Generation of ES cells to meseare DNA repair activity with reporter genes
Project/Area Number |
25550026
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Research Category |
Grant-in-Aid for Challenging Exploratory Research
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Allocation Type | Multi-year Fund |
Research Field |
Risk sciences of radiation and chemicals
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Research Institution | Kyoto University |
Principal Investigator |
KOBAYASHI Junya 京都大学, 放射線生物研究センター, 准教授 (30301302)
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Co-Investigator(Kenkyū-buntansha) |
HONDA Hiroaki 広島大学, 原爆放射線医科学研究所, 教授 (40245064)
KATO Akihiro 京都大学, 放射線生物研究センター, 研究員 (70423051)
KOMATSU Kenshi 京都大学, 放射線生物研究センター, 教授 (80124577)
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Project Period (FY) |
2013-04-01 – 2015-03-31
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Project Status |
Completed (Fiscal Year 2014)
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Budget Amount *help |
¥4,160,000 (Direct Cost: ¥3,200,000、Indirect Cost: ¥960,000)
Fiscal Year 2014: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Fiscal Year 2013: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
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Keywords | DNA修復 / 相同組換え / 非相同末端結合 / 放射線 / DNA損傷 |
Outline of Final Research Achievements |
In order to investigate radiosensitivity in children, we generated the system in ES cells to measure the activity of homologous recombination (HR) repair or non-homologous endjoining (NHEJ) repair. We introduce a specific site of genomic DNA to HR or NHEJ reporter construct. As a result, we got several ES cell lines, which could express NHEJ after generation of DNA double-strand break and possess differentiation potency.
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Report
(3 results)
Research Products
(4 results)
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[Journal Article] Mutations in the FHA-domain of ectopically expressed NBS1 lead to Radiosensitization and to no increase in somatic mutation rates via a partial suppression of homologous recombination2014
Author(s)
Maki Ohara, Yumi Funyu, Shunsuke Ebara, Yuki Sakamoto, Ryota Seki, Kenta Iijima, Akiko Ohishi, Junya Kobayashi, Kenshi Komatsu, Akira Tachibana, and Hiroshi Tauchi
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Journal Title
J. Radiat. Res
Volume: 55
Issue: 4
Pages: 690-698
DOI
Related Report
Peer Reviewed / Open Access
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