FUNCTIONS OF C-FOS PROTEIN IN CELLULAR PHYSIOLOGY
FUNCTIONS OF C-FOS PROTEIN IN CELLULAR PHYSIOLOGY
批准号:
3193009
负责人:
Jeffrey T Holt
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
项目状态:
已结题
起止时间:
1989-01-13 至 1991-12-31
关键词:
DNA binding protein DNA repair DNA replication antibody antisense nucleic acid cell differentiation cell growth regulation fibroblasts gel electrophoresis gene expression gene induction /repression gene mutation genetic manipulation genetic mapping genetic regulation genetic transcription growth factor hematopoietic stem cells immunological substance immunoprecipitation laboratory rabbit molecular cloning molecular genetics mutagen testing nucleic acid hybridization phosphorylation protein structure protooncogene tissue /cell culture
中文摘要
原癌基因具有生产潜力的发现
癌症已经引起了人们对这些功能的极大兴趣
正常的细胞基因。C-fos蛋白特别重要
因为它的核位置、DNA结合能力以及
细胞增殖过程中基因表达的调控
差异化。然而,正常的c-fos蛋白的功能
是未知的。这项提议的总体目标是澄清
C-fos蛋白的特定功能。建议进行的研究
将使用遗传方法来创造和分析细胞突变
通过改变c-fos的表达和cDNA克隆技术来
确定受c-fos表达调控的基因。这个
需要检验的假设是c-fos蛋白是
特定的细胞过程,因为它改变了
具有基本功能的基因。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)确定
正常c-fos蛋白的功能域是必需的
用于胚胎干细胞增殖和/或分化;3)
寻找受c-fos表达调控的基因。这些
研究集中在两者的功能意义上。
C-fos蛋白结构的改变及其可能的诱导作用
C-fos调控基因。这些建议的正常研究
非转换功能域是可行的,基于
初步数据表明,一种突变体(反义RNA
Fos基因反义恢复增殖功能
C-fos RNA抑制成纤维细胞生长。实验将分析
C-fos蛋白特异性突变的功能意义
(例如,假定的磷酸化位点的改变、DNA结合
区域、基本转换域)作为确定
这种蛋白质在细胞过程中的作用,如对数
增殖,生长因子诱导的DNA合成,创伤
回应,和差异化。CDNA克隆技术将是
用于识别受c-fos调控的基因
表情。最终目标是将c-fos蛋白与
基因表达改变所必需的功能结构域
特定基因(AIM 3),以及需要的结构域
增殖和/或分化。
英文摘要
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.
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DOI:
10.1111/j.1749-6632.1992.tb21061.x
发表时间:
1992
期刊:
Annals of the New York Academy of Sciences
影响因子:
5.2
作者:
[Holt,JT]
通讯作者:
Holt,JT
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:
Antisense research and development
影响因子:
--
作者:
[Robinson-Benion,C, Kamata,N, Holt,JT]
通讯作者:
Holt,JT
DOI:
10.1089/ard.1991.1.365
发表时间:
1991
期刊:
Antisense research and development
影响因子:
--
作者:
[Holt,JT]
通讯作者:
Holt,JT
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:
Journal of cellular biochemistry
影响因子:
4
作者:
[Robinson-Benion,C, Salhany,KE, Hann,SR, Holt,JT]
通讯作者:
Holt,JT
IHC Test for BRCA1 Hereditary Ovarian Cancer
-
批准号:8239640
-
项目类别:
-
资助金额:$39.92万
-
财政年份:2010
-
负责人:Jeffrey T Holt
-
依托单位:
