently directly identified G4 DNA formed in vivo. Building upon and extending this result, we now propose to study in detail how G4 DNA forms, how it is eliminated from living cells, and whether G4 DNA contributes to genomic instability. To that end we will pursue the following specific aims: (1) We will ask if G4 DNA forms at two G-rich genes, c-myc and the rDNA repeats; (2) we will ask whether G4 DNA formation contributes to genomic instability in yeast; (3) we will study instability of G-rich repeats in human cells, and the functions of BLM helicase in their maintenance; (4) we will identify the conserved motif(s) within RecQ family helicases that specify G4 DNA interaction, and create the corresponding mutants to study functions of enzymes in this family in vivo;, and (5) we will ask how mismatch repair factors participate in elimination of G4 DNA. Results from experiments in this proposal will extend our understanding of G4 DNA formation in living cells, characterize pathways that promote its elimination, and establish its contribution to genomic instability that leads to genetic disease and development of malignancy.
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