2010 Fiscal Year Final Research Report
Mechanisms of transcriptional repression in response to genome stress-role of histone H3 phosphorylation at T11-
Project/Area Number |
20390083
|
Research Category |
Grant-in-Aid for Scientific Research (B)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
General medical chemistry
|
Research Institution | Nagoya City University |
Principal Investigator |
NAKANISHI Makoto Nagoya City University, 大学院・医学研究科, 教授 (40217774)
|
Project Period (FY) |
2008 – 2010
|
Keywords | 遺伝子 / 核酸 / 癌 / 発現制御 |
Research Abstract |
In this study, we found that dephosphorylation of histone H3-pT11 (H3-pT11) plays an essential role in DNA damage-induced transcriptional repression of various E2F-targeting genes. In the absence of DNA damage, Chk1/GCN5 complexes bound to E2Fs and cooperatively catalyzed T11 phosphorylation and K9 acetylation on E2F promoters, thereby activating their transcription. In the presence of DNA damage, Chk1/GCN5 complexes released from E2Fs and in place, Rb-PP1 gamma-HDAC3 complexes bound to E2Fs, leading to dephosphorylation of T11 and deacetylation of K9, which resulted in the transcriptional repression of E2F-targeting genes.
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Author(s)
中西真
Organizer
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Place of Presentation
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Year and Date
20100922-20100924
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[Presentation] 細胞周期と発がん2008
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Year and Date
20081028-20081030