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Novel Mechanism & Developmental Roles of Repair・Recombination

Novel Mechanism & Developmental Roles of Repair・Recombination
修复重组的新机制和发展作用
批准号:
07044227
负责人:
ENOMOTO Takemi
金额:
$4.54万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for international Scientific Research
财政年份:
1995
资助国家:
日本
项目状态:
已结题
起止时间:
1995 至 1996

项目摘要

项目成果

ENOMOTO Takemi的其他基金

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中文摘要
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英文摘要
DNA helicase Q1 is a human homologue of the Escherichia coli DNA helicase RecQ,which we found in human cells. The existence of a RecQ homologue in human cells indicated that eukaryotic cells had a DNA repair-recombination system involving eukaryotic RecQ.In this study, we intended to clarify functions of eukaryoric RecQ in the novel DNA repair-recombination system and in the process of development using yeast, mouse, and fly.1 Analysis of the function of yeast RecQ (Sgs1) with SGS1 gene disruptantsWe cloned a yeast RecQ gene by using human DNA helicase Q1 cDNA as a probe and found that the cloned gene was identical to SGS1 which was cloned as a suppresser of the slow growth phenotype of topoisomerase III mutants of Saccharomyces cerevisiae. We analyzed the sensitivity of SGS1 gene disruptants to various genotoxic agents. Disruptants showed higher sensitivity to alkylating agents such as methy methanesulfonate and ethyl methanesulfonate (MMS) and hydroxyurea (HU) as compared with wild-t … More ype cells. When homozygous SGS1 disruptants were transferred to sporulation medium, poor sporulation and a reduced frequency of meiotic recombination were observed. In addition, the induction of expression of SGS1 mRNA was observed when wild-type cells were treated with MMS or transferred to sporulation medium to induce meiosis. These results indicates that Sgs1 is involved in the repair of some type of DNA lesions and meiotic DNA recombination.2 cDNA cloning of mouse DNA helicase Q1 and analysis of expression of Q1 mRNAWe cloned a cDNA encoding mouse DNA helicase Q1 and examined expression of Q1 message in various mouse tissues. The mRNA was expressed in the highest level in testis, a higher level in thymus and was poorly expressed in brain, heart, kidney, liver, lung, muscle, ovary, and spleen. When the expression of Q1 mRNA in testis was monitored after birth, an increase in the level of the mRNA was observed 14th day after birth when cells in zygotene and pachytene increased, in which DNA recombination took place.3 cDNA cloning of Dorosophila DNA helicase Q1We have succeeded to isolate a Dorosophila DNA helicase Q1 cDNA.However, the analysis of roles of Q1 during development by making transgenic flies has remained for future study. Less
期刊论文(18)
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会议论文
Ken Matsumoto: "Stimulation of DNA synthesis by mouse DNA helicase B in a DNA replication system containing eukaryotic replication origins." Biochemistry. 34. 7913-7922 (1995)
Ken Matsumoto:“在含有真核复制起点的 DNA 复制系统中,小鼠 DNA 解旋酶 B 刺激 DNA 合成。”
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12
    Analyses of function of RecQ helicase and its related proteins and detection of endogenous DNA damaging agents
    • 批准号:
      26440065
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $3.0万
    • 财政年份:
      2014
    • 负责人:
      ENOMOTO Takemi
    • 依托单位:
    Functions of RECQL1 and RECQL5 in the maintenance of genome stability
    • 批准号:
      23370065
    • 项目类别:
      Grant-in-Aid for Scientific Research (B)
    • 资助金额:
      $12.73万
    • 财政年份:
      2011
    • 负责人:
      ENOMOTO Takemi
    • 依托单位:
    Study on the functions of WRN and WRNIP1 that interacts with WRN
    • 批准号:
      20390020
    • 项目类别:
      Grant-in-Aid for Scientific Research (B)
    • 资助金额:
      $12.48万
    • 财政年份:
      2008
    • 负责人:
      ENOMOTO Takemi
    • 依托单位:
    Studies on the function of Werner syndrome gene product and analyses of the mechanism to induce aging related symptoms
    • 批准号:
      18390019
    • 项目类别:
      Grant-in-Aid for Scientific Research (B)
    • 资助金额:
      $10.7万
    • 财政年份:
      2006
    • 负责人:
      ENOMOTO Takemi
    • 依托单位: