Functional analysis of mature ribosome degradation by RNase T2 in Saccharomyces cerevisiae
Project/Area Number |
25450093
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Applied microbiology
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Research Institution | The University of Tokyo |
Principal Investigator |
Ogawa Tetsuhiro 東京大学, 農学生命科学研究科, 助教 (40323480)
|
Project Period (FY) |
2013-04-01 – 2016-03-31
|
Project Status |
Completed (Fiscal Year 2015)
|
Budget Amount *help |
¥5,200,000 (Direct Cost: ¥4,000,000、Indirect Cost: ¥1,200,000)
Fiscal Year 2015: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2014: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2013: ¥3,120,000 (Direct Cost: ¥2,400,000、Indirect Cost: ¥720,000)
|
Keywords | 出芽酵母 / リボソーム / リボヌクレアーゼ / ストレス応答 |
Outline of Final Research Achievements |
In this study, we tried to elucidate the molecular mechanism of mature ribosome degradation observed in Saccharomyces cerevisiae by the treatment of rapamycin, an antibiotic inducing cellular starvation response. 18S and 25S ribosomal RNA (rRNA) is degraded by Rny1p, which belongs to the conserved RNase T2 family. Ribosomal proteins are also degraded in the same condition. These results indicate that mature ribosomes are actually degraded by the rapamycin treatment, which results in adaptation of host cells to the starvation condition. The degradation partly occurs in the vacuole, which depends on non-selective autophagy pathway. However, most of ribosomes seem to be degraded outside the vacuole.
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Report
(4 results)
Research Products
(6 results)
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[Journal Article] Transfer-messenger RNA and SmpB mediate bacteriostasis in Escherichia coli cells against tRNA cleavage.2015
Author(s)
Sakai, F., Sugita,R., Chang, J.-W., Ogawa, T., Hidaka, M., Masaki, H.
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Journal Title
Microbiology
Volume: 161
Issue: 10
Pages: 2019-2028
DOI
Related Report
Peer Reviewed
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[Journal Article] Evidence for DNA cleavage caused by a transfer-tRNA-targeting toxin.2013
Author(s)
Shigematsu, M., Ogawa, T., Tanaka, W., Takahashi, K., Kitamoto, H.K., Hidaka, M, and Masaki, H,
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Journal Title
PLoS ONE
Volume: 8
Issue: 9
Pages: 75512-75512
DOI
Related Report
Peer Reviewed
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