Mechanisms for all-inclusive controls of cell cycle progression, and IgM H and L-chain gene expressions by GCN5 and HDAC2
Mechanisms for all-inclusive controls of cell cycle progression, and IgM H and L-chain gene expressions by GCN5 and HDAC2
批准号:
16310134
负责人:
NAKAYAMA Tatsuo
金额:
$10.05万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (B)
财政年份:
2004
资助国家:
日本
项目状态:
已结题
起止时间:
2004 至 2006
中文摘要
1.鸡Hira的WD二肽基序和LxxLL基序是与CAF-1p48亚基和HDAC2 I a体内外相互作用所必需的。GCN5通过转录调控多种细胞周期相关基因,全面调控脊椎动物细胞周期进程。Hira的N-末端和C-末端在调控脊椎动物细胞生长的细胞周期相关基因转录调控中发挥不同的作用。HAT1对于复制偶联染色质组装是必不可少的,但有助于恢复脊椎动物细胞复制阻断后造成的DNA损伤。在脊椎动物细胞的DNA复制过程中,ASF1对于活性和染色质组装是必不可少的。CAF-1介导的核小体快速组装是脊椎动物细胞DNA复制和细胞分裂所必需的。HDAC2是通过EBF1、Pax5、Ikaros、Aiolos和E2a基因表达调控IgM H和L链基因表达所必需的。
英文摘要
1. WD dipeptide motifs and LXXLL motif of chicken HIRA are essential for interactions with CAF-1p48 subunit and HDAC2 i a vitro and in vivo.2. GCN5 is a supervisor in all-inclusive control of vertebrate cell cycle progression via transcription regulation of various cell cycle-related genes.3. N-terminal and C-terminal halves of HIRA exhibit different roles in transcription regulation of cell cycle-related genes that contribute to control of vertebrate cell growth.4. HAT1 is dispensable for replication-coupled chromatin assembly but contributes to recover DNA damages created following replication blockage in vertebrate cells.5. ASF1 is essential for viability and chromatin assembly during DNA replication in vertebrate cells.6. CAF-1-mediated rapid nucleosome assembly is essential for DNA replication and cell division in vertebrate cells.7. HDAC2 is necessary for controls of IgM H and L-chain gene expressions via EBF1, Pax5, Ikaros, Aiolos and E2A gene expressions.
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DOI:
10.1016/j.bbrc.2006.05.079
发表时间:
2006-07-14
期刊:
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
影响因子:
3.1
作者:
[Barman, Hirak Kumar, Takami, Yasunari, Nakayama, Tatsuo]
通讯作者:
Nakayama, Tatsuo
Growth inhibition and mutagenesis induced in Escherichia coli by dihydropyrazines with DNA strand-cleaving activity.
具有 DNA 链切割活性的二氢吡嗪可诱导大肠杆菌生长抑制和诱变。
DOI:
--
发表时间:
2004
期刊:
Mutation Research 560
影响因子:
--
作者:
[Takechi, S., Yamaguchi, T., Nomura, H., Minematsu, T., Nakayama, T.]
通讯作者:
T.
DOI:
10.1016/j.gene.2004.12.007
发表时间:
2005-02-28
期刊:
GENE
影响因子:
3.5
作者:
[Kikuchi, H, Takami, Y, Nakayama, T]
通讯作者:
Nakayama, T
DOI:
10.1038/ncb1155
发表时间:
2004-08-01
期刊:
NATURE CELL BIOLOGY
影响因子:
21.3
作者:
[Fukagawa, T, Nogami, M, Oshimura, M]
通讯作者:
Oshimura, M
Essential Role of CAF-1-mediated Rapid Nucleosome Assembly for DNA Replication and Cell Division in Vertebrate Cells.
CAF-1 介导的快速核小体组装对脊椎动物细胞 DNA 复制和细胞分裂的重要作用。
DOI:
--
发表时间:
2007
期刊:
Molecular Biology of the Cell 18
影响因子:
--
作者:
[Kwon, M.S., Hori, T., Okada, M., Fukagawa, T., Mi-Sun Kwon, Michela Zuccolo, Yasunari Takami]
通讯作者:
Yasunari Takami
Functional analyses of chromatin structure changing-related factors in higher eukaryotic cells by gene targeting techniques
-
批准号:19310127
-
项目类别:Grant-in-Aid for Scientific Research (B)
-
资助金额:$13.06万
-
财政年份:2007
-
负责人:NAKAYAMA Tatsuo
-
依托单位:
Joint study on histone modifying enzymes by gene disruption
-
批准号:11694299
-
项目类别:Grant-in-Aid for Scientific Research (B).
-
资助金额:$5.63万
-
财政年份:1999
-
负责人:NAKAYAMA Tatsuo
-
依托单位:
Joint Study on Nature of Histone Variants by Gene Disruption
-
批准号:09044327
-
项目类别:Grant-in-Aid for international Scientific Research
-
资助金额:$5.06万
-
财政年份:1998
-
负责人:NAKAYAMA Tatsuo
-
依托单位:
Functional Analysis of H1 and Core Histone Variants by Gene Targeting Technique
-
批准号:09480152
-
项目类别:Grant-in-Aid for Scientific Research (B)
-
资助金额:$8.0万
-
财政年份:1997
-
负责人:NAKAYAMA Tatsuo
-
依托单位:
Joint study on nature of histone variants by gene targeting
-
批准号:07044283
-
项目类别:Grant-in-Aid for international Scientific Research
-
资助金额:$4.29万
-
财政年份:1995
-
负责人:NAKAYAMA Tatsuo
-
依托单位:
海外基金