| Project/Area Number |
17H03940
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| Research Category |
Grant-in-Aid for Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Insect science
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| Research Institution | The University of Tokyo |
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Principal Investigator |
Suzuki Masataka 東京大学, 大学院新領域創成科学研究科, 准教授 (30360572)
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| Project Period (FY) |
2017-04-01 – 2020-03-31
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| Project Status |
Completed (Fiscal Year 2019)
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| Budget Amount *help |
¥16,900,000 (Direct Cost: ¥13,000,000、Indirect Cost: ¥3,900,000)
Fiscal Year 2019: ¥4,940,000 (Direct Cost: ¥3,800,000、Indirect Cost: ¥1,140,000)
Fiscal Year 2018: ¥4,810,000 (Direct Cost: ¥3,700,000、Indirect Cost: ¥1,110,000)
Fiscal Year 2017: ¥7,150,000 (Direct Cost: ¥5,500,000、Indirect Cost: ¥1,650,000)
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| Keywords | 性決定 / 性分化 / エクダイソン / doublesex / dmrt遺伝子 / Masculinizer / long-non-coding RNA / DMRT遺伝子 / TALEN / CRISPR/Cas9 / 胚致死 / 昆虫 / シグナル伝達 / 遺伝子 / 発現制御 / 発生・分化 / 性ホルモン / カイコ / ホルモン |
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| Outline of Final Research Achievements |
The primary purpose of this research project is to elucidate whether ecdysone, which is known as a typical insect steroid hormone, is involved in the regulation of insect sex differentiation, and if so, what is its mechanism. The results obtained through this project revealed that the expression of dsx, the master regulator for insect sex differentiation, in testis increased in accordance with the concentration of ecdysone. Based on the results of expression site analysis by immunohistochemistry, phenotypic analysis by genome editing, and enhancer analysis, the maleness of internal reproductive organs cannot be explained only by dsx, and its cognate gene dmrt93B is required. Our results also suggested that dmrt93B may be responsible for the ecdysone-dependent regualtion of genes including dsx involved in the sexual development of testis and internal genitalia.
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| Academic Significance and Societal Importance of the Research Achievements |
本研究では、内部生殖器の性分化がdsxだけでは説明できず、その同族遺伝子dmrt93Bが内部生殖器の雄化にとってより重要な働きをもつことを明らかにできた。これは、昆虫性分化のマスター制御因子であるとのこれまでの見解に一石を投じる発見と言える。dsxの精巣における発現がエクダイソン濃度依存的に上昇することを明らかにすると共に、この過程にdmrt93Bが関与するという新たな知見をもたらしたという点でも学術的価値が高い。また本研究では長年謎であった、雄化因子MASCがdsxの雄型アイソフォームの産生を制御する分子機構を解明し、性決定研究にブレークスルーをもたらしたという点で学術的意義が高いと言える。
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