Department of Biochemistry and Molecular Biophysics, Washington University School of Medicine, Saint Louis, MO, USA.
Center for Genomic Integrity, Institute for Basic Science, Ulsan 44919, Republic of Korea.
Nucleic Acids Res. 2020 Sep 4;48(15):8461-8473. doi: 10.1093/nar/gkaa580.
DNA polymerase ζ (Pol ζ) and Rev1 are essential for the repair of DNA interstrand crosslink (ICL) damage. We have used yeast DNA polymerases η, ζ and Rev1 to study translesion synthesis (TLS) past a nitrogen mustard-based interstrand crosslink (ICL) with an 8-atom linker between the crosslinked bases. The Rev1-Pol ζ complex was most efficient in complete bypass synthesis, by 2-3 fold, compared to Pol ζ alone or Pol η. Rev1 protein, but not its catalytic activity, was required for efficient TLS. A dCMP residue was faithfully inserted across the ICL-G by Pol η, Pol ζ, and Rev1-Pol ζ. Rev1-Pol ζ, and particularly Pol ζ alone showed a tendency to stall before the ICL, whereas Pol η stalled just after insertion across the ICL. The stalling of Pol η directly past the ICL is attributed to its autoinhibitory activity, caused by elongation of the short ICL-unhooked oligonucleotide (a six-mer in our study) by Pol η providing a barrier to further elongation of the correct primer. No stalling by Rev1-Pol ζ directly past the ICL was observed, suggesting that the proposed function of Pol ζ as an extender DNA polymerase is also required for ICL repair.
DNA 聚合酶 ζ(Pol ζ)和 Rev1 是修复 DNA 链间交联(ICL)损伤所必需的。我们使用酵母 DNA 聚合酶 η、ζ 和 Rev1 来研究通过氮芥类链间交联(ICL)进行的跨损伤合成(TLS),交联碱基之间有一个 8 个原子的连接链。与单独的 Pol ζ 或 Pol η 相比,Rev1-Pol ζ 复合物在完整的旁路合成中效率最高,增加了 2-3 倍。Rev1 蛋白,而不是其催化活性,是有效进行 TLS 所必需的。在 Rev1-Pol ζ 、Pol ζ 和 Pol η 的作用下,dCMP 残基被忠实插入到 ICL-G 中。Rev1-Pol ζ,特别是单独的 Pol ζ,在 ICL 之前有停顿的趋势,而 Pol η 在插入 ICL 后立即停顿。Pol η 直接通过 ICL 停顿归因于其自动抑制活性,这是由 Pol η 延伸 ICL 未连接的短寡核苷酸(在我们的研究中为六聚体)引起的,为正确引物的进一步延伸提供了障碍。没有观察到 Rev1-Pol ζ 直接通过 ICL 的停顿,这表明 Pol ζ 作为延伸 DNA 聚合酶的提议功能也需要用于 ICL 修复。