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MECHANISMS OF MUTAGENESIS BY CHEMICAL CARCINOGENS

MECHANISMS OF MUTAGENESIS BY CHEMICAL CARCINOGENS
化学致癌物的诱变机制
批准号:
3175791
负责人:
PATRICIA LORRAINE FOSTER
金额:
$14.7万
依托单位国家:
美国
项目类别:
财政年份:
1984
资助国家:
美国
项目状态:
已结题
起止时间:
1984-07-01 至 1994-04-30

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中文摘要
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英文摘要
That a single mutation can change a normal gene into its oncogenic derivative demonstrates the potential importance of mutagenic processes in the etiology of cancer. Thus, understanding how a carcinogen induces mutations may elucidate the basis of its carcinogenicity. The goal of this project is to determine how chemical carcinogens cause mutations, using bacteria as a model system. The research focuses on the mechanisms of mutagenesis of a few environmentally or medically significant genotoxic agents that cause representative classes of DNA damage. Genetic and biochemical methods are used to determine what DNA lesions are induced, how they may be repaired, which give rise to mutations, what cellular functions participate in the mutagenic process, and what mutations result. The specific aims are: 1. To investigate the mechanism of mutagenesis of aflatoxin Bl, which makes bulky lesions to DNA. The effects of defects in bacterial functions affecting both the accurate and mutagenic repair of aflatoxin-induced DNA lesions will be characterized. The mutagenic potential of defined DNA lesions generated in vitro by a direct-acting aflatoxin analog will be determined. 2. To identify the major mutagenic lesions induced by halogenated hydrocarbons. The miscoding lesions demonstrated to be induced by 1,2-dibromoethane will be identified biochemically. Pathways for the repair of these lesions and their induction by other halogenated hydrocarbons will be examined 3. To investigate the mutagenic and toxic potential of the DNA lesions ' induced by the chemotherapeutic agent, cis- diamminedichloroplatinum II. The contribution of repair intermediates to the toxicity and mutagenicity of this agent will be determined.
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UV mutagenesis in Salmonella typhimurium is umuDC dependent despite the presence of samAB.
尽管存在 samAB,鼠伤寒沙门氏菌的紫外线诱变仍依赖于umuDC。
DOI: 10.1128/jb.174.9.2809-2815.1992
发表时间: 1992
期刊: Journal of bacteriology
影响因子: 3.2
作者: [Koch,WH, Cebula,TA, Foster,PL, Eisenstadt,E]
通讯作者: Eisenstadt,E
Sequence analysis and mapping of the Salmonella typhimurium LT2 umuDC operon.
鼠伤寒沙门氏菌 LT2umuDC 操纵子的序列分析和作图。
DOI: 10.1128/jb.172.9.4964-4978.1990
发表时间: 1990
期刊: Journal of bacteriology
影响因子: 3.2
作者: [Smith,CM, Koch,WH, Franklin,SB, Foster,PL, Cebula,TA, Eisenstadt,E]
通讯作者: Eisenstadt,E
Random components in mutagenesis.
诱变中的随机成分。
DOI: 10.1038/299365a0
发表时间: 1982
期刊: Nature
影响因子: 64.8
作者: [Foster,PL, Eisenstadt,E, Cairns,J]
通讯作者: Cairns,J
Loss of an apurinic/apyrimidinic site endonuclease increases the mutagenicity of N-methyl-N'-nitro-N-nitrosoguanidine to Escherichia coli.
无嘌呤/无嘧啶位点核酸内切酶的缺失会增加 N-甲基-N-硝基-N-亚硝基胍对大肠杆菌的致突变性。
DOI: 10.1073/pnas.84.9.2891
发表时间: 1987
期刊: Proceedings of the National Academy of Sciences of the United States of America
影响因子: 11.1
作者: [Foster,PL, Davis,EF]
通讯作者: Davis,EF
9
    Regulation of an Error-Prone Polymerase
    • 批准号:
      8126390
    • 项目类别:
    • 资助金额:
      $25.09万
    • 财政年份:
      2002
    • 负责人:
      PATRICIA LORRAINE FOSTER
    • 依托单位:
    Regulation of an Error-Prone Polymerase
    • 批准号:
      7664335
    • 项目类别:
    • 资助金额:
      $25.68万
    • 财政年份:
      2002
    • 负责人:
      PATRICIA LORRAINE FOSTER
    • 依托单位:
    Regulation of an Error-Prone Polymerase
    • 批准号:
      7320157
    • 项目类别:
    • 资助金额:
      $25.72万
    • 财政年份:
      2002
    • 负责人:
      PATRICIA LORRAINE FOSTER
    • 依托单位:
    Regulation of an Error-Prone Polymerase
    • 批准号:
      6622874
    • 项目类别:
    • 资助金额:
      $21.1万
    • 财政年份:
      2002
    • 负责人:
      PATRICIA LORRAINE FOSTER
    • 依托单位:
    海外基金