Article ID Journal Published Year Pages File Type
2042472 Cell Reports 2013 8 Pages PDF
Abstract

•Architecture of DNA polymerase ζ is now revealed•Enzyme has an elongated structure with separate catalytic and regulatory lobes•The accessory Pol32 and Rev7 subunits are in close spatial proximity•The structure shows why Pol32 and Rev7 are needed for complex formation

SummaryDNA polymerase ζ (Polζ) is specialized for the extension step of translesion DNA synthesis (TLS). Despite its central role in maintaining genome integrity, little is known about its overall architecture. Initially identified as a heterodimer of the catalytic subunit Rev3 and the accessory subunit Rev7, yeast Polζ has recently been shown to form a stable four-subunit enzyme (Polζ-d) upon the incorporation of Pol31 and Pol32, the accessory subunits of yeast Polδ. To understand the 3D architecture and assembly of Polζ and Polζ-d, we employed electron microscopy. We show here how the catalytic and accessory subunits of Polζ and Polζ-d are organized relative to each other. In particular, we show that Polζ-d has a bilobal architecture resembling the replicative polymerases and that Pol32 lies in proximity to Rev7. Collectively, our study provides views of Polζ and Polζ-d and a structural framework for understanding their roles in DNA damage bypass.

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Life Sciences Agricultural and Biological Sciences Agricultural and Biological Sciences (General)
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