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.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA049052-02
Application #
3193008
Study Section
Cellular Biology and Physiology Subcommittee 1 (CBY)
Project Start
1989-01-13
Project End
1991-12-31
Budget Start
1990-01-01
Budget End
1990-12-31
Support Year
2
Fiscal Year
1990
Total Cost
Indirect Cost
Name
Vanderbilt University Medical Center
Department
Type
Schools of Medicine
DUNS #
004413456
City
Nashville
State
TN
Country
United States
Zip Code
37212
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Holt, J T (1992) Antisense promoter mapping. Inhibitory methods of transcriptional analysis. Ann N Y Acad Sci 660:88-94
Kamata, N; Holt, J T (1992) Inhibitory effect of myristylation on transrepression by FBR (Gag-Fos) protein. Mol Cell Biol 12:876-82
Kamata, N; Jotte, R M; Holt, J T (1991) Myristylation alters DNA-binding activity and transactivation of FBR (gag-fos) protein. Mol Cell Biol 11:765-72
Holt, J T (1991) Cutting the chain of command: specific inhibitors of transcription. Antisense Res Dev 1:365-9
Robinson-Benion, C; Salhany, K E; Hann, S R et al. (1991) Antisense inhibition of c-myc expression reveals common and distinct mechanisms of growth inhibition by TGF beta and TNF alpha. J Cell Biochem 45:188-95
Robinson-Benion, C; Kamata, N; Holt, J T (1991) Antisense mapping of the c-fos promoter: role of the serum response element. Antisense Res Dev 1:21-33
Pietenpol, J A; Holt, J T; Stein, R W et al. (1990) Transforming growth factor beta 1 suppression of c-myc gene transcription: role in inhibition of keratinocyte proliferation. Proc Natl Acad Sci U S A 87:3758-62