Rebok Abbey, Torres Mariela C, Ambrose Julia R, Spratt Thomas E
Department of Molecular and Precision Medicine, Penn State College of Medicine, Pennsylvania State University, Hershey 17033, Pennsylvania, United States.
Chem Res Toxicol. 2025 Jun 16;38(6):1103-1112. doi: 10.1021/acs.chemrestox.5c00085. Epub 2025 May 25.
DNA polymerase kappa (pol κ) is an error-prone Y-family polymerase primarily associated with translesion DNA synthesis (TLS), a DNA damage tolerance mechanism that prevents replication fork stalling. Pol κ has been implicated in other DNA repair and tolerance pathways such as nucleotide excision repair (NER). However, the role of error-prone pol κ in the NER pathway remains unclear. We sought to investigate if pol κ had a catalytic role in NER by using the pol κ selective nucleoside analogue, -(4-ethynylbenzyl)-2'-deoxyguanosine (EBndG). Here, we identified robust, cell cycle-independent catalytic activity of pol κ in cells not treated with DNA-damaging agents. We identified approximately 40% of pol κ catalytic activity was reduced with loss of either XPC or XPA, but not CSB, indicating pol κ has a role in global genome-NER. We monitored pol κ catalytic activity after treatment with benzo()pyrene diol epoxide and UVB radiation, and we observed that pol κ catalytic activity increased in an NER-dependent manner. Our study highlights that pol κ is consistently active in cells and possesses a key catalytic role in NER.
DNA聚合酶κ(pol κ)是一种易出错的Y家族聚合酶,主要与跨损伤DNA合成(TLS)相关,TLS是一种防止复制叉停滞的DNA损伤耐受机制。Pol κ还参与了其他DNA修复和耐受途径,如核苷酸切除修复(NER)。然而,易出错的pol κ在NER途径中的作用仍不清楚。我们试图通过使用pol κ选择性核苷类似物-(4-乙炔基苄基)-2'-脱氧鸟苷(EBndG)来研究pol κ在NER中是否具有催化作用。在此,我们在未用DNA损伤剂处理的细胞中鉴定出pol κ具有强大的、不依赖细胞周期的催化活性。我们发现,XPC或XPA缺失会使约40%的pol κ催化活性降低,但CSB缺失则不会,这表明pol κ在全基因组NER中发挥作用。在用苯并[a]芘二醇环氧化物和UVB辐射处理后,我们监测了pol κ的催化活性,发现pol κ催化活性以NER依赖的方式增加。我们的研究强调,pol κ在细胞中持续活跃,并且在NER中具有关键的催化作用。