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鉴定一种新型结构特异性内切酶 AziN,该酶有助于修复阿霉素 B 介导的 DNA 链间交联。

Identification of a novel structure-specific endonuclease AziN that contributes to the repair of azinomycin B-mediated DNA interstrand crosslinks.

机构信息

State Key Laboratory of Agricultural Microbiology, College of Life Science and Technology, Huazhong Agricultural University, Wuhan 430070, China.

出版信息

Nucleic Acids Res. 2020 Jan 24;48(2):709-718. doi: 10.1093/nar/gkz1067.

Abstract

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, Streptomyces sahachiroi, 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 aziN that contributes to drug self-protection in S. sahachiroi. 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 in vitro 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.

摘要

DNA 链间交联(ICLs)由高度遗传毒性的氮霉素 B(AZB)诱导,可导致 DNA 结构严重紊乱,甚至细胞死亡。然而,产生 AZB 的链霉菌似乎对这种危险几乎免疫,因为它具有多样化和独特的自我保护机制。在这里,我们报道了一种新型核酸内切酶样基因 aziN 的鉴定,该基因有助于链霉菌的药物自我保护。aziN 的表达赋予了原生和异源宿主菌株对 AZB 的抗性。根据其与药物结合蛋白的同源性,还验证了 AziN 与 AZB 之间的特异性结合反应,但未检测到药物隔离和失活作用。有趣的是,由于与药物的高亲和力,发现 AziN 对 AZB 介导的 ICL 结构具有特异性识别和结合能力,进一步诱导 DNA 链断裂。随后的体外实验证明了 AziN 的结构特异性内切酶活性,它可在 AZB-ICLs 周围的特定位点切割受损的两条链。揭示 AziN 的核酸酶活性为阐明 AZB-ICL 修复的复杂机制提供了一个很好的切入点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2440/7145581/c6f9da1b4768/gkz1067fig1.jpg

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