Mechanistic insights into the SHU complex and Sgs1 in DNA repair and replication
Mechanistic insights into the SHU complex and Sgs1 in DNA repair and replication
批准号:
8426203
负责人:
Kara A Bernstein
金额:
$0.41万
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:
2009-08-01 至 2014-06-30
关键词:
AddressAllelesBiologicalCell physiologyCellsChromatin StructureComplexDNADNA DamageDNA RepairDNA Sequence RearrangementDNA biosynthesisDefectDependencyDiseaseFellowshipGene MutationGeneticGenetic RecombinationGoalsHumanInstitutionInstructionLaboratoriesMalignant NeoplasmsMediatingMicroscopyMolecularMutateMutationPathway interactionsPhasePhenotypePredispositionProtein AnalysisProteinsRecombinant DNAReplication ErrorResearchRoleRothmund-Thomson syndromeTrainingbasecareerhomologous recombinationhuman diseaseinsightnovelpreventprofessorrepairedresearch studyskillstumorigenesis
中文摘要
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英文摘要
Repair of DNA damage is crucial to prevent accumulation of mutations that can cause human disease, such
as cancer. Many proteins are important for DNA repair including Sgsl, a protein that when mutated in
human cells leads to many devesting diseases (i.e. Bloom, Werner, Rothmund-Thomson syndromes), which
are all fundamentally characterized by cancer predisposition. Sgsl genetically interacts with a group of
proteins collectively called the SHU complex. Although Sgsl has been extensively analyzed, the molecular
mechanism of how it functions to repair DNA damage and its relationship to the SHU complex has remained
elusive, largely because its deletion leads to many pleiotropic phenotypes. During the K99 phase of this
proposal, I will utilize a separation-of-function allele of Sgsl that delineates its role during DNA repair from
DNA replication. My preliminary results suggest that an alternative pathway is used to repair DNA replication
errors that is distinct from the homologous recombination machinery. The experiments proposed here will
use genetic and cell biological approaches to characterize the proteins involved in this novel pathway and
determine how utilization of this pathway is differentially regulated. The second part of the K99 phase will
use flourescent microscopy to place the Sgs1/Top3/Rmi1 proteins in the order of protein assembly utilized
during DNA repair and determine if the genetic requirements for Sgsl foci formation differ depending upon
the type of DNA damage. During the ROO phase, I will focus on the SHU complex and first analyze the role
of one SHU component, Shul, in rDNA repair and rDNA chromatin structure. My second aim will elucidate
the mechanistic role of the SHU complex during DNA repair and replication through its physical interaction
with Srs2. Finally, I will determine if the SHU proteins have unique cellular functions despite forming a
complex and address the significance of complex formation. The training that I receive during the K99
portion of the fellowship will enable me to develop the skills necessary to begin my own laboratory where my
ultimate career goal is to be a tenured professor at a research institution.
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