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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
GCN5 和 HDAC2 全面控制细胞周期进程以及 IgM H 和 L 链基因表达的机制
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

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中文摘要
翻译
1.鸡HIRA的WD二肽基序和LXXLL基序在体内外与CAF-1 p48亚基和HDAC 2相互作用中是必需的. GCN 5是脊椎动物细胞周期进程的一个监督者,它通过转录调控多种细胞周期相关基因来全面控制细胞周期进程. HIRA的N端和C端在细胞周期相关基因的转录调控中表现出不同的作用,这些基因有助于控制脊椎动物细胞的生长. HAT 1是复制偶联染色质组装的关键,但有助于恢复脊椎动物细胞中复制阻断后产生的DNA损伤。ASF 1在脊椎动物细胞DNA复制过程中对生存力和染色质组装至关重要。CAF-1介导的核小体快速组装对于脊椎动物细胞中的DNA复制和细胞分裂是必不可少的。HDAC 2是通过EBF 1、Pax 5、Ikaros、Aiolos和E2 A基因表达控制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.
期刊论文(15)
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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
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:
海外基金