Laboratory of Biochemistry, Department of Medicine, P.le Kolbe 4, 33100 Udine, Italy.
Int J Mol Sci. 2021 Jan 24;22(3):1137. doi: 10.3390/ijms22031137.
The promoter of the () proto-oncogene contains, upstream of the transcription start site, a quadruplex-forming motif called 32R with regulatory functions. As guanine under oxidative stress can be oxidized to 8-oxoguanine (8OG), we investigated the capacity of glycosylases 8-oxoguanine glycosylase (OGG1) and endonuclease VIII-like 1 (Neil1) to excise 8OG from 32R, either in duplex or G-quadruplex (G4) conformation. We found that OGG1 efficiently excised 8OG from oxidized 32R in duplex but not in G4 conformation. By contrast, glycosylase Neil1 showed more activity on the G4 than the duplex conformation. We also found that the excising activity of Neil1 on folded 32R depended on G4 topology. Our data suggest that Neil1, besides being involved in base excision repair pathway (BER), could play a role on transcription.
()原癌基因的启动子在转录起始位点的上游含有一个称为 32R 的四联体形成基序,具有调节功能。由于氧化应激下的鸟嘌呤可以被氧化为 8-氧鸟嘌呤(8OG),我们研究了糖苷酶 8-氧鸟嘌呤糖苷酶(OGG1)和内切核酸酶 VIII 样 1(Neil1)从双链或 G-四联体(G4)构象中切除 32R 中 8OG 的能力。我们发现,OGG1 可以有效地从双链构象中的氧化 32R 中切除 8OG,但不能从 G4 构象中切除。相比之下,糖苷酶 Neil1 在 G4 构象上比双链构象上具有更高的活性。我们还发现,Neil1 在折叠的 32R 上的切除活性取决于 G4 的拓扑结构。我们的数据表明,Neil1 除了参与碱基切除修复途径(BER)外,还可能在转录中发挥作用。