Study on the splicing checkpoint mechanism to prevent pre-mRNA accumulation caused by splicing abnormality
Project/Area Number |
25711001
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Research Category |
Grant-in-Aid for Young Scientists (A)
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Allocation Type | Partial Multi-year Fund |
Research Field |
Molecular biology
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Research Institution | University of Toyama |
Principal Investigator |
Kaida Daisuke 富山大学, 大学院医学薬学研究部(医学), 准教授 (60415122)
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Project Period (FY) |
2013-04-01 – 2017-03-31
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Project Status |
Completed (Fiscal Year 2016)
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Budget Amount *help |
¥26,780,000 (Direct Cost: ¥20,600,000、Indirect Cost: ¥6,180,000)
Fiscal Year 2016: ¥5,200,000 (Direct Cost: ¥4,000,000、Indirect Cost: ¥1,200,000)
Fiscal Year 2015: ¥5,330,000 (Direct Cost: ¥4,100,000、Indirect Cost: ¥1,230,000)
Fiscal Year 2014: ¥5,330,000 (Direct Cost: ¥4,100,000、Indirect Cost: ¥1,230,000)
Fiscal Year 2013: ¥10,920,000 (Direct Cost: ¥8,400,000、Indirect Cost: ¥2,520,000)
|
Keywords | スプライシング / 転写 / RNAポリメラーゼII |
Outline of Final Research Achievements |
mRNA splicing is a fundamental mechanism for the gene expression in eukaryotes. Splicing abnormality might cause pre-mRNA accumulation and diseases. Therefore, I assumed that cells have a checkpoint mechanism that detects splicing abnormality and suppresses transcriptional elongation to prevent pre-mRNA accumulation. I revealed that such a splicing checkpoint mechanism actually exists in this study.
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Report
(5 results)
Research Products
(17 results)
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[Journal Article] U2 snRNP is required for expression of the 3' end of genes2014
Author(s)
Koga, M., Satoh, T., Takasaki, I., Kawamura, Y., Yoshida, M., and Kaida, D
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Journal Title
PloS One
Volume: 9
Issue: 5
Pages: e98015-e98015
DOI
Related Report
Peer Reviewed
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