Schiavone Davide, Jozwiakowski Stanislaw K, Romanello Marina, Guilbaud Guillaume, Guilliam Thomas A, Bailey Laura J, Sale Julian E, Doherty Aidan J
MRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge, CB2 0QH, UK.
Genome Damage and Stability Centre, School of Life Sciences, University of Sussex, Brighton, BN1 9RQ, UK.
Mol Cell. 2016 Jan 7;61(1):161-9. doi: 10.1016/j.molcel.2015.10.038. Epub 2015 Nov 25.
G quadruplexes (G4s) can present potent blocks to DNA replication. Accurate and timely replication of G4s in vertebrates requires multiple specialized DNA helicases and polymerases to prevent genetic and epigenetic instability. Here we report that PrimPol, a recently described primase-polymerase (PrimPol), plays a crucial role in the bypass of leading strand G4 structures. While PrimPol is unable to directly replicate G4s, it can bind and reprime downstream of these structures. Disruption of either the catalytic activity or zinc-finger of PrimPol results in extreme G4-dependent epigenetic instability at the BU-1 locus in avian DT40 cells, indicative of extensive uncoupling of the replicative helicase and polymerase. Together, these observations implicate PrimPol in promoting restart of DNA synthesis downstream of, but closely coupled to, G4 replication impediments.
G-四链体(G4s)会对DNA复制造成强大阻碍。脊椎动物中G4s的准确及时复制需要多种特殊的DNA解旋酶和聚合酶来防止遗传和表观遗传不稳定。在此我们报告,PrimPol,一种最近被描述的引发酶-聚合酶,在前导链G4结构的跨越中起关键作用。虽然PrimPol无法直接复制G4s,但它可以在这些结构的下游结合并重新引发。PrimPol的催化活性或锌指结构的破坏会导致禽DT40细胞中BU-1位点出现极端的G4依赖性表观遗传不稳定,这表明复制解旋酶和聚合酶发生了广泛的解偶联。这些观察结果共同表明,PrimPol在促进G4复制障碍下游但与之紧密偶联的DNA合成重新启动中发挥作用。