| Project/Area Number |
60304097
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| Research Category |
Grant-in-Aid for Co-operative Research (A)
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| Allocation Type | Single-year Grants |
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| Research Field |
分子遺伝学・分子生理学
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| Research Institution | Nagoya University |
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Principal Investigator |
OKAZAKI Tuneko Nagoya University, 理学部, 教授 (10022584)
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| Co-Investigator(Kenkyū-buntansha) |
ARIGA Hiroshi University of Tokyo, 医科学研究所, 助手 (20143505)
SENO Takeshi Saitama Cancer Center, 研究所, 部長 (30076989)
YAMAGUCHI Kazuo Kanazawa University, 遺伝子実験施設, 助教授 (00019879)
HIRAGA Sota Kumamoto University, 医学部, 教授 (40027321)
YOSHIKAWA Hirose Osaka University, 医学部, 教授 (70019876)
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| Project Period (FY) |
1985 – 1987
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| Project Status |
Completed (Fiscal Year 1987)
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| Budget Amount *help |
¥17,300,000 (Direct Cost: ¥17,300,000)
Fiscal Year 1987: ¥1,700,000 (Direct Cost: ¥1,700,000)
Fiscal Year 1986: ¥6,900,000 (Direct Cost: ¥6,900,000)
Fiscal Year 1985: ¥8,700,000 (Direct Cost: ¥8,700,000)
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| Keywords | initiator protein / origin sequence / RAN-DNA transition site / autoregulation / transcription / ARS / 複製開始機構 / Rep蛋白 / ori DNA |
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| Research Abstract |
Mechanism of initiation of DNA replication of various genomes has been studid co-operatively by many investigators. Regulation of the initiation of plasmid DNA replication has been analyzed in emphasis on the interaction between initiator proteins and target DNA sequence at the origin region of each plasmid. Plasmids R6K, F, pSC101, Co1E1, Co1E2, Co1E3, dv and E. coli oriC plasmid have been investigated. Transcription regulation in E. coli oriC has been analyzed in vivo and in vitro. Gene organization of B. subtilis replication origin has been analyzed and high similarities to E. coli genome have been revealed. Priming sites (transition sites from primer RNA to DNA) at replication origins of various genomes have been determined. fermination loci of DNA replication of R6K and E. coli genome have been cloned. Structure and function of the F plasmid genes essential for partitioning has been clarified. Autonomously replicating sequences have been cloned from mammalian cells and possible function of c-myc product in promotion of initiation of replication has been shown. The structure of thymidylate synthase gene has been determined and transcription regulation has been studied. Reverse transcriptase encoded by cauliflower mosaic virus (CaMV) genome has been investigated and involvement of RNA as an intermediate of CaMV DNA replication has been shown.
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