Rudd Sean G, Bianchi Julie, Doherty Aidan J
Genome Damage and Stability Center; University of Sussex ; Brighton, UK.
Present address: Department of Oncology-Pathology; Cancer Center Karolinska; Karolinska Institutet ; Stockholm, Sweden.
Mol Cell Oncol. 2014 Oct 29;1(2):e960754. doi: 10.4161/23723548.2014.960754. eCollection 2014 Apr-Jun.
The DNA-directed primase-polymerase PrimPol of the archaeo-eukaryotic primase superfamily represents an ancient solution to the many problems faced during genome duplication. This versatile enzyme is capable of initiating de novo DNA/RNA synthesis, DNA chain elongation, and has the capacity to bypass modifications that stall the replisome by trans-lesion synthesis or origin-independent re-priming, thus allowing discontinuous synthesis of the leading strand. Recent studies have shown that PrimPol is an important new player in replication fork progression in eukaryotic cells; this review summarizes our current understanding of PrimPol and highlights important questions that remain to be addressed.
古真核生物引发酶超家族的DNA定向引发酶-聚合酶PrimPol是应对基因组复制过程中诸多问题的古老解决方案。这种多功能酶能够从头起始DNA/RNA合成、进行DNA链延伸,并且有能力通过跨损伤合成或不依赖于起始点的重新引发来绕过使复制体停滞的修饰,从而允许前导链的不连续合成。最近的研究表明,PrimPol是真核细胞复制叉进展中的一个重要新角色;本综述总结了我们目前对PrimPol的理解,并突出了有待解决的重要问题。