Epigenetically Modified N-6-Methyladenine Inhibits Dna Replication By Human Dna Polymerase Eta

N-6-methyladenine (6mA), as a newly reported epigenetic marker, plays significant roles in regulation of various biological processes in eukaryotes. However, the effect of 6mA on human DNA replication remain elusive. In this work, we used Y-family human DNA polymerase eta as a model to investigate the kinetics of bypass of 6mA by hPol eta. We found 6mA and its intermediate hypoxanthine (I) on template partially inhibited DNA replication by hPol eta. dTMP incorporation opposite 6mA and dCMP incorporation opposite I can be considered as correct incorporation. However, both 6mA and I reduced correct incorporation efficiency, next-base extension efficiency, and the priority in extension beyond correct base pair. Both dTMP incorporation opposite 6rnA and dCTP opposite I showed fast burst phases. However, 6mA and I reduced the burst incorporation rates (K-pol) and increased the dissociation constant (K-d(,dNTP)), compared with that of dTMP incorporation opposite unmodified A. Biophysical binding assays revealed that both 6mA and I on template reduced the binding affinity of hPol eta to DNA in binary or ternary complex compared with unmodified A. All the results explain the inhibition effects of 6mA and Ion DNA replication by hPol eta, providing new insight in the effects of epigenetically modified 6mA on human DNA replication.