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Publication Detail

Title: Structural insights into the promutagenic bypass of the major cisplatin-induced DNA lesion.

Authors: Ouzon-Shubeita, Hala; Vilas, Caroline K; Lee, Seongmin

Published In Biochem J, (2020 03 13)

Abstract: The cisplatin-1,2-d(GpG) (Pt-GG) intrastrand cross-link is the predominant DNA lesion generated by cisplatin. Cisplatin has been shown to predominantly induce G to T mutations and Pt-GG permits significant misincorporation of dATP by human DNA polymerase β (polβ). In agreement, polβ overexpression, which is frequently observed in cancer cells, is linked to cisplatin resistance and a mutator phenotype. However, the structural basis for the misincorporation of dATP opposite Pt-GG is unknown. Here, we report the first structures of a DNA polymerase inaccurately bypassing Pt-GG. We solved two structures of polβ misincorporating dATP opposite the 5'-dG of Pt-GG in the presence of Mg2+ or Mn2+. The Mg2+-bound structure exhibits a sub-optimal conformation for catalysis, while the Mn2+-bound structure is in a catalytically more favorable semi-closed conformation. In both structures, dATP does not form a coplanar base pairing with Pt-GG. In the polβ active site, the syn-dATP opposite Pt-GG appears to be stabilized by protein templating and pi stacking interactions, which resembles the polβ-mediated dATP incorporation opposite an abasic site. Overall, our results suggest that the templating Pt-GG in the polβ active site behaves like an abasic site, promoting the insertion of dATP in a non-instructional manner.

PubMed ID: 32039434 Exiting the NIEHS site

MeSH Terms: Antineoplastic Agents/chemistry*; Antineoplastic Agents/toxicity; Cisplatin/chemistry*; Cisplatin/toxicity; Crystallography, X-Ray/methods; DNA Damage/drug effects; DNA Damage/physiology*; DNA-Directed DNA Polymerase/chemistry*; DNA-Directed DNA Polymerase/genetics*; Humans; Mutagenesis/drug effects; Mutagenesis/physiology*; Protein Structure, Secondary

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