Analysis of Arabidopsis microRNA biogenesis via posttanslational modification
| Project/Area Number |
17K15416
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| Research Category |
Grant-in-Aid for Young Scientists (B)
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| Allocation Type | Multi-year Fund |
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| Research Field |
Applied molecular and cellular biology
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| Research Institution | Osaka Prefecture University |
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Principal Investigator |
Iwata Yuji 大阪府立大学, 生命環境科学研究科, 准教授 (80704965)
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| Project Period (FY) |
2017-04-01 – 2019-03-31
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| Project Status |
Completed (Fiscal Year 2018)
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| Budget Amount *help |
¥4,290,000 (Direct Cost: ¥3,300,000、Indirect Cost: ¥990,000)
Fiscal Year 2018: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2017: ¥2,600,000 (Direct Cost: ¥2,000,000、Indirect Cost: ¥600,000)
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| Keywords | microRNA / Dicer / シロイヌナズナ / SERRATE / Dicer-Like1 / Serrate |
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| Outline of Final Research Achievements |
miRNA is a 20-22 nucleotide long non-coding RNA that regulates gene regulation via nucleotide complementarity. In plants, miRNA is generated from precursor RNA called pri-miRNA by endonucleolytic cleavage by the RNaseIII family enzyme Dicer-like 1 (DCL1). In the present study, we analyzed the function of Arabidopsis SERRATE (SE), a zinc-finger domain-containing protein that interacts with DCL1. We also performed biochemical characterization of pri-miRNA processing reaction by DCL1 in vitro and clarified the recognition and cleavage mechanisms by which DCL1 cleavages a single-stranded RNA that forms a hairpin structure.
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| Academic Significance and Societal Importance of the Research Achievements |
植物におけるmiRNA生成機構は国内外の多くの研究者によって解析されている。miRNA生成に関与するタンパク質は多数同定されているが、それらがどのように協調してmiRNA生成に寄与しているかに関する詳細な分子メカニズムは不明な点が多い。特に、miRNA生成におけるタンパク質の翻訳後修飾の役割を示した例は少なく、本研究はそれを明らかにした点で意義深いといえる。
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Report
(3 results)
Research Products
(7 results)
