FUNCTIONS OF C-FOS PROTEIN IN CELLULAR PHYSIOLOGY

C-FOS 蛋白在细胞生理学中的功能

基本信息

  • 批准号:
    3193009
  • 负责人:
  • 金额:
    $ 16.88万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    1989
  • 资助国家:
    美国
  • 起止时间:
    1989-01-13 至 1991-12-31
  • 项目状态:
    已结题

项目摘要

The discovery that proto-oncogenes have the potential to produce cancer has created substantial interest in the functions of these normal cellular genes. c-fos protein is of particular importance because of its nuclear location, DNA binding capacity, and modulation of expression during cellular proliferation and differentiation. However, the function of the normal c-fos protein is unknown. The overall goal of this proposal is to elucidate specific functions for the c-fos protein. The proposed studies will employ genetic methods to create and analyze cellular mutants with altered c-fos expression, and cDNA cloning techniques to identify genes which are regulated by c-fos expression. The hypothesis to be tested is that c-fos protein is required for specific cellular processes because it alters the expression of genes with essential functions. The specific aims are: 1) To determine the Functional Domains of the normal c-fos protein which are necessary for fibroblast Proliferation; 2) To determine the Functional Domains of the normal c-fos protein which are necessary for Embryonal stem cell Proliferation and/or Differentiation; 3) To identify Genes which are regulated by c-fos expression. These studies are focused on the functional significance of both alterations in c-fos protein structure and induction of putative c-fos regulated genes. These proposed studies of normal nontransforming functional domains are feasible, based on preliminary data indicating that a mutant (anti-sense RNA resistant) fos gene restores proliferative function to anti-sense c-fos RNA inhibited fibroblasts. Experiments will analyze the functional significance of specific mutations in c-fos protein (e.g. alteration of putative phosphorylation sites, DNA binding regions, essential transforming domains) as a means to determine the role of this protein in such cellular processes as logarithmic proliferation, growth factor-induced DNA synthesis, wounding response, and differentiation. cDNA cloning techniques will be employed for identification of genes which are regulated by c-fos expression. The ultimate goal is to correlate the c-fos protein functional domains which are essential for altered expression of specific genes (AIM 3), with the domains which are required for proliferation and/or differentiation.
原癌基因有可能产生 癌症已经引起了对这些功能的极大兴趣, 正常的细胞基因 c-fos蛋白是特别重要的 因为它的核位置,DNA结合能力, 在细胞增殖过程中调节表达, 分化 然而,正常c-fos蛋白的功能 不明 本提案的总体目标是阐明 c-fos蛋白的特殊功能。 拟议的研究 将采用遗传学方法来创造和分析细胞突变体 改变c-fos的表达,以及cDNA克隆技术, 鉴定受c-fos表达调控的基因。 的 有待检验的假设是c-fos蛋白是 特定的细胞过程,因为它改变了表达 具有重要功能的基因 具体目标是:(1) 确定正常c-fos蛋白的功能结构域, 是成纤维细胞增殖所必需的; 2)为了确定 正常c-fos蛋白的功能结构域是必需的 用于胚胎干细胞增殖和/或分化; 3) 目的:鉴定c-fos表达调控基因。 这些 研究的重点是两者的功能意义 c-fos蛋白结构的改变和诱导假定的 c-fos调控基因。 这些建议的研究正常 非转换功能域是可行的,基于 初步数据表明,突变体(反义RNA fos基因恢复增殖功能的反义 c-fos RNA抑制成纤维细胞。 实验将分析 c-fos蛋白特异性突变的功能意义 (e.g.假定磷酸化位点的改变,DNA结合 区域,必要的转化结构域)作为确定 这种蛋白质在细胞过程中的作用, 增殖,生长因子诱导的DNA合成,创伤 反应和分化。 cDNA克隆技术将是 用于鉴定受c-fos调控的基因 表情 最终的目标是将c-fos蛋白 功能域是改变表达所必需的, 特定的基因(AIM 3),与所需的结构域, 增殖和/或分化。

