Functional study of tRNA mimicry proteins in regulation of protein synthesis
| Project/Area Number |
17310123
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| Research Category |
Grant-in-Aid for Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Living organism molecular science
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| Research Institution | The University of Tokyo |
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Principal Investigator |
ITO Koichi The University of Tokyo, Institute of Medical Science, Associate Professor (10262073)
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| Project Period (FY) |
2005 – 2007
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| Project Status |
Completed (Fiscal Year 2007)
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| Budget Amount *help |
¥17,430,000 (Direct Cost: ¥15,600,000、Indirect Cost: ¥1,830,000)
Fiscal Year 2007: ¥7,930,000 (Direct Cost: ¥6,100,000、Indirect Cost: ¥1,830,000)
Fiscal Year 2006: ¥3,800,000 (Direct Cost: ¥3,800,000)
Fiscal Year 2005: ¥5,700,000 (Direct Cost: ¥5,700,000)
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| Keywords | Translation termination / Translational Control / Ribosome / Recoding / Polypeptide-chain release factor / Protein Synthesis / tRNA mimicry / Regulation of gene expression / 蛋白質合成 |
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| Research Abstract |
Translation termination in eukaryotes is mediated by two eukaryotic release factors, eRF1 and eRF3. eRF1 recognizes all three stop codons and induces polypeptide release, while eRF3 binds to eRF1 and participates in translation termination though the regulatory role of eRF3 is still unknown. Importantly, eRF3 interacts with various proteins of distinct biological functions. Here, we investigated the effect of these binding factors on functionality and stability of eRF3 using a temperature-sensitive mutant eRF3ts, which is susceptible to factor binding to change the growth phenotype or cellular protein level. Of factors tested, Itt1 over-expression and Sla1 knockout severely impaired viability of eRF3ts cell and its protein abundance in permissive and semipermissive conditions. Slat over-expression reversed the phenotype. It is reported that Itt1 and Sla1 bind to the N-terminal extension domain (NED) of eRF3, unlike the other no-effect factors that bind to the C-terminal domain (CTD). Although NED itself is dispensable, NED-less eRF3ts altered in the stability and functionality. Moreover, Itt1-induced eRF3ts lethality was significantly restored by pep4, prb1 and prc1 knockouts that are defective in vacuolar proteolysis. These findings suggest that NED functions to switch the functional mode of eRF3 depending on the nature of binding factors.
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Report
(4 results)
Research Products
(40 results)
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[Journal Article] Chloroplast ribosome release factor 1 (AtcpRF1) is essential for chloroplast development2007
Author(s)
Motohashi, R., Yamazaki, T., Myouga, F., Ito, T., Ito, K., Satou, M., Kobayashi, M., Nagata, N., Yoshida, S., Nagashima, A., Tanaka, K., Takahashi, S., Shinozaki, K.
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Journal Title
Plant Mol Biol. 64
Pages: 481-497
Description
「研究成果報告書概要(欧文)」より
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[Journal Article] Ciliates use both variant and universal genetic codes : An evidence of omnipotent eRF1s in the class Litostomatea
Author(s)
Thi Phuong Kim, O., Sakurai, A., Saito, K., Ito, K., Ikehara, K., Harumoto, T.
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Journal Title
Description
「研究成果報告書概要(欧文)」より
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