Proceedings of the National Academy of Sciences · 1991 · 278 citations · 31 references
Life SciencesBiochemistryMolecular BiologyDna ReplicationEnzyme MechanismEnzymologyDna Polymerase FunctionStructural Enzymology5' To 3' Exonuclease ActivityAmino Acid Sequence EffectsDna Polymerase IEukaryotic Dna Polymerase FunctionProkaryotic Dna Polymerase FunctionProofreading Exonuclease ActivitySequence Motif ConservationSequence Motif Discovery
We have identified an amino-proximal sequence motif, Phe-Asp-Ile-Glu-Thr, in Saccharomyces cerevisiae DNA polymerase II that is almost identical to a sequence comprising part of the 3'----5' exonuclease active site of Escherichia coli DNA polymerase I. Similar motifs were identified by amino acid sequence alignment in related, aphidicolin-sensitive DNA polymerases possessing 3'----5' proofreading exonuclease activity. Substitution of Ala for the Asp and Glu residues in the motif reduced the exonuclease activity of partially purified DNA polymerase II at least 100-fold while preserving the polymerase activity. Yeast strains expressing the exonuclease-deficient DNA polymerase II had on average about a 22-fold increase in spontaneous mutation rate, consistent with a presumed proofreading role in vivo. In multiple amino acid sequence alignments of this and two other conserved motifs described previously, five residues of the 3'----5' exonuclease active site of E. coli DNA polymerase I appeared to be invariant in aphidicolin-sensitive DNA polymerases known to possess 3'----5' proofreading exonuclease activity. None of these residues, however, appeared to be identifiable in the catalytic subunits of human, yeast, or Drosophila alpha DNA polymerases.
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An attempt to unify the structure of polymerases
Marc Delarue, Olivier Poch, Noël Tordo et al. · Protein Engineering Design and Selection · 1990 · 637 citations