课题基金 / 基金详情

Hepatocarcinogesis and Genomic Instability: Functional Analysis of Y-box binding protein.

Hepatocarcinogesis and Genomic Instability: Functional Analysis of Y-box binding protein.
肝癌和基因组不稳定性:Y-box 结合蛋白的功能分析。
批准号:
12670537
负责人:
KAJINO Kazunori
金额:
$2.05万
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
2000
资助国家:
日本
项目状态:
已结题
起止时间:
2000 至 2001

项目摘要

项目成果

KAJINO Kazunori的其他基金

相似基金

相关文献

中文摘要
翻译
我们分离了dbpA,Y-盒结合蛋白家族的成员,作为诱导基因组不稳定性的细胞蛋白的候选者。结果表明:1. DbpA在大肠杆菌中表达,具有弱的链交换活性。近年来,该家族的另一个成员YB-1被报道具有DNA或RNA的退火活性(JBC 276:4484 1-44847),他们的工作和我们的工作都表明该家族可能与DNA重组有关。目前,我们正在研究dbpA在各种癌组织中的表达。(In转录物的水平,已经在HCC中证实了增强的表达。3.构建了dbpA基因的转基因小鼠。在肝脏中过度表达。4.用抗YB-1抗体检测其在人体不同组织中的表达。5.将dbpA启动子区nt-5的T替换为G后,启动子活性增加了2倍。在51例HCC中,3例检测到相同的替代。我们检测到25 kDa的细胞蛋白,其特异性结合到启动子区域的T到A转换,并且目前正在鉴定它。
英文摘要
We isolated dbpA, a member of the Y-box binding protein family, as the candidate for the cellular protein inducing genomic instability. We obtained the following findings about dbpA.1.DbpA expressed in E.coli showed the weak strand exchange activity. Recently, YB-i, another member of this family, is reported to have the annealing activity of DNA or RNA (JBC 276 : 4484 1-44847), and the possible association of this family with DNA recombination is suggested by their work as well as by ours.2.We raised anti-dbpA Ab which recognized dbpA expressed in E.coli with high sensitivity. At present, we are examining the expression of dbpA in various cancer tissue. (In the level of transcripts, the enhanced expression is already confirmed in HCC.)3.We made Transgenic mouse where dbpA is. to be overexpressed in liver. We are going to examine its susceptibility to HCC.4.Using anti-YB-l Ab, we checked its expression in various human tissues. Enhanced expression was detected in several normal tissues including gastrointestinal epithelium, as well as in HCC.5.By replacing T with G at nt -5 of dbpA promoter region, the promoter activity increased twofold. The identical replacement was detected in 3 of 51 HCC cases. We detected the 25 kDa cellular protein which specifically bind to the promoter region with T to A conversion, and currently on the way to identify it.
期刊论文(10)
专著(0)
科研奖励(0)
会议论文
Kajino K: "Hepatocarcinogenesis and genomic instability."Nihon Rinsho. Vol.59. 112-115 (2001)
Kajino K:“肝癌发生和基因组不稳定。”Nihon Rinsho。
DOI: --
发表时间:
期刊:
影响因子: --
作者: []
通讯作者:
Kajino K: "Similarity of the secondary structure with Identical seven bases In the pregenomic/genomic regions required for the replication of hepatitis 13 virus and hepatitis C virus"Proceedings of the Japan Academy. vol.78. 12-14 (2002)
Kajino K:“13型肝炎病毒和丙型肝炎病毒复制所需的前基因组/基因组区域中具有相同七个碱基的二级结构的相似性”日本科学院院刊。
DOI: --
发表时间:
期刊:
影响因子: --
作者: []
通讯作者:
Kajino K: "Recombination hat spot of hepatitis B virus genome binds to members of the HMV domain protein and the Y box binding protein family : Implication of these proteins in genomic Instability"Intervirology. Vol.44. 311-316 (2001)
Kajino K:“乙型肝炎病毒基因组的重组帽点与 HMV 结构域蛋白和 Y 盒结合蛋白家族的成员结合:这些蛋白在基因组不稳定性中的意义”Intervirology。
DOI: --
发表时间:
期刊:
影响因子: --
作者: []
通讯作者:
Hayashi J: "Hepatitis C virus core protein activates the MAPK/ERK cascade synergistically with tumor promoter TPA, but not with epidermal growth factor or transforming growth factor alpha."Hepatology. vol 32,no 5. 958-961 (2000)
Hayashi J:“丙型肝炎病毒核心蛋白与肿瘤启动子 TPA 协同激活 MAPK/ERK 级联,但与表皮生长因子或转化生长因子 α 不协同。”肝病学。
DOI: --
发表时间:
期刊:
影响因子: --
作者: []
通讯作者:
共 9 条
    Role of dbpA in hepatocarcinogenesis
    • 批准号:
      18590748
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $2.57万
    • 财政年份:
      2006
    • 负责人:
      KAJINO Kazunori
    • 依托单位:
    Search of cellular protein(s) binding to the similar structure of HBV epsilon and HCV3'X
    • 批准号:
      15590704
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $2.24万
    • 财政年份:
      2003
    • 负责人:
      KAJINO Kazunori
    • 依托单位:
    海外基金