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Sheila S. David
Professor

Email: david@chem.ucdavis.edu
Phone:(530) 752-4280
Fax:(530) 752-8995

B.A. Saint Olaf College, 1984.
Ph.D. University of Minnesota, 1989.
NIH Postdoctoral Fellow, California Institute of Technology, 1990-1992.
Appointed to Faculty at UC, Davis, 2006.
Beckman Young Investigator
AP Sloan Fellow

Group Page
Principal Research Interests
We use chemical approaches to investigate the fascinating area of DNA repair. Damage to DNA can result in deleterious outcomes, such as cancer and aging; fortunately, most DNA damage is repaired by DNA repair enzymes. Our laboratory focuses on the repair of damaged DNA bases which is mediated by the process of base excision repair. The key enzymes in this pathway are the damage-specific DNA glycosylases that search through the vast amount of normal DNA to find subtle potentially mutagenic base modifications. Our goals are to understand the molecular details associated with the recognition and repair of DNA damage, and how these features impact mutagenesis and carcinogenesis. As chemical biologists interested in DNA repair, we use a variety of approaches, including enzymology, synthesis of modified substrates, spectroscopy, and cell biology. Importantly, putting these approaches together in unique ways allows connections to be made between the molecular insight derived from our in vitro studies, and how these features impact repair in cells. Ultimately this will reveal the critical features of the DNA repair process that prevents deleterious mutations leading to cancer, and how these processes may be manipulated for beneficial therapeutic purposes.
Representative Publications

“Unnatural substrates reveal the importance of 8-oxoguanine for in vivo mismatch repair by MutY,” Livingston, A.L., O’Shea, V.L., Kim, T., Kool, E. T., David, S. S. Nature Chemical Biology, 2008, 4, 51-59.

“Base-excision repair of DNA Damage,” David, S. S., O’Shea, V. L., Kundu, S., Nature, 2007, 941-950.

“Unusual Structural Features of Hydantoin Lesions Translate into Efficient Recognition by Escherichia coli Fpg,” Krishnamurthy, N., Muller, J.G., Burrows, C. J., David, S. S., Biochemistry, 2007, 46, 9355-9365.

“Insight into the Role of Tyrosine 82 and Glycine 253 in the Escherichia coli Adenine Glycosylase MutY,” Livingston, A.L., Kundu, S., Pozzi, M.H., Anderson, D.W., David,S.S., Biochemistry, 2005, 44, 14179-14190.

“A Role for Iron-Sulfur Clusters in DNA Repair,“ Lukianova, O.A., David, S.S., Curr. Op. Chem. Biol., 2005, 9, 145-151.