| Project/Area Number |
61440014
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| Research Category |
Grant-in-Aid for General Scientific Research (A)
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| Allocation Type | Single-year Grants |
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| Research Field |
発酵・醸造
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| Research Institution | HIROSHIMA UNIVERSITY |
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Principal Investigator |
TSUCHIYA Eiko (1988) Fac. Engineering, Hiroshima Univ., Research Assistant, 工学部, 助手 (90127671)
福井 作蔵 (1986-1987) 広島大学, 工学部, 教授 (60013299)
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| Co-Investigator(Kenkyū-buntansha) |
FUKUI Sakuzo Fac. Engineering, Hiroshima Univ., Professor Emelitus, 工学部, 名誉教授 (60013299)
KAMIRYO Tatsuyuki Fac. Integrated Art and Science, Hiroshima Univ., Associate Professor, 総合科学部, 助教授 (50025649)
MIYAJAWA Tokichi Fac. Engineering, Hiroshima Univ., Professor, 工学部, 教授 (10116676)
TOH-E Akio Fac. Engineering, Hiroshima Univ., Professor, 工学部, 教授 (90029249)
土屋 英子 広島大学, 工学部, 助手 (90127671)
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| Project Period (FY) |
1986 – 1988
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| Project Status |
Completed (Fiscal Year 1988)
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| Budget Amount *help |
¥26,000,000 (Direct Cost: ¥26,000,000)
Fiscal Year 1988: ¥2,000,000 (Direct Cost: ¥2,000,000)
Fiscal Year 1987: ¥3,000,000 (Direct Cost: ¥3,000,000)
Fiscal Year 1986: ¥21,000,000 (Direct Cost: ¥21,000,000)
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| Keywords | Sporulation / 2 um DNA / Peroxisome / Transmembrane signaling / Ca^<2+> / calmodulin depandent protein kinase / Cell division cycle / DNA replication / 核膜の物質輸送 / 下等真核生物 / オルガネラ形成 / 核膜ATPase / 性分化 / トランスメンブレンシグナリング機構 / DNAの核内輸送 |
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| Research Abstract |
In the aim of analyzing the controls of gene expression during the cell proliferation and differentiation of yeasts, we accomplished this project and obtained the following findings.
1. Fukui cloned the glucoamylase gene (SGA) specifically expressed during the sporulation of Saccharomyces cerevisiae and determined its DNA sequence.
2.Toh-e isolated 4 novel 2 mum-DNA-like plasmids (pSB2, pSB3, pSR1 and pSM1) from Zygosaccharomyces yeasts and determined the DNA sequences involved in autonomous replication, stable maintenance and recombination of the plasmids. A host-vector system for Zygosaccharomyces rouxii was developed by using pSR1.
3. Kamiryo cloned 9 genes encoding peroxisomal proteins (POXs and OLE) and found that POX2 and POX4, and POX5 and OLE3 formed clusters in Candida tropicalis genom.
4. Miyakawa revealed the involvement of Ca in the transmembrane-signaling system of a sex pheromene rhodotorucin A in Rhodosporidium toruloides a cells as a second messenger. He postulated the possible mechanism for the signal transduction of the pheromone including trigger peptidase, a pheromone receptor, Ca ATPase and Ca /calmodulin dependent protein kinase.
5. Tsuchiya and Miyakawa found that the oscillation of intracellular-free Ca concentration play a regulatory role on the progress of cell division cycle in S. cerevisiae.
6. Miyakawa and Fukui cloned the gene encoding rhodotorucin A and determined its DNA sequence.
7. Tsuchiya established the monoclonal antibody against the yeast nuclear proteins and identified a 70-Kd protein involved in the yeast DNA replication. P70 was found to have a molecular structure resembled to a heat shock protein, hsp70.
8. Tsuchiya and Fukui developed in vitro DNA uptake system of isolated yeast nuclei and found the requirement of ATPase and protein kinase in the trans-nuclear-membrane transport of plasmid DNA. They also identified a nuclear ATPase sensitive to WGA and suggested the involvement of the ATPase in nuclear transport system.
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