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- W3035732249 endingPage "6844" @default.
- W3035732249 startingPage "6831" @default.
- W3035732249 abstract "The N 2 ‐position of deoxyguanosine (dG) in DNA is susceptible to modification by various damaging agents. These modifications (lesions or adducts) can stall the DNA replication by replicative polymerases, and if the common DNA repair pathways do not remove them, it can result in genomic instability. This generally leads to the death or oncogenic transformation of the cell. An important mechanism to deal with this problem is Translesion synthesis (TLS), a bypass mechanism, which involves the tolerance of DNA damage by low‐fidelity DNA polymerases (TLS polymerases). To understand the accuracy of TLS polymerases, a chemical biology approach is required. In this review, we discuss the reliable methods to synthesize specific N 2 ‐dG DNA adducts and how they are tolerated by bacterial TLS polymerase Pol IV and its mammalian orthologue hpol κ. Molecular insights on the accurate bypass of these adducts emerge from the primer extension assays, X‐ray crystallographic, and molecular modeling studies are reviewed here." @default.
- W3035732249 created "2020-06-19" @default.
- W3035732249 creator A5035166900 @default.
- W3035732249 creator A5054425260 @default.
- W3035732249 date "2020-07-13" @default.
- W3035732249 modified "2023-09-26" @default.
- W3035732249 title "Site‐Specific <i>N</i> <sup>2</sup> ‐dG DNA Adducts: Formation, Synthesis, and TLS Polymerase‐Mediated Bypass" @default.
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