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

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 ? (pol?). In agreement, pol? 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 pol? 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 pol? active site, the syn-dATP opposite Pt-GG appears to be stabilized by protein templating and pi stacking interactions, which resembles the pol?-mediated dATP incorporation opposite an abasic site. Overall, our results suggest that the templating Pt-GG in the pol? active site behaves like an abasic site, promoting the insertion of dATP in a non-instructional manner.

SUBMITTER: Ouzon-Shubeita H 

PROVIDER: S-EPMC7534533 | biostudies-literature | 2020 Mar

REPOSITORIES: biostudies-literature