首页> 美国卫生研究院文献>Nucleic Acids Research >Identification of a novel structure-specific endonuclease AziN that contributes to the repair of azinomycin B-mediated DNA interstrand crosslinks
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Identification of a novel structure-specific endonuclease AziN that contributes to the repair of azinomycin B-mediated DNA interstrand crosslinks

机译:新型结构特异性核酸内切酶AziN的鉴定其有助于修复阿奇霉素B介导的DNA链间交联

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摘要

DNA interstrand crosslinks (ICLs) induced by the highly genotoxic agent azinomycin B (AZB) can cause severe perturbation of DNA structure and even cell death. However, , the strain that produces AZB, seems almost impervious to this danger because of its diverse and distinctive self-protection machineries. Here, we report the identification of a novel endonuclease-like gene that contributes to drug self-protection in . AziN expression conferred AZB resistance on native and heterologous host strains. The specific binding reaction between AziN and AZB was also verified in accordance with its homology to drug binding proteins, but no drug sequestering and deactivating effects could be detected. Intriguingly, due to the high affinity with the drug, AziN was discovered to exhibit specific recognition and binding capacity with AZB-mediated ICL structures, further inducing DNA strand breakage. Subsequent assays demonstrated the structure-specific endonuclease activity of AziN, which cuts both damaged strands at specific sites around AZB-ICLs. Unravelling the nuclease activity of AziN provides a good entrance point to illuminate the complex mechanisms of AZB-ICL repair.
机译:高度遗传毒性剂阿奇霉素B(AZB)诱导的DNA链间交联(ICL)可能导致DNA结构的严重扰动,甚至导致细胞死亡。然而,由于其多样化和独特的自我保护机制,产生AZB的菌株似乎几乎无法抵抗这种危险。在这里,我们报告了一种新型的内切核酸酶样基因的鉴定,该基因有助于药物中的自我保护。 AziN表达赋予天然和异源宿主菌株AZB抗性。还根据其与药物结合蛋白的同源性验证了AziN和AZB之间的特异性结合反应,但未检测到药物螯合和失活作用。有趣的是,由于与药物的高度亲和力,AziN被发现对AZB介导的ICL结构具有特异性识别和结合能力,从而进一步诱导DNA链断裂。随后的测定证明了AziN的结构特异性核酸内切酶活性,该活性在AZB-ICL周围的特定位点切割了两条受损链。揭示AziN的核酸酶活性提供了一个很好的切入点,阐明了AZB-ICL修复的复杂机制。

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