PLK1是DNA内切酶CtIP的新相互作用蛋白
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南华大学公共卫生学院,军事医学科学院放射与辐射医学研究所

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PLK1 is a Novel Partner for DNA Endonuclease CtIP
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School of Public Health, University of South China,Beijing Institute of Radiation Medicine

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    摘要:

    CtIP是DNA双链断裂修复中的关键蛋白之一,它能够促进断裂DNA末端切割,并且是一种已知的抑癌基因,与许多参与癌变过程的蛋白质如BRCA1,Rb等相互作用。为了更好地理解CtIP的分子网络,我们用在线工具PrePPI预测CtIP相互作用蛋白,发现PLK1是新的CtIP相互作用蛋白。PLK1在有丝分裂和癌症进展中发挥重要作用。我们进一步通过免疫沉淀法验证了它们的相互作用。 结果显示PLK1与CtIP有较强相互作用。此外,还采用Frodock 2.0工具对接CtIP和PLK1之间的蛋白质相互作用。最后,免疫沉淀测定和免疫荧光染色结果显示这两种蛋白质之间的相互作用与DNA损伤相关。基于这些结果,我们提出CtIP-PLK1相互作用可能在DNA损伤反应以及其他生物过程中发挥重要作用。

    Abstract:

    CtIP is one of the key proteins in DNA double strand breaks repair whereby promoting the end resection. It is a known tumor suppressor and interacts with a number of proteins involved in carcinogenesis such as BRCA1, Rb, etc. To better understand the molecular networks of CtIP, CtIP interaction proteins were predicted with online tool PrePPI and PLK1 was found as the novel CtIP interaction protein which plays an essential role in mitosis and also cancer progression. We further validated the novel interaction by immunoprecipitation method. PLK1 showed strong interaction with CtIP. Moreover, Frodock 2.0 tools for docking protein interactions between CtIP and PLK1 was employed. Finally, the immuoprecipitation assay and immunofluorescence staining results showed the interaction between these two proteins are related to DNA damage. Based on these results, we proposed that the CtIP-PLK1 interaction may play important roles in DNA damage response as well as other biological processes.

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谢煜,金丰,郭宗培,宋志全,高山山,刘晓丹,马腾,周平坤. PLK1是DNA内切酶CtIP的新相互作用蛋白[J].生物化学与生物物理进展,2017,44(4):357-360

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  • 收稿日期:2017-02-16
  • 最后修改日期:2017-03-20
  • 接受日期:2017-04-11
  • 在线发布日期: 2017-04-24
  • 出版日期: 2017-04-20