The experiments in this proposal concern the fate of the genome of polyoma virus in infections of nonpremissive rat cells (Fischer rat F-111). The major question consists of an elucidation of the steps involved in the integration pathway of the viral genome into the host genome. concomitant with stable neoplastic transformation of these cells. Many questions center around the role of interviral recombination and viral DNA replication and the role of the viral large T-antigen in any aspect of the process. There are four major section. The first concerns studies of factors which affect the process. For example we are asking whether the events related to integration occur in specific phases of the cell cycle. The second concerns the role of large T- antigen. For example we are asking whether increasing the amounts of large T-antigen in all cells from the beginning of infection will alter the events correlated with integration. The third section is a study of integrated viral structures. We will make comsid libraries to study whether the viral genome integrate in specific regions of the host chromatin (e.g. DNAse sensitive sites) and whether integration events in a single transformants are independent. The fourth section consists of studies of competition for integration between viral genomes of different parental origin.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
2R01CA029270-07
Application #
3168618
Study Section
Virology Study Section (VR)
Project Start
1981-01-01
Project End
1992-11-30
Budget Start
1987-12-01
Budget End
1988-11-30
Support Year
7
Fiscal Year
1988
Total Cost
Indirect Cost
Name
Michigan State University
Department
Type
Schools of Osteopathy
DUNS #
193247145
City
East Lansing
State
MI
Country
United States
Zip Code
48824
Fluck, Michele M; Schaffhausen, Brian S (2009) Lessons in signaling and tumorigenesis from polyomavirus middle T antigen. Microbiol Mol Biol Rev 73:542-63, Table of Contents
Cheng, Jingwei; DeCaprio, James A; Fluck, Michele M et al. (2009) Cellular transformation by Simian Virus 40 and Murine Polyoma Virus T antigens. Semin Cancer Biol 19:218-28
Chen, Li; Wang, Xiaoyu; Fluck, Michele M (2006) Independent contributions of polyomavirus middle T and small T to the regulation of early and late gene expression and DNA replication. J Virol 80:7295-307
Spink, Kathryn M; Fluck, Michele M (2003) Polyomavirus hr-t mutant-specific induction of a G2/M cell-cycle arrest that is not overcome by the expression of middle T and/or small T. Virology 307:191-203
Chen, L; Fluck, M (2001) Kinetic analysis of the steps of the polyomavirus lytic cycle. J Virol 75:8368-79
Chen, L; Fluck, M M (2001) Role of middle T-small T in the lytic cycle of polyomavirus: control of the early-to-late transcriptional switch and viral DNA replication. J Virol 75:8380-9
Syu, L J; Fluck, M M (1997) Site-specific in situ amplification of the integrated polyomavirus genome: a case for a context-specific over-replication model of gene amplification. J Mol Biol 271:76-99
Fluck, M M; Haslam, S Z (1996) Mammary tumors induced by polyomavirus. Breast Cancer Res Treat 39:45-56
Chen, M C; Redenius, D; Osati-Ashtiani, F et al. (1995) Enhancer-mediated role for polyomavirus middle T/small T in DNA replication. J Virol 69:326-33
Chen, H H; Fluck, M M (1993) Cell cycle control of polyomavirus-induced transformation. J Virol 67:1996-2005

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