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Activation of DNA-PK by hairpinned DNA ends reveals a stepwise mechanism of kinase activation

机译:发夹DNA末端的DNA-PK的激活揭示了激酶活化的逐步机制

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摘要

As its name implies, the DNA dependent protein kinase (DNA-PK) requires DNA double-stranded ends for enzymatic activation. Here, I demonstrate that hairpinned DNA ends are ineffective for activating the kinase toward many of its well-studied substrates (p53, XRCC4, XLF, HSP90). However, hairpinned DNA ends robustly stimulate certain DNA-PK autophosphorylations. Specifically, autophosphorylation sites within the ABCDE cluster are robustly phosphorylated when DNA-PK is activated by hairpinned DNA ends. Of note, phosphorylation of the ABCDE sites is requisite for activation of the Artemis nuclease that associates with DNA-PK to mediate hairpin opening. This finding suggests a multi-step mechanism of kinase activation. Finally, I find that all non-homologous end joining (NHEJ) defective cells (whether deficient in components of the DNA-PK complex or components of the ligase complex) are similarly deficient in joining DNA double-stranded breaks (DSBs) with hairpinned termini.
机译:随着其名称意味着,DNA依赖性蛋白激酶(DNA-PK)需要DNA双链末端用于酶活化。 这里,我证明发出的DNA末端对于激活激酶朝向其许多钻孔基底(P53,XRCC4,XLF,HSP90)是无效的。 然而,发型DNA结束稳健地刺激某些DNA-PK自磷酸化。 具体地,当DNA-PK通过发夹的DNA末端激活时,ABCDE簇内的自磷酸化位点鲁棒地磷酸化。 值得注意的是,ABCDE位点的磷酸化是激活与DNA-PK介导发夹开口的Artemis核酸酶的必要条件。 该发现表明激酶激活的多步机制。 最后,我发现所有非同源末端接合(NHEJ)有缺陷的细胞(无论是缺乏DNA-PK复合物的组分或连接酶复合物的组分)同样缺乏与发夹末端的DNA双链破碎(DSB)相同缺陷 。

著录项

  • 来源
    《Nucleic Acids Research》 |2020年第16期|共11页
  • 作者

    Meek Katheryn;

  • 作者单位

    Michigan State Univ Coll Vet Med Dept Microbiol &

    Mol Genet E Lansing MI 48824 USA;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物化学;
  • 关键词

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