Base excision repair is an important process to understand because damaged DNA bases are known to produce mutations, which can cause hereditary diseases and cancer. A family of alkylation-specific DNA glycosylases is responsible for locating and removing several types of modified bases. Some 3-methyladenine (3-MeA) glycosylases are specific for a certain type of alkylated base, whereas others have a broad specificity. Moreover, these different classes of 3-MeA glycosylases are represented in the large family of helix-hairpin-helix (HhH) glycosylases. The goal of the proposed studies is to understand the structural reason for differences in the substrate specificities of 3-MeA DNA glycosylases that share common folds, and to address the mechanism by which these enzymes locate and remove damaged bases from DNA. To address these questions, the crystal structures of three HhH 3-MeA DNA glycosylases representing two extremes in substrate specificity will be determined in the presence and absence of DNA substrates. H. pylori MagIII is highly specific for 3-MeA residues, while S. cerevisiae MAO and S. pombe MagI have a broad specificity. Crystals of MagIII protein and of MagI/DNA complexes have already been obtained.
| Brieba, Luis G; Eichman, Brandt F; Kokoska, Robert J et al. (2004) Structural basis for the dual coding potential of 8-oxoguanosine by a high-fidelity DNA polymerase. EMBO J 23:3452-61 |
| Eichman, Brandt F; O'Rourke, Eyleen J; Radicella, J Pablo et al. (2003) Crystal structures of 3-methyladenine DNA glycosylase MagIII and the recognition of alkylated bases. EMBO J 22:4898-909 |
