Sobkowiak Katarzyna, Kohzaki Masaoki, Böhm Raphael, Mailler Jonathan, Huber Florian, Emamzadah Soheila, Tropia Laurence, Hiller Sebastian, Halazonetis Thanos D
Department of Molecular and Cellular Biology, University of Geneva, 1205 Geneva, Switzerland.
Department of Molecular and Cellular Biology, University of Geneva, 1205 Geneva, Switzerland.
Cell Rep. 2025 Apr 22;44(4):115431. doi: 10.1016/j.celrep.2025.115431. Epub 2025 Mar 18.
REV7, also named MAD2B or MAD2L2, is a subunit of the DNA translesion polymerase zeta and also part of the 53BP1-shieldin complex, which is present at sites of DNA double-strand breaks. REV7 has high sequence similarity to the MAD2 spindle assembly checkpoint protein, prompting us to examine whether REV7 has a checkpoint function. We observed that, in chicken and human cells exposed to agents that induce DNA replication stress, REV7 inhibits mitotic entry; this effect is most evident when the canonical DNA replication stress checkpoint, mediated by ATR, is inhibited. Similar to MAD2, REV7 undergoes conformational changes upon ligand binding, and its checkpoint function depends on its ability to homodimerize and bind its ligands. Notably, even in unchallenged cells, deletion of the REV7 gene leads to premature mitotic entry, raising the possibility that the REV7 checkpoint monitors ongoing DNA replication.
REV7,也被称为MAD2B或MAD2L2,是DNA跨损伤聚合酶zeta的一个亚基,也是53BP1-保护蛋白复合物的一部分,该复合物存在于DNA双链断裂位点。REV7与MAD2纺锤体组装检查点蛋白具有高度的序列相似性,这促使我们研究REV7是否具有检查点功能。我们观察到,在暴露于诱导DNA复制应激的试剂的鸡和人类细胞中,REV7抑制有丝分裂进入;当由ATR介导的经典DNA复制应激检查点被抑制时,这种效应最为明显。与MAD2类似,REV7在配体结合后会发生构象变化,其检查点功能取决于其同二聚化和结合配体的能力。值得注意的是,即使在未受挑战的细胞中,REV7基因的缺失也会导致有丝分裂过早进入,这增加了REV7检查点监测正在进行的DNA复制的可能性。