Biased distribution of action-at-a-distance mutations by 8-oxo-7,8-dihydroguanine

8-Oxo-7,8-dihydroguanine (8-hydroxyguanine, G?) is a major oxidized base that is considered to play pivotal roles in the pathogenesis of various diseases, including cancer. G? induces G:C -> T:A transversions at the damage site and untargeted (action-at-a-distance) mutations of G bases at 5 '-GpA sequences. In this study, we examined the distribution of the action-at-a-distance mutations and the effects of the replication origin position relative to G? on the untargeted mutagenesis. The G? base was introduced into two shuttle plasmids, each with the SV40 replication origin at a different position with respect to the supF gene. The oxidized base was located at an upstream or downstream site (outside of the gene), or the center of the region encoding the pre-tRNA sequence of the gene, in the sense strand. These shuttle plasmids were introduced into human U2OS cells. The action-at-a-distance mutations were more frequently induced when the G? base was located downstream of the supF gene than upstream of the gene. In addition, more action-at-a-distance mutations were observed when the SV40 origin was present on the 5 '-side of the G? base. These results indicated that the action-at-a-distance mutations are predominantly induced on the 5 '-side of the lesion and occurred more frequently when the damaged base was located on the lagging strand template.

Automated summary

8-Oxo-7,8-dihydroguanine (8-hydroxyguanine, G?) is a major oxidized base that plays pivotal roles in various diseases. The study found that oxidized bases located downstream of genes and on the lagging strand template are more likely to induce action-at-a-distance mutations.