Analysis of protein degradation promoting mechanism derived from abnormal mRNA
Project/Area Number |
26291002
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Research Category |
Grant-in-Aid for Scientific Research (B)
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Allocation Type | Partial Multi-year Fund |
Section | 一般 |
Research Field |
Molecular biology
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Research Institution | Tohoku University |
Principal Investigator |
Inada Toshifumi 東北大学, 薬学研究科(研究院), 教授 (40242812)
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Project Period (FY) |
2014-04-01 – 2017-03-31
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Project Status |
Completed (Fiscal Year 2016)
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Budget Amount *help |
¥16,510,000 (Direct Cost: ¥12,700,000、Indirect Cost: ¥3,810,000)
Fiscal Year 2016: ¥5,980,000 (Direct Cost: ¥4,600,000、Indirect Cost: ¥1,380,000)
Fiscal Year 2015: ¥5,070,000 (Direct Cost: ¥3,900,000、Indirect Cost: ¥1,170,000)
Fiscal Year 2014: ¥5,460,000 (Direct Cost: ¥4,200,000、Indirect Cost: ¥1,260,000)
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Keywords | 遺伝子発現の品質管理 / ナンセンス変異依存分解系 / Upf1 / Sse1 / Hsp70 / ユビキチン化 / プロテアソーム / 品質管理 / ナンセンス変異依存分解 / Upf / ユビキチン / 翻訳アレスト / シャペロン / リボソーム / ノンストップmRNA / 翻訳伸長阻害 / mRNA分解 |
Outline of Final Research Achievements |
Accurate gene expression is the backbone of life phenomenon, and its breakdown and abnormality cause various diseases. In this research project, we aim to elucidate the degradation mechanism (NMPD) of gene products derived from abnormal mRNA, which is the earliest protein quality control mechanism. We analyzed short chain type proteolytic mechanism derived from abnormal mRNA with nonsense mutation, and obtained the following results. Sse1, an exchange factor for ADP/ATP of Hsp70, was required for promoting degradation of short chain type abnormal protein by Upf1. Mutant analysis of Sse1 revealed that interaction with Hsp70 is essential for NMPD. Moreover, it became clear that Sse1 does not promote the ubiquitination itself of short chain type abnormal protein itself. This study has led to an understanding of the molecular mechanism of NMPD, a degradation of truncated protein derived from abnormal mRNA with nonsense mutation.
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Report
(4 results)
Research Products
(13 results)
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[Journal Article] The tRNA splicing endonuclease complex cleaves the mitochondria-localized CBP1 mRNA.2015
Author(s)
Tsuboi, T., Yamazaki, R., Nobuta, R., Ikecuhi, K., Makino, S., Ohtaki, Y., Suzuki, Y., Yoshihisa, T., Trotta, C., and Inada, T.
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Journal Title
Journal of Biological Chemistry
Volume: 290
Issue: 26
Pages: 16021-16030
DOI
Related Report
Peer Reviewed / Int'l Joint Research
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