首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Proliferating cell nuclear antigen (PCNA)-associated KIAA0101/PAF15 protein is a cell cycle-regulated anaphase-promoting complex/cyclosome substrate
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Proliferating cell nuclear antigen (PCNA)-associated KIAA0101/PAF15 protein is a cell cycle-regulated anaphase-promoting complex/cyclosome substrate

机译:增殖细胞核抗原(PCNA)相关的KIAA0101 / PAF15蛋白是细胞周期调控的后期促进复合物/环体底物

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摘要

The anaphase-promoting complex/cyclosome (APC/C) is a cell cycle-regulated E3 ubiquitin ligase that controls the degradation of substrate proteins at mitotic exit and throughout the G1 phase. We have identified an APC/C substrate and cell cycle-regulated protein, KIAA0101/PAF15. PAF15 protein levels peak in the G2/M phase of the cell cycle and drop rapidly at mitotic exit in an APC/C- and KEN-box–dependent fashion. PAF15 associates with proliferating cell nuclear antigen (PCNA), and depletion of PAF15 decreases the number of cells in S phase, suggesting a role for it in cell cycle regulation. Following irradiation, PAF15 colocalized with γH2AX foci at sites of DNA damage through its interaction with PCNA. Finally, PAF15 depletion led to an increase in homologous recombination-mediated DNA repair, and overexpression caused sensitivity to UV-induced DNA damage. We conclude that PAF15 is an APC/C-regulated protein involved in both cell cycle progression and the DNA damage response.
机译:后期促进复合物/环体(APC / C)是细胞周期调节的E3泛素连接酶,可控制有丝分裂出口处和整个G1期的底物蛋白降解。我们已经鉴定出APC / C底物和细胞周期调节蛋白KIAA0101 / PAF15。 PAF15蛋白水平在细胞周期的G2 / M期达到峰值,并在有丝分裂出口以APC / C和KEN-box依赖性的方式迅速下降。 PAF15与增殖细胞核抗原(PCNA)缔合,并且耗尽PAF15会减少S期细胞的数量,提示其在细胞周期调控中的作用。辐照后,PAF15通过与PCNA的相互作用与γH2AX焦点共定位在DNA损伤部位。最后,PAF15耗竭导致同源重组介导的DNA修复增加,而过表达导致对UV诱导的DNA损伤的敏感性。我们得出的结论是,PAF15是一种APC / C调控蛋白,参与细胞周期进程和DNA损伤反应。

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