How a homolog of high-fidelity replicases conducts mutagenic DNA synthesis

Young Sam Lee, Yang Gao, Wei Yang

Research output: Contribution to journalArticlepeer-review

43 Scopus citations

Abstract

All DNA replicases achieve high fidelity by a conserved mechanism, but each translesion polymerase carries out mutagenic DNA synthesis in its own way. Here we report crystal structures of human DNA polymerase ν (Pol ν), which is homologous to high-fidelity replicases yet is error prone. Instead of a simple open-to-closed movement of the O helix upon binding of a correct incoming nucleotide, Pol ν has a different open state and requires the finger domain to swing sideways and undergo both opening and closing motions to accommodate the nascent base pair. A single-amino acid substitution in the O helix of the finger domain improves the fidelity of Pol ν nearly ten-fold. A unique cavity and the flexibility of the thumb domain allow Pol ν to generate and accommodate a looped-out primer strand. Primer loop-out may be a mechanism for DNA trinucloetide-repeat expansion.

Original languageEnglish
Pages (from-to)298-303
Number of pages6
JournalNature Structural and Molecular Biology
Volume22
Issue number4
DOIs
StatePublished - 7 Apr 2015

Bibliographical note

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© 2015 Nature America, Inc. All rights reserved.

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