A DNA Polymerase Mutant That Specifically Causes +1 Frameshift Mutations Within Homonucleotide Runs in Yeast

Corresponding author: M. A. Resnick, National Institute of Environmental Health Sciences (NIEHS), Mail Drop D3-01, 111 T.W. Alexander Dr., P.O. Box 12233, Research Triangle Park, NC 27709., resnick{at}niehs.nih.gov (E-mail)

Communicating editor: L. S. SYMINGTON

The DNA polymerases and are the major replicative polymerases in the yeast Saccharomyces cerevisiae that possess 3' 5' exonuclease proofreading activity. Many errors arising during replication are corrected by these exonuclease activities. We have investigated the contributions of regions of Pol other than the proofreading motifs to replication accuracy. An allele, pol2-C1089Y, was identified in a screen of Pol mutants that in combination with an exonuclease I (exo1) mutation could cause a synergistic increase in mutations within homonucleotide runs. In contrast to other polymerase mutators, this allele specifically results in insertion frameshifts. When pol2-C1089Y was combined with deletions of EXO1 or RAD27 (homologue of human FEN1), mutation rates were increased for +1 frameshifts while there was almost no effect on -1 frameshifts. On the basis of genetic analysis, the pol2-C1089Y mutation did not cause a defect in proofreading. In combination with a deletion of the mismatch repair gene MSH2, the +1 frameshift mutation rate for a short homonucleotide run was increased nearly 100-fold whereas the -1 frameshift rate was unchanged. This suggests that the Pol2-C1089Y protein makes +1 frameshift errors during replication of homonucleotide runs and that these errors can be corrected by either mismatch repair (MMR) or proofreading (in short runs). This is the first report of a +1-specific mutator for homonucleotide runs in vivo. The pol2-C1089Y mutation defines a functionally important residue in Pol.

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