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首页> 外文期刊>Nucleic acids research >Genetics of lagging strand DNA synthesis and maturation in fission yeast: suppression analysis links the Dna2–Cdc24 complex to DNA polymerase δ
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Genetics of lagging strand DNA synthesis and maturation in fission yeast: suppression analysis links the Dna2–Cdc24 complex to DNA polymerase δ

机译:裂变酵母中滞后链DNA合成和成熟的遗传学:抑制分析将Dna2-Cdc24复合物与DNA聚合酶δ联系起来

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The Cdc24 protein is essential for the completion of chromosomal DNA replication in fission yeast. Although its precise role in this process is unclear, Cdc24 forms a complex with Dna2, a conserved endonuclease–helicase implicated in the removal of the RNA–DNA primer during Okazaki fragment processing. To gain further insights into Cdc24–Dna2 function, we screened for chromosomal suppressors of the temperature-sensitive cdc24-M38 allele and mapped the suppressing mutations into six complementation groups. Two of these mutations defined genes encoding the Pol3 and Cdc27 subunits of DNA polymerase δ. Sequence analysis revealed that all the suppressing mutations in Cdc27 resulted in truncation of the protein and loss of sequences that included the conserved C-terminal PCNA binding motif, previously shown to play an important role in maximizing enzyme processivity in vitro. Deletion of this motif is shown to be sufficient for suppression of both cdc24-M38 and dna2-C2, a temperature-sensitive allele of dna2+, suggesting that disruption of the interaction between Cdc27 and PCNA renders the activity of the Cdc24–Dna2 complex dispensable.
机译:Cdc24蛋白对于在裂殖酵母中完成染色体DNA复制至关重要。尽管尚不清楚其在此过程中的确切作用,但Cdc24与Dna2形成复合物,Dna2是一种保守的核酸内切酶-解旋酶,与冈崎片段加工过程中RNA-DNA引物的去除有关。为了进一步了解Cdc24-Dna2功能,我们筛选了对温度敏感的cdc24-M38等位基因的染色体抑制子,并将抑制突变映射为六个互补组。这些突变中的两个定义了编码DNA聚合酶δ的Pol3和Cdc27亚基的基因。序列分析显示,Cdc27中的所有抑制性突变均导致蛋白质的截断和包括保守的C端PCNA结合基序在内的序列丢失,先前显示出在最大化酶体外合成中起重要作用。已表明删除该基序足以抑制cdc24-M38和dna2 + 的温度敏感等位基因dna2-C2,这表明Cdc27和PCNA之间相互作用的破坏使该活性增强。 Cdc24–Dna2复合物可有可无。

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