| Project/Area Number |
06556002
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| Research Category |
Grant-in-Aid for Scientific Research (A)
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| Allocation Type | Single-year Grants |
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| Section | 試験 |
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| Research Field |
Breeding science
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| Research Institution | The University of Tokyo |
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Principal Investigator |
HIRAI Atsushi Graduate School of Agricultural and Life Science Profeesor, 大学院・農学生命科学研究科, 教授 (60023470)
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| Co-Investigator(Kenkyū-buntansha) |
吉羽 洋周 日立製作所, 基礎研究所, 主任研究員
TSUTSUMI Nobuhiro Graduate School of Agricultural and Life Science Asso. Prof., 大学院・農学生命科学研究科, 助教授 (00202185)
NAGATO Yasuo Graduate School of Agricultural and Life Science Profeesor, 大学院・農学生命科学研究科, 教授 (10143413)
YOSHIDA Yosho Hitachi Co. Ltd., Inst. Basic Research Principal Invest.
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| Project Period (FY) |
1994 – 1996
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| Project Status |
Completed (Fiscal Year 1996)
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| Budget Amount *help |
¥14,600,000 (Direct Cost: ¥14,600,000)
Fiscal Year 1996: ¥2,600,000 (Direct Cost: ¥2,600,000)
Fiscal Year 1995: ¥3,000,000 (Direct Cost: ¥3,000,000)
Fiscal Year 1994: ¥9,000,000 (Direct Cost: ¥9,000,000)
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| Keywords | Mitochondrial genome / Plasmid-like DNA / Rice / Transformation / アンチマイシン / エディティング |
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| Research Abstract |
Mitochondria are the sites of energy transduction in eukaryotic cells which carry out aerobic metabolism. Energy transduction is conducted by several kinds of peotein complexes in the mitochondrial membrane. Genetic information of these complexes are stored in the nuclear and mitochondrial genomes. Thus, mitochondrial as well as nuclear genome should be transformed in order to improve mitochondrial activity.
Plasmid DNA was constructed to transform rice mitochondrial DNA.Mitichondrial coded cob gene was mutated to antimycin resistant form by the site directed mutagenesis. The mutated cob gene, together with promoter region of atpl and 3' non-translated region of atp6 were cloned into pBSKS+ plasmid. Plasmid like DNA,B4, in rice mitochondria was also connected to the plasmid in order to accelerate the replication of the plasmid DNA in rice mitochondria. This plasmid DNA for mitochondria transformation was introduced into rice calli by a particle gun. However, transformed cells were not obtained so far. Construction of the improved plasmid is in progress.
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