Elucidation of mechanism underlying synchronization of cellular clocks, an essential process for establishment of circadian clock
| Project/Area Number |
18KT0068
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Multi-year Fund |
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| Section | 特設分野 |
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| Research Field |
Complex Systems Disease Theory
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| Research Institution | Komatsu University |
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Principal Investigator |
Hirayama Jun 公立小松大学, 保健医療学部, 教授 (90510363)
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| Project Period (FY) |
2018-07-18 – 2021-03-31
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| Project Status |
Completed (Fiscal Year 2020)
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| Budget Amount *help |
¥4,550,000 (Direct Cost: ¥3,500,000、Indirect Cost: ¥1,050,000)
Fiscal Year 2020: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2019: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2018: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
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| Keywords | 体内時計 / 転写 / 光 / ゼブラフィッシュ / 細胞時計 / メラトニン / 行動 / 代謝 |
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| Outline of Final Research Achievements |
Circadian clocks are intrinsic, time-tracking systems that bestow upon organisms a survival advantage. Under natural conditions, organisms are trained to follow a 24-h cycle under environmental time cues such as light to maximize their physiological efficiency. The circadian clock is established by cell-autonomous oscillators called cellular clocks which are present in every cell of a living organism. The synchronization of cellular clocks in tissues and organs by environmental signals such as light is required to orchestrate the circadian clock at the organismal level. This study found that zPER2, zCRY1a, and zCRY2a synchronize cellular clocks in a light-dependent manner to form the behavioral rhythms in zebrafish. In addition, we uncovered unforeseen roles for zPER2 and zCRY1a in regulating the total level of locomotor activity, likely via regulating cellular energy metabolism.
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| Academic Significance and Societal Importance of the Research Achievements |
現代産業社会の構造は、ヒトが本来自然サイクルに同調していた生活を、社会構造に合わせた生活時間に順応せざるを得ない状況を作り上げている。そのために生じるシフトワークや夜食の常習化といった生活習慣の乱れが、体内時計を破綻させ、睡眠障害、代謝異常、または高血圧症といった様々な疾患を引き起こすことが明らかになっている。このような背景より、体内時計の重要な制御過程である細胞時計の同調の新規メカニズムを明らかにした本研究成果には、体内時計の異常と関連する様々な疾患の予防法ならびに治療戦略の構築のための有益な知見の提供が期待できる。
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Report
(4 results)
Research Products
(25 results)
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[Journal Article] Expression of sclerostin in the regenerating scales of goldfish and its increase under microgravity during space flight2020
Author(s)
Yamamoto, T., Ikegame, M., Hirayama, J., Kitamura, K., Tabuchi, Y., Furusawa, Y., Sekiguchi, T., Endo, M., Mishima, H., Seki, A., Yano, S., Matsubara H., Hattori, A. and Suzuki, N.
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Journal Title
Biomedical Research
Volume: 41
Issue: 6
Pages: 279-288
DOI
NAID
ISSN
0388-6107, 1880-313X
Year and Date
2020-12-01
Related Report
Peer Reviewed / Open Access
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[Journal Article] Detection of RANKL-producing cells and osteoclastic activation by the addition of exogenous RANKL in the regenerating scales of goldfish.2020
Author(s)
Yamamoto, T., Ikegame, M., Kawago, U., Tabuchi, Y., Hirayama, J., Sekiguchi, T., Furusawa, Y., Yachiguchi, K., Matsubara, H., Urata, M., Hattori, A. and Suzuki, N.
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Journal Title
Biological Science in Space
Volume: 34
Issue: 0
Pages: 34-40
DOI
NAID
Related Report
Peer Reviewed / Open Access
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[Journal Article] The clock components Period2, Cryptochrome1a, and Cryptochrome2a function in establishing light-dependent behavioral rhythms and/or total activity levels in zebrafish2019
Author(s)
Hirayama J, Alifu Y, Hamabe R, Yamaguchi S, Tomita J, Maruyama Y, Asaoka Y , Nakahama K, Tamaru T, Takamatsu K, Takamatsu N, Hattori A, Nishina S, Azuma N, Kawahara A, Kume K, Nishina H.
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Journal Title
Scientific Reports
Volume: 9
Issue: 1
Pages: 196-196
DOI
Related Report
Peer Reviewed / Open Access / Int'l Joint Research
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