Levikova Maryna, Cejka Petr
Institute of Molecular Cancer Research, University of Zurich, Winterthurerstrasse 190, CH-8057 Zurich, Switzerland.
Institute of Molecular Cancer Research, University of Zurich, Winterthurerstrasse 190, CH-8057 Zurich, Switzerland
Nucleic Acids Res. 2015 Sep 18;43(16):7888-97. doi: 10.1093/nar/gkv710. Epub 2015 Jul 14.
During DNA replication, synthesis of the lagging strand occurs in stretches termed Okazaki fragments. Before adjacent fragments are ligated, any flaps resulting from the displacement of the 5' DNA end of the Okazaki fragment must be cleaved. Previously, Dna2 was implicated to function upstream of flap endonuclease 1 (Fen1 or Rad27) in the processing of long flaps bound by the replication protein A (RPA). Here we show that Dna2 efficiently cleaves long DNA flaps exactly at or directly adjacent to the base. A fraction of the flaps cleaved by Dna2 can be immediately ligated. When coupled with DNA replication, the flap processing activity of Dna2 leads to a nearly complete Okazaki fragment maturation at sub-nanomolar Dna2 concentrations. Our results indicate that a subsequent nucleolytic activity of Fen1 is not required in most cases. In contrast Dna2 is completely incapable to cleave short flaps. We show that also Dna2, like Fen1, interacts with proliferating cell nuclear antigen (PCNA). We propose a model where Dna2 alone is responsible for cleaving of RPA-bound long flaps, while Fen1 or exonuclease 1 (Exo1) cleave short flaps. Our results argue that Dna2 can function in a separate, rather than in a Fen1-dependent pathway.
在DNA复制过程中,后随链的合成是以被称为冈崎片段的片段形式进行的。在相邻片段连接之前,冈崎片段5'端DNA位移产生的任何翼片都必须被切割。此前研究表明,在由复制蛋白A(RPA)结合的长翼片加工过程中,Dna2在翼片内切核酸酶1(Fen1或Rad27)的上游发挥作用。在此我们表明,Dna2能精确地在碱基处或紧邻碱基处有效切割长DNA翼片。被Dna2切割的一部分翼片可立即连接。当与DNA复制相结合时,在亚纳摩尔浓度的Dna2下,Dna2的翼片加工活性可使冈崎片段几乎完全成熟。我们的结果表明,在大多数情况下不需要Fen1随后的核酸酶活性。相反,Dna2完全无法切割短翼片。我们还表明,与Fen1一样,Dna2也与增殖细胞核抗原(PCNA)相互作用。我们提出了一个模型,即单独由Dna2负责切割RPA结合的长翼片,而Fen1或核酸外切酶1(Exo1)切割短翼片。我们的结果表明,Dna2可以在一个独立的途径中发挥作用,而不是依赖Fen1的途径。