Molecular mechanisms for micropeptide functions
Project/Area Number |
24370090
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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 |
Developmental biology
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Research Institution | Kobe University |
Principal Investigator |
KAGEYAMA Yuji 神戸大学, 遺伝子実験センター, 准教授 (90335480)
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Project Period (FY) |
2012-04-01 – 2015-03-31
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Project Status |
Completed (Fiscal Year 2014)
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Budget Amount *help |
¥17,940,000 (Direct Cost: ¥13,800,000、Indirect Cost: ¥4,140,000)
Fiscal Year 2014: ¥5,850,000 (Direct Cost: ¥4,500,000、Indirect Cost: ¥1,350,000)
Fiscal Year 2013: ¥5,720,000 (Direct Cost: ¥4,400,000、Indirect Cost: ¥1,320,000)
Fiscal Year 2012: ¥6,370,000 (Direct Cost: ¥4,900,000、Indirect Cost: ¥1,470,000)
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Keywords | マイクロペプチド / ショウジョウバエ / スクリーニング / 遺伝学 / 上皮細胞 / 形態形成 / 分子遺伝学 / 発生生物学 / 細胞増殖 / キイロショウジョウバエ / 短鎖ペプチド / 器官形成 |
Outline of Final Research Achievements |
Eukaryotic gemomes contain a proportional numer of "micropeptide" genes that encode small peptides in extremely short ORFs. Micropeptides are distinguished from canonical active peptide molecules, which are translated as a long precursor and secreted into extracellular spaces, and should therefore function in cytoplasm, although little is known about its molecular mechanisms. In this study, we focused on Drosophila polished rice gene that encode 11- and 32-aa micropeptides. We found that pri is specifically expressed in metamorphic stages and induced by ectopic application of ecdysone. Phenotypic analysis of hypomophic allies of the pri gene demonstrated that pri is essential for progress of metamorphosis and regulate ecdysone-dependent gene network.
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Report
(4 results)
Research Products
(12 results)
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[Journal Article] Pri peptides are mediators of ecdysone for the temporal control of development2014
Author(s)
H. Chanut-Delalande, Y. Hashimoto, A. Pelissier-Monier, R. Spokony, A. Dib, T. Kondo, J. Bohere, K. Niimi, Y. Latapie, S. Inagaki, L. Dubois, P. Valenti, C. Polesello, S. Kobayashi, B. Moussian, K. White, S. Plaza, Y. Kageyama, and F. Payre
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Journal Title
Nature Cell Biol.
Volume: 16
Issue: 11
Pages: 1035-1044
DOI
Related Report
Peer Reviewed
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