Extrinsic proofreading

The high fidelity of replication of the nuclear DNA genome in eukaryotes involves three processes. Correct rather than incorrect dNTPs are almost always incorporated by the three major replicases, DNA polymerases alpha, 8 and e. When an incorrect base is occasionally inserted, the latter Pols 8 and e also have a 3 ' to 5 ' exonuclease activity that can remove the mismatch to allow correct DNA synthesis to proceed. Lastly, rare mismatches that escape proofreading activity and are present in newly replicated DNA can be removed by DNA mismatch repair. In this review, we consider evidence supporting the hypothesis that the second mechanism, proofreading, can operate in two different ways. Primer terminal mismatches made by either Pol 8 or Pol e can be 'intrinsically' proofread. This mechanism occurs by direct transfer of a misinserted base made at the polymerase active site to the exonuclease active site that is located a short distance away. Intrinsic proofreading allows mismatch excision without intervening enzyme dissociation. Alternatively, considerable evidence suggests that mismatches made by any of the three replicases can also be proofread by 'extrinsic' proofreading by Pol 8. Extrinsic proofreading occurs when a mismatch made by any of the three replicases is initially abandoned, thereby allowing the exonuclease active site of Pol 8 to bind directly to and remove the mismatch before replication continues. Here we review the evidence that extrinsic proofreading significantly enhances the fidelity of nuclear DNA replication, and we then briefly consider the implications of this process for evolution and disease.

Automated summary

The high fidelity of replication of the nuclear DNA genome in eukaryotes involves three processes: incorporation of correct dNTPs, removal of mismatches by exonuclease activity, and DNA mismatch repair. This review focuses on two mechanisms of proofreading: intrinsic proofreading and extrinsic proofreading. The evidence suggests that extrinsic proofreading significantly enhances the fidelity of nuclear DNA replication.