2002 Fiscal Year Final Research Report Summary
Screening of bio-active substances by using a peculiar phenotype of yeast mutant
Project/Area Number |
11556017
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Research Category |
Grant-in-Aid for Scientific Research (B)
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Allocation Type | Single-year Grants |
Section | 展開研究 |
Research Field |
応用微生物学・応用生物化学
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Research Institution | HIROSHIMA UNIVERSITY |
Principal Investigator |
MIYAKAWA Tokichi Hiroshima University, Graduate School of Advances Sciences of Matter., Professor, 大学院・先端物質科学研究科, 教授 (10116676)
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Co-Investigator(Kenkyū-buntansha) |
TAKAHASHI Hidetoshi Research Institute of Life Science, Snow Brand Milk Products Co., Ltd., 生物科学研究所, 主任研究員
HIRATA Dai Hiroshima University, Graduate School of Advances Sciences of Matter., Associate Professor, 大学院・先端物質科学研究科, 助教授 (30243603)
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Project Period (FY) |
1999 – 2002
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Keywords | Ca2+ signal / Calcineurin / Drug screening / MAP kinase |
Research Abstract |
An inappropriate activation of a signaling pathway in yeast often has a deleterious physiological effect and causes various defects, including growth defects. In a certain genetic background (Δzdsl) of Saccharomyces cerevisiae, the cell-cycle progression in G2 is specifically blocked in the medium with CaCl_2 by the hyperactivation of the Ca^<2+>-signaling pathways. Here, we developed a novel drug screening procedure designed to detect the active compounds that specifically attenuate the Ca^<2+>-signaling activity on the basis of the ability to abrogate the growth defect of the cells suffering from the hyperactivated Ca^<2+> signal. Using known calcineurin inhibitors as model compounds, we have established the screening conditions for the drugs that suppress the Ca^<2+>-induced growth inhibition. An indicator strain with an increased drug sensitivity was constructed with a syr1/erg3 null mutation.
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