项目成果

期刊论文数量(4)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Antisense promoter mapping. Inhibitory methods of transcriptional analysis.
反义启动子作图。
Antisense mapping of the c-fos promoter: role of the serum response element.
c-fos 启动子的反义图谱:血清反应元件的作用。
  • DOI:
    10.1089/ard.1991.1.21
  • 发表时间:
    1991
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Robinson-Benion,C;Kamata,N;Holt,JT
  • 通讯作者:
    Holt,JT
Cutting the chain of command: specific inhibitors of transcription.
切断指挥链:特异性转录抑制剂。
Antisense inhibition of c-myc expression reveals common and distinct mechanisms of growth inhibition by TGF beta and TNF alpha.
c-myc 表达的反义抑制揭示了 TGF β 和 TNF α 抑制生长的常见且独特的机制。
  • DOI:
    10.1002/jcb.240450210
  • 发表时间:
    1991
  • 期刊:
  • 影响因子:
    4
  • 作者:
    Robinson-Benion,C;Salhany,KE;Hann,SR;Holt,JT
  • 通讯作者:
    Holt,JT
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Jeffrey T Holt其他文献

Jeffrey T Holt的其他文献

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{{ truncateString('Jeffrey T Holt', 18)}}的其他基金

IHC Test for BRCA1 Hereditary Ovarian Cancer
BRCA1 遗传性卵巢癌的 IHC 检测
  • 批准号:
    8239640
  • 财政年份:
    2010
  • 资助金额:
    $ 16.88万
  • 项目类别:
IHC Test for BRCA1 Hereditary Ovarian Cancer
BRCA1 遗传性卵巢癌的 IHC 检测
  • 批准号:
    8259213
  • 财政年份:
    2010
  • 资助金额:
    $ 16.88万
  • 项目类别:
IHC Test for BRCA1 Hereditary Ovarian Cancer
BRCA1 遗传性卵巢癌的 IHC 检测
  • 批准号:
    7804771
  • 财政年份:
    2010
  • 资助金额:
    $ 16.88万
  • 项目类别:
PARP Inhibitor Targeted Therapy for Breast Cancer
PARP抑制剂靶向治疗乳腺癌
  • 批准号:
    7481522
  • 财政年份:
    2008
  • 资助金额:
    $ 16.88万
  • 项目类别:
Development of a BRCA Breast Cancer Diagnostic Test
BRCA 乳腺癌诊断测试的开发
  • 批准号:
    7325640
  • 财政年份:
    2007
  • 资助金额:
    $ 16.88万
  • 项目类别:
BRCA2 Hereditary Ovarian Cancer Tissue Truncation Test
BRCA2 遗传性卵巢癌组织截断试验
  • 批准号:
    7404496
  • 财政年份:
    2007
  • 资助金额:
    $ 16.88万
  • 项目类别:
Mechanisms of Carcinogenesis in BRCA2 Mutant Cells
BRCA2突变细胞的致癌机制
  • 批准号:
    6399060
  • 财政年份:
    2001
  • 资助金额:
    $ 16.88万
  • 项目类别:
Mechanisms of Carcinogenesis in BRCA2 Mutant Cells
BRCA2突变细胞的致癌机制
  • 批准号:
    6559526
  • 财政年份:
    2001
  • 资助金额:
    $ 16.88万
  • 项目类别:
Mechanisms of Carcinogenesis in BRCA2 Mutant Cells
BRCA2突变细胞的致癌机制
  • 批准号:
    6514387
  • 财政年份:
    2001
  • 资助金额:
    $ 16.88万
  • 项目类别:
Mechanisms of Carcinogenesis in BRCA2 Mutant Cells
BRCA2突变细胞的致癌机制
  • 批准号:
    6608872
  • 财政年份:
    2001
  • 资助金额:
    $ 16.88万
  • 项目类别:

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使用古细菌 Sulfolobus 作为模式生物,研究 DNA 复制过程中的 DNA 修复过程。
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