This is an application to continue a 23-year study of eukaryotic DNA polymerases, which originally focused on human polymerase alpha, but now also involves polymerase delta, and their functions in chromosomal DNA replication in vivo. Previous work with DNA polymerase alpha has involved in-depth analysis of the functions of active site residues in every aspect of polymerase function. A central feature of new work will be to test the hypothesis that mutations in genes that play a critical role in DNA replication can be an early event on tumorigenesis and a source of genetic instability observed in cancer cells. The investigators will initially test the mutational effect of altered forms of pol alpha and delta using fission yeast as the model. The progression of alterations in growth properties over generations will be examined. The work will then be developed in human cells and ultimately in an animal model. In another area, they have shown that pol alpha can interact with SV 40T antigen, BPV E1, and HSV UL9 as part of the process of initiation of viral replication. Experiments are proposed to analyze the interaction of pol alpha with the E1 and E2 replication proteins of HPV-11.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA014835-27
Application #
6149992
Study Section
Biochemistry Study Section (BIO)
Program Officer
Okano, Paul
Project Start
1978-07-01
Project End
2002-01-31
Budget Start
2000-02-01
Budget End
2001-01-31
Support Year
27
Fiscal Year
2000
Total Cost
$474,940
Indirect Cost
Name
Stanford University
Department
Pathology
Type
Schools of Medicine
DUNS #
800771545
City
Stanford
State
CA
Country
United States
Zip Code
94305
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Kai, Mihoko; Wang, Teresa S-F (2003) Checkpoint responses to replication stalling: inducing tolerance and preventing mutagenesis. Mutat Res 532:59-73
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Lee, S S; Dong, Q; Wang, T S et al. (1995) Interaction of herpes simplex virus 1 origin-binding protein with DNA polymerase alpha. Proc Natl Acad Sci U S A 92:7882-6

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