This application describes the ongoing research of four investigators who interact extensively, occupy adjoining laboratories, and work on various aspects of the molecular genetics of herpes simplex (HSV) and Epstein-Barr viruses. Project 1 centers on the domains and functions of HSV alpha genes, and on the function of genes nonessential for growth in cell culture. The work entails application of novel insertion/deletion techniques for deletion of genes from the viral genome and construction of cell lines expressing alpha genes for the study of their functions. Project 2 focuses on the HSV glycoproteins that govern the process of viral induced cell fusion. These studies have demonstrated that two glyco-proteins, B and D, play a major role in cell fusion and have led to the discovery and partial nucleotide sequence of a hitherto unidentified gene that also modulates the fusion process. Studies in progress are designed to identify the product of this gene. Project 3 focuses on host gene expression in HSV infected cells. A mutant defective in early host shut-off has been partially mapped and shown to act posttranslationally on both host and viral protein synthesis by destabilizing mRNA. Current studies focus on the product of the gene and on in vitro translational systems to characterize the destablilization of the RNA. Project 4 focuses on the use of HSV vectors to express EBV genes and on the glycoprotein genes of EBV. Current studies center on the characterization of the EBV gene products.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
5P01CA019264-11
Application #
3092822
Study Section
Cancer Special Program Advisory Committee (CAK)
Project Start
1976-06-30
Project End
1989-06-30
Budget Start
1986-07-01
Budget End
1987-06-30
Support Year
11
Fiscal Year
1986
Total Cost
Indirect Cost
Name
University of Chicago
Department
Type
Schools of Medicine
DUNS #
225410919
City
Chicago
State
IL
Country
United States
Zip Code
60637
Chou, J; Roizman, B (1989) Characterization of DNA sequence-common and sequence-specific proteins binding to cis-acting sites for cleavage of the terminal a sequence of the herpes simplex virus 1 genome. J Virol 63:1059-68
Roller, R J; McCormick, A L; Roizman, B (1989) Cellular proteins specifically bind single- and double-stranded DNA and RNA from the initiation site of a transcript that crosses the origin of DNA replication of herpes simplex virus 1. Proc Natl Acad Sci U S A 86:6518-22
Fuller, A O; Santos, R E; Spear, P G (1989) Neutralizing antibodies specific for glycoprotein H of herpes simplex virus permit viral attachment to cells but prevent penetration. J Virol 63:3435-43
Johnson, R M; Spear, P G (1989) Herpes simplex virus glycoprotein D mediates interference with herpes simplex virus infection. J Virol 63:819-27
Kwong, A D; Frenkel, N (1989) The herpes simplex virus virion host shutoff function. J Virol 63:4834-9
WuDunn, D; Spear, P G (1989) Initial interaction of herpes simplex virus with cells is binding to heparan sulfate. J Virol 63:52-8
Kristie, T M; Roizman, B (1988) Differentiation and DNA contact points of host proteins binding at the cis site for virion-mediated induction of alpha genes of herpes simplex virus 1. J Virol 62:1145-57
Arsenakis, M; Campadelli-Fiume, G; Lombardo, M T et al. (1988) The glycoprotein C gene of herpes simplex virus 1 resident in clonal L cell lines manifests two regulatory domains conferring a dominant B and a subordinate gamma 2 regulation. Virology 162:300-10
Hubenthal-Voss, J; Houghten, R A; Pereira, L et al. (1988) Mapping of functional and antigenic domains of the alpha 4 protein of herpes simplex virus 1. J Virol 62:454-62
Arsenakis, M; Campadelli-Fiume, G; Roizman, B (1988) Regulation of glycoprotein D synthesis: does alpha 4, the major regulatory protein of herpes simplex virus 1, regulate late genes both positively and negatively? J Virol 62:148-58

Showing the most recent 10 out of 88 publications