The long-term objective of the proposed research is to understand the cellular mechanisms for the repair of DNA double-strand breaks (DSBs) in eukaryotes, using budding yeast as a model system. The ability to repair DSBs by HR is essential for cell proliferation in vertebrates and for genome stability in all characterized organisms. Central to this process is the Rad51 complex with ssDNA, which is active in the homology search and strand exchange phases of the reaction. However, unregulated recombination is likely to be detrimental to cells and the Rad51 filament appears to be a common target for regulation by a number of proteins. Rad52, Rad54, Rad55 and Rad57 function in formation and/or stabilization of the Rad51 nucleoprotein filament, whereas Srs2 functions to destabilize the filament. Brca2 appears to have complex roles in the regulation of Rad51 by promoting nuclear entry, targeting Rad51 to sites of DNA damage and destabilization of the Rad51 filament. Because of the central role of Rad51 filament dynamics for appropriate recombination in response to DNA damage, it is important to have a complete understanding of the formation and disassembly of the Rad51/DNA complex.
The first aim of this proposal builds on our previous studies of rad51 gain-of-function and altered function alleles to further understand how the Rad51 filament interacts with Rad55, Rad57 and Srs2. The function of residues identified at the protomer interface in the crystal structure of the Rad51 filament will also be determined.
The second aim of the proposal is to characterize known suppressors, and identify additional suppressors of rad57, to determine whether Rad57 functions exclusively at the level of the Rad51 filament, or has additional late roles in recombination. The roles of Rad55 and Rad57 in spontaneous and induced, intra and inter-chromosomal recombination will also be determined. The last aim includes in vitro studies to identify preferred DNA substrates for Rad55:Rad57 binding and stabilization of the Rad51 nucleoprotein by Rad55:Rad57 in the presence or absence of Srs2. ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM054099-10
Application #
7150605
Study Section
Molecular Genetics C Study Section (MGC)
Program Officer
Portnoy, Matthew
Project Start
1997-01-01
Project End
2009-11-30
Budget Start
2006-12-01
Budget End
2007-11-30
Support Year
10
Fiscal Year
2007
Total Cost
$292,038
Indirect Cost
Name
Columbia University (N.Y.)
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
621889815
City
New York
State
NY
Country
United States
Zip Code
10032
Mott, Christina; Symington, Lorraine S (2011) RAD51-independent inverted-repeat recombination by a strand-annealing mechanism. DNA Repair (Amst) 10:408-15
Ho, Chu Kwen; Mazon, Gerard; Lam, Alicia F et al. (2010) Mus81 and Yen1 promote reciprocal exchange during mitotic recombination to maintain genome integrity in budding yeast. Mol Cell 40:988-1000
Smith, Catherine E; Lam, Alicia F; Symington, Lorraine S (2009) Aberrant double-strand break repair resulting in half crossovers in mutants defective for Rad51 or the DNA polymerase delta complex. Mol Cell Biol 29:1432-41
Mimitou, Eleni P; Symington, Lorraine S (2009) Nucleases and helicases take center stage in homologous recombination. Trends Biochem Sci 34:264-72
Fung, Cindy W; Mozlin, Amy M; Symington, Lorraine S (2009) Suppression of the double-strand-break-repair defect of the Saccharomyces cerevisiae rad57 mutant. Genetics 181:1195-206
Mimitou, Eleni P; Symington, Lorraine S (2009) DNA end resection: many nucleases make light work. DNA Repair (Amst) 8:983-95
Mozlin, Amy M; Fung, Cindy W; Symington, Lorraine S (2008) Role of the Saccharomyces cerevisiae Rad51 paralogs in sister chromatid recombination. Genetics 178:113-26
Malik, Punjab S; Symington, Lorraine S (2008) Rad51 gain-of-function mutants that exhibit high affinity DNA binding cause DNA damage sensitivity in the absence of Srs2. Nucleic Acids Res 36:6504-10
Fung, Cindy W; Fortin, Gary S; Peterson, Shaun E et al. (2006) The rad51-K191R ATPase-defective mutant is impaired for presynaptic filament formation. Mol Cell Biol 26:9544-54
Langston, Lance D; Symington, Lorraine S (2005) Opposing roles for DNA structure-specific proteins Rad1, Msh2, Msh3, and Sgs1 in yeast gene targeting. EMBO J 24:2214-23

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