| Project/Area Number |
03044096
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| Research Category |
Grant-in-Aid for international Scientific Research
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| Allocation Type | Single-year Grants |
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| Section | Joint Research |
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| Research Institution | Nara Institute of Science and Technology (1993)
Osaka University (1991-1992) |
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Principal Investigator |
YOSHIKAWA Hiroshi Nara Institute of Science and Technology, Professor, バイオサイエンス研究科, 教授 (70019876)
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| Co-Investigator(Kenkyū-buntansha) |
ALONSO Juan C. National Institute of Biotechnology, Professor
MESSER Walter Max-Planck Institute of Genetics, Professor, 分子生物部, 教授
ATLUNG Tove Technical University of Denmark, Associate Professor, 微生物学部, 助教授
RASUMUSSEN K デンマーク工科大学, 微生物学部, 教授
HANSEN Flemm デンマーク工科大学, 微生物学部, 教授
MORIYA Shigeki Osaka University Medical School, Assistant, 医学部, 助手 (40191051)
OGASAWARA Naotake Nara Institute of Science and Technology, Professor, バイオサイエンス研究科, 教授 (10110553)
HANSEN Flemming G. Technical University of Denmark, Professor
RASMUSSEN Knud V. Technical University of Denmark, Professor
FIRSHEIN Wil ウエスリアン大学, 分子生物学部, 教授
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| Project Period (FY) |
1991 – 1993
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| Project Status |
Completed (Fiscal Year 1993)
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| Budget Amount *help |
¥15,000,000 (Direct Cost: ¥15,000,000)
Fiscal Year 1993: ¥5,000,000 (Direct Cost: ¥5,000,000)
Fiscal Year 1992: ¥5,000,000 (Direct Cost: ¥5,000,000)
Fiscal Year 1991: ¥5,000,000 (Direct Cost: ¥5,000,000)
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| Keywords | chromosomal replication / Bacillus subtilis / Escherichia coli / dnaA gene / oriC plasmid |
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| Research Abstract |
We have found that dnaA gene and its binding sequences(DnaA-box)are conserved in the replication origin region of the chromosome among various bacteria. The aim of this international joint research was to analyze the functional conservation and diversity of DnaA protein and DnaA-boxes through comparative studies of their roles in Bacillus subtilis and Escherichia coli. In collaboration with Dr.Hansen and Dr.Atlung(Technical University of Denmark, Denmark), we have succeeded to isolate an autonomously replicating sequence from the replication origin region of the B.subtilis chromosome. The minimum essential fragment contained two DnaA-box regions separated by the dnaA gene. Requirements of two regions for ARS and the low copy number of the oriC plasmids are in sharp contrast to features exhibited by E. coli oriC. Further studies of replication of the B.subtilis oriC plasmids in vitro, in collaboration with Dr.Firshein (Wesleyan University, USA)and Dr.Messer(Max-Planck Institute, Berlin), revealed the interaction of the two DnaA-box regions through interaction between DnaA proteins bound to them. In collaboration with Dr.Rasmussen(Technical University of Denmark, Denmark), we have analyzed cell cycle control of B.subtilis cells and found that timing of initiation of chromosomal replication is strictly regulated like in E.coli cells. DnaA and DnaB proteins of B.subtilis were found to be responsible for the control. In collaboration with Dr.Alonso(Max-Planck Institute, Berlin), construction of a new B. subtilis mutant cell, in which chromosomal replication is independent of the dnaA gene, is now underway in order to analyze the precise role of DnaA protein in regulation of initiation in vivo.
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