IHC Test for BRCA1 Hereditary Ovarian Cancer
-
批准号:8259213
-
项目类别:
-
资助金额:$39.92万
-
财政年份:2010
-
负责人:Jeffrey T Holt
-
依托单位:
IHC Test for BRCA1 Hereditary Ovarian Cancer
-
批准号:7804771
-
项目类别:
-
资助金额:$16.36万
-
财政年份:2010
-
负责人:Jeffrey T Holt
-
依托单位:
PARP Inhibitor Targeted Therapy for Breast Cancer
-
批准号:7481522
-
项目类别:
-
资助金额:$14.9万
-
财政年份:2008
-
负责人:Jeffrey T Holt
-
依托单位:
Development of a BRCA Breast Cancer Diagnostic Test
-
批准号:7325640
-
项目类别:
-
资助金额:$5.48万
-
财政年份:2007
-
负责人:Jeffrey T Holt
-
依托单位:
BRCA2 Hereditary Ovarian Cancer Tissue Truncation Test
-
批准号:7404496
-
项目类别:
-
资助金额:$16.17万
-
财政年份:2007
-
负责人:Jeffrey T Holt
-
依托单位:
Mechanisms of Carcinogenesis in BRCA2 Mutant Cells
-
批准号:6399060
-
项目类别:
-
资助金额:$30.15万
-
财政年份:2001
-
负责人:Jeffrey T Holt
-
依托单位:
Mechanisms of Carcinogenesis in BRCA2 Mutant Cells
-
批准号:6559526
-
项目类别:
-
资助金额:$3.23万
-
财政年份:2001
-
负责人:Jeffrey T Holt
-
依托单位:
Mechanisms of Carcinogenesis in BRCA2 Mutant Cells
-
批准号:6514387
-
项目类别:
-
资助金额:$37.35万
-
财政年份:2001
-
负责人:Jeffrey T Holt
-
依托单位:
Mechanisms of Carcinogenesis in BRCA2 Mutant Cells
-
批准号:6608872
-
项目类别:
-
资助金额:$26.53万
-
财政年份:2001
-
负责人:Jeffrey T Holt
-
依托单位:
Mechanisms of Carcinogenesis in BRCA2 Mutant Cells
-
批准号:6913605
-
项目类别:
-
资助金额:$22.96万
-
财政年份:2001
-
负责人:Jeffrey T Holt
-
依托单位:
Mechanisms of Carcinogenesis in BRCA2 Mutant Cells
-
批准号:6803434
-
项目类别:
-
资助金额:$23.02万
-
财政年份:2001
-
负责人:Jeffrey T Holt
-
依托单位:
CANCER GENETICS
-
批准号:6103155
-
项目类别:
-
资助金额:$7.03万
-
财政年份:1998
-
负责人:Jeffrey T Holt
-
依托单位:
CORE--VIRAL VECTOR
-
批准号:6103167
-
项目类别:
-
资助金额:$7.03万
-
财政年份:1998
-
负责人:Jeffrey T Holt
-
依托单位:
OVARIAN CANCER GENE THERAPY WITH BRCA1
-
批准号:6115614
-
项目类别:
-
资助金额:$3.64万
-
财政年份:1998
-
负责人:Jeffrey T Holt
-
依托单位:
CANCER GENETICS
-
批准号:6237633
-
项目类别:
-
资助金额:$6.83万
-
财政年份:1997
-
负责人:Jeffrey T Holt
-
依托单位:
OVARIAN CANCER GENE THERAPY WITH BRCA1
-
批准号:6276848
-
项目类别:
-
资助金额:$3.29万
-
财政年份:1997
-
负责人:Jeffrey T Holt
-
依托单位:
TISSUE TARGETED RETROVIRAL VECTORS IN BREAST CANCER
-
批准号:6246734
-
项目类别:
-
资助金额:$3.1万
-
财政年份:1997
-
负责人:Jeffrey T Holt
-
依托单位:
OVARIAN CANCER GENE THERAPY WITH BRCA1
-
批准号:6246777
-
项目类别:
-
资助金额:$3.1万
-
财政年份:1997
-
负责人:Jeffrey T Holt
-
依托单位:
CORE--VIRAL VECTOR
-
批准号:6237645
-
项目类别:
-
资助金额:$6.83万
-
财政年份:1997
-
负责人:Jeffrey T Holt
-
依托单位:
海外基金