The role of DNA repair factor FNACD2 in centrosome duplication maintenance
Project/Area Number |
22710054
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Single-year Grants |
Research Field |
Risk sciences of radiation/Chemicals
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Research Institution | Kyoto University |
Principal Investigator |
SHIMADA Mikio 京都大学, 放射線生物研究センター, 研究員 (20548557)
|
Project Period (FY) |
2010 – 2011
|
Project Status |
Completed (Fiscal Year 2011)
|
Budget Amount *help |
¥4,030,000 (Direct Cost: ¥3,100,000、Indirect Cost: ¥930,000)
Fiscal Year 2011: ¥1,950,000 (Direct Cost: ¥1,500,000、Indirect Cost: ¥450,000)
Fiscal Year 2010: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
|
Keywords | DNA修復 / 中心体 / 発癌 / FANCD2 / 発癌制御 / 染色体異常 |
Research Abstract |
Centrosome is an organelle function as microtubules organizing center. Disfunction of centrosome results in improper cell division and chromosome unstability leads to tumorigenesis. FANCD2 is a cause gene of Fanconi Anemia, which represent predisposition malignancy. In this study, we addressed the role of FNACD2 in centrosome maintence. Defect of FANCD2 by siRNA knockdown in U2OS cells result in centrosome overduplication and reducing of mictorubule assembly function. These results indicated that FANCD2 is involved in centrosome functions.
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Report
(3 results)
Research Products
(24 results)
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[Journal Article] Regulation of homologous recombination by RNF20-dependent H2Bubiquitination2011
Author(s)
Nakamura K, Kato A, Kobayashi J, Yanagihara H, Sakamoto S, Oliveira D, Shimada S, Tauchi H, Suzuki H, Tashiro S, Zou L, Komatsu K.
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Journal Title
Mol Cell
Volume: 41
Issue: 5
Pages: 515-528
DOI
NAID
Related Report
Peer Reviewed
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[Journal Article] Regulation of homologous recombination by RNF20-dependent H2B ubiquitination.2011
Author(s)
K.Nakamura, A.Kato, J.Kobayashi, H.Yanagihara, S.Sakamoto, D.V.N.P.Oliveira, M.Shimada, H.Tauchi, H.Suzuki, S.Tashiro, L.Zou, K.Komatsu
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Journal Title
Molcular Cell
Volume: 41
Pages: 515-528
NAID
Related Report
Peer Reviewed
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