A gene homologous to methionine sulfoxide reductase (msrA) was identified as the predicted open reading frame (cosmid 9379) in chromosome V of Saccharomyces cerevisiae encoding a protein of 184 amino acids. The corresponding protein has been expressed in Escherichia coli and purified to homogeneity. The recombinant yeast MsrA possessed the same substrate specificity as the other known MsrA enzymes from mammalian and bacterial cells. Interruption of the yeast gene resulted in a null mutant, DmsrA::URA3 strain, which totally lost its cellular MsrA activity and was shown to be more sensitive to oxidative stress in comparison to its wild type parent strain. Furthermore, high levels of free and protein-bound methionine sulfoxide were detected in extracts of MsrA mutant cells relative to their wild type parent cells, under various oxidative stresses. These findings show for the first time that MsrA is responsible for the reduction of methionine sulfoxide in vivo as well as in vitro, in eukaryotic cells. Also, the results support the proposition that MsrA possess an antioxidant function. The ability of MsrA to repair oxidative damage in vivo may be of singular importance if methionine residues serve as antioxidants, as has been proposed by Levine et al. (Levine, R.L., Mosoni, L., Berlett, B.S., and Stadtman, E.R. (1996) Proc. Natl. Acad. Sci. USA 93, 15036-15040).
| Moskovitz, J; Poston, J M; Berlett, B S et al. (2000) Identification and characterization of a putative active site for peptide methionine sulfoxide reductase (MsrA) and its substrate stereospecificity. J Biol Chem 275:14167-72 |
| Moskovitz, J; Berlett, B S; Poston, J M et al. (1999) Methionine sulfoxide reductase in antioxidant defense. Methods Enzymol 300:239-44 |
