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Abstract Pol-? catalyzes replication of the genome and other DNA synthetic processes in human cells. However, the precise functions of Pol-? in replication, in repair of endogenous and environmental damage, and in recombination remain to be defined. Further, we lack information on the role of somatic mutations in Pol-? in tumorigenesis and other disease processes. Our goals are to identify the functions of Pol-? in DNA synthesis and the possible role of increased mutation by Pol-? in the generation of human cancer. A major approach will be to exploit mutants of Pol-? that incorporate mutagenic nucleotide analogs and thereby serve as tools to identify DNA synthesized by Pol-? in vivo. We have four specific aims. In Aim 1, we will generate mutants of Pol-? that increase incorporation of a specific nucleotide analog(s). In Aim 2, we will purify wild-type and mutant Pol-? holoenzyme complexes and characterize their catalytic properties in detail, including their fidelity and kinetics of analog incorporation. In Aim 3, we will define the roles of Pol-? in mammalian cells by introducing mutant Pol-?'s that preferentially incorporate mutagenic nucleotide analogs and measuring induced mutation in cells undergoing DNA replication, repair and recombination. The induced mutations will identify the DNA synthesized by Pol-?. In Aim 4, we will assess the role of increased mutagenesis in tumor progression by performing serial transfer experiments to determine if mammalian cells that harbor mutator Pol-? have a competitive advantage, and if there are nucleoside analogs that diminish this advantage. Narrative Our objective is to establish the roles of DNA polymerase-? in replication of the human genome and in repair of damage caused by endogenous and environmental agents. We will determine if mutations in DNA polymerase-? promote genetic instability and accelerate tumor progression in model systems. We aim to identify a new class of chemotherapeutic agents that will retard tumor growth.
期刊论文(8)
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会议论文
DOI: 10.1016/j.semcancer.2010.10.005
发表时间: 2010-10
期刊: Seminars in cancer biology
影响因子: 14.5
作者: [Fox EJ, Loeb LA]
通讯作者: Loeb LA
DOI: 10.1146/annurev-pathol-121808-102113
发表时间: 2010
期刊: Annual review of pathology
影响因子: --
作者: [Salk JJ, Fox EJ, Loeb LA]
通讯作者: Loeb LA
The biochemistry and fidelity of synthesis by the apicoplast genome replication DNA polymerase Pfprex from the malaria parasite Plasmodium falciparum.
来自疟原虫疟原虫疟原虫的生物化学基因组复制DNA聚合酶PfPREX的合成生物化学和忠诚度。
DOI: 10.1016/j.jmb.2011.04.071
发表时间: 2011-07-01
期刊: Journal of molecular biology
影响因子: 5.6
作者: [Kennedy SR, Chen CY, Schmitt MW, Bower CN, Loeb LA]
通讯作者: Loeb LA
DOI: 10.1016/j.sbi.2009.10.008
发表时间: 2009-12
期刊: CURRENT OPINION IN STRUCTURAL BIOLOGY
影响因子: 6.8
作者: [Erie, Dorothy A., Kennedy, Scott R.]
通讯作者: Kennedy, Scott R.
6
    Mutator Phenotype in Colon Cancer
    • 批准号:
      9208748
    • 项目类别:
    • 资助金额:
      $35.53万
    • 财政年份:
      2016
    • 负责人:
      LAWRENCE A LOEB
    • 依托单位:
    Mutator Phenotype in Colon Cancer
    • 批准号:
      9390042
    • 项目类别:
    • 资助金额:
      $35.53万
    • 财政年份:
      2016
    • 负责人:
      LAWRENCE A LOEB
    • 依托单位:
    Validation and Advanced Development of Duplex Sequencing
    • 批准号:
      8735349
    • 项目类别:
    • 资助金额:
      $38.49万
    • 财政年份:
      2014
    • 负责人:
      LAWRENCE A LOEB
    • 依托单位:
    Biochemistry
    • 批准号:
      8277942
    • 项目类别:
    • 资助金额:
      $31.08万
    • 财政年份:
      2011
    • 负责人:
      LAWRENCE A LOEB
    • 依托单位:
    海外基金