ANALYSIS OF TARGET GENES ACTIVATED--JUN ONCOPROTEIN
激活靶基因分析--JUN ONCOPROTEIN
基本信息
- 批准号:2094497
- 负责人:
- 金额:$ 9.11万
- 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:1989-08-01 至 1995-05-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
The mechanisms governing the regulation of cell growth are fundamental to
the understanding of tumorigenesis. These mechanisms include signal chains
that can be affected by oncogenes. In order to analyze these mechanisms,
one must know normal and aberrant functions of oncogenes, their targets and
effects on cellular signalling. The long term objective of this work is to
gain insight into the mechanisms by which oncogenes turn normal cells into
cancer cells. The specific aims focus on the identification and molecular
characterization of oncogenically important target genes activated by the
jun oncoprotein. This knowledge will be invaluable in understanding the
process by which oncogenes induce cell transformation as well as the steps
involved in normal growth control.
This study will be divided into three parts. The first involves the
identification of primary target genes activated by jun. This will be done
by subtraction screening of a cDNA library generated immediately after
induction of expression of v-jun, against an uninduced library. The second
area involves the determination of oncogenic potential of each target
identified. This will be performed by assaying for cell transformation in
the potential large number of targets, these assays will be performed with
pools of DNA. Important targets from transformation positive pools can then
be sorted out. The third area deals with a molecular analysis of
oncogenically important target gene(s) and a structural and functional
characterization of their products.
控制细胞生长调节的机制对于
对肿瘤发生的理解。这些机制包括信号链
会受到致癌基因的影响。为了分析这些机制,
人们必须了解癌基因的正常和异常功能,它们的靶点,
对细胞信号的影响。这项工作的长期目标是
深入了解致癌基因将正常细胞转化为
癌细胞具体目标集中在鉴定和分子
表征致癌重要的靶基因激活的
jun癌蛋白。这些知识对于理解
癌基因诱导细胞转化的过程以及
参与正常生长控制。
本研究将分为三个部分。第一个涉及
识别jun激活的主要靶基因。这将在
通过差减筛选后立即产生的cDNA文库
针对未诱导文库诱导v-jun的表达。第二
区域涉及确定每个靶点的致癌潜力
鉴定这将通过测定细胞转化来进行,
由于潜在的大量靶标,这些试验将使用
DNA池转化阳性样本池中的重要靶标可以
解决问题第三个领域涉及的分子分析,
致癌重要的靶基因和结构和功能
他们的产品特征。
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)
In vivo viral and cellular Jun complexes exhibit differential interaction with a number of in vitro generated 'AP-1- and CREB-like' target sequences.
体内病毒和细胞 Jun 复合物与许多体外生成的“AP-1 和 CREB 样”靶序列表现出不同的相互作用。
- DOI:
- 发表时间:1993
- 期刊:
- 影响因子:8
- 作者:Hadman,M;Loo,M;Bos,TJ
- 通讯作者:Bos,TJ
Modifications to the differential display technique reduce background and increase sensitivity.
对差分显示技术的修改减少了背景并提高了灵敏度。
- DOI:10.1006/abio.1995.1243
- 发表时间:1995
- 期刊:
- 影响因子:0
- 作者:Hadman,M;Adam,BL;WrightJr,GL;Bos,TJ
- 通讯作者:Bos,TJ
Heterodimerization with c-Fos is not required for cell transformation of chicken embryo fibroblasts by Jun.
Jun 提出的鸡胚成纤维细胞的细胞转化不需要 c-Fos 异二聚化。
- DOI:
- 发表时间:1992
- 期刊:
- 影响因子:0
- 作者:Hughes,M;Sehgal,A;Hadman,M;Bos,T
- 通讯作者:Bos,T
Isolation and cloning of JTAP-1: a cathepsin like gene upregulated in response to V-Jun induced cell transformation.
JTAP-1 的分离和克隆:一种组织蛋白酶样基因,响应 V-Jun 诱导的细胞转化而上调。
- DOI:
- 发表时间:1996
- 期刊:
- 影响因子:8
- 作者:Hadman,M;Gabos,L;Loo,M;Sehgal,A;Bos,TJ
- 通讯作者:Bos,TJ
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{{ truncateString('TIMOTHY J BOS', 18)}}的其他基金
Cancer Education Program:Student Research Experiences
癌症教育计划:学生研究经验
- 批准号:
6748166 - 财政年份:1996
- 资助金额:
$ 9.11万 - 项目类别:
Cancer Education Program:Student Research Experiences
癌症教育计划:学生研究经历
- 批准号:
6897313 - 财政年份:1996
- 资助金额:
$ 9.11万 - 项目类别:
Cancer Education Program:Student Research Experiences
癌症教育计划:学生研究经验
- 批准号:
7067069 - 财政年份:1996
- 资助金额:
$ 9.11万 - 项目类别:
Cancer Education Program:Student Research Experiences
癌症教育计划:学生研究经历
- 批准号:
6604331 - 财政年份:1996
- 资助金额:
$ 9.11万 - 项目类别:
ANALYSIS OF TARGET GENES ACTIVATED--JUN ONCOPROTEIN
激活靶基因分析--JUN ONCOPROTEIN
- 批准号:
3459836 - 财政年份:1989
- 资助金额:
$ 9.11万 - 项目类别:
ANALYSIS OF TARGET GENES ACTIVATED--JUN ONCOPROTEIN
激活靶基因分析--JUN ONCOPROTEIN
- 批准号:
3459837 - 财政年份:1989
- 资助金额:
$ 9.11万 - 项目类别:
ANALYSIS OF TARGET GENES ACTIVATED--JUN ONCOPROTEIN
激活靶基因分析--JUN ONCOPROTEIN
- 批准号:
3459835 - 财政年份:1989
- 资助金额:
$ 9.11万 - 项目类别:
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