| Project/Area Number |
24620001
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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 | 一般 |
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| Research Field |
宇宙生命学
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| Research Institution | Tohoku University |
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Principal Investigator |
Teranishi Mika 東北大学, 生命科学研究科, 助教 (10333832)
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| Co-Investigator(Kenkyū-buntansha) |
HIDEMA Jun 東北大学, 大学院生命科学研究科, 准教授 (20250855)
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| Project Period (FY) |
2012-04-01 – 2016-03-31
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| Project Status |
Completed (Fiscal Year 2015)
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| Budget Amount *help |
¥5,330,000 (Direct Cost: ¥4,100,000、Indirect Cost: ¥1,230,000)
Fiscal Year 2014: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Fiscal Year 2013: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Fiscal Year 2012: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
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| Keywords | 放射線 / 植物 / DNA / 損傷 / ゲノム不安定化 / 変異 / 不安定化 |
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| Outline of Final Research Achievements |
In this study, we measured the number of DNA damages induced by ionizing radiation (gamma ray and x-ray) and non-ionizing radiation (UV-B radiation) in Arabidopsis seedlings. After irradiation, whole plants used for preparing an agarose plug. The agarose plugs were subjected to denature and non-denature agarose gel electrophoresis. The number of DNA double strand break (DSB), single strand break (SSB) and cyclobutane pyrimidine dimer (CPD)were calculated using the molecular length standard curve and the quantity of DNA at each migration position as shown by the quantitative image data. As a result, the number of DNA damages increased with increasing dose of radiation. DSB, SSB and CPD were induced by irradiation with gamma ray, x-ray and UV-B radiation. However, induction efficiency was different among the types of radiation. Furthermore, we constructed the transgenic Marchantia polymorpha which has marker gene as a recombination substrate for detect a homologous recombination.
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