National Research Center "Kurchatov Institute", Kurchatov sq. 2, 123182 Moscow, Russia; Institute of Gene Biology, Russian Academy of Sciences, Vavilova 34 / 5, 119334 Moscow, Russia.
Eppley Institute for Research in Cancer and Allied Diseases, Fred & Pamela Buffett Cancer Center, University of Nebraska Medical Center, Omaha, NE 68198, USA.
J Mol Biol. 2024 May 1;436(9):168542. doi: 10.1016/j.jmb.2024.168542. Epub 2024 Mar 15.
PrimPol is a human DNA primase-polymerase which restarts DNA synthesis beyond DNA lesions and non-B DNA structures blocking replication. Disfunction of PrimPol in cells leads to slowing of DNA replication rates in mitochondria and nucleus, accumulation of chromosome aberrations, cell cycle delay, and elevated sensitivity to DNA-damaging agents. A defective PrimPol has been suggested to be associated with the development of ophthalmic diseases, elevated mitochondrial toxicity of antiviral drugs and increased cell resistance to chemotherapy. Here, we describe a rare missense PrimPol variant V102A with altered biochemical properties identified in patients suffering from ovarian and cervical cancer. The Val102 to Ala substitution dramatically reduced both the primase and DNA polymerase activities of PrimPol as well as specifically decreased its ability to incorporate ribonucleotides. Structural analysis indicates that the V102A substitution can destabilize the hydrophobic pocket adjacent to the active site, affecting dNTP binding and catalysis.
PrimPol 是一种人类 DNA 引发酶-聚合酶,可在 DNA 损伤和阻止复制的非 B 型 DNA 结构之外重新启动 DNA 合成。细胞中 PrimPol 的功能障碍导致线粒体和细胞核中 DNA 复制速度减慢、染色体畸变积累、细胞周期延迟以及对 DNA 损伤剂的敏感性增加。有研究表明,功能缺陷的 PrimPol 与眼科疾病的发展、抗病毒药物的线粒体毒性升高以及细胞对化疗的耐药性增加有关。在这里,我们描述了一种罕见的错义 PrimPol 变体 V102A,该变体在患有卵巢癌和宫颈癌的患者中被发现,具有改变的生化特性。缬氨酸 102 到丙氨酸的取代极大地降低了 PrimPol 的引发酶和 DNA 聚合酶活性,并且特异性地降低了其掺入核糖核苷酸的能力。结构分析表明,V102A 取代可以使邻近活性位点的疏水性口袋失稳,从而影响 dNTP 的结合和催化。