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Enzymology
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- DNA and ChromosomesOpen Access
Structural and Kinetic Analysis of Miscoding Opposite the DNA Adduct 1,N6-Ethenodeoxyadenosine by Human Translesion DNA Polymerase η
Journal of Biological ChemistryVol. 291Issue 27p14134–14145Published online: May 16, 2016- Amritraj Patra
- Yan Su
- Qianqian Zhang
- Kevin M. Johnson
- F.Peter Guengerich
- Martin Egli
Cited in Scopus: 121,N6-Ethenodeoxyadenosine (1,N6-ϵdA) is the major etheno lesion formed in the reaction of DNA with epoxides substituted with good leaving groups (e.g. vinyl chloride epoxide). This lesion is also formed endogenously in DNA from lipid oxidation. Recombinant human DNA polymerase η (hpol η) can replicate oligonucleotide templates containing 1,N6-ϵdA. In steady-state kinetic analysis, hpol η preferred to incorporate dATP and dGTP, compared with dTTP. Mass spectral analysis of incorporation products also showed preferred purine (A, G) incorporation and extensive −1 frameshifts, suggesting pairing of the inserted purine and slippage before further replication.