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首页> 外文期刊>BMC Molecular Biology >An in vivo analysis of the localisation and interactions of human p66 DNA polymerase δ subunit
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An in vivo analysis of the localisation and interactions of human p66 DNA polymerase δ subunit

机译:人p66 DNA聚合酶δ亚基的定位和相互作用的体内分析

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Background DNA polymerase δ is essential for eukaryotic DNA replication and also plays a role in DNA repair. The processivity of this polymerase complex is dependent upon its interaction with the sliding clamp PCNA and the polymerase-PCNA interaction is largely mediated through the p66 polymerase subunit. We have analysed the interactions of the human p66 DNA polymerase δ subunit with PCNA and with components of the DNA polymerase δ complex in vivo. Results Using the two-hybrid system, we have mapped the interaction domains for binding to the p50 polymerase δ subunit and with PCNA to the N-terminus and the C-terminus of p66, respectively. Co-immunoprecipitation experiments confirm that these interaction domains are functional in vivo. Expression of EGFP-p66 shows that it is a nuclear protein which co-localises with PCNA throughout the cell cycle. p66 is localised to sites of DNA replication during S phase and to repair foci following DNA damage. We have identified a functional nuclear localisation sequence and shown that localisation to replication foci is not dependent upon active nuclear import. Sub-domains of p66 act as dominant negative suppressors of colony formation, suggesting that p66 forms an essential structural link between the p50 subunit and PCNA. Analysis of the C-terminal PCNA binding motif shows that deletion of the QVSITGFF core motif results in a reduced affinity for PCNA, while deletion of a further 20 amino acids completely abolishes the interaction. A reduced affinity for PCNA correlates with reduced targeting to replication foci. We have confirmed the p66-PCNA interaction in vivo using fluorescence resonance energy transfer (FRET) techniques. Conclusion We have defined the regions of p66 required for its interaction with PCNA and the p50 polymerase subunit. We demonstrate a functional link between PCNA interaction and localisation to replication foci and show that there is a direct interaction between p66 and PCNA in living cells during DNA replication. The dominant negative effect upon growth resulting from expression of p66 sub-domains confirms that the p66-PCNA interaction is essential in vivo.
机译:背景DNA聚合酶δ对于真核DNA复制至关重要,并且在DNA修复中也起作用。该聚合酶复合物的持续合成能力取决于其与滑动钳PCNA的相互作用,而聚合酶-PCNA的相互作用主要通过p66聚合酶亚基介导。我们已经分析了人p66 DNA聚合酶δ亚基与PCNA以及DNA聚合酶δ复合物在体内的相互作用。结果使用双杂交系统,我们将相互作用域与p50聚合酶δ亚基结合,并将PCNA与PCNA分别映射到p66的N端和C端。免疫共沉淀实验证实,这些相互作用域在体内具有功能。 EGFP-p66的表达表明它是一种核蛋白,在整个细胞周期中都与PCNA共定位。 p66在S期定位于DNA复制位点,并在DNA损伤后修复病灶。我们已经确定了功能性核定位序列,并表明复制复制灶的定位不依赖于主动核导入。 p66的亚结构域充当集落形成的主要负抑制因子,表明p66在p50亚基和PCNA之间形成必不可少的结构联系。 C末端PCNA结合基序的分析表明,QVSITGFF核心基序的缺失导致对PCNA的亲和力降低,而另外20个氨基酸的缺失则完全消除了相互作用。对PCNA的亲和力降低与针对复制灶的靶向降低有关。我们已经使用荧光共振能量转移(FRET)技术在体内证实了p66-PCNA的相互作用。结论我们已经定义了其与PCNA和p50聚合酶亚基相互作用所需的p66区域。我们展示了PCNA相互作用与复制灶定位之间的功能联系,并表明在DNA复制过程中,活细胞中的p66和PCNA之间存在直接相互作用。由p66亚结构域表达引起的对生长的显性负作用证实了p66-PCNA相互作用在体内是必不可少的。

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