Structural Basis of Eukaryotic Replication Initiation by Cryo-EM
Structural Basis of Eukaryotic Replication Initiation by Cryo-EM
批准号:
8958866
负责人:
Huilin Li
金额:
$31.21万
依托单位国家:
美国
项目类别:
财政年份:
2015
资助国家:
美国
项目状态:
已结题
起止时间:
2015-08-01 至 2019-03-31
关键词:
ArchitectureBindingBiological ModelsBiologyCell CycleCell ProliferationCellsChromatin StructureCollaborationsComplexComputer softwareCrystallographyDNADNA BindingDNA biosynthesisDNA replication forkDNA replication originDiseaseElectronsEnsureEukaryotaEventFailureGenerationsGenomeGoalsHumanInterruptionKnowledgeLaboratoriesLeadLearningLicensing FactorMCM2 geneMalignant NeoplasmsMapsMedical ResearchMolecularMolecular BiologyMolecular ConformationPeptidesPre-Replication ComplexProcessProteinsPublishingRecruitment ActivityReplication InitiationReplication LicensingReplication OriginReportingResolutionRoentgen RaysS PhaseSeriesStructureSystemTestingTherapeutic InterventionTitanUniversitiesWorkX-Ray CrystallographyYeastsbasechromosome replicationdetectords-DNAflexibilityhelicaseimprovedmanmeltingmutantorigin recognition complexprotein complexpublic health relevanceskillssmall moleculetumortumorigenesis
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Initiation of the eukaryotic chromosome replication is a tightly regulated multi-step process. Failure to ensure once and once only initiation event per cell division cycle can result in uncontrolled cell proliferation and tumorigenesis. Central to the
replication initiation is the origin recognition complex (ORC) that recognizes the chromosomal origins of replication. With the help of replication initiator Cdc6 and replication licensing facto Cdt1, ORC recruits and loads the Mcm2-7 helicase onto DNA, forming a highly stable Mcm2-7 double hexamer. This completes the first milestone - formation of pre-replication complex (pre-RC). A series of subsequent events culminate to formation of pre-initiation complex (pre-IC) and leading cell to enter into the S phase. X-ray crystal structures have been reported for key proteins involved in prokaryotic replication initiation, but little is known about the structures o the corresponding eukaryotic complexes. This is so because the eukaryotic replication initiators assemble into large and transient complexes, which have been exceedingly difficult for crystallography. Recent advance in hardware and software has made cryo-EM an ideal approach to studying these complexes at much improved resolution. We therefore propose to study how the pre- Replication Complex is established by cryo-EM. This work will advance our knowledge in the initiation of eukaryotic chromosome replication.
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