The goal of this research is to elucidate the mechanisms underlying how DNA repair proteins locate and repair damaged DNA. The health implications of this process extend to breast and ovarian cancers, as these cancers are associated with defects in this pathway. Improved understanding of homologous recombination and DNA repair will in turn allow better understanding of the development of human cancers. The focus of this proposal is to determine how the DNA repair proteins Rad51 and Rad54 interact with DNA and with other protein components of homologous recombination, and how DNA molecules are aligned during homologous recombination. This proposal hypothesizes that the presynaptic complex formed by Rad51, Rad54, and ssDNA searches dsDNA for regions of homology using ATP hydrolysis to drive translocation. In addition, it is hypothesized that ATP hydrolysis is a vehicle for the removal of nucleosomes and other DNA binding proteins from the dsDNA that would otherwise hinder access to homologous regions of dsDNA.
The specific aims of this project are to (1) investigate the biochemical mechanism used by the presynaptic complex to probe dsDNA for homologous sequence and to (2) detail the interaction of the presynaptic complex with nucleosomes bound to the dsDNA. To test this hypothesis, reactions involving fluorescently labeled DNA molecules, Rad51, and Rad54 will be observed using total internal reflection fluorescent microscopy. This technique is able to directly visualize individual proteins interacting with individual molecules of DNA. DNA repair is an absolutely essential process to maintain cellular health. The proposed research is directly relevant to cancer biology, and the successful completion of the experiments contained in this research will contribute immensely to understanding of various types of cancers.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32GM084587-02
Application #
7588802
Study Section
Special Emphasis Panel (ZRG1-F08-G (20))
Program Officer
Carter, Anthony D
Project Start
2008-04-01
Project End
2009-09-30
Budget Start
2009-04-01
Budget End
2009-09-30
Support Year
2
Fiscal Year
2009
Total Cost
$27,530
Indirect Cost
Name
Columbia University (N.Y.)
Department
Biochemistry
Type
Schools of Medicine
DUNS #
621889815
City
New York
State
NY
Country
United States
Zip Code
10032
Robertson, Ragan B; Moses, Dana N; Kwon, YoungHo et al. (2009) Visualizing the disassembly of S. cerevisiae Rad51 nucleoprotein filaments. J Mol Biol 388:703-20
Robertson, Ragan B; Moses, Dana N; Kwon, YoungHo et al. (2009) Structural transitions within human Rad51 nucleoprotein filaments. Proc Natl Acad Sci U S A 106:12688-93
Chi, Peter; Kwon, Youngho; Moses, Dana N et al. (2009) Functional interactions of meiotic recombination factors Rdh54 and Dmc1. DNA Repair (Amst) 8:279-84