首页> 外文期刊>Nucleic Acids Research >The Saccharomyces cerevisiae Dna2 can function as a sole nuclease in the processing of Okazaki fragments in DNA replication
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The Saccharomyces cerevisiae Dna2 can function as a sole nuclease in the processing of Okazaki fragments in DNA replication

机译:酿酒酵母Dna2在DNA复制的冈崎片段加工中可以作为唯一的核酸酶

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摘要

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 fragmentmaturation at subnanomolar 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.
机译:在DNA复制过程中,落后链的合成发生在称为Okazaki片段的片段中。连接相邻片段之前,必须先切割冈崎片段5'DNA末端位移产生的任何襟翼。以前,Dna2参与了由复制蛋白A(RPA)结合的长皮瓣加工中皮瓣内切核酸酶1(Fen1或Rad27)的上游功能。在这里,我们显示Dna2有效地在碱基正好或紧邻碱基的地方有效地切割了长条DNA瓣。 Dna2裂解的一部分皮瓣可以立即结扎。当与DNA复制结合时,Dna2的皮瓣加工活性导致亚纳摩尔Dna2浓度下几乎完全的Okazaki片段成熟。我们的结果表明,在大多数情况下,不需要Fen1的后续溶核活性。相反,Dna2完全不能裂解短的皮瓣。我们显示,Dna2,像Fen1,与增殖细胞核抗原(PCNA)相互作用。我们提出了一个模型,其中仅Dna2负责RPA结合的长皮瓣的切割,而Fen1或核酸外切酶1(Exo1)则切割短皮瓣。我们的结果认为,Dna2可以在单独的途径中发挥作用,而不是在Fen1依赖性途径中起作用。

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