The overall, long-term objective of this research program is to use genetic, immunological, and molecular approaches to define the functions that the various type 12 adenovirus (Ad12) E1A and E1B proteins play in transforming rat and mouse cells in vitro, and to understand the basis for the strong oncogenicity of this serotype and the very striking difference in viral oncogenicity between this serotype and non-oncogenic serotypes such as 2 and 5. We are also interested in determining the roles of these E1 gene products in regulating the progress of infection in permissive human cells.
Our specific aims over the next five years are to: 1) Analyze the roles of the Ad12 E1b 54Kd protein in the early phase of productive infection in human cells, and in ocogenic transformation of rodent cells. 2) Extend phenotypic analysis of the Ad12 E1B 19Kd mutants with a view to determining the basis for their differential DNA degradation and transformation phenotypes and defining the role of this protein in productive infection and transformation. 3) Extend mutational analysis of the roles of Ad12 E1A gene product functions in productive infection of human cells and oncogenic transformation of rodent cells. 4) Prepare and characterize monoclonal antibodies specific for each of the various Ad12 E1A and E1B proteins.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA032940-09
Application #
3170824
Study Section
Virology Study Section (VR)
Project Start
1982-08-01
Project End
1993-06-30
Budget Start
1990-07-01
Budget End
1991-06-30
Support Year
9
Fiscal Year
1990
Total Cost
Indirect Cost
Name
Carnegie-Mellon University
Department
Type
Schools of Arts and Sciences
DUNS #
052184116
City
Pittsburgh
State
PA
Country
United States
Zip Code
15213
Williams, J F; Zhang, Y; Williams, M A et al. (2004) E1A-based determinants of oncogenicity in human adenovirus groups A and C. Curr Top Microbiol Immunol 273:245-88
Williams, J; Williams, M; Liu, C et al. (1995) Assessing the role of E1A in the differential oncogenicity of group A and group C human adenoviruses. Curr Top Microbiol Immunol 199 ( Pt 3):149-75
Telling, G C; Perera, S; Szatkowski-Ozers, M et al. (1994) Absence of an essential regulatory influence of the adenovirus E1B 19-kilodalton protein on viral growth and early gene expression in human diploid WI38, HeLa, and A549 cells. J Virol 68:541-7
Telling, G C; Williams, J (1994) Constructing chimeric type 12/type 5 adenovirus E1A genes and using them to identify an oncogenic determinant of adenovirus type 12. J Virol 68:877-87
Lamberti, C; Williams, J (1990) Differential requirement for adenovirus type 12 E1A gene products in oncogenic transformation. J Virol 64:4997-5007
Byrd, P J; Grand, R J; Breiding, D et al. (1988) Host range mutants of adenovirus type 12 E1 defective for lytic infection, transformation, and oncogenicity. Virology 163:155-65
Breiding, D E; Edbauer, C A; Tong, J Y et al. (1988) Isolation and characterization of adenovirus type 12 E1 host-range mutants defective for growth in nontransformed human cells. Virology 164:390-402
Edbauer, C; Lamberti, C; Tong, J et al. (1988) Adenovirus type 12 E1B 19-kilodalton protein is not required for oncogenic transformation in rats. J Virol 62:3265-73
Eager, K B; Williams, J; Breiding, D et al. (1985) Expression of histocompatibility antigens H-2K, -D, and -L is reduced in adenovirus-12-transformed mouse cells and is restored by interferon gamma. Proc Natl Acad Sci U S A 82:5525-9