Molecular mechanisms of mRNA decay that is triggered by translation arrest.
Project/Area Number |
22770129
|
Research Category |
Grant-in-Aid for Young Scientists (B)
|
Allocation Type | Single-year Grants |
Research Field |
Functional biochemistry
|
Research Institution | Nagoya City University |
Principal Investigator |
HOSODA Nao 名古屋市立大学, 大学院・薬学研究科, 講師 (40438198)
|
Project Period (FY) |
2010 – 2011
|
Project Status |
Completed (Fiscal Year 2011)
|
Budget Amount *help |
¥4,290,000 (Direct Cost: ¥3,300,000、Indirect Cost: ¥990,000)
Fiscal Year 2011: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Fiscal Year 2010: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
|
Keywords | mRNA分解 / 翻訳制御 / G蛋白質 / リボソーム / mRNA品質管理 |
Research Abstract |
In this study, we examined quality control mechanisms for mRNA lacking in-frame termination codons(non-stop mRNA) using mammalian cells. The non-stop mRNA is unstable and degraded in a translation-dependent manner. The decay requires another eRF3-eRF1 family member Hbs1-Dom34.Also, the elimination of aberrant proteins produced from the non-stop transcripts requires Listerin, which functions as an E3 ubiquitin ligase.
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Report
(3 results)
Research Products
(22 results)