Involvement of 3-methyladenine DNA glycosylases Mag1p and Mag2p in base excision repair of methyl methanesulfonate-damaged DNA in the fission yeast Schizosaccharomyces pombe

• Published in: Genes & Genetic Systems Vol. 82; no. 6; pp. 489 - 494
• Main Authors: Kanamitsu, K.(Okayama Univ. of Science (Japan)), Tanihigashi, H, Tanita, Y, Inatani, S, Ikeda, S
• Format: Journal Article
• Language: English
• Published: Japan The Genetics Society of Japan 2007; Japan Science and Technology Agency
• Subjects: 3-methyladenine DNA glycosylase; Alkylation; alkylation damage; Base excision repair; DNA damage; DNA Damage - physiology; DNA glycosylase; DNA Glycosylases - genetics; DNA Glycosylases - metabolism; DNA Repair; Enzymes; Escherichia coli; EXPRESION GENICA; EXPRESSION DES GENES; Gene deletion; GENE EXPRESSION; Genetic analysis; Homology; mag1; mag2; Methyl methanesulfonate; Methyl Methanesulfonate - toxicity; MMS; Mutagens - toxicity; MUTANT; MUTANTES; MUTANTS; NTH1 protein; Nucleotide excision repair; REPAIRING; REPARACION; REPARATION; Schizosaccharomyces - drug effects; Schizosaccharomyces - enzymology; Schizosaccharomyces - genetics; SCHIZOSACCHAROMYCES POMBE; Schizosaccharomyces pombe Proteins - genetics; Schizosaccharomyces pombe Proteins - metabolism
• DOI: 10.1266/ggs.82.489
• ISSN: 1341-7568; 1880-5779

Schizosaccharomyces pombe has two paralogues of 3-methyladenine DNA glycosylase, Mag1p and Mag2p, which share homology with Escherichia coli AlkA. To clarify the function of these redundant enzymes in base excision repair (BER) of alkylation damage, we performed several genetic analyses. The mag1 and mag2 single mutants as well as the double mutant showed no obvious methyl methanesulfonate (MMS) sensitivity. Deletion of mag1 or mag2 from an nth1 mutant resulted in tolerance to MMS damage, indicating that both enzymes generate AP sites in vivo by removal of methylated bases. A rad16 mutant that is deficient in nucleotide excision repair (NER) exhibited moderate MMS sensitivity. Deletion of mag1 from the rad16 mutant greatly enhanced MMS sensitivity, and the mag2 deletion also weakened the resistance to MMS of the rad16 mutant. A mag1/mag2/rad16 triple mutant was most sensitive to MMS. These results suggest that the NER pathway obscures the mag1 and mag2 functions in MMS resistance and that both paralogues initiate the BER pathway of MMS-induced DNA damage at the same level in NER-deficient cells or that Mag2p tends to make a little lower contribution than Mag1p. Mag1p and Mag2p functioned additively in vivo. Expression of mag1 and mag2 in the triple mutant confirmed the contribution of Mag1p and Mag2p to BER of MMS resistance.